Ano Brasil. Brasil ?

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Sandra Jatahy Pesavento

2005-06-01

Full Text Available 2005, Ano Brasil na França. E, para assinalar a data, o prestigioso Grand Palais de Paris abriga Brésil indien, uma exposição que se propõe a combater os clichês. Perguntaria o visitante, curioso: clichês sobre o Brasil?  Não, sobre os povos indígenas, que hoje correspondem a 0,3% da população brasileira, informa o primeiro cartaz explicativo já desde o início do percurso. Uma exposição que se anuncia para dar a ver e sentir uma experiência estética construída como visão de mundo, complement...

Identificação de roedores silvestres como hospedeiros do Angiostrongylus costaricensis no sul do Brasil Identification of wild rodents as hosts of Angiostrongylus costaricensis in the South of Brazil

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Carlos Graeff-Teixeira

1990-06-01

Full Text Available Um número crescente de casos de angiostrongilíase abdominal tem sido detectado no sul do Brasil. O principal hospedeiro do Angiostrongylus costaricensis na América Central, o rato do algodão (Sigmodon hispidus, não ocorre na América do Sul, exceto no norte do Peru, Colômbia e Venezuela. Foram realizadas capturas na área endêmica do Rio Grande do Sul (RS, visando identificar hospedeiros para obtenção de vermes em laboratório e produção de antígeno. Pela primeira vez no Brasil foi constatada a infecção em roedores: Oryzomys nigripes e Oryzomys ratticeps. O. nigripes é um roedor silvestre de pequeno porte e parece ser o principal hospedeiro definitivo do A. costaricensis na região serrana do RS.Increasing number of human cases of abdominal angiostrongyliasis has been diagnosed in the south of Brazil. The main definitive host of Angiostrongylus costaricensis in Central America is the cotton rat (Sigmodon hispidus that does not occur in South America, except in the north of Colombia, Peru and Venezuela. Rodents were captured in the endemic area in Rio Grande do Sul (RS and definitive hosts were identified for the first time in Brazil: Oryzomys nigripes and Oryzomys ratticeps. O. nigripes is a small wild rodent and it appears to be the main definitive host of A. costaricensis in the highlands of RS, Brazil's southermost State.

RS CVn binary systems

International Nuclear Information System (INIS)

Linsky, J.L.

1984-01-01

The author attempts to place in context the vast amount of data obtained in the last few years as a result of X-ray, ultraviolet, optical, and microwave observations of RS CVn and similar spectroscopic binary systems. He concentrates on the RS CVn systems and their long-period analogs, and restricts the scope by attempting to answer on the basis of the recent data and theory following questions: (1) Are the original defining characteristics still valid and still adequate? (2) What is the evidence for discrete active regions? (3) Have we derived any meaningful physical properties for the atmospheres of RS CVn systems? (4) What are the flare observations telling us about magnetic fields in the RS CVn systems? (5) Is there evidence for systematic trends in RS CVn systems with spectral type?

RS-WebPredictor

DEFF Research Database (Denmark)

Zaretzki, J.; Bergeron, C.; Huang, T.-W.

2013-01-01

Regioselectivity-WebPredictor (RS-WebPredictor) is a server that predicts isozyme-specific cytochrome P450 (CYP)-mediated sites of metabolism (SOMs) on drug-like molecules. Predictions may be made for the promiscuous 2C9, 2D6 and 3A4 CYP isozymes, as well as CYPs 1A2, 2A6, 2B6, 2C8, 2C19 and 2E1....... RS-WebPredictor is the first freely accessible server that predicts the regioselectivity of the last six isozymes. Server execution time is fast, taking on average 2s to encode a submitted molecule and 1s to apply a given model, allowing for high-throughput use in lead optimization projects.......Availability: RS-WebPredictor is accessible for free use at http://reccr.chem.rpi.edu/ Software/RS-WebPredictor....

Association between ACE (rs4646994), FABP2 (rs1799883), MTHFR (rs1801133), FTO (rs9939609) Genes Polymorphism and Type 2 Diabetes with Dyslipidemia.

Science.gov (United States)

Raza, Syed Tasleem; Abbas, Shania; Siddiqi, Zeba; Mahdi, Farzana

2017-01-01

Diabetic dyslipidemia is one of the leading causes of coronary artery disease (CAD) death. Genetic and environmental factors play an important role in the development of type 2 diabetes mellitus (T2DM) and dyslipidemia. The present study was aimed to investigate the association of ACE (rs4646994), FABP2 (rs1799883), MTHFR (rs1801133) and FTO (rs9939609) genes polymorphism in T2DM with dyslipidemia. Totally, 559 subjects including 221 T2DM cases with dyslipidemia, 158 T2DM without dyslipidemia and 180 controls were enrolled. ACE genes polymorphism was evaluated by polymerase chain reaction (PCR), while MTHFR , FABP2 , FTO genes polymorphisms were evaluated by PCR and restriction fragment length polymorphism (RFLP). Significant association of ACE and MTHFR genes polymorphisms were found in both group of cases [T2DM with dyslipidemia (Pgenes polymorphisms were significantly associated with T2DM without dyslipidemia (P=0.038, and P= 0.019, respectively). This study concludes that ACE , FABP2 , FTO and MTHFR genes are associated with T2DM. Additionally, it also seems that ACE and MTHFR genes might be further associated with the development of dyslipidemia in T2DM cases.

Turismo de Eventos na Serra Gaúcha: O Caso da Festa Nacional da Uva de Caxias do Sul, RS / Tourism Events in Serra Gaucha: The Case of Caxias do Sul, RS, National Grape Festival

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Fabrício Silva Barbosa

2015-07-01

Full Text Available Eventos são, cada vez mais, utilizados como instrumentos de promoção de destinos e de localidades turísticas. O rápido crescimento do setor é considerado um fenômeno global, pois os eventos impulsionam a economia local, sendo uma alternativa para minimizar os efeitos da sazonalidade nos centros receptores de turismo. Este estudo teve como objetivo investigar como ocorre o planejamento da Festa da Uva de Caxias do Sul, RS, tomando como base as fases do pré-evento, trans-evento e pós- evento propostas por Allen et al (2008. Trata-se de um estudo de caso, em pesquisa de viés qualitativo e descritivo. Os resultados da pesquisa apontam para a existência de um planejamento logístico do evento estruturado e organizado com divisão de tarefas e atividades que contribuem para o sucesso da festa. Palavras-chaves: Turismo. Turismo de Eventos. Festa Nacional da Uva. Caxias do Sul, RS. Tourism Events in Serra Gaucha: The Case of Caxias do Sul, RS, National Grape Festival - Events are increasingly being used to promoting tourism destinations and localities. Events help the local economy as alternative for decreasing the effects caused by seasonality in the major host centers of tourism. This article investigates the planning of the Grape Festival of Caxias do Sul, it’s pre-event, trans-event and post-event structure as proposed by Allen et al (2008. It’s a qualitative and exploratory study. The results point the presence of a logistic plan well-organized, with the division of tasks and activities that contribute to the success of the festival. Keywords: Tourism. Events Tourism.  National Grape Festival. Caxias do Sul, RS, Brasil.

Colesterolemia, trigliceridemia e excesso de peso em escolares de Santa Maria, RS, Brasil Blood lipids abnormalities and overweight prevalence in students of Santa Maria, RS, Brazil

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Cláudia Cruz Lunardi

2010-08-01

Full Text Available INTRODUÇÃO: O nível de colesterol na infância é um preditor do nível de colesterol na vida adulta. As consequências do colesterol elevado, somadas a outros fatores de risco constituem problema mundial de saúde pública. OBJETIVO: Estimar a prevalência de hipercolesterolemia, hipertrigliceridemia e excesso de peso em estudantes do município de Santa Maria-RS. Métodos: Estudo transversal com 374 crianças de 10 a 12 anos de idade, de escolas das redes pública e privada, realizado no segundo semestre de 2005 na cidade de Santa Maria-RS. Foram determinados os níveis de colesterol total, triglicerídeos e estado nutricional. RESULTADOS: As prevalências de hipercolesterolemia, hipertrigliceridemia e excesso de peso encontradas foram de 4,7%, 8,9% e 20,7%, respectivamente. Não houve diferença significante entre sexo e rede pública e privada. As crianças com excesso de peso apresentaram maior prevalência de alterações lipídicas. CONCLUSÕES: A prevalência de alterações lipídicas pode ser considerada baixa, mas a prevalência de excesso de peso dos estudantes de Santa Maria mostrou-se relativamente alta, alertando à importância de políticas públicas e à necessidade de assistência pediátrica nessa faixa etária, visando o seu diagnóstico precoce e, principalmente, o aconselhamento nutricional e incentivo à prática esportiva, uma vez que as dislipidemias e o excesso de peso têm sido apontados como fatores de risco para as doenças cardiovasculares.INTRODUCTION: Cholesterol level in childhood is a predictor of cholesterol level in adult life. The consequences of high cholesterol levels summed to other risk factors constitute a worldwide public health problem. OBJECTIVE: To estimate the prevalence of blood lipid abnormalities and overweight among school students of the city of Santa Maria, RS, Brazil. Methods: A cross-sectional study with 374 children, aged between 10 and 12 years, from public and private schools of the

Ocorrência de ixodidae parasitos de capivara (Hydrochoerus hydrochaeris linnaeus, 1766 na estação ecológica do Taim, Rio Grande - RS, Brasil Occurence of ixodidae parasites of capybara (Hydrochoeurus hydrochaeris linnaeus, 1766 in the ecologic area of Taim, Rio Grande - RS, Brazil

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Afonso Lodovico Sinkoc

1997-03-01

Full Text Available O objetivo deste trabalho foi identificar as espécies de carrapatos observadas sobre capivaras na Estação Ecológica do Taim, Rio Grande- RS, Brasil. Foram examinadas 27 capivaras encontradas mortas por atropelamento na BR 471, em seu trecho que corta a Estação, sendo cole lados 497 carrapatos das espécies Amblyomma cooperi (=A. lutzi; = A. ypisilophorum, Amblyomma triste, Amblyomma tigrinum e ninfas do gênero Amblyomma. A. cooperi representou 68,41% dos carrapatos identificados, com uma freqüência de parasitismo de 92,60% dos hospedeiros, enquanto A. triste representou 24,75% dos carrapatos em 44,43% dos hospedeiros e A. tigrinum foi coletado em 14,81% dos hospedeiros, totalizando 1,21% dos carrapatos. As ninfas de Amblyomma sp. foram cotetadas em 18,51% dos hospedeiros apresentando um percentual de 5,63% do total de carrapatos. A relação macho : fêmea apresentou valores de 2,3 : 1 e 2 : l para o A. cooperi e A. triste, respectivamente. Todos hospedeiros apresentavam-se parasitados, com uma média de 18,4 carrapatos, variando de 1 a 64 carrapatos coletados por hospedeiro.The aim of this article was the identification ofthe tick species observed on capybara in wildlife in the Ecologic Area of Taim, Rio Grande - RS; Brazil. Twenly seven capybaras found dead by trample in the road BR 471 in the Ecologic Area, wereexamined ticks coilected of the species Amblyomma cooperi (= A. lutzi and = A. ypisilophorum, Amblyomma triste, Amblyomma tigrinum and ninphs of the Genus Amblyomma. Amblyomma cooperi represented 68.41% of the ticks with a frequency of parasitism of 92.60% of the hosts; Amblyomma triste species represented 24.75% of the collected ticks m 44.43% of the hosts; Amblyomma tigrinum species were coilected m 14.81% of the hosts from a total of 1.21% of the found ticks and, the nimphs of Amblyomma were coilected in 18.51% of the hosts per forming 5.63% of the ali ticks coilected. The relation mate .female showed values of 2.3:1 and 2

AVALIAÇAO DA QUALIDADE DAS ÁGUAS SUBTERRÂNEAS DA BACIA HIDROGRÁFICA DO RIO PARDO, SISTEMA AQUÍFERO GUARANI, RS, BRASIL

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Marluce Purper

2011-08-01

Full Text Available O objetivo desta pesquisa foi avaliar a qualidade das águas subterrâneas em áreas de preservação permanente (Sistema Aquífero Guarani – SAG da Bacia Hidrográfica do Rio Pardo, RS, Brasil, através de variáveis físicas, químicas e microbiológicas. Nove pontos de coleta foram distribuídos ao longo da bacia, nos quais as águas subterrâneas foram classificadas quanto aos íons de maior ocorrência quantitativa. Os resultados indicaram que a maioria dos poços avaliados enquadraram-se na Classe 4 de usos da água, correspondendo a águas de usos menos restritivos (como recreação de contato secundário. Entretanto, deve-se considerar que os aquíferos são caracterizados por diferentes condições geológicas, com características físicas, químicas e biológicas intrínsecas, e também variações hidrogeoquímicas, sendo necessário que as suas classes de qualidade sejam determinadas com base nessas especificidades. As amostras P1, P2, P3, P5 e P9 classificaram-se como bicarbonatadas cálcicas; as águas dos pontos P4, P6, P7 como bicarbonatadas sódicas; e P8 como sulfatada. Verificou-se que a qualidade das águas de poços com profundidade inferior a 6 m está mais vulnerável, devido a alterações antrópicas em função da concentração de nitrato, coliformes totais e termotolerantes, enquanto a qualidade das águas de poços mais profundos depende basicamente de suas características hidrogeológicas e hidrogeoquímicas naturais, em função das variáveis sulfato e sódio.

COX-2 rs689466, rs5275, and rs20417 polymorphisms and risk of head and neck squamous cell carcinoma: a meta-analysis of adjusted and unadjusted data

International Nuclear Information System (INIS)

Leng, Wei-Dong; Wen, Xiu-Jie; Kwong, Joey S. W.; Huang, Wei; Chen, Jian-Gang; Zeng, Xian-Tao

2016-01-01

Numerous case–control studies have been performed to investigate the association between three cyclooxygenase-2 (COX-2) polymorphisms (rs20417 (−765G > C), rs689466 (−1195G > A), and rs5275 (8473 T > C)) and the risk of head and neck squamous cell carcinoma (HNSCC). However, the results were inconsistent. Therefore, we conducted this meta-analysis to investigate the association. We searched in PubMed, Embase, and Web of Science up to January 20, 2015 (last updated on May 12, 2016). Two independent reviewers extracted the data. Odds ratios (ORs) with their 95 % confidence intervals (CIs) were used to assess the association. All statistical analyses were performed using the Review Manager (RevMan) 5.2 software. Finally 8 case–control studies were included in this meta-analysis. For unadjusted data, an association with increased risk was observed in three genetic models in COX-2 rs689466 polymorphism; however, COX-2 rs5275 and rs20417 polymorphisms were not related to HNSCC risk in this study. The pooled results from adjusted data all revealed non-significant association between these three polymorphisms and risk of HNSCC. We also found a similar result in the subgroup analyses, based on both unadjusted data and adjusted data. Current results suggest that COX-2 rs689466, rs5275, and rs20417 polymorphisms are not associated with HNSCC. Further large and well-designed studies are necessary to validate this association

RENEWABLE ENERGY PROJECTS UNDER THE CDM – PROFILE PROJECTS LOCATED IN RS

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Alice de Moraes Falleiro

2014-09-01

Full Text Available Há 13 anos entrava em vigor o acordo climático global denominado Protocolo de Quioto, como uma tentativa de frear as emissões de gases do efeito estufa (GEE a partir de três mecanismos de flexibilização, entre eles, o Mecanismos de Desenvolvimento Limpo (MDL, único aplicado aos países em desenvolvimento. O Brasil está entre os países com maior número de projetos de MDL registrados durante o primeiro período do acordo. O Rio Grande do Sul apresenta o maior número de projetos aptos a comercializar créditos de carbono do País. Dentro desse contexto, este artigo tem por objetivo mapear e realizar um perfil prévio dos projetos de energia renováveis, desenvolvidos conforme a ferramenta metodológica ACM 0002“Consolidated baseline methodology for grid-connected electricity generation from renewable sources”, localizados no Rio Grande do Sul comparando-os com os dados desse segmento no Brasil. Para isso, foram realizadas pesquisas em artigos, livros bibliografias e buscas nos sites da United Nations Framework Convention Climate Changes (UNFCCC e do Ministério da Ciência, Tecnologia e Inovação (MTCI, entidades responsáveis pelo registro e aprovação dos projetos, respectivamente. Os projetos localizados no RS são de larga escala e apresentam período de venda de crédito renovável seguindo o perfil desse segmento no País.

Correlation of Fetuin-A gene rs1071592 and rs2593813 single nucleotide polymorphisms with polycystic ovary syndrome

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Juan YI

2016-10-01

Full Text Available Objective 　To investigate the relations of Fetuin-A gene rs1071592 and rs2593813 single nucleotide polymorphisms (SNPs with the affect ability to polycystic ovary syndrome (PCOS and its endocrine and metabolic characteristics in Chongqing Han population. Methods 　A case-control study was performed in Chinese Han subjects. The clinical data of 156 cases of normal control and 147 cases of PCOS patients were collected, and their blood glucose, lipids, sex hormone and other biochemical indexes were determined, the SNPs of rs1071592 and rs2593813 were genotyped by TaqMan SNP Genotyping Assay. Hyperinsulinemic-euglycemic clamp was performed in 147 PCOS women and 20 controls. The relative risk of developing PCOS in women with rs1071592 genotype was assessed using a binary logistic regression analysis. Results 　The distribution frequency of Fetuin-A gene homozygous rs1071592 AA genotype and A allele was significantly increased in PCOS patients than in controls (Pc0.05. Binary logistic regression analysis showed that the risk of developing PCOS was 4.93 times high in women with AA genotype of rs1071592 (OR=4.933, 95%CI 1.593-15.278, P0.05. Conclusion 　People with SNPs variants of rs1071592 in Fetuin-A gene may have an increased genetic susceptibility to PCOS. However, there won't be significant relationship between SNP of rs2593813 at Fetuin-A gene and PCOS. DOI: 10.11855/j.issn.0577-7402.2016.09.07

Os efeitos da carga tributária indireta e das políticas públicas agrícolas sobre os preços dos alimentos em Porto Alegre (RS, Brasil

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Sibele Vasconcelos de Oliveira

2012-12-01

Full Text Available No Brasil, a vasta experiência e aptidão para os agronegócios geram reflexões sobre as implicações das políticas agrícolas e fiscais sobre a formação de preços dos alimentos e, por conseguinte, sobre a segurança alimentar. Destarte, o presente estudo visa avaliar o impacto da Política de Garantia de Preço Mínimos Agrícolas, do crédito rural e da carga tributária indireta sobre os preços dos principais alimentos da cesta básica de Porto Alegre (RS, Brasil. Para tanto, as estatísticas descritiva e inferencial foram empregadas na identificação de relações de causalidade entre as variáveis no período de janeiro/2005 a abril/2011. Observou-se que as regressões lineares múltiplas demonstraram significância estatística, com exceção das estimadas para os preços do café e farinha de trigo. Ainda, a oferta dos produtos amostrados tende a ser elástica, considerando-se o relacionamento positivo entre preços dos alimentos e as proxies dos subsídios públicos agrícolas. Percebeu-se que variações na carga tributária indireta implicam em variações no mesmo sentido no preço do arroz, feijão, leite, óleo e pão. Por fim, considerando-se o grau moderado de associação linear entre as variáveis explanatórias e os preços dos alimentos, sugere-se que variações nestes podem ser também explicadas por fatores relacionados ao processo produtivo e concorrencial.In Brazil, the vast experience and ability for agribusiness generate reflections regarding implications of fiscal and agricultural policies on the food pricing and, consequently, on food security. Thus, this study aims to evaluate the impact of the Minimum Price Policy for Agriculture, rural credit and indirect taxes on prices of some of the more important food from the Food Basket of Porto Alegre (RS, Brazil. To this end, descriptive and inferential statistics were used to identify causal relationships between variables in the period from January/2005 to April

RS CV sub n binary systems

International Nuclear Information System (INIS)

Linsky, J.L.

1984-01-01

An attempt is made to place in context the vast amount of data obtained as a result of X-ray, ultraviolet, optical, and microwave observations of RS CVn and similar spectroscopic binary systems. Emphasis is on the RS CVn systems and their long period analogs. The following questions are considered: (1) are the original defining characteristics still valid and still adequate; (2) what is the evidence for discrete active regions; (3) have any meaningful physical properties for the atmospheres of RS CVn systems been derived; (4) what do the flare observations tell about magnetic fields in RS CVn systems; (5) is there evidence for systematic trends in RS CVn systems with spectral type

MARCA BRASIL - FICÇÃO OU REALIDADE?: uma análise das iniciativas da APEX-Brasil para a construção da marca Brasil

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DANIELA MOTTA R. KHAUAJA

2007-01-01

Full Text Available Vivemos em uma economia global e é urgente que o Brasil, por meio de seus governantes e empresariado, busque a inserção nessa economia de forma mais efetiva. A marca-país pode ajudar na criação de uma forte identidade para o país, o que tende a colaborar com a venda de produtos oriundos desse país. O presente estudo se propõe a analisar como a marca Brasil foi construída e como ela tem sido explorada pelo governo brasileiro para ajudar na inserção de produtos nacionais no comércio internacional. Para tal, foi feita uma revisão da literatura, abordando conceitos relevantes e relativos ao marketing global, a produtos e marcas globais e à marca-país. Em seguida, explicitou-se o método do estudo e fez-se a análise da construção da marca Brasil e das iniciativas do governo brasileiro, mais especificamente da Agência de Promoção de Exportações do Brasil (Apex-Brasil, à construção da marca Brasil. A iniciativa da criação da marca Brasil, embora tardia, parece muito louvável, mas, por sua tímida utilização, a marca Brasil ainda parece mais ficção do que realidade.

40 CFR 180.1114 - Pseudomonas fluorescens A506, Pseudomonas fluorescens 1629RS, and Pseudomonas syringae 742RS...

Science.gov (United States)

2010-07-01

... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Pseudomonas fluorescens A506, Pseudomonas fluorescens 1629RS, and Pseudomonas syringae 742RS; exemptions from the requirement of a tolerance... Tolerances § 180.1114 Pseudomonas fluorescens A506, Pseudomonas fluorescens 1629RS, and Pseudomonas syringae...

Multiple infestation of Dioctophyme renale in dogs with leishmaniasis in Uruguaiana, RS - Report of five cases

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Maria Lígia de Arruda Mistieri

2014-06-01

Full Text Available ABSTRACT. Mistieri M.L. de A., Pascon J.P. da E. & dos Santos F.P. [Multiple infestation of Dioctophyme renale in dogs with leishmaniasis in Uruguaiana, RS - Report of five cases.] Infestação múltipla de Dioctophyme renale em cães portadores de leishmaniose em Uruguaiana, RS - Relato de cinco casos. Revista Brasileira de Medicina Veterinária, 36(2:195-198, 2014. Universidade Federal do Pampa, BR 472, Km 592, Caixa Postal 118, Uruguaiana, RS 97500-970, Brasil. Email: mariamistieri@unipampa.edu.br Dioctophyme renale is a parasite of different animal species, including human beings. The parasite life cycle can be complex, involving intermediate hosts, definitive hosts and paratenic hosts, represented by different species of frog, rat and fish, specially. The domestic dogs are considered unusual and terminal hosts because they commonly present single parasite, enabling its reproduction and the cycle maintenance. This report presents a multiple infestation of D. renale (male and female specimens in five of nine dogs that underwent to euthanasia due to leishmaniasis. It was noticed two to eight parasites in each affected dog, summing 27 specimens, 12 males measuring between 9.0 and 21.5 cm in length and 15 females with 23.5 to 42.0 cm. In all dogs, the right kidney was completely destroyed. Actual epidemiological studies are necessary to check the real prevalence of the dioctophimosis in the region of Uruguaiana and the determination of the local parasite cycle. Deficient sanitary and hygiene conditions are commonly observed in the progression of D. renale and Leishmania sp. infections. It is possible that those conditions are the link between both disorders in the studied dogs.

Comunidade de Syrphidae (Diptera: diversidade e preferências florais no Cinturão Verde (Santa Cruz do Sul, RS, Brasil Syrphidae (Diptera community: diversity and floral preferences in the Green Belt (Santa Cruz do Sul, RS, Brazil

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Mírian Nunes Morales

2008-01-01

Full Text Available Objetivou-se investigar a comunidade de Syrphidae, do Cinturão Verde de Santa Cruz do Sul, RS, Brasil, permitindo a obtenção de informações acerca da composição e estrutura desta comunidade, suas preferências florais e interações entre as espécies na utilização de recursos alimentares. Realizaram-se coletas com rede entomológica, entre setembro/2001 a janeiro/2005. Foram capturados 1.283 espécimes de Syrphidae, representados por 88 espécies, distribuídos em 21 gêneros. Eristalinae apresentou o maior número de espécies coletadas, seguida por Syrphinae e Microdontinae. O gênero Palpada Macquart e a espécie P. urotaenia (Curran foram os mais abundantes. As coletas alcançaram cerca de 80% do que se estima para a área de estudo. Coletaram-se 1.187 sirfídeos (74 espécies visitantes de 51 espécies de plantas, de 23 famílias, onde Apiaceae e Asteraceae apresentaram o maior número de visitantes. O grau de especialização alimentar variou de acordo com os tipos de flores visitadas. A facilidade do acesso aos recursos florais e a coloração clara das flores são os principais responsáveis pela atração dos sirfídeos em Apiaceae, Asteraceae, Lauraceae, Malvaceae, Meliaceae, Oleaceae, Poaceae e Solanaceae. A diversidade da comunidade de Syrphidae é regulada por interações locais entre as espécies, principalmente entre as condições ambientais e disponibilidade de recursos alimentares.The aim of this study was to investigate the Syrphidae community in the area of the Green Belt of Santa Cruz do Sul, RS, Brazil, as well as to obtain information on the structure and composition of this community, its floral preferences and the interactions between the species in the food resource utilization. The specimens were collected with entomological net, from September/2001 to January/2005. A total of 1.283 syrphid specimens were collected, totaling 88 species distributed in 21 genera. Eristalinae presented the highest number of

Association of PTPN22 (rs2476601) and STAT4 (rs7574865) polymorphisms with Rheumatoid Arthritis in the Western Algerian population.

Science.gov (United States)

Fodil, M; Benzaoui, A; Zemani-Fodil, F; Aberkane, M; Boughrara, W; Saidi-Mehtar, N; Petit-Teixeira, E; Boudjema, A

2015-01-01

The aim of the present study was to replicate the association of five risk gene polymorphisms (PTPN22-rs2476601, STAT4-rs7574865, 6q23-rs6927172, IRF5-rs2004640 and TRAF1/C5-rs10818488) with RA in a specific population of the Western Algeria. The study group comprised 110 patients with RA and 197 ethnically matched healthy control subjects. All polymorphisms were genotyped using predesigned TaqMan® assays. Allele and genotype frequencies in patients and control subjects were compared by chi-square test and odds ratios with 95% confidence intervals. Correction for multiple testing was carried out using the Bonferroni adjustment. Statistically significant associations with RA were detected. The strongest signal was obtained for PTPN22-rs2476601 with an allelic Pvalue 3.32 x 10(-11) (OR = 9.83, 95% CI [4.28 - 22.56]). A second significant association was obtained with STAT4-rs7574865 (allelic Pvalue = 4 x 10(-3); OR = 1.75, 95% CI [1.16 - 2.63]). The third SNP, 6q23-rs6927172, showed a significant result of association with RA, but missed our criteria for significance at allelic level after Bonferroni's correction (allelic Pvalue = 0.027; OR = 0.64, 95% CI [0.42 - 0.97]). Finally, IRF5-rs2004640 and TRAF1/C5-rs10818488 showed a significant association only at genotypic level (Pvalues: 3 x 10(-4) and 2.9 x 10(-3) respectively) but did not reach statistical significance when comparing allele frequencies (Pvalues: 0.96 and 0.21 respectively). From this initial study, we can conclude that PTPN22-rs2476601 and STAT4-rs7574865 polymorphisms are clearly associated with the risk of RA in the Western Algerian population.

Association of PTPN22 (rs2476601 and STAT4 (rs7574865 polymorphisms with Rheumatoid Arthritis in the Western Algerian population

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Mostefa FODIL

2015-01-01

Full Text Available Aim: The aim of the present study was to replicate the association of five risk gene polymorphisms (PTPN22-rs2476601, STAT4-rs7574865, 6q23-rs6927172, IRF5-rs2004640 and TRAF1/C5-rs10818488 with RA in a specific population of the Western Algeria. Material and methods: The study group comprised 110 patients with RA and 197 ethnically matched healthy control subjects. All polymorphisms were genotyped using predesigned TaqMan® assays. Allele and genotype frequencies in patients and control subjects were compared by chi-square test and odds ratios with 95% confidence intervals. Correction for multiple testing was carried out using the Bonferroni adjustment. Results: Statistically significant associations with RA were detected. The strongest signal was obtained for PTPN22-rs2476601 with an allelic Pvalue 3.32 x 10-11 (OR = 9.83, 95% CI [4.28 – 22.56]. A second significant association was obtained with STAT4-rs7574865 (allelic Pvalue = 4 x 10-3; OR = 1.75, 95% CI [1.16 – 2.63]. The third SNP, 6q23-rs6927172, showed a significant result of association with RA, but missed our criteria for significance at allelic level after Bonferroni’s correction (allelic Pvalue = 0.027; OR = 0.64, 95% CI [0.42 – 0.97]. Finally, IRF5-rs2004640 and TRAF1/C5-rs10818488 showed a significant association only at genotypic level (Pvalues: 3 x 10-4 and 2.9 x 10-3 respectively but did not reach statistical significance when comparing allele frequencies (Pvalues: 0.96 and 0.21 respectively. Conclusions: From this initial study, we can conclude that PTPN22-rs2476601 and STAT4-rs7574865 polymorphisms are clearly associated with the risk of RA in the Western Algerian population.

Amenazas y oportunidades del comercio brasileño con China. Lecciones para Brasil

OpenAIRE

Fernando Augusto Mansor de Mattos; Marcelo Dias Carcanholo

2012-01-01

En 2009, China se convirtió en el principal socio comercial de Brasil. La intensificación de las relaciones comerciales entre ambos países en los últimos años ha provocado rápidos cambios en los resultados agregados y en el perfil de la balanza comercial brasileña. Por un lado, ha permitido una importante expansión de las exportaciones brasileñas, pero muy concentradas en productos de bajo contenido tecnológico, como las materias primas agrícolas y minerales. Por otra parte, se ha producido u...

Matrizes progressivas coloridas de Raven - escala especial: normas para Porto Alegre, RS The Raven's coloured progressive matrices: norms for Porto Alegre, RS

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Denise Ruschel Bandeira

2004-12-01

Full Text Available O Teste das Matrizes Progressivas Coloridas de Raven destina-se à avaliação do desenvolvimento intelectual de crianças de 5 a 11 anos de idade. O presente trabalho teve como objetivo estabelecer normas para as crianças de Porto Alegre - RS. A amostra foi composta por 779 crianças matriculadas em escolas estaduais, de 4 anos e 9 meses a 11 anos e 9 meses. Foi constatado aumento progressivo nas médias de pontos com o aumento da idade e não foram encontradas diferenças entre meninos e meninas. Na comparação com as crianças de escolas públicas de São Paulo, as médias das crianças de Porto Alegre foram mais altas, mas em geral foram inferiores às das escolas particulares de São Paulo. Foram estabelecidas as normas em percentis para cada faixa etária. Os resultados reforçam a necessidade do estabelecimento de normas distintas para as diferentes regiões do Brasil, principalmente em relação aos testes de inteligência.The Raven's Coloured Progressive Matrices was proposed standards to Porto Alegre (RS children. The sample was composed by 779 children from Porto Alegre state public schools, aged from 4 years and 9 months to 11 years and 9 months. It was found a progressive increase in average scores as age increased and it was not verified differences between boys and girls. Comparing average scores between children from São Paulo and Porto Alegre public schools we found that the average scores from Porto Alegre children was higher, but they were lower than the scores from São Paulo private schools children. Percentile ranks were obtained to each age level with range of six months. Research results show the need to establish specific norms to different Brazilian regions, mainly concerning intelligence tests.

The NC3Rs gateway: Accelerating scientific discoveries with new 3Rs models and technologies.

Science.gov (United States)

Percie du Sert, Nathalie; Robinson, Vicky

2018-01-01

This editorial introduces the NC3Rs gateway, which publishes articles and reviews on new models and technologies emerging from NC3Rs-funded research. The aim is to raise awareness about these approaches, increase confidence in their capability, and provide sufficient information to facilitate their uptake by others.

HLA variants rs9271366 and rs9275328 are associated with systemic lupus erythematosus susceptibility in Malays and Chinese.

Science.gov (United States)

Chai, H C; Phipps, M E; Othman, I; Tan, L P; Chua, K H

2013-02-01

Human leukocyte antigen (HLA) antigens and genes have long been reported associated with systemic lupus erythematosus (SLE) susceptibility in many populations. With the advance in technologies such as genome-wide association studies, many newly discovered SLE-associated single-nucleotide polymorphisms (SNPs) have been reported in recent years. These include HLA-DRB1/HLA-DQA1 rs9271366 and HLA-DQB1/HLA-DQA2 rs9275328. Our aim was to investigate these SNPs in a Malaysian SLE cohort. SNPs rs9271366 and rs9275328 were screened across 790 Malaysian citizens from three ethnic groups (360 patients and 430 healthy volunteers) by Taqman SNP genotyping assays. Allele and genotyping frequencies, Hardy-Weinberg equilibrium, Fisher's exact test and odds ratio were calculated for each SNP and ethnic group. Linkage disequilibrium and interaction between the two SNPs were also evaluated. The minor allele G and its homozygous genotype GG of HLA-DRB1/HLA-DQA1 rs9271366 significantly increased the SLE susceptibility in Malaysian patients, including those of Malay and Chinese ethnicity (odds ratio (OR) > 1, p < 0.05). As for HLA-DQB1/HLA-DQA2 rs9275328, the minor allele T and the heterozygous genotype CT conferred protective effect to SLE in Malaysians, as well as in Malays and Chinese, by having OR < 1 and p value <0.05. Both SNPs did not show associations to SLE in Indians. D' and r (2) values for the two SNPs in LD analysis were 0.941 and 0.065, respectively, with haplotype GC and AT being significantly associated with SLE (p < 5.0 × 10(-4)) after 10,000 permutations were performed. The MDR test clustered the genotype combinations of GG and CC, and AG and CC of rs9271366 and rs9275328, accordingly, as high-risk group, and the two SNPs interacted redundantly by removing 1.96% of the entropy. Our findings suggest that in addition to some classical HLA variants, rs9271366 and rs9275328 are additional polymorphisms worth considering in the Malaysian and possibly in

Evaluation of transcobalamin II rs1801198 and transcobalamin II receptor rs2336573 gene polymorphisms in recurrent spontaneous abortion.

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Hashemi, Mohammad; Mokhtari, Mojgan; Yazdani-Shahrbabaki, Vajiheh; Danesh, Hiva; Bizhani, Fatemeh; Taheri, Mohsen

2018-03-14

It has been proposed that transcobalamin 2 (TCN2) and the transcobalamin 2 receptor (TCN2R) are associated with idiopathic recurrent spontaneous abortion (RSA). The aim of the present study was to investigate the impact of TCN2 rs1801198 and TCN2R rs2336573 polymorphism on RSA in a sample of Iranian population. This case-control study was done on 92 RSA patients and 93 normal, fertile women. Genotyping of the TCN2 rs1801198 and TCN2R rs2336573 variants was done by polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP). The findings showed no significant association between the TCN2 rs1801198 and TCN2R rs2336573 polymorphisms and the risk/protection of RSA. Our results did not support an association between the TCN2 polymorphism and the risk of RSA in a sample of southeast Iranian population. Larger studies with different ethnicities are needed to evaluate the possible impact of TCN2 and TCN2R polymorphisms on the pathogenesis of RSA. Impact statement What is already known on this subject? Recurrent spontaneous abortion (RSA), a multifactorial condition, is one of the most common complications of pregnancy. It has been proposed that genetic polymorphisms play a role in the pathogenesis of RSA. Few studies have examined the association between TNC2 and TCN2R polymorphisms and the RSA risk and the findings were inconsistent. The aim of the current study was to determine the possible association between the TCN2 rs1801198 and TCN2R rs2336573 polymorphisms and the RSA in a sample of the southeast Iranian population. What do the results of the study add? The findings of the present case-control study did not support an association between the TCN2 rs1801198 and TCN2R rs2336573 polymorphisms and the risk of RSA in a sample of the Iranian population. What are the implications of these findings for clinical practice and future research? The findings of this study may provide a basis for future studies with larger sample sizes and different ethnicities

Exceptional longevity and muscle and fitness related genotypes: a functional in vitro analysis and case-control association replication study with SNPs THRH rs7832552, IL6 rs1800795 and ACSL1 rs6552828

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Noriyuki eFuku

2015-05-01

Full Text Available There are several gene variants that are candidates to influence functional capacity in long-lived individuals. As such, their potential association with exceptional longevity (EL, i.e., reaching 100+ years deserves analysis. Among them are rs7832552 in the thyrotropin-releasing hormone receptor (TRHR gene, rs1800795 in the interleukin-6 (IL6 gene and rs6552828 in the coenzyme A synthetase long-chain 1 (ACSL1 gene. To gain insight into their functionality (which is yet unknown, here we determined for the first time luciferase gene reporter activity at the muscle tissue level in rs7832552 and rs6552828. We then compared allele/genotype frequencies of the 3 abovementioned variants among centenarians [n=138, age range 100-111 years (114 women] and healthy controls [n=334, 20-50 years (141 women] of the same ethnic and geographic origin (Spain. We also studied healthy centenarians [n=79, 100-104 years (40 women] and controls [n=316, 27-81 years (156 women] from Italy, and centenarians [n=742, 100-116 years (623 women] and healthy controls [n=499, 23-59 years (356 women] from Japan. The THRH rs7832552 T-allele and ACSL1 rs6552828 A-allele up-regulated luciferase activity compared to the C and G-allele, respectively (P≤0.001. Yet we found no significant association of EL with rs7832552, rs1800795 or rs6552828 in any of the 3 cohorts. Further research is needed with larger cohorts of centenarians of different origin as well as with younger old people.

Prevalência de alterações posturais em escolares de ensino médio de São Leopoldo (RS), Brasil

OpenAIRE

Fonseca, Cíntia Detsch

2015-01-01

Objetivos estimar a prevalência de alterações posturais laterais e ântero-posteriores em adolescentes do sexo feminino da cidade de São Leopoldo, Rio Grande do Sul, Brasil, no ano de 2004 e verificar se os fatores sócio-econômicos, demográficos, antropométricos e comportamentais estão associados a estas alterações posturais. Métodos Inquérito epidemiológico de base escolar com amostra representativa de 495 alunas de 14 a 18 anos de idade, estudantes de escolas de ensino médio regular diurno, ...

Riscos ocupacionais autorreferidos por trabalhadores de uma indústria de produção de fertilizantes – RS – Brasil

OpenAIRE

Liane Silveira da Rosa; Leticia Machado Pereira; Leticia Silveira Cardoso; Marta Regina Cezar-Vaz; Valdecir Zavarese da Costa

2016-01-01

Objetivo: descrever a exposição a riscos ocupacionais autorreferida por trabalhadores de uma indústria de fertilizantes sólido e líquido no Extremo Sul do Rio Grande do Sul – Brasil. Método: estudo descritivo, realizado com 78 trabalhadores, dos quais 49 atuavam no setor de produção e 29 no de movimentação e ensaque. Produziu-se uma análise quantitativa, aplicando-se a estatística descritiva para apresentar as características dos trabalhadores e a exposição aos riscos ocupacionais autorreferi...

Role of redoximiRs in fibrogenesis.

Science.gov (United States)

Fierro-Fernández, Marta; Miguel, Verónica; Lamas, Santiago

2016-04-01

Fibrosis can be defined as an excessive accumulation of extracellular matrix (ECM) components, ultimately leading to stiffness, scarring and devitalized tissue. MicroRNAs (miRNAs) are short, 19-25 nucleotides (nt), non-coding RNAs involved in the post-transcriptional regulation of gene expression. Recently, miRNAs have also emerged as powerful regulators of fibrotic processes and have been termed "fibromiRs". Oxidative stress represents a self-perpetuating mechanism in fibrogenesis. MiRNAs can also influence the expression of genes responsible for the generation of reactive oxygen species (ROS) and antioxidant defence and are termed "redoximiRs". Here, we review the current knowledge of mechanisms by which "redoximiRs" regulate fibrogenesis. This new set of miRNAs may be called "redoxifibromiRs". Copyright © 2015 The Authors. Published by Elsevier B.V. All rights reserved.

Marca Brasil: ficção ou realidade? uma análise das iniciativas da APEX- Brasil para a construção da marca Brasil

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Daniela Motta R. Khauaja

2008-01-01

Full Text Available We live in a global economy and it is urgent for Brazil, through its governors and entrepreneurs, to increase its share in this economy. Branding the country can help create a strong identity for the country, which tends to collaborate with the exports of products made in this place. This study has the purpose of analyzing how brand Brasil was built and how it has been used by the Brazilian government to help its exports. In order to accomplish this objective, there was a review of the literature, concerning relevant concepts relative to global marketing, global branding and country as a brand. After this, the research method was explained and there was an analysis about the built of Brasil brand and the initiatives of the Brazilian government, more specifically of the Agência de Promoção de Exportações do Brasil (Apex-Brasil, for building Brazil as a brand. The initiative of creating brand Brasil, although quite late, was good, but, due to the lack of usage, the brand still seems to be more fiction than reality.

Polymorphism of rs7688672 and rs10033237 in cGKII/PRKG2 and gout susceptibility of Han population in northern China.

Science.gov (United States)

Guo, Min; Cheng, Zhifeng; Li, Changgui; Li, Shanshan; Li, Ming; Wang, Mingli; Xu, Jinmei; Tang, Yingying; Wang, Yujing; Qiu, Wenli; Liu, Xiaomin

2015-05-10

Gout is a genetic or acquired metabolic disease caused by increase of uric acid synthesis resulted from purine metabolic abnormalities. Whether cGMP-dependent protein kinase 2 (cGKII/PRKG2) is correlated with gout remains controversial. The objective of the present study was to investigate whether there is a correlation between polymorphism of cGKII/PRKG2 and gout susceptibility of Han population in northern China. Four hundred and five male patients with gout in the case group and 429 controls in the control group were collected from the Department of Endocrinology and Metabolic Disease, the Fourth Affiliated Hospital of Harbin Medical University. A case-control study method was used to study the correlation between cGKII/PRKG2 polymorphism rs7688672 and rs10033237 and gout susceptibility. The genotype frequencies of rs7688672 and rs10033237 polymorphisms of cGKII/PRKG2 in the case group and the control group both were in accordance with Hardy-Weinberg equilibrium. There were significant differences of rs10033237 in the allele frequencies and genotype distributions (Pgout. Combined mutation sites AA(*) from rs7688672 and rs10033237 were negatively correlated with gout susceptibility, whereas haplotype GG(*) was positively correlated with gout susceptibility. In conclusion, patients with rs10033237 polymorphism of cGKII/PRKG2 gene are more likely to suffer from gout. With regard to haplotypes of rs10033237 and rs7688672, both AA(*) and GG(*) are related to gout. AA(*) is a gout susceptible gene, whereas GG(*) is a protective gene. Copyright © 2015 Elsevier B.V. All rights reserved.

The Two-Component System CprRS Senses Cationic Peptides and Triggers Adaptive Resistance in Pseudomonas aeruginosa Independently of ParRS

DEFF Research Database (Denmark)

Fernandez, Luca; Jenssen, Håvard; Bains, Manjeet

2012-01-01

dependency on the CprRS and ParRS systems in a concentration-dependent manner. It was further demonstrated that, following exposure to inducing antimicrobial peptides, cprRS mutants did not become adaptively resistant to polymyxins as was observed for wild-type cells. Our microarray studies demonstrated...

ANÁLISE DO DESEMPENHO E PARTICIPAÇÃO DA AGRICULTURA FAMILIAR NA AVICULTURA DE CORTE NA REGIÃO SUL DO RIO GRANDE DO SUL / BRASIL

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Sérgio Renato Ferreira Decker

2016-03-01

Full Text Available RESUMO O presente estudo foi realizado junto à cadeia produtiva da avicultura de corte estabelecida na região sul do Rio Grande do Sul / Brasil, cuja indústria integradora está localizada no município de Morro Redondo/RS. O artigo, a partir de uma pesquisa bibliográfica e documental, apresenta uma análise da avicultura de corte no Brasil, no Rio Grande do Sul e por fim na Região Sul do RS. Realizou-se uma caracterização dos elos produtores e indústria, evidenciando-se no trabalho dados como: número de produtores, capacidade de produção, volume de produção e outros dados que revelam a importância econômica e social deste segmento. A base de produtores é essencialmente constituída por agricultores familiares e a avicultura é uma das principais atividades que garantem a sustentabilidade das oitenta e nove famílias que compõe a base de fornecimento da cadeia. Constata-se que a existe uma perspectiva promissora de crescimento, haja visto que a indústria está atuando no limite de sua capacidade e já possui projeto de duplicação da planta para os próximos anos. Desta forma, entendemos que a integração dos produtores familiares revela-se uma boa alternativa para o desenvolvimento da agricultura familiar da região.

Relatório das atividades de campo do Projeto de Salvamento Arqueológico do Centro Histórico de Pelotas-RS/Brasil (período 2006-2007

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Fábio Vergara Cerqueira

2012-09-01

Full Text Available O Projeto de Salvamento Arqueológico do Centro Histórico de Pelotas-Rs/Brasil  consiste em uma pesquisa de arqueologia histórica em meio urbano que realiza atividades de levantamento e preservação de sítios arqueológicos desde o ano de 2002. Inicialmente, o projeto foi desenvolvido para atender as demandas do Programa  Monumenta  (o qual prevê a restauração da Praça Cel. Pedro Osório e dos mais imponentes prédios de seu entorno e atuou nos projetos de restauração dos casarões 8 (sítio PSGPe-1, escavado em 2002 e 2 (Sítio PSGPe-2, escavado em 2003. Atualmente, o projeto atende a todas as obras de impactação em prédios históricos e sítios arqueológicos da área urbana pelotense, bem como do patrimônio histórico das áreas periféricas. A responsabilidade  técnica pelo trabalho, junto ao  Instituto do Patrimônio Histórico e Artístico Nacional (IPHAN  -  registrado sob número de processo 01512.000006/2005  –  92  -  é do  Laboratório de Ensino e Pesquisa em Antropologia e Arqueologia da Universidade Federal de Pelotas (LEPAARQ  –  UFPEL,  coordenado pelo  Arqueólogo Dr. Fábio Vergara Cerqueira (CERQUEIRA  et  al., 2004a; CERQUEIRA e LOUREIRO, 2004b. PALAVRAS-CHAVE:  Arqueologia histórica  –  Salvamento Arqueológico  – Pelotas oitocentista

Comparação gráfica entre curvas de índice de sítio para Pinus elliottii e Pinus taeda desenvolvidas no sul do Brasil

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Helio Tonini

2002-01-01

Full Text Available This research had as main objective to study the dominant height growth of Pinus elliottii and Pinus taeda through site index curves comparisons in some regions of Rio Grande do Sul State and other states of the country. These comparisons showed that the site index curves made by Tonini (2000, for the southeastern mountain and coast land in Rio Grande do Sul State did not show the same pattern of those by Scolforo e Machado (1988, for Paraná and Santa Catarina, Brazil (1989a for Passo Fundo RS, Marcolin (1990, for the Parana’s Second Upland and Selle (1993 for Cambará do Sul RS. However, the same growth pattern was observed for curves by Brasil (1989b for S ão Francisco de Paula which only level differences were observed.

RURALIDADES E TURISMO: A cultura rural no município de São João do Polêsine/RS

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Michele Lindner

2011-11-01

Full Text Available Resumo: O turismo possui íntima relação com a cultura, pois ele se utiliza dela como um atrativo. Conhecer diferentes culturas é prática instigante. O turismo rural no Brasil vem chamando a atenção dos habitantes de áreas urbanas, como uma forma de vivenciar experiências diversas de seu cotidiano, assim como conhecer a cultura e os modos de vida das populações rurais. A cultura rural, dessa maneira, se manifestada através das ruralidades. É nesse sentido que este artigo busca analisar como as ruralidades vem sendo exploradas como produto turístico no município de São João do Polêsine/RS. Palavras chave: Turismo Rural. Ruralidades. Cultura. 

Association of 5-HT2C (rs3813929) and UCP3 (rs1800849) gene polymorphisms with type 2 diabetes in obese women candidates for bariatric surgery.

Science.gov (United States)

Schnor, Noa Pereira Prada; Verlengia, Rozangela; Novais, Patrícia Fátima Sousa; Crisp, Alex Harley; Leite, Celso Vieira de Souza; Rasera-Junior, Irineu; Oliveira, Maria Rita Marques de

2017-01-01

Obesity can cause systemic arterial hypertension (SAH) and type 2 diabetes mellitus (DM2) factor that is also influenced by genetic variability. The present study aims to investigate the association between gene polymorphisms related with obesity on the prevalence of SAH and DM2 in the preoperative period and 1 year after Roux-en-Y gastric bypass surgery. In total, 351 obese women in a Brazilian cohort completed the study. The clinical diagnosis of SAH and DM2 was monitored from medical records. Twelve gene polymorphisms (rs26802; rs572169; rs7799039; rs1137101; rs3813929; rs659366; rs660339; rs1800849; rs7498665; rs35874116; rs9701796; and rs9939609) were determined using real-time polymerase chain reaction and TaqMan assay. In the preoperative period, prevalence of SAH and DM2 was 57% and 22%, respectively. One year postoperatively, 86.8% subjects had remission of DM2 and 99.5% had control of SAH. Subjects with T allele from the serotonin receptor gene (5-HT2C, rs3813929) had five times greater chance of DM2, and the CC genotype from uncoupling protein 3 gene (UCP3, rs1800849) had three times greater chance in the preoperative period. These findings indicate that polymorphisms rs3813929 and rs1800849 from 5-HT2C and UCP3 genes were related to DM2 prevalence among the Brazilian obese women candidates for bariatric surgery.

Genetic polymorphisms of IL-18 rs1946518 and IL-1β rs16944 are associated with prognosis and survival of acute myeloid leukemia.

Science.gov (United States)

Wang, Hong; Hua, Mingqiang; Wang, Shukang; Yu, Jie; Chen, Chen; Zhao, Xueyun; Zhang, Chen; Zhong, Chaoqin; Wang, Ruiqing; He, Na; Hou, Ming; Ma, Daoxin

2017-03-01

Though the pathogenesis of AML is still unknown, accumulating evidence revealed that immune response plays a vital part in it. NLRP3 inflammasome as a component of immune system has been found related to several cancers. The single nucleotide polymorphisms (SNPs) of NLRP3 inflammasome genes may be related to pathogenesis and prognosis of AML. We determined polymorphisms of NLRP3 (rs35829419), CARD8 (rs2043211), IL-1β (rs16944), IL-18 (rs1946518) and NF-κB -94 ins/del ATTG in de novo AML patients to find out whether they play roles in the susceptibility and severity of AML. In our study, 383 AML cases and 300 randomly selected healthy individuals were examined for the polymorphisms and expression of NLRP3 genes. IL-1β (rs16944) polymorphism in different risk AML subgroups was found statistically different, with more GA genotype in favorable-risk cytogenetics group. We also demonstrated that the bone marrow blasts of patients carrying IL-18 (rs1946518) GG or GT genotype were higher than patients of TT genotype. IL-18 plasma level of patients with IL-18 (rs1946518) GT or TT genotype was higher than GG genotype. Moreover, the GT genotype of IL-18 (rs1946518) led to statistically poorer AML-specific survival. IL-1β (rs16944) and IL-18 (rs1946518) may be served as potential predictors for AML.

The obesity-associated polymorphisms FTO rs9939609 and MC4R rs17782313 and endometrial cancer risk in non-Hispanic white women.

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Galina Lurie

2011-02-01

Full Text Available Overweight and obesity are strongly associated with endometrial cancer. Several independent genome-wide association studies recently identified two common polymorphisms, FTO rs9939609 and MC4R rs17782313, that are linked to increased body weight and obesity. We examined the association of FTO rs9939609 and MC4R rs17782313 with endometrial cancer risk in a pooled analysis of nine case-control studies within the Epidemiology of Endometrial Cancer Consortium (E2C2. This analysis included 3601 non-Hispanic white women with histologically-confirmed endometrial carcinoma and 5275 frequency-matched controls. Unconditional logistic regression models were used to assess the relation of FTO rs9939609 and MC4R rs17782313 genotypes to the risk of endometrial cancer. Among control women, both the FTO rs9939609 A and MC4R rs17782313 C alleles were associated with a 16% increased risk of being overweight (p = 0.001 and p = 0.004, respectively. In case-control analyses, carriers of the FTO rs9939609 AA genotype were at increased risk of endometrial carcinoma compared to women with the TT genotype [odds ratio (OR  = 1.17; 95% confidence interval (CI: 1.03-1.32, p = 0.01]. However, this association was no longer apparent after adjusting for body mass index (BMI, suggesting mediation of the gene-disease effect through body weight. The MC4R rs17782313 polymorphism was not related to endometrial cancer risk (per allele OR = 0.98; 95% CI: 0.91-1.06; p = 0.68. FTO rs9939609 is a susceptibility marker for white non-Hispanic women at higher risk of endometrial cancer. Although FTO rs9939609 alone might have limited clinical or public health significance for identifying women at high risk for endometrial cancer beyond that of excess body weight, further investigation of obesity-related genetic markers might help to identify the pathways that influence endometrial carcinogenesis.

APOC3 rs2070666 Is Associated with the Hepatic Steatosis Independently of PNPLA3 rs738409 in Chinese Han Patients with Nonalcoholic Fatty Liver Diseases.

Science.gov (United States)

Zhang, Rui-Nan; Zheng, Rui-Dan; Mi, Yu-Qiang; Zhou, Da; Shen, Feng; Chen, Guang-Yu; Zhu, Chan-Yan; Pan, Qin; Fan, Jian-Gao

2016-08-01

The association between nonalcoholic fatty liver disease (NAFLD) and apolipoprotein C3 gene (APOC3) promoter region single-nucleotide polymorphisms (SNPs) rs2854117 and rs2854116 is controversial. The aim of this study was to investigate the relationship between other polymorphisms of APOC3 and NAFLD in Chinese. Fifty-nine liver biopsy-proven NAFLD patients and 72 healthy control subjects were recruited to a cohort representing Chinese Han population. The polymorphisms in the exons and flanking regions of APOC3 and patatin-like phospholipase domain-containing protein 3 (PNPLA3) rs738409 polymorphisms were genotyped. Among the five SNPs (rs4225, rs4520, rs5128, rs2070666, and rs2070667) in APOC3, only rs2070666 (c.179 + 62 T/A) was significantly different in genotype and allele frequency (both p steatosis (OR 4.986, 95 % CI 1.020-24.371), but neither to liver stiffness measurement values nor to hepatic histological activity and fibrosis in NAFLD patients. The APOC3 rs2070666 A allele is a risk factor for NAFLD independent of obesity, dyslipidemia, and PNPLA3 rs738409, and it might contribute to increased liver fat content in Chinese Han population.

Association of PTPN22 rs2476601 and STAT4 rs7574865 polymorphisms with rheumatoid arthritis: A meta-analysis update.

Science.gov (United States)

Elshazli, Rami; Settin, Ahmad

2015-08-01

Rheumatoid arthritis (RA) is a common autoimmune disease with a complex genetic background. The genes encoding protein tyrosine phosphatase non-receptor type 22 (PTPN22) and signal transducer and activator of transcription 4 (STAT4) have been reported to be associated with RA in several ethnic populations. This work aims to assess the association between PTPN22 rs2476601 and STAT4 rs7574865 polymorphisms with RA susceptibility through an updated meta-analysis of available case-control studies. A literature search of all relevant studies published from January 2007 up to December 2014 was conducted using Pubmed and Science Direct databases. The observed studies that were related to an association between PTPN22 rs2476601 and STAT4 rs7574865 polymorphisms with RA susceptibility were identified. Meta-analysis of the pooled and stratified data was done and assessed using varied genetic models. Thirty-seven case-control studies with a total of 47 comparisons (29 for PTPN22 rs2476601 polymorphism and 18 for STAT4 rs7574865 polymorphism) met our inclusion criteria. The meta-analysis showed an association between PTPN22 T allele, CT+TT and TT genotypes with RA susceptibility. Furthermore, The meta-analysis showed an association between STAT4 T allele, GT+TT and TT genotypes with RA susceptibility. Stratification of RA patients according to ethnic groups showed that PTPN22 T allele, CT+TT genotypes, STAT4 T allele and STAT4 GT+TT were significantly associated with RA in European, Asian, African subjects, while PTPN22 TT genotype was significantly associated with RA in European but not in Asian and African subjects and STAT4 TT genotype was significantly associated with RA in European and Asian but not in African subject. A subgroup analysis according to the presence or absence of rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) antibodies revealed that the association between PTPN22 rs2476601 and STAT4 rs7574865 polymorphisms with RA susceptibility

Ocorrência de Trypanosoma evansi em eqüinos no município de Cruz Alta, RS, Brasil Occurrence of Trypanosoma evansi in equines in Cruz Alta, RS, Brazil

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Régis Adriel Zanette

2008-08-01

Full Text Available O objetivo deste trabalho foi relatar a ocorrência de Trypanosoma evansi em eqüinos no município de Cruz Alta, Estado do Rio Grande do Sul, abordando aspectos epidemiológicos e sinais clínicos da infecção. A tripanosomose ocorreu em uma propriedade rural no município de Cruz Alta. Ao exame clínico, observou-se que quatro dos animais apresentavam marcha oscilante, com incoordenação dos membros posteriores. No entanto, eles estavam em bom estado nutricional, sem febre, bem hidratados e alimentavam-se normalmente. Foram coletadas amostras de sangue das éguas para hemograma, sendo identificado aumento das proteínas plasmáticas, leucocitose, eosinofilia e linfocitose em animais com sinais clínicos. No esfregaço sangüíneo periférico, observou-se a forma flagelada do T. evansi em três dos eqüinos.This study aimed at describing the occurrence of Trypanosoma evansi in equines from the city of Cruz Alta, RS, Brazil, relating epidemiological aspects and clinical signs of the infection. The tripanosomiasis occurred in a rural area of Cruz Alta, RS. Clinical signs presented by four animals were stiff and incoordinated gait of the pelvic members, although they were in good nutritional status, without fever, well-hydrated and eating normally. Blood samples were collected from the mares for hemogram. Increased levels of plasmatic proteins, leukocytosis, eosinophilia, and limphocytosis were observed in animals with clinical signs. Flagellated forms of T. evansi were observed in the blood smear of three animals.

Association of TNF-α rs1799964 and IL-1β rs16944 polymorphisms with multiple system atrophy in Chinese Han population.

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Zhou, Xin; Wang, Chunrong; Chen, Zhao; Peng, Yun; Peng, Huirong; Hou, Xuan; Ye, Wei; Qiu, Rong; Xia, Kun; Tang, Beisha; Jiang, Hong

2018-01-07

Recent evidence suggested that several single nucleotide polymorphisms (SNPs) of inflammation-related genes (TNF-α rs1799964, IL-1α rs1800587, IL-1β rs16944, IL-8 rs4073, ICAM-1 rs5498) were associated with multiple system atrophy (MSA). Herein, we conducted this case-control study to evaluate the possible correlation between the five SNPs related to inflammation and MSA in Chinese Han population. We recruited 154 sporadic patients with MSA and 223 health controls in this study. All subjects were genotyped for the five SNPs using polymerase chain reaction amplification and Sanger sequencing. TNF-α rs1799964, genotype distribution and minor allele frequency (MAF) showed significant differences between patients and controls, which might illustrate the minor allele C may increase the risk for MSA (genotype, P = 0.006, OR = 1.245, 95% CI = [1.066-1.455]; allele, P = 0.001, OR = 1.887, 95% CI = [1.303-2.733]). For rs16944, patients carrying AA genotype showed a nearly 5-year early age at onset (AAO) than GG genotype (50.52 ± 7.45 years vs. 54.90 ± 7.21 years, P = 0.037). No differences were found in genotype distribution and MAF of the five SNPs between patients with MSA with predominant cerebellar ataxia (MSA-C) and with predominant Parkinsonism (MSA-P). Our study suggests that rs1799964 of TNF-α may act as a risk factor for MSA and the IL-1β rs16944 might be a genetic factor that modifies the AAO in MSA. Moreover, the exact mechanism of neuroinflammatory response in MSA deserves further exploration.

El Brasil y Alberdi

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Enrique de Gandia

1968-12-01

Full Text Available Alberdi fue amigo de Chile, del Paraguay, de España y de otras naciones; pero nunca lo fue del Brasil. Tenía hacia esta nación una desconfianza innata que lo llevaba a temores y suposiciones impropias de su talento. En marzo de 1865 publicó en París un opúsculo sobre Las disensiones de las Repúblicas del Plata y las maquinaciones del Brasil.

Polymorphisms of transforming growth factor beta 1 (RS#1800468 and RS#1800471) and esophageal squamous cell carcinoma among Zhuangese population, China.

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Tang, Ren-Guang; Huang, Yong-Zhi; Yao, Li-Min; Xiao, Jian; Lu, Chuan; Yu, Qian

2013-01-01

Epidemiological evidence has shown two polymorphisms (namely RS#1800468G>A and RS#1800471G>C) of transforming growth factor-beta 1 (TGF-β1) gene may be involved in the cancer development. However, their role in the carcinogenic process of esophageal squamous cell carcinoma (ESCC) has been less well elaborated. We conducted a hospital-based case-control study including 391 ESCC cases and 508 controls without any evidence of tumors to evaluate the association between these two polymorphisms and ESCC risk and prognosis for Zhuangese population by means of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and amplification refractory mutation system (ARMS)-PCR techniques. We found that individuals with the genotypes with RS#1800471 C allele (namely RS#1800471-GC or -CC) had an increased risk of ESCC than those without above genotypes (namely RS#1800471-GG, adjusted odds ratio 3.26 and 5.65, respectively). Further stratification analysis showed that this polymorphism was correlated with tumor histological grades and TNM (tumor, node, and metastasis) stage, and modified the serum levels of TGF-β1. Additionally, RS#1800471 polymorphism affected ESCC prognosis (hazard ratio, 3.40), especially under high serum levels of TGF-β1 conditions. However, RS#1800468 polymorphism was not significantly related to ESCC risk. These findings indicated that TGF-β1 RS#1800471G>C polymorphism may be a genetic modifier for developing ESCC in Zhuangese population. Copyright © 2012 Elsevier B.V. All rights reserved.

Genetic polymorphisms of surfactant protein D rs2243639, Interleukin (IL)-1β rs16944 and IL-1RN rs2234663 in chronic obstructive pulmonary disease, healthy smokers, and non-smokers.

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Issac, Marianne Samir M; Ashur, Wafaa; Mousa, Heba

2014-06-01

Chronic obstructive pulmonary disease (COPD) is a complex chronic inflammatory disease that involves the activity of various inflammatory cells and mediators. It has been suggested that susceptibility to COPD is, at least in part, genetically determined. The primary aim of this study was to investigate the association between surfactant protein D (SFTPD) rs2243639, interleukin (IL)-1β rs16944 and IL-1 receptor antagonist (IL-1RN) rs2234663 gene polymorphisms and COPD susceptibility, as well as examining the association between the various IL-1RN/IL-1β haplotypes and pulmonary function tests (PFT). Secondly, we aimed to examine the influence of SFTPD rs2243639 polymorphism on serum surfactant protein D (SP-D) level. A total of 114 subjects were recruited in this study and divided into three groups: 63 COPD patients, 25 asymptomatic smokers, and 26 healthy controls. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was performed for the detection of SFTPD rs2243639 and IL-1β rs16944 polymorphisms. Detection of variable numbers of an 86-bp tandem repeat (VNTR) of IL-1RN was done using PCR. Serum SP-D level was measured using enzyme linked-immunosorbent assay. PFTs were measured by spirometry. Carriers of the SFTPD AG and AA polymorphic genotypes constituted 71.4 % of COPD patients versus 48 % in asymptomatic smokers, with a statistically significant difference between the two groups (p = 0.049). Smokers who were carriers of the polymorphic SFTPD rs2243639 A allele (AG and AA genotypes) have a 2.708 times risk of developing COPD when compared with wild-type GG genotype carriers [odds ratio (OR) 2.708 (95 % CI 1.041-7.047)]. Forced expiratory flow (FEF) 25-75 % predicted was higher in IL-1RN*1/*1 when compared with *1/*2 (p = 0.013). FEF25-75 % predicted in carriers of haplotype IL-1RN *1/IL-1β T (49.21 ± 10.26) was statistically significantly higher than in carriers of IL-1RN *2/IL-1β T (39.67 ± 12.64) [p = 0

Association of the matrix metalloproteinase-3 polymorphisms rs679620 and rs3025058 with ischemic stroke risk: a meta-analysis

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Zhang Q

2018-01-01

Full Text Available Qi-Wei Zhang Department of Neurosurgery, The Affiliated Hospital of Jilin Medical University, Jilin, People’s Republic of China Purpose: The relationship of the matrix metalloproteinase-3 (MMP-3 polymorphisms rs679620 and rs3025058 with ischemic stroke has received much attention. The aim of the present study was to perform a meta-analysis of published case–control studies to evaluate the cumulative evidence.Methods: We performed a search of ISI Web of Science, Embase, PubMed, and China National Knowledge Infrastructure databases. Pooled odds ratios (ORs were appropriately derived from fixed-effects or random-effects models.Results: We identified seven eligible studies including 5,204 subjects. The pooled analysis showed that the MMP-3 rs679620 A allele carriers had increased risk of ischemic stroke compared with homozygotes for the G allele in Asians (AA + GA vs GG: OR =1.42, 95% CI: 1.05–1.91, P=0.022. Concerning the rs3025058 polymorphism, the results did not suggest an association between rs3025058 genotypes and ischemic stroke risk (5A5A + 6A5A vs 6A6A: OR =1.04, 95% CI: 0.73–1.47, P=0.844; 5A5A vs 6A5A + 6A6A: OR =1.14, 95% CI: 0.74–1.77, P=0.556; and 5A5A vs 6A6A: OR =1.11, 95% CI: 0.68–1.80, P=0.677. In subgroup analysis by ethnicity, no statistically significant associations were demonstrated for rs3025058 in Asians and Caucasians, respectively. There was no evidence for publication bias.Conclusion: Our findings indicate that the rs679620 A allele carriers have increased risk of ischemic stroke in Asians, but there is no association between rs3025058 and ischemic stroke risk. Keywords: ischemic stroke, meta-analysis, MMP-3, polymorphism

Determination of IL-1B (rs16944) and IL-6 (rs1800796) genetic polymorphisms in IgA nephropathy in a northwest Chinese Han population.

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Zhang, Daofa; Xie, Maowei; Yang, Xiaohong; Zhang, Yin; Su, Yan; Wang, Yanni; Huang, Haiyang; Han, Hui; Li, Wenning; Fu, Keying; Su, Huiluan; Xu, Wentan; Han, Yeguang; Wang, Ru; Zhang, Pei; Wu, Wei; Huang, Yun; Chen, Daojun; Jin, Tianbo; Wei, Jiali

2017-09-22

IgA nephropathy (IgAN) is the most common form of primary glomerulonephritis worldwide, but etiology and pathogenesis continue to be poorly understood. Polymorphisms in the cytokine genes may play a role in the etiology and pathogenesis of IgAN. The incidence of different between diverse ethnic groups suggested important genetic influences on its pathogenesis. We genotype 10 single nucleotide polymorphisms (SNPs) in IL-1B and IL-6 gene using Sequenom Mass-ARRAY technology from 417 IgAN patients and 463 healthy controls of the Chinese Han population. We evaluated these SNPs associated with IgAN utilising the chi-square tests and genetic model analysis. We identified that the minor alleles of rs16944 ("A"), rs1800796 ("G") in IL-1B, IL-6 were involved in an increasingly risk of IgAN in allelic model analysis, respectively. The rs16944 in IL-1B and rs1800796 in IL-6 were associated with 1.23-fold (95% CI, 1.02-1.48, P = 0.031) and 1.33-fold (95% CI, 1.11-1.66, P = 0.003) increases in the risk of developing IgAN, respectively. There was only rs1800796 still correlated with IgAN in the allelic model after adjustment by age and gender and the Bonferroni correction. In addition, Haplotype G rs1800796 A rs2069837 G rs2069840 ( P = 0.037) and G rs1800796 A rs2069837 C rs2069840 ( P = 0.042) in IL-6 were considered to be associated with increased IgAN risk. This study verified the IL-6, IL-1B genetic variants polymorphisms contributed to IgAN susceptibility in a Chinese Han population. Although we identified SNPs susceptibility, however, replication studies and functional research are required to confirm the genetic contribution in IgAN.

Mundo Braz. El devenir-mundo de Brasil y el devenir-Brasil del mundo

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Rodrigo Martínez Reinoso

2015-02-01

Full Text Available Reseña: Mundo Braz. El devenir-mundo de Brasil y el devenir-Brasil del mundo   MundoBraz. El devenir-mundo de Brasil y el devenir-Brasil del mundo es el título que lleva la obra del filósofo italiano radicado en Brasil Giuseppe Cocco. Fue publicada originalmente en portugués (Río de Janeiro, 2009 y editada en español por la Editorial Traficantes de Sueños tres años después (Madrid, 2012. Sus principales aportaciones se relacionan con el análisis político y social de nuestra realidad contemporánea bajo una línea de investigación neo-marxista que ha dado origen a dos emblemáticas publicaciones, las cuales son en rigor los antecedentes inmediatos del espíritu crítico, transdisciplinario y altermundista que caracteriza a MundoBraz. [1] Cocco, Giuseppe (2012: MundoBraz. El devenir-mundo de Brasil y el devenir-Brasil del mundo. Traficantes de Sueños, Madrid. Giuseppe Cocco se formó en Italia y Francia y fue activista político en los años 70 de Autonomía Obrera. Es Licenciado en Ciencias Políticas (Università degli Studi di Padova, 1981, Licenciado en Ciencias Políticas (Université de Paris VIII, 1984, Master of Science Technologie et Société (Conservatoire National des Arts et Métiers, 1988, MA en Historia Social (Universidad de París I (Panthéon-Sorbonne, 1986 y Doctor en Historia Social (Universidad Paris I Panthéon-Sorbonne, 1993. Ejerce como profesor de la Universidad Federal de Río de Janeiro y es editor de diversas revistas de perfil neomarxista y altermundista: Global Brasil, Common Place y Multitudes. Un modo de resumir el valor de esta bella y asombrosa obra quizás consista en decir que cumple a cabalidad con el sentido de lo que Deleuze y Guattari han denominado como una política menor. La cual, paradójicamente, si bien derriba una serie de dogmas del liberalismo y del marxismo, tal mirada no se queda en un diagnóstico fatídico y determinista (como sería el economicismo que acusa al neoliberalismo de

Four therapeutic cases of RS3PE syndrome

International Nuclear Information System (INIS)

Nakajima, Naoya; Fukuda, Yukiko; Yang, Kwang-Seok; Aiba, Miyoji; Tsuda, Hiroshi

2007-01-01

RS3PE syndrome (Remitting Seronegative Symmetrical Synovitis with Pitting Edema Syndrome) is one of the disorders which present as polyarthritis. It is important to be aware of RS3PE syndrome when encountering elderly patients with polyarthritis who are negative for rheumatoid factor. We report 4 cases of RS3PE syndrome. All cases shared common clinical findings, such as acute onset, symmetrical polyarthritis, pitting edema of the hands and feet, and being negative for rheumatoid factor in serum. Treatment with corticosteroid was very effective in all cases. However, two patients showed a deteriorated clinical condition during the tapering of corticosteroid. Corticosteroid should be tapered off cautiously in patients with RS3PE syndrome. (author)

Association of rs6265 and rs2030324 polymorphisms in brain-derived neurotrophic factor gene with Alzheimer's disease: a meta-analysis.

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Yan Lin

Full Text Available BACKGROUND: The association between polymorphisms rs6265 and rs2030324 in brain-derived neurotrophic factor (BDNF and Alzheimer's disease (AD has been widely reported, but the results remain controversial. METHODS: A comprehensive search of Pubmed, Web of Science, China National Knowledge Infrastructure (CNKI, Wanfang Med Online and China Biology Medical literature database (CBM was performed. Pooled odds ratios (ORs with 95% confidence intervals (CIs were calculated using fixed or random-effects models. We excluded the studies with OR>3.0 or OR<0.3 for sensitive analysis. Subgroup analysis by ethnicity, form of AD and gender was carried out. Meta-regression was conducted to explore the potential sources of between-study heterogeneity. RESULTS: 29 articles with 7548 cases and 7334 controls concerning rs6265 and 22 articles with 5796 cases and 5706 controls concerning rs2030324 were included in this meta-analysis. The combined evidence suggested rs6265 contributing significantly to the increased risk of AD in females (codominant: fixed-effects model (FEM: OR = 1.13, 95% CI = 1.04-1.23; dominant: FEM: OR = 1.17, 95% CI = 1.05-1.31, especially for Caucasian females (codominant: FEM: OR = 1.18, 95% CI = 1.03-1.34; dominant: FEM: OR = 1.18, 95% CI = 1.01-1.37 and female late-onset Alzheimer's disease (LOAD patients (codominant: FEM: OR = 1.22, 95% CI = 1.05-1.41; dominant: FEM: OR = 1.23, 95% CI = 1.03-1.46. No evidence indicated an association between rs2030324 with AD in codominant (random-effects model (REM: OR = 1.06, 95% CI = 0.89-1.26 and dominant (REM: OR = 1.05, 95% CI = 0.86-1.27 models. CONCLUSION: This meta-analysis suggested A allele of rs6265 might increase the risk of AD in Caucasian females and female LOAD patients. In addition, no evidence indicated an association between rs2030324 with AD. Further studies are needed to confirm these results.

Genetic Association for P2X7R rs3751142 and CARD8 rs2043211 Polymorphisms for Susceptibility of Gout in Korean Men: Multi-Center Study.

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Lee, Sung Won; Lee, Shin Seok; Oh, Dong Ho; Park, Dong Jin; Kim, Hyun Sook; Choi, Jung Ran; Chae, Soo Cheon; Yun, Ki Jung; Chung, Won Tae; Choe, Jung Yoon; Kim, Seong Kyu

2016-10-01

The aim of this study was to determine the association between P2X7R rs3751142 and CARD8 rs2043211 polymorphisms and gout susceptibility in male Korean subjects. This study enrolled a total of 242 male patients with gout and 280 healthy controls. The polymorphisms of two individual genes including rs3751142(C>A) in the P2X7R gene and rs2043211(A>T) in the CARD8 gene were assessed using Taq-Man analysis. Statistical analyses were performed using the Chi-square test, Kruskal-Wallis test, and logistic regression analyses. A difference in genotypic frequency of the P2X7R rs3751142 and CARD8 rs2043211 genes was not detected between gout and control patients. Clinical parameters including age, onset age, disease duration, body mass index, and serum uric acid levels were not different among the three genotypes for either P2X7R or CARD8 (P > 0.05 for all). A pair-wise comparison of P2X7R rs3751142 and CARD8 rs2043211 genotype combinations revealed that subjects with the CA P2X7R rs3751142 genotype and the TT CARD8 rs2043211 genotype had a trend toward a higher risk of gout compared to the CC/AA combination (P = 0.056, OR = 2.618, 95% CI 0.975 - 7.031). In conclusion, this study revealed that genetic variability of the P2X7R rs3751142 and CARD8 rs2043211 genes might, in part, be associated with susceptibility for gout.

Design Report for Isolated RS-485 Bus Node

Science.gov (United States)

2016-07-01

TERMS Android , RS-485, isolated, USB, smartphone 16. SECURITY CLASSIFICATION OF: 17. LIMITATION OF ABSTRACT UU 18. NUMBER...controlled wired RS-485 network. The Android -based smartphone or tablet is used in conjunction with a USB to serial bridge to operate as the bus master in...the system. The Android device operates in USB Host mode and communicates to the RS-485 bus as if a single peripheral on the USB bus. 15. SUBJECT

RS485 optical router for HIRFL-CSR

International Nuclear Information System (INIS)

Zhang Shuocheng; Wang Dan; Jing Lan; Qiao Weimin

2007-01-01

A communication equipment-RS485 optical router has been developed to satisfy requirements of control system communication network of HIRFL-CSR (Heavy Ion Research Facility at Lanzhou-Cooling Storage Ring). The equipment is compatible with multiple communication protocols, such as Ethernet, RS232 and RS485 standard. It can be used to setup the RS485 communication network quickly and connected to the Ethernet easily. The fiber optical interface is introduced to facilitate the connection with the network of industrial Fiber Optics Communication (FOC), which expands the application field of the equipment in a large extent. This paper introduces the details of the equipment, including the design of the circuit and software, features of the equipment and how it works in the whole control system network. Its application in the HIRFL-CSR control system shows that the equipment is in accordance with the general requirement of automatic control communication system. It could also be used in other industrial automatic control fields. (authors)

Aspectos fitossociológicos de um fragmento da floresta natural de Astronium balansae engl., no município de Bossoroca, RS

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Boligon Alexandra Augusti

2005-01-01

Full Text Available Este estudo objetivou conhecer a composição florística e a estrutura fitossociológica de um fragmento da Floresta Natural de Astronium balansae Engl., no município de Bossoroca, RS, Brasil. Foram demarcadas 7 unidades amostrais de 10x100m (1000m2 onde observou-se a ocorrência de 476 indivíduos com Circunferência à Altura do Peito (CAP = 30cm, distribuídos em 35 espécies e 25 famílias. As espécies mais características e importantes da floresta foram Astronium balansae, Myrcianthes pungens, Patagonula americana, Eugenia uniflora e Parapiptadenia rigida. As famílias Myrtaceae, Meliaceae e Euphorbiaceae foram as mais representativas do fragmento florestal estudado. O valor do Índice de diversidade de Shannon foi 3.

Associations of polymorphisms in the cytokine genes IL1β (rs16944), IL6 (rs1800795), IL12b (rs3212227) and growth factor VEGFA (rs2010963) with anthracosilicosis in coal miners in Russia and related genotoxic effects.

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Volobaev, Valentin P; Larionov, Aleksey V; Kalyuzhnaya, Ekaterina E; Serdyukova, Ekaterina S; Yakovleva, Svetlana; Druzhinin, Vladimir G; Babich, Olga O; Hill, Elena G; Semenihin, Victor A; Panev, Nikolay I; Minina, Varvara I; Sivanesan, Saravana Devi; Naoghare, Pravin; da Silva, Juliana; Barcelos, Gustavo R M; Prosekov, Alexander Y

2018-04-13

Anthracosilicosis (AS), a prevalent form of pneumoconiosis among coal miners, results from the accumulation of carbon and silica in the lungs from inhaled coal dust. This study investigated genotoxic effects and certain cytokine genes polymorphic variants in Russian coal miners with АS. Peripheral leukocytes were sampled from 129 patients with AS confirmed by X-ray and tissue biopsy and from 164 asymptomatic coal miners. Four single-nucleotide polymorphisms were genotyped in the extracted DNA samples: IL1β T-511C (rs16944), IL6 C-174G (rs1800795), IL12b A1188C (rs3212227) and VEGFA C634G (rs2010963). Genotoxic effects were assessed by the analysis of chromosome aberrations in cultured peripheral lymphocytes. The mean frequency of chromatid-type aberrations and chromosome-type aberrations, namely, chromatid-type breaks and dicentric chromosomes, was found to be higher in AS patients [3.70 (95% confidence interval {CI}, 3.29-4.10) and 0.28 (95% CI, 0.17-0.38)] compared to the control group [2.41 (95% CI, 2.00-2.82) and 0.09 (95% CI, 0.03-0.15)], respectively. IL1β gene T/T genotype (rs16944) was associated with AS [17.83% in AS patients against 4.35% in healthy donors, odds ratio = 4.77 (1.88-12.15), P < 0.01]. A significant increase in the level of certain chromosome interchanges among AS donors is of interest because such effects are typical for radiation damage and caused by acute oxidative stress. IL1β T allele probably may be considered as an AS susceptibility factor among coal miners.

Multirate Filter Bank Representations of RS and BCH Codes

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Van Meerbergen Geert

2008-01-01

Full Text Available Abstract This paper addresses the use of multirate filter banks in the context of error-correction coding. An in-depth study of these filter banks is presented, motivated by earlier results and applications based on the filter bank representation of Reed-Solomon (RS codes, such as Soft-In Soft-Out RS-decoding or RS-OFDM. The specific structure of the filter banks (critical subsampling is an important aspect in these applications. The goal of the paper is twofold. First, the filter bank representation of RS codes is now explained based on polynomial descriptions. This approach allows us to gain new insight in the correspondence between RS codes and filter banks. More specifically, it allows us to show that the inherent periodically time-varying character of a critically subsampled filter bank matches remarkably well with the cyclic properties of RS codes. Secondly, an extension of these techniques toward the more general class of BCH codes is presented. It is demonstrated that a BCH code can be decomposed into a sum of critically subsampled filter banks.

Multirate Filter Bank Representations of RS and BCH Codes

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Marc Moonen

2009-01-01

Full Text Available This paper addresses the use of multirate filter banks in the context of error-correction coding. An in-depth study of these filter banks is presented, motivated by earlier results and applications based on the filter bank representation of Reed-Solomon (RS codes, such as Soft-In Soft-Out RS-decoding or RS-OFDM. The specific structure of the filter banks (critical subsampling is an important aspect in these applications. The goal of the paper is twofold. First, the filter bank representation of RS codes is now explained based on polynomial descriptions. This approach allows us to gain new insight in the correspondence between RS codes and filter banks. More specifically, it allows us to show that the inherent periodically time-varying character of a critically subsampled filter bank matches remarkably well with the cyclic properties of RS codes. Secondly, an extension of these techniques toward the more general class of BCH codes is presented. It is demonstrated that a BCH code can be decomposed into a sum of critically subsampled filter banks.

A Combination of CD28 (rs1980422 and IRF5 (rs10488631 Polymorphisms Is Associated with Seropositivity in Rheumatoid Arthritis: A Case Control Study.

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Lucia Vernerova

Full Text Available The aim of the study was to analyse genetic architecture of RA by utilizing multiparametric statistical methods such as linear discriminant analysis (LDA and redundancy analysis (RDA.A total of 1393 volunteers, 499 patients with RA and 894 healthy controls were included in the study. The presence of shared epitope (SE in HLA-DRB1 and 11 SNPs (PTPN22 C/T (rs2476601, STAT4 G/T (rs7574865, CTLA4 A/G (rs3087243, TRAF1/C5 A/G (rs3761847, IRF5 T/C (rs10488631, TNFAIP3 C/T (rs5029937, AFF3 A/T (rs11676922, PADI4 C/T (rs2240340, CD28 T/C (rs1980422, CSK G/A (rs34933034 and FCGR3A A/C (rs396991, rheumatoid factor (RF, anti-citrullinated protein antibodies (ACPA and clinical status was analysed using the LDA and RDA.HLA-DRB1, PTPN22, STAT4, IRF5 and PADI4 significantly discriminated between RA patients and healthy controls in LDA. The correlation between RA diagnosis and the explanatory variables in the model was 0.328 (Trace = 0.107; F = 13.715; P = 0.0002. The risk variants of IRF5 and CD28 genes were found to be common determinants for seropositivity in RDA, while positivity of RF alone was associated with the CTLA4 risk variant in heterozygous form. The correlation between serologic status and genetic determinants on the 1st ordinal axis was 0.468, and 0.145 on the 2nd one (Trace = 0.179; F = 6.135; P = 0.001. The risk alleles in AFF3 gene together with the presence of ACPA were associated with higher clinical severity of RA.The association among multiple risk variants related to T cell receptor signalling with seropositivity may play an important role in distinct clinical phenotypes of RA. Our study demonstrates that multiparametric analyses represent a powerful tool for investigation of mutual relationships of potential risk factors in complex diseases such as RA.

A Combination of CD28 (rs1980422) and IRF5 (rs10488631) Polymorphisms Is Associated with Seropositivity in Rheumatoid Arthritis: A Case Control Study.

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Vernerova, Lucia; Spoutil, Frantisek; Vlcek, Miroslav; Krskova, Katarina; Penesova, Adela; Meskova, Milada; Marko, Andrea; Raslova, Katarina; Vohnout, Branislav; Rovensky, Jozef; Killinger, Zdenko; Jochmanova, Ivana; Lazurova, Ivica; Steiner, Guenter; Smolen, Josef; Imrich, Richard

2016-01-01

The aim of the study was to analyse genetic architecture of RA by utilizing multiparametric statistical methods such as linear discriminant analysis (LDA) and redundancy analysis (RDA). A total of 1393 volunteers, 499 patients with RA and 894 healthy controls were included in the study. The presence of shared epitope (SE) in HLA-DRB1 and 11 SNPs (PTPN22 C/T (rs2476601), STAT4 G/T (rs7574865), CTLA4 A/G (rs3087243), TRAF1/C5 A/G (rs3761847), IRF5 T/C (rs10488631), TNFAIP3 C/T (rs5029937), AFF3 A/T (rs11676922), PADI4 C/T (rs2240340), CD28 T/C (rs1980422), CSK G/A (rs34933034) and FCGR3A A/C (rs396991), rheumatoid factor (RF), anti-citrullinated protein antibodies (ACPA) and clinical status was analysed using the LDA and RDA. HLA-DRB1, PTPN22, STAT4, IRF5 and PADI4 significantly discriminated between RA patients and healthy controls in LDA. The correlation between RA diagnosis and the explanatory variables in the model was 0.328 (Trace = 0.107; F = 13.715; P = 0.0002). The risk variants of IRF5 and CD28 genes were found to be common determinants for seropositivity in RDA, while positivity of RF alone was associated with the CTLA4 risk variant in heterozygous form. The correlation between serologic status and genetic determinants on the 1st ordinal axis was 0.468, and 0.145 on the 2nd one (Trace = 0.179; F = 6.135; P = 0.001). The risk alleles in AFF3 gene together with the presence of ACPA were associated with higher clinical severity of RA. The association among multiple risk variants related to T cell receptor signalling with seropositivity may play an important role in distinct clinical phenotypes of RA. Our study demonstrates that multiparametric analyses represent a powerful tool for investigation of mutual relationships of potential risk factors in complex diseases such as RA.

Telenovela y cultura en Brasil

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Fadul, Anamaria

1993-01-01

Trabajo sobre el surgimiento de la telenovela en Brasil. Se habla del papel de la telenovela en la cultura brasileña, de su audiencia, del panorama televisivo en ese país y de sus estrategias de programación. A la par del artículo, se presentan cuadros con información sobre las telenovelas mexicanas. Se incluyen ilustraciones de Lucía Maya, reproducidas en blanco y negro.

Perfil das intoxicações na infância atendidas pelo Centro de Informação Toxicológica do Rio Grande do Sul (CIT/RS, Brasil Caseload of poisoning among children treated by the Rio Grande do Sul State Toxicology Information Center (CIT/RS, Brazil

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Carla Luiza Job Ramos

2005-08-01

Full Text Available Estudo transversal descritivo analítico para estabelecer perfil das intoxicações em crianças de 0 a 4 anos, registradas no Centro de Informação Toxicológica do Rio Grande do Sul (CIT/RS, Porto Alegre, Brasil, 2003. Selecionados 1.311 casos, extraíram-se dados de crianças que sofreram intoxicação acidental individual dentro de suas residências. Em uma amostra do tipo aleatória sistemática de 286 pacientes, foram realizadas 21 entrevistas com responsáveis legais das crianças, utilizando-se instrumento estruturado. O perfil da intoxicação apresentou faixa etária de um ano; gênero masculino; via de exposição oral; agente tóxico localizado no chão da sala de estar ou no quarto; altura do móvel inferior a 30cm; horário da intoxicação entre 18h01-22h; tempo entre o acidente e a busca por uma conduta médica menor que 30 minutos; medicamento analgésico como agente tóxico; avaliação da intoxicação como não tóxica, evoluindo para a cura. Os dados indicam características relevantes quanto ao horário da intoxicação e local em que se encontravam os agentes tóxicos. A definição do perfil permite orientar e incrementar campanhas de prevenção de acidentes tóxicos na infância promovidas pelos órgãos públicos de saúde.This was an analytical, descriptive, cross-sectional study to establish the profile of poisonings among children 0 to 4 years of age reported to the Rio Grande do Sul State Toxicology Information Center (CIT/RS in Porto Alegre, Brazil, 2003. A total of 1,311 cases were selected and data were extracted on children who had suffered individual accidental poisoning inside the home. From a systematic random sample of 286 patients, 21 interviews were held with the children's parents or guardians, using a structured instrument. The typical profile of poisoning featured: < 1 year age bracket; male gender; oral exposure; poisonous agent located on living room or bedroom floor; furniture height < 30cm; time

Association between rs3087243 and rs231775 polymorphism within the cytotoxic T-lymphocyte antigen 4 gene and Graves' disease: a case/control study combined with meta-analyses

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Dai, Yu; Zeng, Tianshu; Xiao, Fei; Chen, Lulu; Kong, Wen

2017-01-01

We conducted a case/control study to assess the impact of SNP rs3087243 and rs231775 within the CTLA4 gene, on the susceptibility to Graves' disease (GD) in a Chinese Han dataset (271 cases and 298 controls). The frequency of G allele for rs3087243 and rs231775 was observed to be significantly higher in subjects with GD than in control subjects (p = 0.005 and p = 0.000, respectively). After logistic regression analysis, a significant association was detected between SNP rs3087243 and GD in the additive and recessive models. Similarly, association for the SNP rs231775 could also be detected in the additive model, dominant model and recessive model. A meta-analysis, including 27 published datasets along with the current dataset, was performed to further confirm the association. Consistent with our case/control results, rs3087243 and rs231775 showed a significant association with GD in all genetic models. Of note, ethnic stratification revealed that these two SNPs were associated with susceptibility to GD in populations of both Asian and European descent. In conclusion, our data support that the rs3087243 and rs231775 polymorphisms within the CTLA4 gene confer genetic susceptibility to GD. PMID:29299173

Polymorphisms rs12998 and rs5780218 in KiSS1 Suppressor Metastasis Gene in Mexican Patients with Breast Cancer

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Edhit Guadalupe Cruz Quevedo

2015-01-01

Full Text Available Aims. KiSS1 is a metastasis suppressor gene associated with inhibition of cellular chemotaxis and invasion attenuating the metastasis in melanoma and breast cancer cell lines. Along the KiSS-1 gene at least 294 SNPs have been described; however the association of these polymorphisms as genetic markers for metastasis in breast cancer studies has not been investigated. Here we describe two simple PCR-RFLPs protocols to identify the rs5780218 (9DelT and the rs12998 (E20K KiSS1 polymorphisms and the allelic, genotypic, and haplotypic frequencies in Mexican general population (GP and patients with benign breast disease (BBD or breast cancer (BC. Results. The rs5780218 polymorphism was individually associated with breast cancer (P=0.0332 and the rs12998 polymorphism shows statistically significant differences when GP versus case (BC and BBD groups were compared (P<0.0001. The H1 Haplotype (G/- occurred more frequently in BC group (0.4256 whereas H2 haplotype (G/T was the most prevalent in BBD group (0.4674. Conclusions. Our data indicated that the rs5780218 polymorphism individually confers susceptibility for development of breast cancer in Mexican population and a possible role as a genetic marker in breast cancer metastasis for H1 haplotype (Wt/variant in KiSS1 gene must be analyzed in other populations.

Pentatomídeos (Hemiptera associados a espécies nativas em Itaara, RS, Brasil

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Juliana Garlet

2010-04-01

Full Text Available http://dx.doi.org/10.5007/2175-7925.2010v23n1p91 Com o objetivo de determinar qualitativamente e quantitativamente os pentatomídeos associados a diferentes espécies botânicas nativas, no período de setembro de 2005 a setembro de 2006, foram coletados insetos em nove espécies: Gochnatia polymorpha (Less. (cambará, Eugenia uniflora Berg. (pitangueira, Acca selowiana (Berg Burret (goiaba-da-serra, Psidium cattleianum Sabine (araçá, Baccharis spp., Solanaum mauritianum Scop. (fumo-bravo, Micanea cinerascens Miq. (passiquinho, Calliandra brevipes Bhent. (caliandra, Schinus molle L. (aroeira, localizadas na barragem Rodolfo da Costa e Silva, município de Itaara, RS. Foram realizadas coletas quinzenais, com o auxílio de um funil cônico confeccionado com folha de flandres (2mm, com 70cm de diâmetro na maior abertura e 63cm de altura. Retirou-se uma amostra por espécie botânica por data de coleta, obtida através de dez sacudidas dos ramos sobre o funil. Realizadas as coletas, o material foi levado ao Laboratório de Entomologia do Departamento de Defesa Fitossanitária da Universidade Federal de Santa Maria, onde foi realizada a triagem e identificação do material. Foram identificadas nove espécies de Pentatomidae. Edessa rufomarginata (De Geer, 1773 foi à espécie com maior ocorrência, seguida de Thyanta humilis Bergroth, 1891. A espécie botânica S. mauritianum foi a que apresentou o maior número de espécies de Pentatomidae coletados, representando 26,9% do total.

Relationships between FTO rs9939609, MC4R rs17782313, and PPARγ rs1801282 polymorphisms and the occurrence of selected metabolic and hormonal disorders in middle-aged and elderly men – a preliminary study

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Rotter I

2016-11-01

Full Text Available Iwona Rotter,1 Karolina Skonieczna-Żydecka,2 Danuta Kosik-Bogacka,3 Grażyna Adler,2 Aleksandra Rył,4 Maria Laszczyńska4 1Department of Medical Rehabilitation, 2Department of Gerontobiology, 3Department of Biology and Medical Parasitology, 4Department of Histology and Developmental Biology, Pomeranian Medical University, Szczecin, Poland Purpose: Metabolic disorders, including MetS, obesity, and lipid disorders, may be related to genetic factors. Metabolic disorders are associated with decreased TS levels in aging men. The aim of this study was to evaluate the relationship between FTO rs9939609, MC4R rs17782313, and PPARɣ rs1801282 polymorphisms and the presence of MetS and its components, the concurrent lipid disorders, as well as sex hormone concentrations. Subjects and methods: This study involved 272 men of Caucasian descent aged 50–75 years. Lipid profile, including TCh, LDL, HDL, and TG, was evaluated by spectrophotometric method. Anthropometric measurements concerned WC and blood pressure. MetS was diagnosed according to the criteria of the IDF. Sex hormone profile, including TST, FTS, E2, DHEAS, and SHBG, was examined using enzyme-linked immunosorbent assay. Polymorphisms within FTO, MC4R, and PPARɣ genes were identified using polymerase chain reaction-restriction fragments length polymorphism. Results: This study did not show links between the analyzed genetic polymorphisms and the presence of MetS, T2DM, HT, and obesity. However, higher concentrations of TCh and LDL were found in men with the FTO rs9939609 polymorphism in the recessive mode of inheritance (P=0.03 and P=0.05, respectively. Lower WC was found to be associated with MC4R rs17782313 gene inherited in the same model (P=0.005. Conclusion: FTO rs9939609, MC4R rs17782313, and PPARɣ rs1801282 polymorphisms seem to have little effect on the incidence of metabolic malfunctions and no effect on androgen-related disorders in the examined middle-aged and elderly men

Frequency of suspected cases of neurocysticercosis detected by computed skull tomography in Santa Maria, RS, Brazil Freqüência de casos suspeitos de neurocisticercose em tomografias computadorizadas de crânio em Santa Maria, RS, Brasil

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José Edson Paz da SILVA

2000-02-01

Full Text Available Due to the lack of studies about neurocysticercosis in the South of Brazil, an investigation was conducted to determine the percentage of suspected cases of neurocysticercosis in computed tomography diagnoses in Santa Maria, RS, from January 1997 to December 1998. Of 6300 computed tomographies (CT of the skull performed at the private Hospital de Caridade Astrogildo de Azevedo, 80, i.e., 1.27% were suspected of neurocysticercosis. Fifty were women (62.5% and 30 were men (37.5%. The most frequent radiological manifestation indicating neurocysticercosis was the presence of calcifications (isolated or associated, with a 95% rate (76 cases, while the presence of hypodense lesions reached a 5% rate (4 cases. After routine analysis, each CT was evaluated again and the suspected cases were confirmed. The percentage of suspected cases of neurocysticercosis detected by CT in the present study carried out in Santa Maria was considered low (1.27%. This can be explained by the fact that tomography is not accessible to the economically underprivileged population of Santa Maria. We hope that the present study can alert the population and the professionals to the fact that neurocysticercosis is a more frequent disease than indicated by the few diagnoses made.Com o objetivo de iniciar um estudo sobre a neurocisticercose no Sul do Brasil, foi verificada a porcentagem de casos suspeitos de neurocisticercose em tomografia computadorizada de crânio (TCC em Santa Maria, entre janeiro de 1997 e dezembro de 1998. Os resultados mostraram que entre 6300 TCC realizadas no Hospital de Caridade Astrogildo de Azevedo, 80, isto é, 1,27% eram suspeitas de neurocisticercose. Constatamos que 50 eram mulheres (62,5% e 30 homens (37,5%. A manifestação radiológica mais freqüente para indicar neurocisticercose foi a calcificação (isolada ou associada com 95% (76 casos, enquanto a presença de lesões hipodensas foi de 5% (4 casos. Após a análise de rotina cada TCC foi

Ser Gitano y Brasileño: migración, interculturalidad y ciudadanía en el sureste de Brasil, 1936-2007

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Cairus, Brigitte Grossmann

2010-01-01

Full Text Available Este ensayo explora la manera en la que los gitanos del este europeo definen su identidad dentro de la nación brasileña en relación con otros inmigrantes, ya sean estos de su mismo continente de origen o de otra parte del mundo. Aunque la “gitanidad” ha sido reconocida como un elemento vital de la cultura brasileña, los romanís brasileños han ejercido presión para obtener apoyo político, visibilidad y derechos de ciudadanía. Analizando esta lucha, examinaremos la construcción de la identidad que los gitanos mantienen basándose en mitos, lenguaje, valores, creencias, símbolos y lazos de parentesco dentro y fuera de Brasil. Asimismo, también analizaremos el ethos de deambular, hecho persistente a pesar de que muchos romanís brasileños han adquirido propiedades privadas y negocios en las principales ciudades del país. Por último, es necesario mencionar que el proceso de aculturación ha sido ambiguo para los gitanos, quienes siguen siendo tratados con un alto grado de indeseabilidad y exclusión dentro de la sociedad brasileña, a pesar de su presencia en el país desde el siglo XVI. Al mismo tiempo, los gitanos mantienen un aura de libertad y misticismo en el imaginario cultural brasileño, la cual puede encontrarse en literatura, telenovelas e incluso en Umbanda, es decir, prácticas religiosas afrobrasileñas.

STAT4 rs7574865 G/T and PTPN22 rs2488457 G/C polymorphisms influence the risk of developing juvenile idiopathic arthritis in Han Chinese patients.

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Fan, Zhi-Dan; Wang, Fei-Fei; Huang, Hui; Huang, Na; Ma, Hui-Hui; Guo, Yi-Hong; Zhang, Ya-Yuan; Qian, Xiao-Qing; Yu, Hai-Guo

2015-01-01

Juvenile idiopathic arthritis (JIA) is a common autoimmune disease characterized by environmental influences along with several predisposing genes in the pathogenesis. The protein tyrosine phosphatase nonreceptor 22 (PTPN22) and signal transducer and activator of transcription factor 4 (STAT4) have been recognized as susceptibility genes for numerous autoimmune diseases. Associations of STAT4 rs7574865 G/T and PTPN22 (rs2488457 G/C and rs2476601 C/T) polymorphisms with JIA have repeatedly been replicated in several Caucasian populations. The aim of this study was to investigate the influence of three polymorphisms mentioned above on the risk of developing JIA in Han Chinese patients. Genotyping was performed on a total of 137 Chinese patients with JIA (JIA group) and 150 sex and age frequency-matched healthy volunteers (Control group). The single-nucleotide polymorphisms (SNP) were determined by using direct sequencing of PCR-amplified products. There were significant differences of PTPN22 rs2488457 G/C and STAT4 rs7574865 G/T polymorphisms between both groups. However, no significant difference was observed in distribution frequencies of PTPN22 rs2476601 polymorphism. The association with the PTPN22 rs2488457 G/C polymorphism remained significant in the stratifications by age at onset, ANA status, splenomegaly, lymphadenectasis and involvement joints. As with the STAT4 rs7574865 G/T polymorphisms, the enthesitis-related arthritis and presence of hepatomegaly had strong effect on the association. Our data strengthen STAT4 rs7574865 G/T and PTPN22 rs2488457 G/C polymorphisms as susceptibility factors for JIA.

STAT4 rs7574865 G/T and PTPN22 rs2488457 G/C polymorphisms influence the risk of developing juvenile idiopathic arthritis in Han Chinese patients.

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Zhi-Dan Fan

Full Text Available Juvenile idiopathic arthritis (JIA is a common autoimmune disease characterized by environmental influences along with several predisposing genes in the pathogenesis. The protein tyrosine phosphatase nonreceptor 22 (PTPN22 and signal transducer and activator of transcription factor 4 (STAT4 have been recognized as susceptibility genes for numerous autoimmune diseases. Associations of STAT4 rs7574865 G/T and PTPN22 (rs2488457 G/C and rs2476601 C/T polymorphisms with JIA have repeatedly been replicated in several Caucasian populations. The aim of this study was to investigate the influence of three polymorphisms mentioned above on the risk of developing JIA in Han Chinese patients. Genotyping was performed on a total of 137 Chinese patients with JIA (JIA group and 150 sex and age frequency-matched healthy volunteers (Control group. The single-nucleotide polymorphisms (SNP were determined by using direct sequencing of PCR-amplified products. There were significant differences of PTPN22 rs2488457 G/C and STAT4 rs7574865 G/T polymorphisms between both groups. However, no significant difference was observed in distribution frequencies of PTPN22 rs2476601 polymorphism. The association with the PTPN22 rs2488457 G/C polymorphism remained significant in the stratifications by age at onset, ANA status, splenomegaly, lymphadenectasis and involvement joints. As with the STAT4 rs7574865 G/T polymorphisms, the enthesitis-related arthritis and presence of hepatomegaly had strong effect on the association. Our data strengthen STAT4 rs7574865 G/T and PTPN22 rs2488457 G/C polymorphisms as susceptibility factors for JIA.

mir-126 rs4636297 and TGFβRI rs334348 functional gene variants are associated with susceptibility to endometriosis and its severity.

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Sepahi, Neda; Kohan, Leila; Jahromi, Athar Rasekh; Daneshbod, Yahya; Hoveidi, Elahe Nimi

2017-06-01

microRNAs (miRNAs) are negative regulators in a variety of cellular processes that occur in endometriosis. Therefore, functional polymorphisms in miRNA and miRNA binding sites may affect gene expression and contribute to susceptibility of endometriosis. In this study, we evaluated the association of two miRNA related polymorphisms, mir-126 rs4636297 and TGFβRI rs334348, with endometriosis risk and its severity. This case-control study was done on 157 endometriosis patients and 252 healthy women as a control group. Tetra amplification refractory mutation system-polymerase chain reaction (tetra-ARMS PCR) was designed to determine the polymorphisms. Our finding showed significant differences in genotype frequency of mir-126 rs4636297 between the groups (χ 2  = 6.26, p = 0.044). A significant protection against endometriosis was found for mir-126 rs4636297 in allele (G versus A allele: OR = 0.695, 95% CI = 0.519-0.931, p = 0.015) and genotype (GG versus AA genotype: OR = 0.451, 95%CI = 0.233-0.873, p = 0.018). Significant association was also observed between the A allele and severity of endometriosis (OR = 0.478, 95%CI = 0.297-0.768, p = 0.002). Moreover, we found a significant association between AA genotype with the risk of endometriosis (OR = 0.493, 95%CI = 0.250-0.970, p = 0.041) and its severity (OR = 0.240, 95%CI = 0.065-0.883, p = 0.032) regarding TGFβRI rs334348 polymorphism. These finding suggest that, for the first time, mir-126 rs4636297 and TGFβRI rs334348 polymorphisms may influence individual's susceptibility to endometriosis and its severity.

Prevalência de consumo alimentar entre hipertensos e diabéticos na cidade de Nova Boa Vista, Rio Grande do Sul, Brasil, 2013

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Kelli Destri

Full Text Available Resumo OBJETIVO: descrever o consumo alimentar em uma população de hipertensos e diabéticos de uma cidade do sul do Brasil. MÉTODOS: estudo transversal descritivo, realizado na cidade de Nova Boa Vista-RS, Brasil, entre junho e setembro de 2013; dados sobre consumo alimentar foram coletados utilizando-se o questionário do Sistema de Vigilância Alimentar e Nutricional (SISVAN, a adequação foi baseada no Guia Alimentar para a População Brasileira de 2008. RESULTADOS: foram incluídos 422 participantes (≥18 anos de idade; os alimentos que tiveram maior frequência de consumo recomendada foram salada crua (60,7%, frutas (73,0%, lácteos (61,4%, frituras (57,3%, salgados (66,4% e refrigerantes (76,3%; embutidos e doces foram os alimentos que tiveram maior frequência de consumo não recomendado, 34,8% e 23,9% respectivamente; a prevalência de consumo semanal recomendado de frutas foi 19% maior entre mulheres (p=0,004. CONCLUSÃO: o consumo alimentar na população do estudo parece estar de acordo com as frequências recomendadas, especialmente entre mulheres.

Association of ADORA1 rs2228079 and ADORA2A rs5751876 Polymorphisms with Gilles de la Tourette Syndrome in the Polish Population.

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Piotr Janik

Full Text Available Gilles de la Tourette syndrome (GTS is a neurodevelopmental disorder characterized by motor and vocal tics. Hyperactivity of dopaminergic transmission is considered a prime abnormality in the pathophysiology of tics. There are reciprocal antagonistic interactions between adenosine and dopamine transmission. The aim of the study was to analyze the association of two polymorphisms, rs2228079 in ADORA1 and rs5751876 in ADORA2A, with the risk of GTS and co-morbid disorders.A total of 162 Polish GTS patients and 270 healthy persons were enrolled in the study. Two polymorphisms were selected on the basis of knowledge of SNPs frequencies in ADORA1 and ADORA2A. Chi-square test was used for allelic and genotypic association studies. Association of genotypes with age of tic onset was analyzed with Mann-Whitney test. Multivariate logistic regression was used to find independent predictors of GTS risk.We found that the risk of GTS was associated with rs2228079 and rs5751876 polymorphisms. The GG+GT genotypes of rs2228079 in ADORA1 were underrepresented in GTS patients (p = 0.011, whereas T allele of rs5751876 in ADORA2A was overrepresented (p = 0.017. The GG genotype of rs2228079 was associated with earlier age of tic onset (p = 0.046. We found also that the minor allele G of rs2228079 was more frequent in GTS patients with depression as compared to the patients without depression (p = 0.015. Also the genotype GG was significantly more frequent in patients with obsessive compulsive disorder/behavior (OCD/OCB, p = 0.021 and depression (p = 0.032, as compared to the patients without these co-morbidities. The minor allele T frequency of rs5751876 was lower in GTS patients with co-morbid attention deficit hyperactivity disorder (p = 0.022, and TT+TC genotypes were less frequent in the non-OCD anxiety disorder group (p = 0.045.ADORA1 and ADORA2A variants are associated with the risk of GTS, co-morbid disorders, and may affect the age of tic onset.

The optimal algorithm for Multi-source RS image fusion.

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Fu, Wei; Huang, Shui-Guang; Li, Zeng-Shun; Shen, Hao; Li, Jun-Shuai; Wang, Peng-Yuan

2016-01-01

In order to solve the issue which the fusion rules cannot be self-adaptively adjusted by using available fusion methods according to the subsequent processing requirements of Remote Sensing (RS) image, this paper puts forward GSDA (genetic-iterative self-organizing data analysis algorithm) by integrating the merit of genetic arithmetic together with the advantage of iterative self-organizing data analysis algorithm for multi-source RS image fusion. The proposed algorithm considers the wavelet transform of the translation invariance as the model operator, also regards the contrast pyramid conversion as the observed operator. The algorithm then designs the objective function by taking use of the weighted sum of evaluation indices, and optimizes the objective function by employing GSDA so as to get a higher resolution of RS image. As discussed above, the bullet points of the text are summarized as follows.•The contribution proposes the iterative self-organizing data analysis algorithm for multi-source RS image fusion.•This article presents GSDA algorithm for the self-adaptively adjustment of the fusion rules.•This text comes up with the model operator and the observed operator as the fusion scheme of RS image based on GSDA. The proposed algorithm opens up a novel algorithmic pathway for multi-source RS image fusion by means of GSDA.

Quantitative evaluation of pairs and RS steganalysis

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Ker, Andrew D.

2004-06-01

We give initial results from a new project which performs statistically accurate evaluation of the reliability of image steganalysis algorithms. The focus here is on the Pairs and RS methods, for detection of simple LSB steganography in grayscale bitmaps, due to Fridrich et al. Using libraries totalling around 30,000 images we have measured the performance of these methods and suggest changes which lead to significant improvements. Particular results from the project presented here include notes on the distribution of the RS statistic, the relative merits of different "masks" used in the RS algorithm, the effect on reliability when previously compressed cover images are used, and the effect of repeating steganalysis on the transposed image. We also discuss improvements to the Pairs algorithm, restricting it to spatially close pairs of pixels, which leads to a substantial performance improvement, even to the extent of surpassing the RS statistic which was previously thought superior for grayscale images. We also describe some of the questions for a general methodology of evaluation of steganalysis, and potential pitfalls caused by the differences between uncompressed, compressed, and resampled cover images.

The origin of the RS CVn binaries

International Nuclear Information System (INIS)

Biermann, P.

1976-01-01

Six possible origins for the RS CVn binaries are considered based on the following possibilities. RS CVn binaries might now be either pre-main-sequence or post-main-sequence. A pre-main-sequence binary might not always have been a binary but might have resulted from fission of a rapidly rotating single pre-main-sequence star. The main-sequence counterparts might be either single stars or binaries. To decide which of the six origins is possible, the following observed data for the RS CVn binaries are considered: total mass, total angular momentum, lack of observed connection with regions of star formation, large space density, kinematical age, and the visual companion of WW Dra. In addition lifetimes and space densities of single stars and other types of binaries are considered. The only origin possible is that the RS CVn binaries are in a thermal phase following fission of a main-sequence single star. In this explanation the single star had a rapidly rotating core which became unstable due to the core contraction which made it begin to evolve off the main sequence. The present Be stars might be examples of such parent single stars. (Auth.)

COMPARAÇÃO GRÁFICA ENTRE CURVAS DE ÍNDICE DE SÍTIO PARA Pinus elliottii E Pinus taeda DESENVOLVIDAS NO SUL DO BRASIL

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Helio Tonini

2002-04-01

Full Text Available Este trabalho teve como objetivos estudar o crescimento em altura dominante para Pinus elliottii e Pinus taeda, mediante comparações entre as curvas de índice de sítio construídas para algumas regiões do estado do Rio Grande do Sul e outros Estados da Federação. Essas comparações indicaram que as curvas feitas por Tonini (2000 para as regiões da Serra do Sudeste e Litoral no estado do Rio Grande do Sul, não apresentaram o mesmo desenvolvimento em relação às curvas feitas por Scolforo e Machado (1988, para os estados do Paraná e Santa Catarina; Brasil (1989a, para a região de Passo Fundo RS, Marcolin (1990, para o Segundo Planalto Paranaense e Selle (1993, para a região de Cambará do Sul. No entanto, o comportamento em relação às curvas de índice de sítio feitas por Brasil (1989b, para a região de São Francisco de Paula mostraram-se semelhantes, havendo somente uma diferença de nível entre estas.

Petrography and geochemistry of the volcanic rocks of the Rodeio Velho Member, Ordovician of the Camaqua basin (RS-Brazil): preliminary results

International Nuclear Information System (INIS)

Almeida, Delia del Pilar M. de; Lopes, Ricardo da C.; Gomes, Cristiane H.; Lima, Larissa de.

2000-01-01

A geochemical study based in REE, minor elements and petrographic analyses from the volcanic rocks pertaining to the Rodeio Velho Member, comprising lava flows and epizonal intrusive bodies, both corresponding to andesites, subalkaline and alkaline basalts and trachyandesites; and stratified pyroclastic deposits, showed that fractional crystallization of deep source magma is the fundamental mechanism controlling the relationships among these rocks. This igneous event occurred in an alkaline intraplate environment, associated to a widespread extension tectonics, probably corresponding to a final stage of the Pan African - Brasiliano Orogeny during the Middle Ordovician. (author)

O Flúor nas águas subterrâneas da Formação Santa Maria, na região de Santa Cruz do Sul e Venâncio Aires, RS, Brasil

OpenAIRE

Maria Paula Casagrande Marimon

2006-01-01

Concentrações de fluoreto, até 11 mg L-1, têm sido detectadas no aqüífero da Formação Santa Maria, Sistema Aqüífero Guarani, na região central do Estado do Rio Grande do Sul, Brasil. As águas subterrâneas são utilizadas para abastecimento público e levaram a incidência de fluorose dental. Esta área é a maior produtora de tabaco no Brasil, com uma longa história de aplicação de fertilizantes. Duas hipóteses são investigadas na busca de elucidar a origem das anomalias de flúor, a primeira, se r...

[Medical assessments and measurements in ELSA-Brasil].

Science.gov (United States)

Mill, Jose Geraldo; Pinto, Karina; Griep, Rosane Härter; Goulart, Alessandra; Foppa, Murilo; Lotufo, Paulo A; Maestri, Marcelo K; Ribeiro, Antonio Luiz; Andreão, Rodrigo Varejão; Dantas, Eduardo Miranda; Oliveira, Ilka; Fuchs, Sandra C; Cunha, Roberto de Sá; Bensenor, Isabela M

2013-06-01

The article describes assessments and measurements performed in the Brazilian Longitudinal Study for Adult Health (ELSA-Brasil). Some assessments including anthropometric assessment, casual blood pressure measurement, and ankle-brachial index have an established clinical application while others including pulse wave velocity, heart rate variability, and carotid intima-media thickness have no established application and do not have reference values for healthy Brazilian population but may be important predictors of cardiovascular outcomes. Blood pressure measurement following postural change maneuver was included in the ELSA-Brasil because it has not been much tested in epidemiological studies. Innovative approaches were developed for assessing the ankle-brachial index using an automatic device instead of the mercury column to measure blood pressure and for assessing the anterior-posterior diameter of the right lobe of the liver by ultrasound for quantitative assessment of nonalcoholic fatty liver disease. All ELSA-Brasil subjects were younger (35 years or more) than those included in other cohorts studying subclinical atherosclerosis. The inclusion of younger individuals and a variety of assessments make the ELSA-Brasil a relevant epidemiology study nationwide and worldwide.

ROBATEL RS 24 packaging

International Nuclear Information System (INIS)

Robatel, M.; Bochard, C.

1986-01-01

The ROBATEL RS 24 packaging for light-water reactor fuel assemblies is discussed. The cask uses a strength frame of carbon steel sheets, lead gamma ray shielding, neutron shielding of aluminous concrete, a thermal protection system for the gamma shielding, and a natural convection thermal transfer system

Variedades da Democracia no Brasil

Directory of Open Access Journals (Sweden)

Fernando Bizzarro

Full Text Available Resumo Neste artigo apresentamos resultados coletados pelo projeto Variedades da Democracia para o Brasil. Descrevemos a evolução histórica da democracia brasileira entre 1900 e 2015 enfocando seus cinco principais componentes (eleitoral, liberal, participativo, deliberativo e igualitário e duas dimensões adjacentes ao regime (corrupção e partidos políticos. Por fim, nós comparamos os dados para o Brasil com resultados obtidos para outros países da América do Sul. A análise dos dados aponta: a. a existência de uma trajetória “em espiral” dos regimes políticos no Brasil, na qual novas experiências democráticas tendem a superar experiências anteriores em todos os quesitos; b. os avanços e limites da experiência democrática contemporânea em que se combinam bons resultados nos indicadores eleitoral, liberal e deliberativo da democracia, e resultados menos elevados nos componentes igualitário e participativo do regime, bem como em suas dimensões adjacentes.

Vad ersätter företagets avbrottsförsäkring?

OpenAIRE

Rosenqvist, Felix

2010-01-01

I arbetet redogörs för hur en avbrottsförsäkring är uppbyggd och hur ersättningen räknas ut i praktiken. I teoridelen behandlas försäkringshistoria, de frivilliga skadeförsäkringarna och mera djupgående avbrottsförsäkringen. Skadehanteringsprocessen beskrivs också i teoridelen. För att åskådliggöra ämnet har själva resultatredovisnigen förverkligats genom en fiktiv fallstudie. Detta för att göra det enklare för läsaren att förstå hur avbrottsförsäkringen fungerar i praktiken...

Association of the ENPP1 rs997509 polymorphism with obesity in ...

African Journals Online (AJOL)

) polymorphisms have been associated with metabolic traits. There is no data on the effect of ENPP1 in South African children or adults. Objective: To investigate the role of K121Q (rs1044498), rs997509 and rs9402349 in obesity and other ...

RS-34 (Peacekeeper Post Boost Propulsion System) Orbital Debris Application Concept Study

Science.gov (United States)

Esther, Elizabeth A.; Burnside, Christopher G.

2013-01-01

The Advanced Concepts Office (ACO) at the NASA Marshall Space Flight Center (MSFC) lead a study to evaluate the Rocketdyne produced RS-34 propulsion system as it applies to an orbital debris removal design reference mission. The existing RS-34 propulsion system is a remaining asset from the de-commissioned United States Air Force Peacekeeper ICBM program; specifically the pressure-fed storable bi-propellant Stage IV Post Boost Propulsion System. MSFC gained experience with the RS-34 propulsion system on the successful Ares I-X flight test program flown in the Ares I-X Roll control system (RoCS). The heritage hardware proved extremely robust and reliable and sparked interest for further utilization on other potential in-space applications. Subsequently, MSFC is working closely with the USAF to obtain all the remaining RS-34 stages for re-use opportunities. Prior to pursuit of securing the hardware, MSFC commissioned the Advanced Concepts Office to understand the capability and potential applications for the RS-34 Phoenix stage as it benefits NASA, DoD, and commercial industry. Originally designed, the RS-34 Phoenix provided in-space six-degrees-of freedom operational maneuvering to deploy multiple payloads at various orbital locations. The RS-34 Concept Study, preceded by a utilization study to understand how the unique capabilities of the RS-34 Phoenix and its application to six candidate missions, sought to further understand application for an orbital debris design reference mission as the orbital debris removal mission was found to closely mimic the heritage RS-34 mission. The RS-34 Orbital Debris Application Concept Study sought to identify multiple configurations varying the degree of modification to trade for dry mass optimization and propellant load for overall capability and evaluation of several candidate missions. The results of the RS-34 Phoenix Utilization Study show that the system is technically sufficient to successfully support all of the missions

Antimicrobial susceptibility among Enterococcus isolates from the city of Porto Alegre, RS, Brazil Sensibilidade aos antimicrobianos entre amostras de Enterococcus isolados na cidade de Porto Alegre, RS, Brasil

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Pedro Alves d'Azevedo

2004-09-01

Full Text Available Resistance to several classes of antimicrobial agents is a remarkable characteristic of enterococcal strains increasingly reported worldwide. Information about strains isolated in the southern region of Brazil is still limited. In this study, a total of 455 consecutive enterococcal isolates recovered from patients living in Porto Alegre, Brazil, were identified at species level and evaluated for their antimicrobial susceptibilities by agar diffusion testing. The most frequent species was E. faecalis (92.8%, followed by E. faecium (2.9%, E. gallinarum (1.5%, E. avium (1.1%, E. hirae (0.7%, E. casseliflavus (0.4%, E. durans (0.4%, and E. raffinosus (0.2%. According to the results of disk tests 62.0% of the strains were resistant to tetracycline, 42.6% to erythromycin, 24.8% to chloramphenicol, 22.6% to ciprofloxacin, 22.0% to norfloxacin, 3.5% to ampicillin, 3.5% to nitrofurantoin. High level resistance to aminoglycosides was found in 37.8% of the isolates, with 23.5% being resistant to gentamicin, 14.3% to streptomycin, and 2.8% to both gentamicin and streptomycin. No vancomycin resistant or b-lactamase producing isolates were found. The results indicate that a significant percentage of isolates are resistant to different antimicrobials, pointing out the need for control strategies to avoid dissemination of resistant isolates and for continuous surveillance for the detection of emerging resistance traits.A resistência a várias classes de agentes antimicrobianos é uma característica marcante dos enterococos observada em diferentes regiões geográficas. Informações sobre amostras isoladas na região sul do Brasil ainda são limitadas. No presente estudo, 455 enterococos isolados consecutivamente de pacientes moradores na cidade de Porto Alegre, Brasil, foram identificados ao nível de espécie e testados em relação a sua sensibilidade aos antimicrobianos através de testes de difusão em agar. As espécies mais freqüentes foram E

Consumo de nutrientes em idosos residentes em Porto Alegre (RS, Brasil: um estudo de base populacional

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Carina Duarte Venturini

2015-12-01

Full Text Available Resumo Para descrever o perfil de consumo de nutrientes e verificar a sua associação com as variáveis sociodemográficas e de saúde, desenvolveu-se um estudo transversal, de base populacional em uma amostra aleatória de 427 idosos residentes em Porto Alegre, Brasil. O consumo alimentar foi avaliado através do Inquérito Recordatório de 24 Horas e Investigação da História Dietética. Dos idosos entrevistados, 70% eram mulheres; 48,5% possuíam entre 60 e 69 anos; 68,8% possuíam menos de 8 anos de escolaridade; 39,0%, renda familiar entre 2 e 5 salários mínimos; e 58,4% não praticava exercício físico. A hipertensão foi a doença mais prevalente, e 54,9% dos idosos estavam abaixo do peso. Os homens consumiam mais calorias, proteínas, fibras, minerais e vitaminas do que as mulheres. O consumo de carboidrato e cálcio aumentou conforme o avanço da idade, assim como diminuiu a ingestão de zinco. A prática de exercício físico elevou o consumo de calorias, magnésio, potássio e fósforo. Quanto maior a escolaridade, maior é o consumo de vitaminas B6 e B12; quanto maior a renda familiar, maior o consumo de vitamina B6 e ácido fólico. Os resultados demonstram que há deficiências nutricionais na alimentação diária da nossa população de idosos, principalmente entre as mulheres e os indivíduos acima de 80 anos.

Eudragit RS PO nanoparticles for sustained release of pyridostigmine bromide

International Nuclear Information System (INIS)

Hoobakht, Fatemeh; Ganji, Fariba; Vasheghani-Farahani, Ebrahim; Mousavi, Seyyed Mohammad

2013-01-01

Pyridostigmine bromide (PB) is an inhibitor of cholinesterase, which is used in the treatment of myasthenia gravis and administered for protection against exposure to toxic nerve agents. Tests were done to investigate prolonging the half-life of PB and improving its release behavior. PB was loaded in nanoparticles (NPs) of Eudragit RS PO (Eu-RS) prepared using the technique of quasi emulsion solvent diffusion. Variables of output power of the sonicator, bath temperature and mixing time, were chosen as the optimization factors to obtain the minimum sized NPs. In addition, emulsions were tested at different ratios of drug-to-polymer by dynamic light scattering to determine size and zeta potential of NPs. UV-spectroscopy was used to determine PB content of the NPs. Drug-loaded NPs were characterized by scanning electron microscopy, X-ray diffraction, and Fourier transform infrared spectra. Results determined that mixing time had a significant impact on the size of Eu-RS NPs, but power output of sonicator and bath temperature had no significant effect. The particle size obtained at the optimum condition (power output of 70 W, bath temperature of 33 °C, and mixing time of 7 min) was less than 200 nm (optimum sizes were 138.9 and 179.5 nm for Eu-RS and PB-loaded Eu-RS NPs, respectively). The optimum PB-loaded Eu-RS NPs at the PB to Eu-RS weight ratio of 1–4 and 20 % of loaded PB released from the nanocarriers within 100 h

Eudragit RS PO nanoparticles for sustained release of pyridostigmine bromide

Energy Technology Data Exchange (ETDEWEB)

Hoobakht, Fatemeh; Ganji, Fariba, E-mail: fganji@modares.ac.ir; Vasheghani-Farahani, Ebrahim [Tarbiat Modares University, Biomedical Engineering Group, Chemical Engineering Department (Iran, Islamic Republic of); Mousavi, Seyyed Mohammad [Tarbiat Modares University, Biotechnology Group, Chemical Engineering Department (Iran, Islamic Republic of)

2013-09-15

Pyridostigmine bromide (PB) is an inhibitor of cholinesterase, which is used in the treatment of myasthenia gravis and administered for protection against exposure to toxic nerve agents. Tests were done to investigate prolonging the half-life of PB and improving its release behavior. PB was loaded in nanoparticles (NPs) of Eudragit RS PO (Eu-RS) prepared using the technique of quasi emulsion solvent diffusion. Variables of output power of the sonicator, bath temperature and mixing time, were chosen as the optimization factors to obtain the minimum sized NPs. In addition, emulsions were tested at different ratios of drug-to-polymer by dynamic light scattering to determine size and zeta potential of NPs. UV-spectroscopy was used to determine PB content of the NPs. Drug-loaded NPs were characterized by scanning electron microscopy, X-ray diffraction, and Fourier transform infrared spectra. Results determined that mixing time had a significant impact on the size of Eu-RS NPs, but power output of sonicator and bath temperature had no significant effect. The particle size obtained at the optimum condition (power output of 70 W, bath temperature of 33 Degree-Sign C, and mixing time of 7 min) was less than 200 nm (optimum sizes were 138.9 and 179.5 nm for Eu-RS and PB-loaded Eu-RS NPs, respectively). The optimum PB-loaded Eu-RS NPs at the PB to Eu-RS weight ratio of 1-4 and 20 % of loaded PB released from the nanocarriers within 100 h.

[Polymorphisms of TLR7 rs3853839 and rs179010 are associated with susceptibility to and severity of hand, foot and mouth disease caused by enterovirus 71 in male children].

Science.gov (United States)

Li, Yaping; Zhai, Song; Li, Mei; Wang, Yuan; Lu, Tong; Deng, Huiling; Zhang, Xin; Dang, Shuangsuo

2017-07-01

Objective To investigate whether the polymorphisms of TLR7/MyD88 signaling pathway is associated with the susceptibility to and severity of hand, foot and mouth disease (HFMD) caused by enterovirus 71 (EV71) in children. Methods We collected 180 EV71 HFMD cases and 201 healthy controls from both the Second Affiliated Hospital of Xi'an Jiaotong University and Xi'an Children's Hospital. The genotypes including rs3853839, rs179010 of TLR7, and rs7744 of MyD88 were detected in the 381 samples by SNPscan kit. Results The susceptibility risk (OR=2.343, 95%CI:1.516-3.621) and severity risk (OR=1.939, 95%CI: 1.064-3.521) of TLR7 rs3853839 allele C significantly increased in the male children with EV71 HFMD. Also, the susceptibility risk (OR=1.701, 95%CI: 1.142-2.535) and severity risk (OR=1.852, 95%CI: 1.038-3.305) of TLR7 rs179010 allele T significantly increased in the male children with EV71 HFMD. But there was no significant difference in the distribution of TLR7 rs179010 and rs3853839 genes between female children with EV71 HFMD and female controls. There was no correlation between the genetic polymorphisms of MyD88 rs7744 and the susceptibility to and severity of EV71 HFMD in the children. Conclusion Polymorphisms of TLR7 rs3853839 and rs179010 are correlated to the susceptibility to and severity of EV71 HFMD in male children.

Infrared observations of RS CVn stars

International Nuclear Information System (INIS)

Berriman, G.; De Campli, W.M.; Werner, M.W.; Hatchett, S.P.

1983-01-01

Infrared photometry is presented of the RS CVn binary stars AR Lac (1.2-10 μm) and MM Her (1.2-3.5 μm) as they egressed from their primary and secondary eclipses; of the eclipsing systems RS CVn and Z Her at maximum light (1.2-10 μm) and of the non-eclipsing systems UX Ari and HR 1099 (1.2-10 μm). An analysis of these and published V data based on flux ratio diagrams (linear analogues of colour-colour diagrams) shows that G and K stars supply the infrared light of these systems. None of these systems shows infrared emission from circumstellar matter. (author)

RS-Predictor models augmented with SMARTCyp reactivities

DEFF Research Database (Denmark)

Zaretzki, Jed; Rydberg, Patrik; Bergeron, Charles

2012-01-01

(82.3%) and merged(86.0%). Comprehensive datamining of each substrate set and careful statistical analyses of the predictions made by the different models revealed new insights into molecular features that control metabolic regioselectivity and enable accurate prospective prediction of likely SOMs.......RS-Predictor is a tool for creating pathway-independent, isozyme-specific site of metabolism (SOM) prediction models using any set of known cytochrome P450 substrates and metabolites. Until now, the RS-Predictor method was only trained and validated on CYP 3A4 data, but in the present study we...... report on the versatility the RS-Predictor modeling paradigm by creating and testing regioselectivity models for substrates of the nine most important CYP isozymes. Through curation of source literature, we have assembled 680 substrates distributed among CYPs 1A2, 2A6, 2B6, 2C19, 2C8, 2C9, 2D6, 2E1 and 3...

Do Schüler-Zeitung ao O Ateneu: marcas da cultura escolar nas páginas dos periódicos (São Leopoldo/RS, 1964-1973 - the Schüler-Zeitung ao The Athenaeum: marks school of culture on pages of periodicals (São Leopoldo/RS, 1964-1973

Directory of Open Access Journals (Sweden)

Luciane Sgarbi Santos Grazziotin

2013-04-01

Full Text Available O trabalho investiga o periódico O Ateneu, produzido pelos alunos de uma escola de São Leopoldo/RS, entre os anos de 1937 e 1973. O recorte escolhido foi as décadas de 1964 a 1973. A investigação de propôs a analisar os discursos referentes ao contexto da ditadura militar no Brasil. O Ateneu é tomado como um elemento da cultura material escolar que representa a possibilidade de tangenciar alguns aspectos referentes à cultura escolar de uma instituição de confissão luterana, representativa da Região do Vale do Rio dos Sinos. Observa-se que O Ateneu foi um espaço de afirmação e construções identitárias de um grupo de jovens estudantes secundaristas. Quanto aos discursos relativos ao regime ditatorial, percebe-se que as manifestações presentes no periódico aparecem, em sua maioria, de forma velada. No entanto, também é possível entender que os estudantes preocupavam-se com as questões sociais e políticas do país, pois, no ano de 1963, há registros de que nessa escola formou-se o Departamento de Estudos Políticos e Sociais Brasileiros - DEPSB - como órgão do Grêmio Estudantil. Nos registros do caderno de atas do DEPSB não só alunos, mas também um professor se reuniam normalmente no turno da noite para debater o que eles registraram como sendo temas atuais da política brasileira e internacional.Palavras-chave: cultura escolar, periódicos estudantis, memória, ditadura militar. THE SCHÜLER-ZEITUNG AO THE ATHENAEUM: MARKS SCHOOL OF CULTURE ON PAGES OF PERIODICALS (SÃO LEOPOLDO/RS, 1964-1973AbstractThe work investigates the journalTheAthenaeum, produced bystudents of a schooling São Leopoldo/RS, between the years1937 and1973.The clippingwashosent the decades from 1964 to 1973. Theresearchproposed to analyze thediscourses presentrelated to the contextof the military dictatorship in Brazil. TheAthenaeumis taken as an elementofmaterial cultureschoolthat represents thetangentpossibility ofsome aspects of the school

Association of IL28B SNPs rs12979860 and rs8099917 on Hepatitis C Virus-RNA Status in Donors/Recipients of Living Donor Liver Transplantation.

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King-Wah Chiu

Full Text Available To investigate the effect of IL28B single nucleotide polymorphisms (SNPs (rs8099917 and rs12979860 in the donors and recipients on the outcome of Hepatitis C virus-RNA clearance after living donor liver transplantation (LDLT. The rs8099917 and rs12979860 genotypes in 50 donor and recipients pairs were explored on the pre-operative day (POD and post-operative day 30 (POD30. There was a significant difference in HCV-RNA clearance before (12%, 6/50 and after (48%, 24/50 liver transplantation (P < 0.001. The rs8099917 genotype TT was dominant in both the recipients (82%, 41/50 and donors (86%, 43/50, but had no significant effect on HCV-RNA clearance (87.5%, 21/24 and recurrence (76.9%, 20/26 after LDLT. One recipient was detected with genotype GG on POD, which changed to genotype GT on POD30. Prevalence of rs12979860 genotype CT was 98% (49/50 recipient and 92% (46/50 donor and prevalence of genotype CC was 2% (1/50 recipient and 8% (4/50 donor on POD and POD30, respectively. Of the 4 recipients with rs12979860 genotype CC on POD30, 3 recipients (12.5%, 3/24 exhibited HCV clearance and 1 experienced recurrence (3.9%, 1/26, however, this was not statistically significant. In conclusion, alterations in IL28B SNP genotype may occur after LDLT, leading to modifications in the host genome or donor proteome by HCV. This predicted mechanism will need to be investigated further.

RS-485 Bus Design of a Missile Simulation Training System

Directory of Open Access Journals (Sweden)

Liu Fang

2013-07-01

Full Text Available In a missile simulation training system with one-master and multi-slaves distributed system structure, a universal controller is necessary due to the system composed with several controllers. In this research, the designed controllers communicate with each other and upper control computer through RS-485 field bus. RS-485 bus including interface circuits, transmission protocol, Cyclic Redundancy Check (CRC method and upper control test software is designed and proposed. The universal controller adopting the designed RS-485 interface circuits is connected through twisted-pair and makes the simulation system, then the controller is tested in line. The results show that the RS-485 bus communicates effectively using the protocol and CRC method, data transmission rates reaches 115.2 kbps, and has a good stability.

MARGEM DENTRO DA MARGEM: OLHAR ANGOLANO PARA O BRASIL

OpenAIRE

Montaury, Alexandre

2008-01-01

O ARTIGO PROPÕE UMA ANÁLISE DE UM DOS MAIS RECENTES TRABALHOS DO ESCRITOR RUY DUARTE DE CARVALHO, DESMEDIDA – LUANDA, SÃO PAULO, SÃO FRANCISCO E VOLTA: CRÓNICAS DO BRASIL (2006), PARA FORMULAR ENTENDIMENTOS ACERCA DO REDIMENSIONAMENTO DOS TRÂNSITOS CULTURAIS ENTRE O BRASIL E ANGOLA, NA EXPERIÊNCIA CONTEMPORÂNEA. O OBJETIVO DESTA PROPOSTA É PÔREM QUESTÃO A ESPECIFICIDADE DE UM OLHAR ANGOLANO PARA O BRASIL QUE, ALÉM DE LER A MARGEM DE DENTRO DA MARGEM, ATUALIZA AS FORMAS DE “COMUNHÃO DA EXPERIÊ...

The Drosha rs10719 T>C polymorphism is associated with preeclampsia susceptibility.

Science.gov (United States)

Rezaei, Mahnaz; Eskandari, Fatemeh; Mohammadpour-Gharehbagh, Abbas; Teimoori, Batool; Yaghmaei, Minoo; Mokhtari, Mojgan; Salimi, Saeedeh

2018-01-01

Drosha is a member of the micro RNA (miRNA) processing machinery that affects miRNA processing. Single-nucleotide polymorphisms (SNPs) in the Drosha gene might affect microRNA processing and the expression of various genes. The aim of this study is to investigate the association between SNPs in the Drosha gene and preeclampsia (PE) in the southeast of Iran. Genotyping of Drosha rs10719 and rs6877842 was performed using blood samples from 219 PE women and 205 healthy control subjects by a polymerase chain reaction-restriction fragment length polymorphism method. The Drosha rs10719TC genotype was significantly associated with 1.6-fold higher risk of PE (odds ratio (OR, 1.6 [95% CI, 1.1-2.4], P = 0.026). In addition, the frequency of the Drosha rs10719CC genotype was significantly higher in PE women and was associated with threefold higher risk of PE (OR 3 [95% CI 1.4-6.3], P = 0.004). There was no association between the Drosha rs6877842 polymorphism and PE susceptibility. The CC-GG combined genotype was associated with 3.4-fold higher risk of PE (OR 3.4 [95% CI 1.4-8.1], P = 0.007). The haplotype-based association analysis showed higher frequency of C-G haplotype of Drosha rs10719 and rs6877842 polymorphisms with the increased risk of PE 1.5-fold (OR 1.5 [95% CI 1.1 - 2], P = 0.01). The Drosha rs10719TC and CC genotypes were associated with PE risk. The CC-GG combined genotype and C-G haplotype of Drosha rs10719 and rs6877842 polymorphisms may increase PE susceptibility.

Association between MC4R rs17782313 polymorphism and overeating behaviors.

Science.gov (United States)

Yilmaz, Z; Davis, C; Loxton, N J; Kaplan, A S; Levitan, R D; Carter, J C; Kennedy, J L

2015-01-01

Melanocortins have a crucial role in appetite and weight regulation. Although the melanocortin 4 receptor (MC4R) gene has been repeatedly linked to obesity and antipsychotic-induced weight gain, the mechanism behind how it leads to this effect in still undetermined. The goal of this study was to conduct an in-depth and sophisticated analysis of MC4R polymorphisms, body mass index (BMI), eating behavior and depressed mood. We genotyped 328 individuals of European ancestry on the following MC4R markers based on the relevant literature on obesity and antipsychotic-induced weight gain: rs571312, rs17782313, rs489693, rs11872992, and rs8087522. Height and weight were measured, and information on depressed mood and overeating behaviors was obtained during the in-person assessment. BMI was associated with rs17782313 C allele; however, this finding did not survive correction for multiple testing (P = 0.018). Although rs17782313 was significantly associated with depressed mood and overeating behaviors, tests of indirect effects indicated that emotional eating and food cravings, rather than depressed mood, uniquely accounted for the effect of this marker and BMI (n = 152). To our knowledge, this is the first study to investigate the link between MC4R rs17782313, mood and overeating behavior, as well as to demonstrate possible mechanisms behind MC4R's influence on body weight. If replicated in a larger sample, these results may have important clinical implications, including potential for the use of MC4R agonists in the treatment of obesity and disordered eating.

FTO gene polymorphisms (rs9939609 and rs17817449) as predictors of Type 2 Diabetes Mellitus in obese Iraqi population.

Science.gov (United States)

Younus, Laith A; Algenabi, Abdul Hussein A; Abdul-Zhara, Mohammed S; Hussein, Majid K

2017-09-05

The variation of the SNPs in FTO (fat mass and obesity associated) gene are improved to be associated with obesity and type 2 diabetes (T2DM) in some ethnic groups for example in European while, this consistency is controversial in Asians and there were few studies in Iraqi population about the effect of this gene on the development of T2DM in obese patients. Therefore, the objective of this study is to investigate the impact of the two common FTO gene variants in the development of T2DM in obese Iraqi patients. A case-control study in which the FTO gene variants rs9939609 and rs17817449 were genotyping in a total of 800 individuals, 400 T2DM obese patients (patients group) and 400 healthy control obese volunteers (control group) to explore the relation of these SNPs with T2DM in obese Iraqi population. The patients group was enrolled from diabetic clinic in Al Najaf al Ashraf based on WHO guidelines of T2DM. From whole blood the DNA was extraction and genotyped by using ScaI and AlwNI enzymes respectively in the PCR-RFLP technique. Multinomial logistic regression was applied to compare the proportions of genotypes and alleles. The odd's ratio, t-test P value at 95% confidence interval were measured before and after adjustment of BMI, age and sex adjustment. The genetic power, Hardy Weinberg equilibrium and haplotype analysis were tested in the present study. It was observed that the presence of T allele in the two SNPs rs9939609 and rs17817449 in the FTO gene polymorphisms was associated with increased risk for the development of T2DM in Iraqi obese individuals. The minor allele (T) in rs9939609 was significantly higher (P=0.0001) in T2DM (31.25%) when compared with that of the control obese group (20%). The Homozygous genotype (TT) significantly (OR=3.25, CI 95% 1.87-5.64, P=0.000) increased the risk of T2DM by three folds with respect to those of wild type (AA) after adjustment for age, sex and BMI, furthermore, it was significantly increased the risk in the

Manganelli "posfaciado" no Brasil

Directory of Open Access Journals (Sweden)

Andrea Santurbano

2017-10-01

Full Text Available É sabido como o escritor italiano Giorgio Manganelli (1922-1990 amava escrever para seus livros orelhas e contracapas que, de alguma forma, dialogavam e integravam o próprio texto. Já em dois dos seus três livros traduzidos no Brasil – Hilarotragoedia (Imago, 1993 e Centúria (Iluminuras, 1995 –, encontram- se prefácios e introduções, sendo reposicionados ou parcialmente omitidos os peritextos, de acordo com a definição de Genette, originais. Este artigo, portanto, pretende analisar a diferente articulação dos paratextos nas edições traduzidas, a fim de refletir sobre as estratégias pensadas para a recepção no Brasil de um autor, sem dúvida, de difícil acesso.

Comparação gráfica entre curvas de índice de sítio para Pinus elliottii e Pinus taeda desenvolvidas no sul do Brasil.

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Helio Tonini

2010-08-01

Full Text Available Este trabalho teve como objetivos estudar o crescimento em altura dominante para Pinus elliottii e Pinus taeda, mediante comparações entre as curvas de índice de sítio construídas para algumas regiões do estado do Rio Grande do Sul e outros Estados da Federação. Essas comparações indicaram que as curvas feitas por Tonini (2000 para as regiões da Serra do Sudeste e Litoral no estado do Rio Grande do Sul, não apresentaram o mesmo desenvolvimento em relação às curvas feitas por Scolforo e Machado (1988, para os estados do Paraná e Santa Catarina; Brasil (1989a, para a região de Passo Fundo RS, Marcolin (1990, para o Segundo Planalto Paranaense e Selle (1993, para a região de Cambará do Sul. No entanto, o comportamento em relação às curvas de índice de sítio feitas por Brasil (1989b, para a região de São Francisco de Paula mostraram-se semelhantes, havendo somente uma diferença de nível entre estas.

Validation of Omron RS8, RS6, and RS3 home blood pressure monitoring devices, in accordance with the European Society of Hypertension International Protocol revision 2010.

Science.gov (United States)

Takahashi, Hakuo; Yoshika, Masamichi; Yokoi, Toyohiko

2013-01-01

Allowing patients to measure their blood pressure at home is recognized as being of clinical value. However, it is not known how often these measurements are taken correctly. Blood pressure monitors for home use fall into two types based on the position of the cuff, ie, at the upper arm or the wrist. The latter is particularly convenient, as measurements can be taken fully clothed. This study aimed to evaluate the performance of the wrist-type blood pressure monitors Omron RS8 (HEM-6310F-E), Omron RS6 (HEM-6221-E), and Omron RS3 (HEM-6130-E). A team of three trained doctors validated the performance of these devices by comparing the measurements obtained from these devices with those taken using a standard mercury sphygmomanometer. All the devices met the validation requirements of the European Society of Hypertension International Protocol revision 2010. The difference in blood pressure readings between the tested device and the standard mercury sphygmomanometer was within 3 mmHg, which is acceptable according to the European Society of Hypertension guidelines. All the home devices tested were found to be suitable for measuring blood pressure at home because their performance fulfilled the requirement of the guidelines.

Association between MC4R rs17782313 Polymorphism and Overeating Behaviours

Science.gov (United States)

Yilmaz, Zeynep; Davis, Caroline; Loxton, Natalie J.; Kaplan, Allan S.; Levitan, Robert D.; Carter, Jacqueline C.; Kennedy, James L.

2014-01-01

Background/Objectives Melanocortins play a crucial role in appetite and weight regulation. Although the melanocortin 4 receptor (MC4R) gene has been repeatedly linked to obesity and antipsychotic-induced weight gain, the mechanism behind how it leads to this effect in still undetermined. The goal of this study was to conduct an in-depth and sophisticated analysis of MC4R polymorphisms, body mass index (BMI), eating behaviour, and depressed mood. Subjects/Methods We genotyped 328 individuals of European ancestry on the following MC4R markers based on the relevant literature on obesity and antipsychotic-induced weight gain: rs571312, rs17782313, rs489693, rs11872992, and rs8087522. Height and weight were measured, and information on depressed mood and overeating behaviours was obtained during the in-person assessment. Results BMI was associated with rs17782313 C allele; however this finding did not survive correction for multiple testing (p=0.018). Although rs17782313 was significantly associated with depressed mood and overeating behaviours, tests of indirect effects indicated that emotional eating and food cravings, rather than depressed mood, uniquely accounted for the effect of this marker and BMI (n=152). Conclusions To our knowledge, this is the first study to investigate the link between MC4R rs17782313, mood and overeating behaviour, as well as to demonstrate possible mechanisms behind MC4R’s influence on body weight. If replicated in a larger sample, these results may have important clinical implications, including potential for the use of MC4R agonists in the treatment of obesity and disordered eating. PMID:24827639

Investigating the Correlation between rs1049305 and ‏rs10244884 Polymorphisms of AQP-1 Gene and Menorrhagia ‎in Adolescents

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S Madani

2014-02-01

Results: Regarding ‏‎rs1049305, the C minor allele showed more frequency in patients' group‏ (0.47 vs. 0.37.‎‎ The results revealed that GG genotype presents less probable risk ‎for menorrhagia. ‎‎ rs10244884‎ also shows the same frequency. Conclusion: It can be concluded that both variants are important in pathogenesis of menorrhagia and the results confirm the important role of Aquqporin–1 channel in menstruation as well as endometrium physiology.

The ARIES-RS power core - recent development in Li/V designs

International Nuclear Information System (INIS)

Sze Dai-Kai; Billone, M.C.; Hua, T.Q.; Tillack, M.; Najmabadi, F.; Wang Xueren; Malang, S.; El-Guebaly, L.A.; Sviatoslavsky, I.N.; Blanchard, J.P.; Crowell, J.A.; Khater, H.Y.; Mogahed, E.A.; Waganer, L.M.; Lee, D.; Cole, D.

1998-01-01

The ARIES-RS fusion power plant design study is based on reversed-shear (RS) physics with a Li/V (lithium breeder and vanadium structure) blanket. The reversed-shear discharge has been documented in many large tokamak experiments. The plasma in the RS mode has a high beta, low current, and low current drive requirement. Therefore, it is an attractive physics regime for a fusion power plant. The blanket system based on Li/V has high temperature operating capability, good tritium breeding, excellent high heat flux removal capability, long structural life time, low activation, low after heat and good safety characteristics. For these reasons, the ARIES-RS reactor study selected Li/V as the reference blanket. The combination of attractive physics and attractive blanket engineering is expected to result in a superior power plant design. This paper summarizes the power core design of the ARIES-RS power plant study. (orig.)

The Calcium-Sensing Receptor Gene Polymorphism rs1801725 and Calcium-Related Phenotypes in Hemodialysis Patients

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Alicja E. Grzegorzewska

2018-05-01

Full Text Available Background/Aims: The calcium-sensing receptor gene (CASR rs1801725 variant is responsible for a non-conservative amino-acid change (A986S in the calcium-sensing receptor cytoplasmic tail. We hypothesized that rs1801725 polymorphism might be helpful in understanding Ca-related abnormalities in HD patients. Methods: In 1215 subjects (245 on cinacalcet, we determined the associations of rs1801725 with secondary hyperparathyroidism (sHPT-related laboratory parameters, PTH-decreasing effect of cinacalcet hydrochloride, coronary artery disease (CAD, myocardial infarction (MI, nephrolithiasis-related ESRD, and mortality. CASR rs7652589(Ars1801725(G>T haplotypes and rs1801725 epistatic interactions with vitamin D signaling pathway genes were examined for associations with selected phenotypes. Results: The rs1801725 variant allele showed an increasing independent effect on plasma PTH (Pcorrected = 0.009. CASR rs7652589_rs1801725 AT haplotype was associated with 1.7-fold higher frequency of PTH levels over 437 pg/mL than the reference haplotype GG (P = 0.001. CASR rs7652589_rs1801725 AG haplotype was 1.5-fold more frequent in nephrolithiasis-related ESRD than the GG haplotype (P = 0.004. There were no significant associations between rs1801725, CAD, MI, and response to cinacalcet. Variant homozygosity of rs1801725 correlated independently with higher infection-related mortality compared with heterozygosity (HR 7.95, 95%CI 2.15 – 29.37, P = 0.003 and major homozygosity (HR 5.89, 95%CI 1.69 – 20.55, P = 0.040. CASR rs1801725 did not show epistatic interactions with vitamin D signaling pathway genes concerning tested associations. Conclusion: The variant allele of CASR rs1801725 solely and together with the variant allele of rs7652589 increases risk of more advanced sHPT. Homozygosity of the rs1801725 variant allele contributes to infection-related mortality in HD patients.

Physical activity in Brazil: lessons from ELSA-Brasil. Narrative review.

Science.gov (United States)

Pitanga, Francisco José Gondim; Almeida, Maria Conceição Chagas; Queiroz, Ciro Oliveira; Aquino, Estela Maria Leão de; Matos, Sheila Maria Alvim

2017-01-01

The Brazilian Longitudinal Study of Adult Health (ELSA-Brasil) was conducted among civil servants at six higher education institutions located in six Brazilian state capitals. The objective of this review was to identify the publications produced within the scope of ELSA-Brasil that analyzed the participants' physical activity. Review study using baseline data from ELSA-Brasil. Narrative review of Brazilian studies on physical activity produced using data from ELSA-Brasil participants. The prevalence of leisure-time physical activity (LTPA) among ELSA-Brasil participants was low (44.1% among men and 33.8% among women). The main factors associated were social (higher schooling and family income), environmental (living in places with conditions and opportunities for physical activity) and individual (not being obese, being retired, not smoking and positive perception of body image). The perception of facilities for walking in the neighborhood was positively associated with both LTPA and commuting-related physical activity. An active lifestyle was a protective factor against several cardiometa-bolic variables (hypertension, diabetes, lipid abnormalities and cardiovascular risk over the next 10 years). Comparison between LTPA and commuting-related physical activity showed that only LTPA had a protective effect against arterial hypertension. The prevalence of physical activity among ELSA-Brasil participants was low. The main determinants were social, environmental and personal. LTPA had a greater protective efect on cardio-metabolic outcomes than did commuting-related physical activity.

Genetic association of polymorphism rs1333049 with gout.

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Wang, Binbin; Meng, Dongmei; Wang, Jing; Liu, Shiguo; Zhou, Sirui; Miao, Zhimin; Han, Lin; Chu, Nan; Zhang, Kun; Ma, Xu; Li, Changgui

2011-09-01

We suspect that genes or loci that contribute to coronary artery disease (CAD) may also play a role in the pathogenesis of gout, since hyperuricaemia leads to gout, and serum uric acid (SUA) levels are potential risk factors for CAD. The single nucleotide polymorphism (SNP) rs1333049 (C/G) on chromosome 9p21 has been implicated in previous studies to be associated with CAD. The aim of this study was to evaluate the relationship between this SNP and gout pathogenesis. Nine hundred Chinese Han were recruited for this study (461 gout patients and 439 gout-free individuals). The rs1333049 SNP and surrounding sequences were PCR sequenced. There was a clear link between the rs1333049 genotypic and allelic frequencies between gout cases and controls (χ(2) = 6.81, df = 2, P = 0.033 by genotype; χ(2) = 6.63, df = 1, P = 0.01 by allele). There was a significantly increased risk of gout in carriers of the CC genotype (odds ratio = 1.43, 95% CI 1.07, 1.91). To the best of our knowledge, our findings are the first to establish an association of rs1333049 with gout in a Chinese Han population. Meanwhile, this SNP is homologous to miR-519 and miR-520.

O IDRC no Brasil

International Development Research Centre (IDRC) Digital Library (Canada)

sociais. Um destes pesquisadores finan- ciados pelo IDRC, Fernando Henrique. Cardoso, serviu o Brasil como ... Outorgado: Rede para a Pesquisa em. Sistemas e Serviços de ... e parcerias entre os setores público e privado. Maio de 2010.

Association of STAT4 rs7574865 and PTPN22 rs2476601 polymorphisms with rheumatoid arthritis and non-systemically reacting antibodies in Egyptian patients.

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El-Lebedy, Dalia; Raslan, Hala; Ibrahim, Alshaymaa; Ashmawy, Ingy; El-Aziz, Shereen Abd; Mohammed, Asmaa M

2017-09-01

The aim of this study was to investigate association of protein tyrosine phosphatase non-receptor type 22 (PTPN22) rs2476601 and signal transducer and activator of transcription 4 (STAT4) rs7574865 polymorphisms with rheumatoid arthritis (RA) susceptibility and to assess potential association with the status of rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) antibodies, serum neopterin, and disease activity. RF, anti-CCP antibodies, and neopterin were assayed in serum of 100 unrelated RA patients and 114 controls. STAT4 rs7574865 G/T and PTPN22 rs2476601 C/T polymorphisms were genotyped by the TaqMan allelic discrimination method. The frequency of STAT4 variant allele was significantly higher in RA patients than in controls (p = 0.01), while the variant allele of PTPN22 was identified in only two RA patients, in a heterozygous form and in none of control subjects. The frequency of STAT4 variant allele carrier genotypes (GT+TT) was significantly higher among RA patients than in controls (43.7 vs. 10.5%, p = 0.02) and associated with RA under additive and dominant models. The frequency of RF and anti-CCP positivity was significantly higher among RA patients carrying T allele genotypes compared to patients carrying wild genotype (P = 0.02 and 0.04, respectively). No significant associations between STAT4 variant and serum neopterin or disease activity parameters were identified. Our study confirmed the association of STAT4 rs7574865 polymorphism with RA and was the first to indicate an association with RF and anti-CCP antibodies positivity. We also found PTPN22 rs2476601 has no role in susceptibility to RA in Egyptian patients.

El IDRC en Brasil

International Development Research Centre (IDRC) Digital Library (Canada)

en 1985, el IDRC ayudó a intelectuales de ideas democráticas ... más sostenible. □ los países ... CENTRO INTERNACIONAL DE INVESTIGACIONES PARA EL DESARROLLO. El IDRC en Brasil ... a las personas y al medio ambiente. Investi-.

Polymorphic Variants rs3088442 and rs2292334 in the Organic Cation Transporter 3 (OCT3) Gene and Susceptibility Against Type 2 Diabetes: Role of their Interaction.

Science.gov (United States)

Mahrooz, Abdolkarim; Alizadeh, Ahad; Hashemi-Soteh, Mohammad Bagher; Ghaffari-Cherati, Maryam; Hosseyni-Talei, Seyyedeh Raheleh

2017-02-01

In this study, we investigated whether two common variants (rs3088442G>A and rs2292334G>A) in the organic cation transporter 3 (OCT3) gene, a high-capacity transporter widely expressed in various tissues, affect susceptibility to type 2 diabetes (T2D) in patients newly diagnosed with T2D. We performed a study with 150 newly diagnosed patients with T2D and 152 controls. The genetic analyses were performed using the restricted fragment length polymorphism (RFLP) after PCR amplification. For the rs3088442G>A variant, A allele carriers had a significantly lower odds ratio (OR) vs. GG homozygotes in the BMI A variant was associated with a decreased risk of T2D (OR = 0.016, p A in the 3'-untranslated region of the OCT3 gene in susceptibility to T2D, and that the protective role is maintained in the presence of risky alleles of the variant rs2292334G>A. The association of the A allele of rs3088442G>A with T2D become weaker in obese people than that of non-obese. If confirmed in other populations, the rs3088442G>A variant as a genetic marker may potentially assist in the identification of individuals at an increased risk of T2D. Copyright © 2017 IMSS. Published by Elsevier Inc. All rights reserved.

HISTÓRIA DAS IDÉIAS PEDAGÓGICAS NO BRASIL

OpenAIRE

Aline Perazzoli; Maristela Ferreira da Rocha; Sandino Hoff

2015-01-01

A interrogação sobre a história da educação no Brasil, as idéias educacionais componentes e o lugar a ela conferida na pesquisa e no ensino universitário constitui-se no tema central do livro História das idéias Pedagógicas no Brasil, elaborado a partir dos resultados da investigação conduzida pelo autor com Bolsa de Produtividade em Pesquisa do CNPq. Cobre o conjunto de idéias pedagógicas no Brasil desde 1549 até nossos dias. O professor Saviani é formado em Filosofia pela PUC − SP, é dou...

Physical activity in Brazil: lessons from ELSA-Brasil. Narrative review

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Francisco José Gondim Pitanga

2017-07-01

Full Text Available ABSTRACT CONTEXT AND OBJECTIVE: The Brazilian Longitudinal Study of Adult Health (ELSA-Brasil was conducted among civil servants at six higher education institutions located in six Brazilian state capitals. The objective of this review was to identify the publications produced within the scope of ELSA-Brasil that analyzed the participants’ physical activity. DESIGN AND SETTING: Review study using baseline data from ELSA-Brasil. METHODS: Narrative review of Brazilian studies on physical activity produced using data from ELSA-Brasil participants. RESULTS: The prevalence of leisure-time physical activity (LTPA among ELSA-Brasil participants was low (44.1% among men and 33.8% among women. The main factors associated were social (higher schooling and family income, environmental (living in places with conditions and opportunities for physical activity and individual (not being obese, being retired, not smoking and positive perception of body image. The perception of facilities for walking in the neighborhood was positively associated with both LTPA and commuting-related physical activity. An active lifestyle was a protective factor against several cardiometa-bolic variables (hypertension, diabetes, lipid abnormalities and cardiovascular risk over the next 10 years. Comparison between LTPA and commuting-related physical activity showed that only LTPA had a protective effect against arterial hypertension. CONCLUSIONS: The prevalence of physical activity among ELSA-Brasil participants was low. The main determinants were social, environmental and personal. LTPA had a greater protective efect on cardio-metabolic outcomes than did commuting-related physical activity.

High-Speed RaPToRS

Science.gov (United States)

Henchen, Robert; Esham, Benjamin; Becker, William; Pogozelski, Edward; Padalino, Stephen; Sangster, Thomas; Glebov, Vladimir

2008-11-01

The High-Speed Rapid Pneumatic Transport of Radioactive Samples (HS-RaPToRS) system, designed to quickly and safely move radioactive materials, was assembled and tested at the Mercury facility of the Naval Research Laboratory (NRL) in Washington D.C. A sample, which is placed inside a four-inch-diameter carrier, is activated before being transported through a PVC tube via airflow. The carrier travels from the reaction chamber to the end station where it pneumatically brakes prior to the gate. A magnetic latch releases the gate when the carrier arrives and comes to rest. The airflow, optical carrier-monitoring devices, and end gate are controlled manually or automatically with LabView software. The installation and testing of the RaPToRS system at NRL was successfully completed with transport times of less than 3 seconds. The speed of the carrier averaged 16 m/s. Prospective facilities for similar systems include the Laboratory for Laser Energetics and the National Ignition Facility.

Genetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish population

International Nuclear Information System (INIS)

Peña-Chilet, Maria; Ribas, Gloria; Blanquer-Maceiras, Maite; Ibarrola-Villava, Maider; Martinez-Cadenas, Conrado; Martin-Gonzalez, Manuel; Gomez-Fernandez, Cristina; Mayor, Matias; Aviles, Juan Antonio; Lluch, Ana

2013-01-01

Few high penetrance genes are known in Malignant Melanoma (MM), however, the involvement of low-penetrance genes such as MC1R, OCA2, ASIP, SLC45A2 and TYR has been observed. Lately, genome-wide association studies (GWAS) have been the ideal strategy to identify new common, low-penetrance susceptibility loci. In this case–control study, we try to validate in our population nine melanoma associated markers selected from published GWAS in melanoma predisposition. We genotyped the 9 markers corresponding to 8 genes (PARP1, MX2, ATM, CCND1, NADSYN1, CASP8, IRF4 and CYP2R1) in 566 cases and 347 controls from a Spanish population using KASPar probes. Genotypes were analyzed by logistic regression and adjusted by phenotypic characteristics. We confirm the protective role in MM of the rs3219090 located on the PARP1 gene (p-value 0.027). Additionally, this SNP was also associated with eye color (p-value 0.002). A second polymorphism, rs12203592, located on the IRF4 gene was associated with protection to develop MM for the dominant model (p-value 0.037). We have also observed an association of this SNP with both lentigines (p-value 0.014) and light eye color (p-value 3.76 × 10 -4 ). Furthermore, we detected a novel association with rs1485993, located on the CCND1 gene, and dark eye color (p-value 4.96 × 10 -4 ). Finally, rs1801516, located on the ATM gene, showed a trend towards a protective role in MM similar to the one firstly described in a GWAS study. To our knowledge, this is the first time that these SNPs have been associated with MM in a Spanish population. We confirmed the proposed role of rs3219090, located on the PARP1 gene, and rs12203592, located on the IRF4 gene, as protective to MM along the same lines as have previous genome-wide associated works. Finally, we have seen associations between IRF4, PARP1, and CCND1 and phenotypic characteristics, confirming previous results for the IRF4 gene and presenting novel data for the last two, suggesting that

Possíveis interações medicamentosas em pacientes polimedicados de Novo Hamburgo, RS, Brasil

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Denis Tasso da SILVA

2018-04-01

Full Text Available A expectativa de vida da população mundial tem aumentado e consequentemente, tem ocorrido aumento no nível de doenças crônico degenerativas e acréscimo no uso concomitantemente de medicamentos, caracterizando a polifarmácia, o que aumenta o risco de interações medicamentosas (IM. Desta forma, este trabalho teve como objetivo identificar possíveis IM entre os medicamentos utilizados por um grupo de pacientes polimedicados de Novo Hamburgo, RS. Foi realizado um estudo transversal com voluntários de um projeto de pesquisa durante sua entrevista inicial. Foram avaliados dados sócio-demográficos, patologias, medicamentos utilizados e suas IM. As doenças de base foram classificadas de acordo com o código internacional de doenças (CID-10 e os medicamentos utilizados classificados conforme os padrões Anatomical Therapeutic Chemical (ATC. As IM foram identificadas e classificadas conforme literatura e pelo sistema Micromedex®. Participaram do estudo 67 pacientes (62±9 anos, maioria do sexo feminino,74,6%, sendo que 76,1% dos pacientes apresentaram probabilidade de desenvolverem algum tipo de IM. Ao todo foram identificadas 157 possíveis IM, sendo 3,0±2,2 interações por paciente. Destas, 69,4% foram consideradas moderadas, 19,8% graves e 10,8% leves. 51,6% das interações ocorrem por mecanismo farmacodinâmico, 31,9% farmacocinético e 16,5% apresentam ambos mecanismos. A IM mais prevalente foi entre ácido acetilsalicílico e hidroclorotiazida. A maioria das IM identificadas foi do tipo grave ou moderada, com riscos consideráveis à saúde do paciente. Assim, as IM identificadas podem comprometer a segurança do paciente, evidenciando a relevância deste tema e a necessidade de avaliar e monitorar a terapêutica medicamentosa.

Association of interferon regulatory factor 4 gene polymorphisms rs12203592 and rs872071 with skin cancer and haematological malignancies susceptibility: a meta-analysis of 19 case–control studies

International Nuclear Information System (INIS)

Wang, Songtao; Yan, Qing; Chen, Pin; Zhao, Peng; Gu, Aihua

2014-01-01

Research has indicated that the rs12203592 and rs872071 interferon regulatory factor 4 (IRF4) gene polymorphisms correlate with the risk of cancer, especially skin cancer and haematological malignancies, but the results remain controversial. To understand better the effects of these two polymorphisms on skin cancer and haematological malignancies susceptibility, a cumulative meta-analysis was performed. We conducted a search using the PubMed and Web of Science databases for relevant case-control studies published before April 2014. Summary odds ratios (ORs) and corresponding 95% confidence intervals (CIs) were estimated using fixed- or random-effects models where appropriate. Heterogeneity test, publication bias test, and sensitivity analysis were also performed. In total, 11 articles comprised of 19 case–control studies were identified; five focused on the rs12203592 polymorphism with 7,992 cases and 8,849 controls, and six were on the rs872071 polymorphism with 3108 cases and 8300 controls. As for rs12203592, a significant correlation with overall skin cancer and haematological malignancies risk was found with the homozygote comparison model (OR = 1.566, 95% CI 1.087-2.256) and recessive model (OR = 1.526, 95% CI 1.107-2.104). For rs872071, a significantly elevated haematological malignancies risk was observed in all genetic models (homozygote comparison: OR = 1.805, 95% CI 1.402-2.323; heterozygote comparison: OR = 1.427, 95% CI 1.203-1.692; dominant: OR = 1.556, 95% CI 1.281-1.891; recessive: OR = 1.432, 95% CI 1.293-1.587; additive: OR = 1.349, 95% CI 1.201-1.515). Similarly, increased skin cancer and haematological malignancies risk was also identified after stratification of the SNP data by cancer type, ethnicity and source of controls for both polymorphisms. Our meta-analysis indicated that the rs12203592 and rs872071 IRF4 gene polymorphisms are associated with individual susceptibility to skin cancer and haematological malignancies. Moreover, the effect

Převodník Ethernet na RS-232

OpenAIRE

Dreiseitel, Jiří

2012-01-01

Práce je věnována problematice konstrukce převodníku Ethernet na RS-232 za pomocí jednočipového mikrokontroléru. Cílem je seznámit čtenáře se síťovou technologií Ethernet a technologií pro sériový přenos založený na protokolu RS-232 a zároveň s technologií vestavěných systémů pro konstrukci zařízení. Součástí práce je kompletní návrh převodníku Ethernet na RS-232 včetně návrhu a implementace firmware v jazyce C za využití LwIP TCP/IP stacku. Převodník je postaven na základě vývojového kitu ST...

Brasil y "América Latina" Brazil and "Latin America"

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Leslie Bethell

2012-06-01

Full Text Available Este ensayo, en parte historia de las ideas y en parte historia de las relaciones internacionales, examina la relación del Brasil con América Latina en perspectiva histórica. Durante más de un siglo, con posterioridad a la independencia, ni los intelectuales ni los gobiernos hispanoamericanos consideraron al Brasil como parte de "América latina". En cuanto a los intelectuales y los gobiernos brasileños, excepto por su relación con el Río de la Plata, sólo tenían ojos para Europa y, cada vez más después de 1889, los Estados Unidos. Cuando, en especial durante la Guerra Fría, los Estados Unidos, y por extensión el resto del mundo, comenzaron a tratar al Brasil como parte de América Latina, los gobiernos brasileños y los intelectuales brasileños, con la excepción de algunos de izquierda, seguían sin pensar al Brasil como parte integral de esta región. Desde el fin de la Guerra Fría, el Brasil ha comenzado a poner en práctica por primera vez una política de compromiso con sus vecinos en América del Sur.This essay, part history of ideas and part history of international relations, examines Brazil's relationship with Latin America in historical perspective. For more than a century after independence neither Spanish American intellectuals nor Spanish American governments considered Brazil part of 'America Latina'. For their part, Brazilian intellectuals and Brazilian governments, except for the Rio de la Plata, only had eyes for Europe and increasingly, after 1889, the United States. When, especially during the Cold War, the United States, and by extension the rest of the world, began to regard and treat Brazil as part of 'Latin America', Brazilian governments and Brazilian intellectuals, except some on the Left, still did not think of Brazil as an integral part of it. Since the end of the Cold War Brazil has for the first time pursued a policy of engagement with its neighbours -in South America.

Study on parallel and distributed management of RS data based on spatial database

Science.gov (United States)

Chen, Yingbiao; Qian, Qinglan; Wu, Hongqiao; Liu, Shijin

2009-10-01

With the rapid development of current earth-observing technology, RS image data storage, management and information publication become a bottle-neck for its appliance and popularization. There are two prominent problems in RS image data storage and management system. First, background server hardly handle the heavy process of great capacity of RS data which stored at different nodes in a distributing environment. A tough burden has put on the background server. Second, there is no unique, standard and rational organization of Multi-sensor RS data for its storage and management. And lots of information is lost or not included at storage. Faced at the above two problems, the paper has put forward a framework for RS image data parallel and distributed management and storage system. This system aims at RS data information system based on parallel background server and a distributed data management system. Aiming at the above two goals, this paper has studied the following key techniques and elicited some revelatory conclusions. The paper has put forward a solid index of "Pyramid, Block, Layer, Epoch" according to the properties of RS image data. With the solid index mechanism, a rational organization for different resolution, different area, different band and different period of Multi-sensor RS image data is completed. In data storage, RS data is not divided into binary large objects to be stored at current relational database system, while it is reconstructed through the above solid index mechanism. A logical image database for the RS image data file is constructed. In system architecture, this paper has set up a framework based on a parallel server of several common computers. Under the framework, the background process is divided into two parts, the common WEB process and parallel process.

ANÁLISE DENDROECOLÓGICA DE Ocotea pulchella Nees et Mart. ex Nees (CANELA LAGEANA NA SERRA GERAL DE SANTA MARIA, RS, BRASIL

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Peter Spathelf

2000-06-01

Full Text Available Foram estudadas as relações entre variáveis climáticas e o incremento em diâmetro do tronco de cinco árvores de Ocotea pulchella localizadas às margens de uma barragem no município de Itaára, RS. Os dados de crescimento, em diâmetro, foram obtidos mediante análise de tronco, utilizando-se seções transversais retiradas na altura de 1,3 m (DAP, sendo os incrementos radiais determinados por meio da média de quatro raios, diametralmente, opostos. As seqüências médias dos incrementos foram estandartizadas para salientar a variação a curto prazo. Os dados climáticos são oriundos da estação meteorológica do município de Santa Maria, RS. Foram calculadas grandezas climáticas compostas, como a evapotranspiração e o balanço hídrico, para melhor descrever as condições hídricas de crescimento das árvores. Foram determinados anéis de crescimento característicos e sensitividades das seqüências de crescimento. Possíveis mudanças no estado de competição das árvores e seu efeito no crescimento foram estudados. Além disso, foram relacionados o incremento radial e as variáveis climáticas selecionadas por intermédio de análise de correlação. Não foi possível identificar nenhuma variável climática que, coerentemente, tenha influenciado no incremento durante o período observado. Os resultados mostram que o excesso de água influencia no crescimento diamétrico das árvores.

Polymorphism of glucagon-like peptide-1 receptor gene (rs1042044 ...

African Journals Online (AJOL)

patience

2015-02-16

Feb 16, 2015 ... turnover via GLP-1 receptors (GLP1Rs) in postmenopausal state. Furthermore, polymorphisms in. GLP1R gene were suggested to affect the function of GLP1Rs and be associated with many diseases. However, the relationships between GLP1R polymorphisms and osteoporosis susceptibility and bone.

Polymorphism of glucagon-like peptide-1 receptor gene (rs1042044 ...

African Journals Online (AJOL)

Previous investigations indicated that glucagon-like peptide-1 (GLP-1) played important roles in bone turnover via GLP-1 receptors (GLP1Rs) in postmenopausal state. Furthermore, polymorphisms in GLP1R gene were suggested to affect the function of GLP1Rs and be associated with many diseases. However, the ...

Configuration control plan for the ports NCS IBM RS/6000

International Nuclear Information System (INIS)

Brown, A.S.

1996-01-01

This document describes the actions and responsibilities for maintaining the quality and integrity of the NS software resident on the IBM RS/6000 workstation managed by the Nuclear Criticality Safety group at the Portsmouth Gaseous Diffusion Plant. This document does not address the validation of NS software packages for the RS/6000

ASPECTOS FITOSSOCIOLÓGICOS DE FRAGMENTO DE FLORESTA ESTACIONAL DECIDUAL, SANTA MARIA, RS

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Solon Jonas Longhi

2000-08-01

Full Text Available Foi realizado estudo da vegetação em fragmento de floresta estacional decidual em processo de sucessão, em área da Associação Tabor (29o43'S; 53o47'W, no município de Santa Maria (RS, Brasil. Utilizaram-se dezesseis unidades amostrais de 10 x 20 m distribuídas de forma sistemática para avaliação (medição e identificação dos indivíduos com Circunferência à Altura do Peito (CAP igual ou maior de 30 cm e subunidades circulares com raios de 1,78 m para identificação e contagem da regeneração (indivíduos menores de 30 cm. Observou-se a ocorrência de 64 espécies arbóreas e arbustivas de 54 gêneros e 31 famílias. As espécies com maior valor de importância foram Myrocarpus frondosus, Cupania vernalis, Ocotea puberula, Patagonula americana, Casearia sylvestris, Luehea divaricata, Enterolobium contortisiliquum e Helietta apiculata. Na regeneração, as espécies com maior densidade de indivíduos foram Trichilia elegans, Nectandra megapotamica, Actinostemon concolor, Piper gaudichaudianum, Cupania vernalis, Hybanthus bigibbosus, Aiouea saligna e Parapiptadenia rigida. Constatou-se o contínuo processo de sucessão por meio da substituição de espécies nos estratos da floresta e algumas bem-representadas desde a regeneração até o estrato superior.

BDNF rs6265 methylation and genotype interact on risk for schizophrenia.

Science.gov (United States)

Ursini, Gianluca; Cavalleri, Tommaso; Fazio, Leonardo; Angrisano, Tiziana; Iacovelli, Luisa; Porcelli, Annamaria; Maddalena, Giancarlo; Punzi, Giovanna; Mancini, Marina; Gelao, Barbara; Romano, Raffaella; Masellis, Rita; Calabrese, Francesca; Rampino, Antonio; Taurisano, Paolo; Di Giorgio, Annabella; Keller, Simona; Tarantini, Letizia; Sinibaldi, Lorenzo; Quarto, Tiziana; Popolizio, Teresa; Caforio, Grazia; Blasi, Giuseppe; Riva, Marco A; De Blasi, Antonio; Chiariotti, Lorenzo; Bollati, Valentina; Bertolino, Alessandro

2016-01-01

Epigenetic mechanisms can mediate gene-environment interactions relevant for complex disorders. The BDNF gene is crucial for development and brain plasticity, is sensitive to environmental stressors, such as hypoxia, and harbors the functional SNP rs6265 (Val(66)Met), which creates or abolishes a CpG dinucleotide for DNA methylation. We found that methylation at the BDNF rs6265 Val allele in peripheral blood of healthy subjects is associated with hypoxia-related early life events (hOCs) and intermediate phenotypes for schizophrenia in a distinctive manner, depending on rs6265 genotype: in ValVal individuals increased methylation is associated with exposure to hOCs and impaired working memory (WM) accuracy, while the opposite is true for ValMet subjects. Also, rs6265 methylation and hOCs interact in modulating WM-related prefrontal activity, another intermediate phenotype for schizophrenia, with an analogous opposite direction in the 2 genotypes. Consistently, rs6265 methylation has a different association with schizophrenia risk in ValVals and ValMets. The relationships of methylation with BDNF levels and of genotype with BHLHB2 binding likely contribute to these opposite effects of methylation. We conclude that BDNF rs6265 methylation interacts with genotype to bridge early environmental exposures to adult phenotypes, relevant for schizophrenia. The study of epigenetic changes in regions containing genetic variation relevant for human diseases may have beneficial implications for the understanding of how genes are actually translated into phenotypes.

Santificado a una judía comunista: la recomodación de la identidad brasileña en Olga (Monjardin, Brasil, 2004

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Tzvi Tal

2006-01-01

Full Text Available El éxito del film “Olga” en el público brasileño y las contrapuestas interpretaciones de la figura histórica de Olga Benario Prestes que su exhibición provocó, indican su relevancia en los procesos de la identidad brasileña actual. El artículo propone una lectura alegórica del texto cinematográfico, donde el vaciamiento ideológico y político del pasado de la militancia revolucionaria en un film producido por el complejo mediático Globo, representa el acomodamiento de la identidad brasileña ante la frustración de las expectativas históricas: la presidencia de “Lula” no pone en marcha un proyecto de justicia social alternativo al sistema neoliberal imperante.

The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.

Science.gov (United States)

Schnitzler, Fabian; Friedrich, Matthias; Wolf, Christiane; Angelberger, Marianne; Diegelmann, Julia; Olszak, Torsten; Beigel, Florian; Tillack, Cornelia; Stallhofer, Johannes; Göke, Burkhard; Glas, Jürgen; Lohse, Peter; Brand, Stephan

2014-01-01

Very recently, a sub-analysis of genome-wide association scans revealed that the non-coding single nucleotide polymorphism (SNP) rs12212067 in the FOXO3A gene is associated with a milder course of Crohn's disease (CD) (Cell 2013;155:57-69). The aim of our study was to evaluate the clinical value of the SNP rs12212067 in predicting the severity of CD by correlating CD patient genotype status with the most relevant complications of CD such as stenoses, fistulas, and CD-related surgery. We genotyped 550 CD patients for rs12212067 (FOXO3A) and the three common CD-associated NOD2 mutations rs2066844, rs2066847, and rs2066847 and performed genotype-phenotype analyses. No significant phenotypic differences were found between the wild-type genotype TT of the FOXO3A SNP rs12212067 and the minor genotypes TG and GG independently from NOD2 variants. The allele frequency of the minor G allele was 12.7%. Age at diagnosis, disease duration, body mass index, surgery rate, stenoses, fistula, need for immunosuppressive therapy, and disease course were not significantly different. In contrast, the NOD2 mutant p.Leu1007fsX1008 (rs2066847) was highly associated with penetrating CD (p = 0.01), the development of fistulas (p = 0.01) and stenoses (p = 0.01), and ileal disease localization (p = 0.03). Importantly, the NOD2 SNP rs2066847 was a strong separator between an aggressive and a mild course of CD (p = 2.99×10(-5)), while the FOXO3A SNP rs12212067 did not separate between mild and aggressive CD behavior in our cohort (p = 0.35). 96.2% of the homozygous NOD2 p.Leu1007fsX1008 carriers had an aggressive disease behavior compared to 69.3% of the patients with the NOD2 wild-type genotype (p = 0.007). In clinical practice, the NOD2 variant p.Leu1007fsX1008 (rs2066847), in particular in homozygous form, is a much stronger marker for a severe clinical phenotype than the FOXO3A rs12212067 SNP for a mild disease course on an individual patient level despite its

Vascular endothelial growth factor (VEGF-related single nucleotide polymorphisms rs10738760 and rs6921438 are not associated with diabetic retinopathy (DR in Slovenian patients with type 2 diabetes mellitus (T2DM

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Rifet Terzić

2017-11-01

Full Text Available Diabetic retinopathy (DR is a complication of diabetes characterized by vascular permeability, increased tissue ischemia, and angiogenesis. One of the most important proteins involved in angiogenesis is vascular endothelial growth factor (VEGF, also known as VEGFA. A previous study demonstrated that two single nucleotide polymorphisms (SNPs, rs6921438 and rs10738760, account for nearly half the variation in circulating VEGF levels. The aim of our study was to assess the association between rs6921438 and rs10738760 and DR in Slovenian patients with type 2 diabetes mellitus (T2DM. This case-control study enrolled 1037 unrelated Slovenian individuals (Caucasians with T2DM. DR group included 415 T2DM patients with DR, while control group included 622 T2DM patients with no clinical signs of DR. The clinical and laboratory data were obtained from the medical records of the patients. The genotyping of rs6921438 and rs10738760 SNPs was carried out with real-time PCR assays. Significant differences were observed between patients with DR and controls in the duration of diabetes (p < 0.001, insulin therapy (p < 0.001, glycated hemoglobin (p = 0.001, body mass index (p = 0.002, total cholesterol (p = 0.002, and low-density lipoprotein cholesterol (p < 0.001. However, we did not observe significant differences in the genotype and allele distribution of the two SNPs, between DR and control group (p < 0.05. Logistic regression analysis showed that rs6921438 and rs10738760 were not independent genetic risk factors for DR in the co-dominant model adjusted for the above-mentioned clinical and laboratory data. In conclusion, VEGF-related SNPs rs10738760 and rs6921438 are not associated with DR in our group of Slovenian patients (Caucasians with T2DM.

Enhancement and feature extraction of RS images from seismic area and seismic disaster recognition technologies

Science.gov (United States)

Zhang, Jingfa; Qin, Qiming

2003-09-01

Many types of feature extracting of RS image are analyzed, and the work procedure of pattern recognizing in RS images of seismic disaster is proposed. The aerial RS image of Tangshan Great Earthquake is processed, and the digital features of various typical seismic disaster on the RS image is calculated.

Maternal mortality due to hemorrhage in Brazil Mortalidad materna en Brasil debida a hemorragia Mortalidade materna por hemorragia no Brasil

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Maria de Lourdes de Souza

2013-06-01

Full Text Available OBJECTIVE: to analyze the rates of maternal mortality due to hemorrhage identified in Brazil from 1997 to 2009. Methods: the time series and population data from the Brazilian Health Ministry, Mortality Information System and Live Birth Information System were examined. From the Mortality Information System, we initially selected all reported deaths of women between 10 and 49 years old, which occurred from January 1, 1997 to December 31, 2009 in Brazil, recorded as a "maternal death". RESULTS: during the research period, 22,281 maternal deaths were identified, among which 3,179 were due to hemorrhage, accounting for 14.26% of the total deaths. The highest rates of maternal mortality were found in the North and Northeast areas of Brazil. CONCLUSIONS: the Brazilian scenario shows regional inequalities regarding maternal mortality. It presents hemorrhaging as a symptom and not as a cause of death. OBJETIVO: analizar las tasas de mortalidad materna debida a hemorragia, identificadas en Brasil durante el periodo de 1997 a 2009. MÉTODOS: fueron examinados los datos de series temporales y de población del Ministerio de la Salud de Brasil, del Sistema de Información de Mortalidad y del Sistema de Información de Nacidos Vivos. Del Sistema de Información de Mortalidad, inicialmente seleccionamos todos los informes sobre muerte de mujeres con edad entre 10 y 49 años, que ocurrieron entre el 01 de enero de 1997 y el 31 de diciembre de 2009, en Brasil, clasificadas como "muertes maternas". RESULTADOS: durante el periodo de investigación, fueron identificadas 22.281 muertes maternas, entre las cuales 3.179 se debieron a hemorragia, siendo responsables por 14,26% del total de muertes. La tasa más alta de mortalidad materna fue encontrada en las regiones Norte y Noreste de Brasil. CONCLUSIONES: el escenario brasileño muestra desigualdades regionales en lo que se refiere a mortalidad materna; este presenta la hemorragia como un síntoma y no como la

Estratégias de desenvolvimento do Brasil e da China

OpenAIRE

Oliveira Júnior, Alcides Mário Amaral de

2011-01-01

Resumo: Este trabalho visa analisar as estratégias de desenvolvimento econômico de longo prazo, observando as experiências do Brasil e da China. O mundo era diferente três décadas atras. A economia do Brasil era maior do que a da China. Os anos de 1980 marcaram uma trajetória diferente entre estes dois países. A China cresceu nas últimas três décadas a taxas médias de 8% enquanto o Brasil ficou com uma média de 3% no mesmo período. O objetivo do presente trabalho é analisar quais os motivos d...

Association analysis of APOA5 rs662799 and rs3135506 polymorphisms with obesity in Moroccan patients.

Science.gov (United States)

Lakbakbi El Yaagoubi, F; Charoute, H; Bakhchane, A; Ajjemami, M; Benrahma, H; Errouagui, A; Kandil, M; Rouba, H; Barakat, A

2015-12-01

The aim of the present study is to explore the association between the APOA5 polymorphisms and haplotypes with obesity in Moroccan patients. The study was performed in 459 subjects, Obese (n=164) and non-obese (n=295). All subjects were genotyped for the APOA5 -1131T>C (rs662799) and c.56C>G (rs3135506) polymorphisms. The contribution of APOA5 polymorphisms and haplotypes in the increased risk of obesity were explored using logistic regression analyses. The -1131T>C and c.56C>G polymorphisms were significantly associated with obesity. Both polymorphisms were strongly associated with increased BMI. Analysis of constructed haplotypes showed a significant association between CG haplotype and susceptibility to obesity (OR [95%CI]=3.09 [1.93-4.97]; P<0.001). These results support a potential role for APOA5 common variants and related haplotypes as risk factors for obesity. Copyright © 2015 Elsevier Masson SAS. All rights reserved.

Evaluation of IFITM3 rs12252 Association With Severe Pediatric Influenza Infection.

Science.gov (United States)

Randolph, Adrienne G; Yip, Wai-Ki; Allen, Emma Kaitlynn; Rosenberger, Carrie M; Agan, Anna A; Ash, Stephanie A; Zhang, Yu; Bhangale, Tushar R; Finkelstein, David; Cvijanovich, Natalie Z; Mourani, Peter M; Hall, Mark W; Su, Helen C; Thomas, Paul G

2017-07-01

Interferon-induced transmembrane protein 3 (IFITM3) restricts endocytic fusion of influenza virus. IFITM3 rs12252_C, a putative alternate splice site, has been associated with influenza severity in adults. IFITM3 has not been evaluated in pediatric influenza. The Pediatric Influenza (PICFLU) study enrolled children with suspected influenza infection across 38 pediatric intensive care units during November 2008 to April 2016. IFITM3 was sequenced in patients and parents were genotyped for specific variants for family-based association testing. rs12252 was genotyped in 54 African-American pediatric outpatients with influenza (FLU09), included in the population-based comparisons with 1000 genomes. Splice site analysis of rs12252_C was performed using PICFLU and FLU09 patient RNA. In PICFLU, 358 children had influenza infection. We identified 22 rs12252_C homozygotes in 185 white non-Hispanic children. rs12252_C was not associated with influenza infection in population or family-based analyses. We did not identify the Δ21 IFITM3 isoform in RNAseq data. The rs12252 genotype was not associated with IFITM3 expression levels, nor with critical illness severity. No novel rare IFITM3 functional variants were identified. rs12252 was not associated with susceptibility to influenza-related critical illness in children or with critical illness severity. Our data also do not support it being a splice site. © The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail journals.permissions@oup.com.

A Radish Basic Helix-Loop-Helix Transcription Factor, RsTT8 Acts a Positive Regulator for Anthocyanin Biosynthesis

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Sun-Hyung Lim

2017-11-01

Full Text Available The MYB-bHLH-WDR (MBW complex activates anthocyanin biosynthesis through the transcriptional regulation. RsMYB1 has been identified as a key player in anthocyanin biosynthesis in red radish (Raphanus sativus L., but its partner bHLH transcription factor (TF remains to be determined. In this study, we isolated a bHLH TF gene from red radish. Phylogenetic analysis indicated that this gene belongs to the TT8 clade of the IIIF subgroup of bHLH TFs, and we thus designated this gene RsTT8. Subcellular localization analysis showed that RsTT8-sGFP was localized to the nuclei of Arabidopsis thaliana protoplasts harboring the RsTT8-sGFP construct. We evaluated anthocyanin biosynthesis and RsTT8 expression levels in three radish varieties (N, C, and D that display different red phenotypes in the leaves, root flesh, and root skins. The root flesh of the C variety and the leaves and skins of the D variety exhibit intense red pigmentation; in these tissues, RsTT8 expression showed totally positive association with the expression of RsMYB1 TF and of five of eight tested anthocyanin biosynthesis genes (i.e., RsCHS, RsCHI, RsF3H, RsDFR, and RsANS. Heterologous co-expression of both RsTT8 and RsMYB1 in tobacco leaves dramatically increased the expression of endogenous anthocyanin biosynthesis genes and anthocyanin accumulation. Furthermore, a yeast two-hybrid assay showed that RsTT8 interacts with RsMYB1 at the MYB-interacting region (MIR, and a transient transactivation assay indicated that RsTT8 activates the RsCHS and RsDFR promoters when co-expressed with RsMYB1. Complementation of the Arabidopsis tt8-1 mutant, which lacks red pigmentation in the leaves and seeds, with RsTT8 restored red pigmentation, and resulted in high anthocyanin and proanthocyanidin contents in the leaves and seeds, respectively. Together, these results show that RsTT8 functions as a regulatory partner with RsMYB1 during anthocyanin biosynthesis.

Brasil y Argentina, 1990-2005

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Marina Gabriela Zunino

2008-01-01

Full Text Available Con el objetivo de analizar la mortalidad por armas de fuego en Brasil y Argentina entre 1990 y 2005, se realizó un estudio epidemiológico descriptivo utilizando datos oficiales de mortalidad de ambos países. Se analizaron número, proporción y tasas crudas y ajustadas para cada tipo de muerte (catalogadas según la CIE-9a y CIE-10a, el total por año y el promedio anual del período, sexo y edad. Los perfiles globales de los dos países presentaron tendencia creciente, pero Brasil mostró valores superiores de muertes y homicidios por armas de fuego en todo el período. A partir de los resultados se discute la hipótesis: el perfil de Brasil, particularmente el de homicidios por armas de fuego, es consecuencia no solo de la violencia social que responde a la persistentemente alta desigualdad y exclusión en que vive gran parte de la población, sino también al surgimiento, expansión y fortalecimiento de diversos grupos armados en ese país. El perfil argentino resultaría en parte del aumento de la violencia social también como respuesta al deterioro socioeconómico imperante, y por otra parte, sería consecuencia de la histórica monopolización de la violencia por parte del Estado

Association between rs6812193 polymorphism and sporadic Parkinson's disease susceptibility.

Science.gov (United States)

Huo, Qiang; Li, Tao; Zhao, Peiqing; Wang, Lianqing

2015-08-01

Recently, the association of a single nucleotide polymorphism rs6812193 C/T with sporadic Parkinson's disease (PD) susceptibility has been widely evaluated, but the results remained inconsistent. This association should be clarified because of the importance of it on human health and quality of life. We performed a comprehensive meta-analysis to evaluate the association between the rs6812193 polymorphism and sporadic PD. PubMed was used to retrieve articles published up to June 2014 for all studies evaluating the rs6812193 polymorphism and PD in humans. Ethnicity-specific subgroup analysis was also performed based on ethnicity susceptibility. A total of 17 independent study samples (15 Caucasians and 2 Asians) including 17,956 cases and 52,751 controls were used in the presented study. The MAFT (minor allele T frequency) in PD patients of European descent is obviously higher than Asian cases (p susceptibility among overall samples (OR 0.882, 95 % CI 0.856-0.908) and Caucasian population (OR 0.881, 95 % CI 0.856-0.907), but not in Asian samples (OR 0.918, 95 % CI 0.721-1.168). No evidence of publication bias was observed. Throughout our analysis, the rs6812193 polymorphism is significantly associated with sporadic PD susceptibility in Caucasian samples, and ethnicity might be the key point of inconsistency in rs6812193 studies. Further studies are warranted to re-examine the observed associations, especially in different ethnicities.

rs3806268 of NLRP3 gene polymorphism is associated with the development of primary gout.

Science.gov (United States)

Deng, Jianping; Lin, Wen; Chen, Yunpeng; Wang, Xin; Yin, Zhong; Yao, Chunhong; Liu, Tangbing; Lv, Yonghong

2015-01-01

The aim of the present study was to investigate the association between seven functional SNPs in NALP3 gene and the susceptibility to primary gout. A total of 247 patients with primary gout and 247 controls were selected in this study. Genotyping of NALP3 rs4612666, rs3806268, rs12239046, rs10754558, rs7512998, rs12137901 and rs12565738 was performed using the Sequenom MassARRAY platform. Comparison analysis showed that primary gout patients were more likely to have a higher body mass index, DBP, SBP, TG, urea nitrogen and uric acid (P gout when compared with the AA genotype (OR=1.83, 95% CI=1.03-3.26). However, no significant associations were identified for the remaining SNPs. In conclusion, we found a significant association between rs3806268 in NLRP3 gene and the risk of primary gout in a Chinese population. Further clinical and genetic studies are required to investigate the mechanisms underlying the association between NALP3 polymorphisms and the development of primary gout.

La experiencia brasileña

OpenAIRE

Barbosa, Phidias

2011-01-01

16 transparencias.-- Presentado en: Tercer Seminario internacional TECMERIN "Televisión digital terrestre: confrontando las experiencias brasileña y española", celebrado del 18 al 20 de enero de 2011 en la Universidad Carlos III de Madrid

Polymorphisms in TRPV1 and TAS2Rs associate with sensations from sampled ethanol.

Science.gov (United States)

Allen, Alissa L; McGeary, John E; Hayes, John E

2014-10-01

Genetic variation in chemosensory genes can explain variability in individual's perception of and preference for many foods and beverages. To gain insight into variable preference and intake of alcoholic beverages, we explored individual variability in the responses to sampled ethanol (EtOH). In humans, EtOH elicits sweet, bitter, and burning sensations. Here, we explore the relationship between variation in EtOH sensations and polymorphisms in genes encoding bitter taste receptors (TAS2Rs) and a polymodal nociceptor (TRPV1). Caucasian participants (n = 93) were genotyped for 16 single nucleotide polymorphisms (SNPs) in TRPV1, 3 SNPs in TAS2R38, and 1 SNP in TAS2R13. Participants rated sampled EtOH on a generalized Labeled Magnitude Scale. Two stimuli were presented: a 16% EtOH whole-mouth sip-and-spit solution with a single time-point rating of overall intensity and a cotton swab saturated with 50% EtOH on the circumvallate papillae (CV) with ratings of multiple qualities over 3 minutes. Area-under-the-curve (AUC) was calculated for the time-intensity data. The EtOH whole-mouth solution had overall intensity ratings near "very strong." Burning/stinging had the highest mean AUC values, followed by bitterness and sweetness. Whole-mouth intensity ratings were significantly associated with burning/stinging and bitterness AUC values on the CV. Three TRPV1 SNPs (rs224547, rs4780521, rs161364) were associated with EtOH sensations on the CV, with 2 (rs224547 and rs4780521) exhibiting strong linkage disequilibrium. Additionally, the TAS2R38 SNPs rs713598, rs1726866, and rs10246939 formed a haplotype, and were associated with bitterness on the CV. Last, overall intensity for whole-mouth EtOH associated with the TAS2R13 SNP rs1015443. These data suggest genetic variation in TRPV1 and TAS2Rs influence sensations from sampled EtOH and may potentially influence how individuals initially respond to alcoholic beverages. Copyright © 2014 by the Research Society on Alcoholism.

A atenção em saúde mental aos adolescentes em conflito com a lei no Brasil

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Nilson do Rosário Costa

Full Text Available Resumo O trabalho analisa a utilização de medicamentos psicoativos por adolescentes infratores em unidades socioeducativas (USES no Brasil. Descreve as diretrizes da política pública nacional e a qualidade da coordenação da atenção em saúde mental pelos governos subnacionais. O artigo tem como hipótese que a governança verticalizada da USES está associada à utilização de medicação psicoativa. O modelo da pesquisa foi estudo comparado dos casos do Rio Grande do Sul (RS e Minas Gerais. Os dados resultaram da coleta em prontuários e entrevistas com informantes-chave. O artigo demonstra que a governança vertical observada no RS está associada à alta prevalência de diagnósticos de transtorno mental, uso de medicamentos psicoativos e de medicalização psiquiátrica pelos adolescentes privados de liberdade. As evidências revelam que as sanções de privação de liberdade por atos infracionais produzem decisões de medicalização que ameaçam o direito dos adolescentes no campo da saúde. As diretrizes da política nacional incentivam escolhas mais cautelosas. As psicoterapias e as ações de reabilitação são as intervenções de primeira linha defendidas. O manejo pouco cuidadoso da intervenção psicofarmacológica favorece a múltiplas prescrições.

Impact of Gene rs7422339 Polymorphism in Argentine Patients With Hyperhomocysteinemia

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Silene M. Silvera-Ruiz BSc

2015-05-01

Full Text Available Carbamoyl phosphate synthetase 1 ( CPS1 is a key gene in the first step of urea cycle and has been correlated with nitric oxide level and vascular smooth muscle activity. A functional single-nucleotide polymorphism C/A at position 4217 in CPS1 (National Center for Biotechnology Information SNP database no. rs7422339, T1405N was reported to be associated with high homocysteine (Hcy plasma values. Although genetic variants of methylenetetrahydrofolate reductase ( MTHFR gene are known to influence Hcy concentration, other genetic determinants of Hcy remain largely unknown. The association between the CPS1 rs7422339 and the risk of hyperhomocysteinemia in Latin American populations is unknown. Here, we study this association in 100 patients having hyperhomocysteinemia without MTHFR c.677C>T polymorphism and 100 controls. CPS1 rs7422339 was studied using polymerase chain reaction and enzymatic restriction. Comparisons of the CPS1 rs7422339 genotype distributions revealed a significant difference between groups ( P = 2.3 × 10 −3 . Patients carrying polymorphic allele showed almost 3 times higher risk (odds ratio [OR] = 2.47 of hyperhomocysteinemia than wild-type allele, suggesting that rs7422339 SNP is associated with high Hcy levels in the Argentine population.

The NOD2 p.Leu1007fsX1008 mutation (rs2066847 is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.

Directory of Open Access Journals (Sweden)

Fabian Schnitzler

Full Text Available Very recently, a sub-analysis of genome-wide association scans revealed that the non-coding single nucleotide polymorphism (SNP rs12212067 in the FOXO3A gene is associated with a milder course of Crohn's disease (CD (Cell 2013;155:57-69. The aim of our study was to evaluate the clinical value of the SNP rs12212067 in predicting the severity of CD by correlating CD patient genotype status with the most relevant complications of CD such as stenoses, fistulas, and CD-related surgery.We genotyped 550 CD patients for rs12212067 (FOXO3A and the three common CD-associated NOD2 mutations rs2066844, rs2066847, and rs2066847 and performed genotype-phenotype analyses.No significant phenotypic differences were found between the wild-type genotype TT of the FOXO3A SNP rs12212067 and the minor genotypes TG and GG independently from NOD2 variants. The allele frequency of the minor G allele was 12.7%. Age at diagnosis, disease duration, body mass index, surgery rate, stenoses, fistula, need for immunosuppressive therapy, and disease course were not significantly different. In contrast, the NOD2 mutant p.Leu1007fsX1008 (rs2066847 was highly associated with penetrating CD (p = 0.01, the development of fistulas (p = 0.01 and stenoses (p = 0.01, and ileal disease localization (p = 0.03. Importantly, the NOD2 SNP rs2066847 was a strong separator between an aggressive and a mild course of CD (p = 2.99×10(-5, while the FOXO3A SNP rs12212067 did not separate between mild and aggressive CD behavior in our cohort (p = 0.35. 96.2% of the homozygous NOD2 p.Leu1007fsX1008 carriers had an aggressive disease behavior compared to 69.3% of the patients with the NOD2 wild-type genotype (p = 0.007.In clinical practice, the NOD2 variant p.Leu1007fsX1008 (rs2066847, in particular in homozygous form, is a much stronger marker for a severe clinical phenotype than the FOXO3A rs12212067 SNP for a mild disease course on an individual patient level despite

Hsa-miR-34b/c rs4938723 T>C and hsa-miR-423 rs6505162 C>A polymorphisms are associated with the risk of esophageal cancer in a Chinese population.

Directory of Open Access Journals (Sweden)

Jun Yin

Full Text Available Esophageal cancer is the eighth most common cancer and sixth leading cause of cancer associated death worldwide. Besides environmental risk factors, genetic factors might play an important role in the esophageal cancer carcinogenesis. We conducted a hospital based case-control study to evaluate the genetic susceptibility of functional single nucleotide polymorphisms (SNPs in the microRNAs on the development of esophageal cancer. A total of 629 esophageal squamous cell carcinoma (ESCC cases and 686 controls were recruited for this study. The hsa-miR-34b/c rs4938723 T>C, pri-miR-124-1 rs531564 C>G, pre-miR-125a rs12975333 G>T and hsa-miR-423 rs6505162 C>A genotypes were determined using Ligation Detection Reaction (LDR method. Our results demonstrated that hsa-miR-34b/c rs4938723 CC genotype had a decreased risk of ESCC. The association was evident among patients who never drinking. Hsa-miR-423 rs6505162 C>A might associated with a significantly increased risk of ESCC in patients who smoking. These findings indicated that functional polymorphisms hsa-miR-34b/c rs4938723 T>C and hsa-miR-423 rs6505162 C>A might alter individual susceptibility to ESCC. However, our results were obtained with a limited sample size. Future larger studies with other ethnic populations are required to confirm current findings.

The common variant rs11646213 is associated with preeclampsia in Han Chinese women.

Directory of Open Access Journals (Sweden)

Ji-peng Wan

Full Text Available BACKGROUND: Preeclampsia, characterized by hypertension and proteinuria, is a multifactorial disease caused by complex interactions between environmental and genetic factors. A recent genome-wide association study of blood pressure reported an association between hypertension and rs11646213. This study evaluated the association between preeclampsia and rs11646213. METHODS: A total of 454 cases and 460 controls were recruited to participate in this study. The single nucleotide polymorphism (SNP rs11646213 was genotyped by polymerase chain reaction (PCR and direct sequencing. RESULTS: The allele frequency of rs11646213 was significantly different between the preeclampsia and control groups (P = 0.017, OR = 1.36, 95% CI = 1.06-1.76. Differences were particularly significant in the severe preeclampsia subgroup (P = 0.002, OR = 1.54, 95% CI = 1.17-2.03 and the early-onset preeclampsia subgroup (P = 0.004, OR = 1.57, 95% CI = 1.16-2.13. Genotyping analysis showed that the T allele of rs11646213 could confer a risk for preeclampsia, severe preeclampsia and early-onset preeclampsia. CONCLUSIONS: Rs11646213 upstream of the CDH13 gene is associated with preeclampsia in Han Chinese women.

Resiliency Scale (RS): Scale Development, Reliability and Validity Study

OpenAIRE

GÜRGAN, Uğur

2003-01-01

The purpose of this study was to develop a new Resiliency Scale (RS) for Turkish samples. Various items from some major resiliency scales, most of them with some partial change, were collected and a pool of 228 items containing almost all possible resilience areas were obtained. This item-pool was administered to a college sample of 419. Resulting of analysis 50 item RS were obtained and administered to a new college sample of 112 participants. This second sample has also received the Rosenba...

The 3Rs principle – mind the ethical gap!

DEFF Research Database (Denmark)

Olsson, I. Anna S.; Franco, Nuno H.; Weary, Daniel M.

2012-01-01

to believe that full implementation is merely a matter of time, and once the 3Rs are widely implemented, the public will fully support any continued laboratory animal use that is deemed necessary. In this paper, we argue that these conclusions are unlikely to be correct, in part because the 3Rs are rich...... effects of repeated exposure to harmful procedures). We conclude that there is now a need for a more thorough ethical discussion on how to resolve these issues....

Potências emergentes na ordem de redes: o caso do Brasil

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Daniel Flemes

2014-12-01

Full Text Available Na última década, mudanças e inovações foram introduzidas nas redes intergovernamentais de política externa. Novas potências como Brasil adquiriram um peso relativo devido ao seu novo status atuando como definidor de agendas, moderador e construtor de coalizões. Esse artigo examina a relevância de diferentes redes de política externa como o Fórum Índia-Brasil-África do Sul (IBAS e Brasil-África do Sul-Índia-China (BASIC para a política externa brasileira desde 2003.

Inclusão de Surdos na Escola Municipal Marechal Castelo Branco de Jaguarão-Rs

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Helena Beatriz Costa De Oliveira

2016-12-01

Full Text Available O trabalho tem como meta mapear as ações e os materiais usados na Escola Municipal Marechal Castelo Branco na cidade de Jaguarão –RS -Brasil, que desenvolve praticas pedagógicas voltadas a alfabetização   de alunos surdos inclusos na classe do sistema regular de ensino, recebendo alunos advindos de outras escolas do referido município. Os objetivos assentam-se em refletir sobre os materiais usados pelos educadores, educandos e demais profissionais envolvidos nas  praticas pedagógicas. Como metodologia usamos o método qualitativo, analisamos o que está disponível na referida escola. Primamos pela necessidade de problematizarmos a atuação do autor deste trabalho durante o tempo de implantação das aulas, ressaltando as possibilidades de aprendizagem salientando as habilidades da escrita, da leitura e matemática em libras que são trabalhadas pelos educadores. Destacamos que durante suas atuações este profissional trabalha junto com um interprete em libras. Podemos concluir que a sociabilidade gerada através do processo de inclusão destes indivíduos nas classes regulares faz com que o material disponibilizado em libras e a convivência se tornam uma unidade caminhando juntas e trazendo um bom modelo a ser seguido.

Os investimentos públicos em saúde e a mortalidade dos idosos no sul do Brasil:uma análise regionalizada

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Marilia Patta Ramos

2010-05-01

Full Text Available Este artigo teve como objetivo examinar o efeito dos investimentos públicos em saúde na mortalidade dos idosos no Rio Grande do Sul, controlando-se pelas características socioeconômicas dos municípios. A base de dados foi extraída do Censo Demográfico do IBGE de 2000 e do Datasus, o qual inclui informações sobre recursos regionais para a saúde em 7 meso-regiões do RS. Foi criada uma tipologia para classificar as regiões do RS com base na taxa de dependência idosa. Modelos de regressões lineares estimaram o efeito dos investimentos públicos na mortalidade dos idosos separadamente por grupos de taxa de dependência controlando-se pelo PIB per capita, o índice de Gini, renda per capita, média de anos de estudo e a taxa de urbanização (variáveis independentes. Apesar de ter a expectativa de vida mais alta do Brasil, os resultados desse estudo revelam significativa diferença na mortalidade dos idosos entre as 7 meso-regiões que compõem o Estado do Rio Grande do Sul. os resultados mostram que os investimentos públicos federais em saúde são maiores em regiões com baixa taxa de dependência idosa. Também observamos uma associação frágil entre os investimentos públicos em saúde e a mortalidade dos idosos.

Genetic Variant rs10757278 on Chromosome 9p21 Contributes to Myocardial Infarction Susceptibility

Directory of Open Access Journals (Sweden)

Guangyuan Chen

2015-05-01

Full Text Available Large-scale genome-wide association studies (GWAS have revealed that rs10757278 polymorphism (or its proxy rs1333049 on chromosome 9p21 is associated with myocardial infarction (MI susceptibility in individuals of Caucasian ancestry. Following studies in other populations investigated this association. However, some of these studies reported weak or no significant association. Here, we reevaluated this association using large-scale samples by searching PubMed and Google Scholar databases. Our results showed significant association between rs10757278 polymorphism and MI with p = 6.09 × 10−22, odds ratio (OR = 1.29, 95% confidence interval (CI 1.22–1.36 in pooled population. We further performed a subgroup analysis, and found significant association between rs10757278 polymorphism and MI in Asian and Caucasian populations. We identified that the association between rs10757278 polymorphism and MI did not vary substantially by excluding any one study. However, the heterogeneity among the selected studies varies substantially by excluding the study from the Pakistan population. We found even more significant association between rs10757278 polymorphism and MI in pooled population, p = 3.55 × 10−53, after excluding the study from the Pakistan population. In summary, previous studies reported weak or no significant association between rs10757278 polymorphism and MI. Interestingly, our analysis suggests that rs10757278 polymorphism is significantly associated with MI susceptibility by analyzing large-scale samples.

Predicting pKa for proteins using COSMO-RS

DEFF Research Database (Denmark)

Andersson, Martin Peter; Jensen, Jan Halborg; Stipp, Susan Louise Svane

2013-01-01

We have used the COSMO-RS implicit solvation method to calculate the equilibrium constants, pKa, for deprotonation of the acidic residues of the ovomucoid inhibitor protein, OMTKY3. The root mean square error for comparison with experimental data is only 0.5 pH units and the maximum error 0.8 p......H units. The results show that the accuracy of pKa prediction using COSMO-RS is as good for large biomolecules as it is for smaller inorganic and organic acids and that the method compares very well to previous pKa predictions of the OMTKY3 protein using Quantum Mechanics/Molecular Mechanics. Our approach...

Two-Component Signal Transduction System SaeRS Positively Regulates Staphylococcus epidermidis Glucose Metabolism

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Qiang Lou

2014-01-01

Full Text Available Staphylococcus epidermidis, which is a causative pathogen of nosocomial infection, expresses its virulent traits such as biofilm and autolysis regulated by two-component signal transduction system SaeRS. In this study, we performed a proteomic analysis of differences in expression between the S. epidermidis 1457 wild-type and saeRS mutant to identify candidates regulated by saeRS using two-dimensional gel electrophoresis (2-DE combined with matrix-assisted laser desorption/lonization mass spectrometry (MALDI-TOF-MS. Of 55 identified proteins that significantly differed in expression between the two strains, 15 were upregulated and 40 were downregulated. The downregulated proteins included enzymes related to glycolysis and TCA cycle, suggesting that glucose is not properly utilized in S. epidermidis when saeRS was deleted. The study will be helpful for treatment of S. epidermidis infection from the viewpoint of metabolic modulation dependent on two-component signal transduction system SaeRS.

Soft-decision decoding of RS codes

DEFF Research Database (Denmark)

Justesen, Jørn

2005-01-01

By introducing a few simplifying assumptions we derive a simple condition for successful decoding using the Koetter-Vardy algorithm for soft-decision decoding of RS codes. We show that the algorithm has a significant advantage over hard decision decoding when the code rate is low, when two or more...

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African Journals Online (AJOL)

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Influence of VEGFA gene polymorphisms rs2010963 and rs699947 on clinical and laboratory indicators in diabetic retinopathy among patients with type 2 diabetes mellitus

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A.S. Gudz

2017-10-01

Full Text Available Background. A key factor of neoangiogenesis deve­lopment in diabetic retinopathy (DR among patients with type 2 diabetes mellitus (DM is vascular endothelial growth factor A (VEGFA. The important role of genetic polymorphisms of the VEGFA gene indicates a number of studies and meta-analyzes, that have shown their association with DR, especially with its proliferative variant, which varies in different populations. Accordingly, the purpose of this work was to find out the influence of the polymorphic genotypes rs2010963 and rs699947 of the VEGFA gene on clinical and laboratory parameters of DR in DM patients from Ukrainian population. Materials and methods. The study involved 302 patients with type 2 diabetes mellitus and DR. Diagnosis was established according to the international clinical classification adopted by the American Academy of Ophthalmology (2003. The control group consisted of 98 people who did not have DM and DR, as well as other ophthalmic diseases. All patients were operated on cataract. In the intraocular fluid collected during the surgery, the VEGFA content was determined by the immunoassay method. Analysis of the polymorphic DNA loci of the VEGFA gene: rs2010963 and rs699947 was performed in a real time polymerase chain reaction using TaqMan Mutation Detection Assays (Thermo Fisher Scientific, USA. Results. An analysis of the study results showed that rs2010963 polymorphism had an effect on the intraocular fluid VEGFA level (maximum — under the C/C risk genotype. This polymorphism was related to the sex (the genotype C/C was more common in men than in women: 3 : 1, the presence of proliferative DR (most often was determined by the presence of the genotype C/C: 45.4 % and neovascularization of the optic disc (most often determined by the pre­sence of heterozygotes G/C: 21.4 %. Polymorphism rs699947 had an effect on the visual acuity (the minimum was available in the genotype C/C, the thickness of the retina (the maximum

Role of the SaeRS two-component regulatory system in Staphylococcus epidermidis autolysis and biofilm formation

Science.gov (United States)

2011-01-01

Background Staphylococcus epidermidis (SE) has emerged as one of the most important causes of nosocomial infections. The SaeRS two-component signal transduction system (TCS) influences virulence and biofilm formation in Staphylococcus aureus. The deletion of saeR in S. epidermidis results in impaired anaerobic growth and decreased nitrate utilization. However, the regulatory function of SaeRS on biofilm formation and autolysis in S. epidermidis remains unclear. Results The saeRS genes of SE1457 were deleted by homologous recombination. The saeRS deletion mutant, SE1457ΔsaeRS, exhibited increased biofilm formation that was disturbed more severely (a 4-fold reduction) by DNase I treatment compared to SE1457 and the complementation strain SE1457saec. Compared to SE1457 and SE1457saec, SE1457ΔsaeRS showed increased Triton X-100-induced autolysis (approximately 3-fold) and decreased cell viability in planktonic/biofilm states; further, SE1457ΔsaeRS also released more extracellular DNA (eDNA) in the biofilms. Correlated with the increased autolysis phenotype, the transcription of autolysis-related genes, such as atlE and aae, was increased in SE1457ΔsaeRS. Whereas the expression of accumulation-associated protein was up-regulated by 1.8-fold in 1457ΔsaeRS, the expression of an N-acetylglucosaminyl transferase enzyme (encoded by icaA) critical for polysaccharide intercellular adhesin (PIA) synthesis was not affected by the deletion of saeRS. Conclusions Deletion of saeRS in S. epidermidis resulted in an increase in biofilm-forming ability, which was associated with increased eDNA release and up-regulated Aap expression. The increased eDNA release from SE1457ΔsaeRS was associated with increased bacterial autolysis and decreased bacterial cell viability in the planktonic/biofilm states. PMID:21702925

Role of the SaeRS two-component regulatory system in Staphylococcus epidermidis autolysis and biofilm formation

Directory of Open Access Journals (Sweden)

Francois Patrice

2011-06-01

Full Text Available Abstract Background Staphylococcus epidermidis (SE has emerged as one of the most important causes of nosocomial infections. The SaeRS two-component signal transduction system (TCS influences virulence and biofilm formation in Staphylococcus aureus. The deletion of saeR in S. epidermidis results in impaired anaerobic growth and decreased nitrate utilization. However, the regulatory function of SaeRS on biofilm formation and autolysis in S. epidermidis remains unclear. Results The saeRS genes of SE1457 were deleted by homologous recombination. The saeRS deletion mutant, SE1457ΔsaeRS, exhibited increased biofilm formation that was disturbed more severely (a 4-fold reduction by DNase I treatment compared to SE1457 and the complementation strain SE1457saec. Compared to SE1457 and SE1457saec, SE1457ΔsaeRS showed increased Triton X-100-induced autolysis (approximately 3-fold and decreased cell viability in planktonic/biofilm states; further, SE1457ΔsaeRS also released more extracellular DNA (eDNA in the biofilms. Correlated with the increased autolysis phenotype, the transcription of autolysis-related genes, such as atlE and aae, was increased in SE1457ΔsaeRS. Whereas the expression of accumulation-associated protein was up-regulated by 1.8-fold in 1457ΔsaeRS, the expression of an N-acetylglucosaminyl transferase enzyme (encoded by icaA critical for polysaccharide intercellular adhesin (PIA synthesis was not affected by the deletion of saeRS. Conclusions Deletion of saeRS in S. epidermidis resulted in an increase in biofilm-forming ability, which was associated with increased eDNA release and up-regulated Aap expression. The increased eDNA release from SE1457ΔsaeRS was associated with increased bacterial autolysis and decreased bacterial cell viability in the planktonic/biofilm states.

Mass and Reliability System (MaRS)

Science.gov (United States)

Barnes, Sarah

2016-01-01

The Safety and Mission Assurance (S&MA) Directorate is responsible for mitigating risk, providing system safety, and lowering risk for space programs from ground to space. The S&MA is divided into 4 divisions: The Space Exploration Division (NC), the International Space Station Division (NE), the Safety & Test Operations Division (NS), and the Quality and Flight Equipment Division (NT). The interns, myself and Arun Aruljothi, will be working with the Risk & Reliability Analysis Branch under the NC Division's. The mission of this division is to identify, characterize, diminish, and communicate risk by implementing an efficient and effective assurance model. The team utilizes Reliability and Maintainability (R&M) and Probabilistic Risk Assessment (PRA) to ensure decisions concerning risks are informed, vehicles are safe and reliable, and program/project requirements are realistic and realized. This project pertains to the Orion mission, so it is geared toward a long duration Human Space Flight Program(s). For space missions, payload is a critical concept; balancing what hardware can be replaced by components verse by Orbital Replacement Units (ORU) or subassemblies is key. For this effort a database was created that combines mass and reliability data, called Mass and Reliability System or MaRS. The U.S. International Space Station (ISS) components are used as reference parts in the MaRS database. Using ISS components as a platform is beneficial because of the historical context and the environment similarities to a space flight mission. MaRS uses a combination of systems: International Space Station PART for failure data, Vehicle Master Database (VMDB) for ORU & components, Maintenance & Analysis Data Set (MADS) for operation hours and other pertinent data, & Hardware History Retrieval System (HHRS) for unit weights. MaRS is populated using a Visual Basic Application. Once populated, the excel spreadsheet is comprised of information on ISS components including

RsComm User Manual. Data system for the control of continuous recording measuring instruments (monitors); RsComm brukermanual. Datasystem for kontroll av kontinuerlig registrerende maaleinstrumenter (monitorer)

Energy Technology Data Exchange (ETDEWEB)

Marsteen, L.

1996-02-01

Norwegian Institute for Air Research (NILU) has, as a part of the quality control systems, developed an automatic system of data recording. This report describes the installation and use of the RsComm software. Using RsComm and a NILU data recorder it is possible to run system tests on air quality analyzers via a telephone line. Test reports are generated. 17 figs.

THREE-DIMENSIONAL DOPPLER TOMOGRAPHY OF THE RS VULPECULAE INTERACTING BINARY

International Nuclear Information System (INIS)

Richards, Mercedes T.; Sharova, Olga I.; Agafonov, Michail I.

2010-01-01

Three-dimensional Doppler tomography has been used to study the Hα emission sources in the RS Vulpeculae (RS Vul) interacting binary. The two-dimensional tomogram of this binary suggested that most of the emission arises from the cool mass losing star with additional evidence of a gas stream flowing close to its predicted trajectory. However, the three-dimensional tomogram revealed surprising evidence that the gas stream has an average velocity of -85 km s -1 relative to the central velocity plane at V z = 0 km s -1 , unlike U CrB in which the stream was prominent along this central plane. These unexpected V z motions may result from the interaction between magnetic activity on the cool star and the gravitationally induced Roche lobe overflow from that star. Evidence of a loop prominence on the cool star close to the L1 point has been found in the three-dimensional tomogram of RS Vul; hence, the magnetic field lines may have deflected the gas stream relative to the central plane. This result is consistent with earlier detections of RS Vul as both an X-ray and a radio source, and represents the first detection of a loop prominence in an interacting binary based on tomography. Moreover, recent radio images of β Per, the prototype of the Algols, show that the magnetic field of the mass losing star is asymmetric and extends well beyond the orbital plane of the binary, so it is now plausible that the gas flow between the stars in RS Vul could be deflected in an asymmetric way by the magnetic field.

Crosstalk XVI, basic data communication and RS-232C

International Nuclear Information System (INIS)

Hwang, Hui Yung

1988-10-01

This book is divided into three parts, which deals with compatible software of data communication with IBM PC XT/AT. The first part consists of an introduction to crosstalk XVI, getting start for user, crosstalk practice, call with crosstalk, terminal feature, switch of communication parameter, terminal emulation, capturing data, transmission of text file answer mode, file transfer, command file and script file, command summary and examples. The second part deals with basic personal computer communication, RS-232C and explanation of communication control : RS-232C interface, transmission device and interrupt controller 8259.

Telenovelas y culturas híbridas en Brasil

Directory of Open Access Journals (Sweden)

Thomas Tufte

2015-01-01

Full Text Available Las telenovelas han sido categorizadas como productos comerciales alienantes. Solo en los últimos años se les ha prestado una atención académica seria. Este trabajo, presenta los lados socialmente dinámicos y culturalmente expresivos de este género fascinante, en el Brasil contemporáneo. La literatura de cordel y la narrativa oral constituyen las matrices históricas fundamentales de la telenovela. La sociabilidad, la actividad colectiva y el entretenimiento son algunos de los denominadores comunes que se encuentran al analizar la función desempeñada por estas expresiones culturales populares en la historia brasileña. El rol mediador de las telenovelas en el Brasil actual es una extensión de viejas prácticas sociales y culturales. La forma de vivir con la televisión y las telenovelas, contribuye específicamente a reunirse, Hecho que influye en la constitución y desarrollo de las culturas híbridas que caracterizan a las masas urbanas de Latinoamérica.

Parallel data grabbing card based on PCI bus RS422

International Nuclear Information System (INIS)

Zhang Zhenghui; Shen Ji; Wei Dongshan; Chen Ziyu

2005-01-01

This article briefly introduces the developments of the parallel data grabbing card based on RS422 and PCI bus. It could be applied for grabbing the 14 bits parallel data in high speed, coming from the devices with RS422 interface. The methods of data acquisition which bases on the PCI protocol, the functions and their usages of the chips employed, the ideas and principles of the hardware and software designing are presented. (authors)

Caminha, Meirelles, e Mauro : narrativas do (re) descobrimento do Brasil; decifrando as imagens do paraiso

OpenAIRE

Carolina Cavalcanti Bezerra

2008-01-01

Resumo: Essa dissertação tem como propositura uma nova leitura sobre o descobrimento do Brasil através das imagens/representações do Paraíso na Terra. A permanência dessa imagem no imaginário coletivo foi a base para o desenvolvimento dessa dissertação, partindo dos seguintes documentos: a Carta de Caminha sobre o descobrimento do Brasil (1500), o quadro A Primeira Missa no Brasil de Meirelles (1860/1) e O Descobrimento do Brasil (1937), filme de Humberto Mauro. A presente incursão pelas narr...

Polymorphisms of Interlukin-1β rs16944 confer susceptibility to myelodysplastic syndromes.

Science.gov (United States)

Yin, Congcong; He, Na; Li, Peng; Zhang, Chen; Yu, Jie; Hua, Mingqiang; Ji, Chunyan; Ma, Daoxin

2016-11-15

Genetic factors have been shown to be associated with Myelodysplastic syndromes (MDS) susceptibility. In recent years, the role of inflammation in the promotion of tumor growth is supported by a broad range of experimental and clinical evidence. But the relationship between polymorphisms in NOD-like receptor protein 3 (NLRP3) inflammasome and MDS is rarely reported. Thus, we conducted a case-control study, and genotyped five single nucleotide polymorphisms (SNPs) (NLRP3, IL-1β, IL-18, CARD8, and NF-κB) in MDS patients and healthy controls. The association of different genotypes with patient characteristics was analyzed. Comparing MDS patients with controls, GG genotype of IL-1β (rs16944) was observed to be associated with a significantly increased risk of MDS 78/166 (48.8%) vs 26/96 (27.0%), OR=2.1, CI (1.0-4.4). No significant association was identified regarding the rest of investigated polymorphisms and MDS susceptibility. Complex karyotypes were more frequent in patients with GG genotype of IL-1β (rs16944). Patients with IL-1β polymorphisms (rs16944) GG and GA had lower hemoglobin than those without. Patients with IL-1β polymorphisms (rs16944) GG had higher IPSS scores than those without IL-1β polymorphisms. In conclusion, our present data shows that the IL-1β polymorphisms (rs16944) GG were frequently occurred in MDS. IL-1β (rs16944) GG genotype might serve as a novel biomarker and potential targets for MDS. Copyright © 2016 Elsevier Inc. All rights reserved.

Olhando futebol: jeitos Xavantes de torcer Mirando el fútbol: modos Xavantes de apoyo Looking football: Xavante's ways of support

Directory of Open Access Journals (Sweden)

Luciano Jahnecka

2013-03-01

Full Text Available Diferente dos estudos que tratam das torcidas dos clubes das grandes cidades, esta pesquisa teve como objetivo central descrever e analisar os torcedores do Grêmio Esportivo Brasil (Pelotas, RS, Brasil. Inspirado na perspectiva da etnografia contemporânea, que contou com um trabalho de campo realizado nos anos de 2007 e 2008 que envolveu observações, entrevistas e registros fotográficos, realizou-se uma descrição cuidadosa, acompanhada de uma análise das práticas torcedoras que ocorrem antes, durante e após os jogos. Concluímos que a torcida do Grêmio Esportivo Brasil contempla uma diversidade de grupos de torcedores que se relacionam com o futebol e com o clube de distintas maneiras, produzindo diferentes jeitos Xavantes de torcer.Diferente de los estudios que se ocupan de los aficionados de los clubes en las grandes ciudades, esta investigación tuvo como objetivo describir y analizar la hinchada de Grêmio Esportivo Brasil (Pelotas, RS, Brasil. Inspirados en la perspectiva de la etnografía contemporánea a través del trabajo de campo realizado en los años 2007 y 2008 con observaciones participantes, entrevistas y registros fotográficos, hicimos una minuciosa descripción y análisis de las practicas de los aficionados antes, durante y después de los juegos. Se concluye que la hinchada de Grêmio Esportivo Brasil ofrece una variedad de modos en se relacionar al fútbol y con el club, produciendo diferentes maneras de apoyar Xavante.Different from studies about fans from clubs located in big cities, this research aimed to describe and to analize the fans of Grêmio Esportivo Brasil (Pelotas, RS, Brazil. Inspired by the perspective of contemporary ethnography, through a fieldwork conducted in the years of 2007 and 2008 which involved observations, interviews and photographic records, we made a careful description and analysis of fans practices before, during and after the games. We concluded that the crowd of Grêmio Esportivo

REBATIMENTOS EM NATAL, BRASIL

Directory of Open Access Journals (Sweden)

Fábio Fonseca Figueiredo

2013-01-01

Full Text Available El artículo presenta la gestión de los residuos sólidos en Brasil y sus implicaciones en la ciudad de Natal/ RN, analizando sus aspectos ambientales, económicos y sociales. El fracaso del programa oficial de recogi - da selectiva constatado en las bajas tasas de recuperación de materiales; la poca relevancia de la inclusión socioeconómica de los trabajadores que participan en el programa asistencialista oficial; la inexistencia de estrategias oficiales para que se disminuya la cantidad de residuos que se generan cada día y el aumento exagerado del gasto público, especialmente con el tratamiento de los residuos en el relleno sanitario, demues - tran que la gestión de residuos en Natal, que tiene como parámetro los dictámenes de la Política Brasileña para los Residuos Sólidos, tiene como objetivo el control de los residuos en la ciudad y la consolidación del modelo de tratamiento finalista de residuos mediante el envío de éstos al relleno sanitario.

The prostate cancer risk stratification (ProCaRS) project: Recursive partitioning risk stratification analysis

International Nuclear Information System (INIS)

Rodrigues, George; Lukka, Himu; Warde, Padraig; Brundage, Michael; Souhami, Luis; Crook, Juanita; Cury, Fabio; Catton, Charles; Mok, Gary; Martin, Andre-Guy; Vigneault, Eric; Morris, Jim; Warner, Andrew; Gonzalez Maldonado, Sandra; Pickles, Tom

2013-01-01

Background: The Genitourinary Radiation Oncologists of Canada (GUROC) published a three-group risk stratification (RS) system to assist prostate cancer decision-making in 2001. The objective of this project is to use the ProCaRS database to statistically model the predictive accuracy and clinical utility of a proposed new multi-group RS schema. Methods: The RS analyses utilized the ProCaRS database that consists of 7974 patients from four Canadian institutions. Recursive partitioning analysis (RPA) was utilized to explore the sub-stratification of groups defined by the existing three-group GUROC scheme. 10-fold cross-validated C-indices and the Net Reclassification Index were both used to assess multivariable models and compare the predictive accuracy of existing and proposed RS systems, respectively. Results: The recursive partitioning analysis has suggested that the existing GUROC classification system could be altered to accommodate as many as six separate and statistical unique groups based on differences in BFFS (C-index 0.67 and AUC 0.70). GUROC low-risk patients would be divided into new favorable-low and low-risk groups based on PSA ⩽6 and PSA >6. GUROC intermediate-risk patients can be subclassified into low-intermediate and high-intermediate groups. GUROC high-intermediate-risk is defined as existing GUROC intermediate-risk with PSA >=10 AND either T2b/c disease or T1T2a disease with Gleason 7. GUROC high-risk patients would be subclassified into an additional extreme-risk group (GUROC high-risk AND (positive cores ⩾87.5% OR PSA >30). Conclusions: Proposed RS subcategories have been identified by a RPA of the ProCaRS database

Infrared observations of RS CVn stars

Science.gov (United States)

Berriman, G.; De Campli, W. M.; Werner, M. W.; Hatchett, S. P.

1983-01-01

The paper presents infrared photometry of the RS CVn binary stars AR Lac (1.2-10 microns) and MM Her (1.2-3.5 microns) as they egressed from their primary and secondary eclipses; of the eclipsing systems RS CVn and Z Her at maximum light (1.2-10 microns) and of the non-eclipsing systems UX Ari and HR 1099 (1.2-10 microns). An analysis of these and published V data based on flux ratio diagrams (linear analogues of color-color diagrams) shows that G and K stars supply the infrared light of these systems. In AR Lac, the combined light of a G5-K0 subgiant and either a late F dwarf or an early F subgiant can account for the observed visual and infrared light curves. None of these systems shows infrared emission from circumstellar matter. This result is simply understood: dust grains would not be expected to form in the physical conditions surrounding the subgiant, and the corona and chromosphere (whose properties have been deduced from spectroscopic X-ray observations) should not produce appreciable infrared emission.

Working in partnership to advance the 3Rs in toxicity testing

International Nuclear Information System (INIS)

Holmes, Anthony M.; Creton, Stuart; Chapman, Kathryn

2010-01-01

Toxicological assessment of pharmaceutical and non-pharmaceutical chemicals is a regulatory requirement to ensure all compounds likely to be exposed to humans or the environment are safe. These studies rely on the use of large numbers of animals and involve a number of assumptions and extrapolations that remain controversial in assuring consumer safety. The UK's National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs) has taken a collaborative approach to identify opportunities for implementation of the 3Rs principles (Replacement, Reduction and Refinement) to drive innovation and support animal welfare in toxicity testing. This review highlights the mechanisms by which the NC3Rs is working with the pharmaceutical and chemical industries and regulatory authorities to achieve these goals.

Medidas higienistas adotadas no Patronato Agrícola Visconde da Graça (1923-34 - Pelotas/RS

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Magda de Abreu Vicente

2012-09-01

Full Text Available Esta pesquisa foi desenvolvida como parte de trabalho de mestrado junto ao Programa dePós-Graduação da Universidade Federal de Pelotas, Faculdade de Educação. Tem comoobjetivo analisar as normas higiênicas no Patronato Agrícola Visconde da Graça, noperíodo de 1923 até 1934, na cidade de Pelotas-RS e entender o enquadramento dasdiscussões higiênicas em voga no Brasil, a partir das notícias vinculadas no jornal DiárioPopular e das fichas dos alunos desta instituição. O texto, inicialmente, esboça asdiscussões brasileiras que elaboram o discurso higienista. Usa, para tal, referênciasbibliográficas que buscaram explicitar esta questão. Posteriormente, adentramos nestadiscussão em parâmetros locais, especificamente na cidade de Pelotas, através das notíciaspublicadas no jornal pelotense Diário Popular e também através de alguns pesquisadoresque aqui buscam entender as questões referentes às normas de higiene na cidade e naescola. Ao mesmo tempo analisamos como estas questões eram abordadas dentro doPatronato, através dos registros anotados nas fichas dos alunos que ali estiveram noperíodo estudado, pesquisadas no Acervo Escolar.

PCSK1 rs6232 Is Associated with Childhood and Adult Class III Obesity in the Mexican Population

Science.gov (United States)

Villalobos-Comparán, Marisela; Villamil-Ramírez, Hugo; Villarreal-Molina, Teresa; Larrieta-Carrasco, Elena; León-Mimila, Paola; Romero-Hidalgo, Sandra; Jacobo-Albavera, Leonor; Liceaga-Fuentes, Adriana E.; Campos-Pérez, Francisco J.; López-Contreras, Blanca E.; Tusié-Luna, Teresa; del Río-Navarro, Blanca E.; Aguilar-Salinas, Carlos A.; Canizales-Quinteros, Samuel

2012-01-01

Background Common variants rs6232 and rs6235 in the PCSK1 gene have been associated with obesity in European populations. We aimed to evaluate the contribution of these variants to obesity and related traits in Mexican children and adults. Methodology/Principal Findings Rs6232 and rs6235 were genotyped in 2382 individuals, 1206 children and 1176 adults. Minor allele frequencies were 0.78% for rs6232 and 19.99% for rs6235. Rs6232 was significantly associated with childhood obesity and adult class III obesity (OR = 3.01 95%CI 1.64–5.53; P = 4×10−4 in the combined analysis). In addition, this SNP was significantly associated with lower fasting glucose levels (P = 0.01) and with increased insulin levels and HOMA-B (P = 0.05 and 0.01, respectively) only in non-obese children. In contrast, rs6235 showed no significant association with obesity or with glucose homeostasis parameters in any group. Conclusion/Significance Although rs6232 is rare in the Mexican population, it should be considered as an important risk factor for extreme forms of obesity. PMID:22737226

Role of ArlRS in autolysis in methicillin-sensitive and methicillin-resistant Staphylococcus aureus strains.

Science.gov (United States)

Memmi, Guido; Nair, Dhanalakshmi R; Cheung, Ambrose

2012-02-01

Autolysis plays an essential role in bacterial cell division and lysis with β-lactam antibiotics. Accordingly, the expression of autolysins is tightly regulated by several endogenous regulators, including ArlRS, a two component regulatory system that has been shown to negatively regulate autolysis in methicillin-sensitive Staphylococcus aureus (MSSA) strains. In this study, we found that inactivation of arlRS does not play a role in autolysis of methicillin-resistant S. aureus (MRSA) strains, such as community-acquired (CA)-MRSA strains USA300 and MW2 or the hospital-acquired (HA)-MRSA strain COL. This contrasts with MSSA strains, including Newman, SH1000, RN6390, and 8325-4, where autolysis is affected by ArlRS. We further demonstrated that the striking difference in the roles of arlRS between MSSA and MRSA strains is not due to the methicillin resistance determinant mecA. Among known autolysins and their regulators, we found that arlRS represses lytN, while no effect was seen on atl, lytM, and lytH expression in both CA- and HA-MRSA strains. Transcriptional-fusion assays showed that the agr transcripts, RNAII and RNAIII, were significantly more downregulated in the arlRS mutant of MW2 than the MSSA strain Newman. Importantly, provision of agr RNAIII in trans to the MW2 arlRS mutant via a multicopy plasmid induced autolysis in this MRSA strain. Also, the autolytic phenotype in the arlRS mutant of MSSA strain Newman could be rescued by a mutation in either atl or lytM. Together, these data showed that ArlRS impacts autolysis differently in MSSA and MRSA strains.

THE HISTORY OF LABORATORY ANIMALS AND THE 3RS

DEFF Research Database (Denmark)

Alstrup, Aage Kristian Olsen

This talk will give an introduction to the history of the use of laboratory animals with focus on the history of the three Rs (3Rs). We will see how animal experimentation has been performed early in our civilization, and how the suffering of animals has been justified. This will include Rene...... Descartes´s mechanical view of animals in the seventeenth century, and Charles Darwin's ambivalent relationship to animal experimentation, which he views as cruel but necessary. In the 1870s the Danish Foundation for Protection of Animals (“Dyrenes Beskyttelse”) and Professor Peter Panum discussed the use...

Abundância e sazonalidade de Bothriurus signatus (Arachnida, Scorpiones em diferentes formações vegetais em São Francisco de Paula, RS, Brasil

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Ricardo Ott

2014-03-01

Full Text Available Foi realizado levantamento de escorpiões em serrapilheira de três tipos de formações vegetais (florestas primárias, florestas secundárias e silviculturas em área de Floresta com Araucária no Sul do Brasil. Para a coleta foram utilizadas armadilhas de queda ao longo de 20 meses. No total foram amostrados 165 escorpiões de apenas uma espécie identificada como Bothriurus signatus Pocock, 1893. Machos foram mais abundantes que fêmeas e jovens. A espécie foi mais abundante em áreas de floresta primária e silvicultura do que na floresta secundária. A maior atividade dos escorpiões foi registrada durante a primavera. O comprimento total dos escorpiões adultos coletados variou de 3,05 a 4,52 cm sendo que machos foram significativamente maiores que fêmeas. Nenhuma fêmea grávida foi registrada entre os indivíduos coletados.

Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus.

Science.gov (United States)

Sakiyama, Masayuki; Matsuo, Hirotaka; Nakaoka, Hirofumi; Yamamoto, Ken; Nakayama, Akiyoshi; Nakamura, Takahiro; Kawai, Sayo; Okada, Rieko; Ooyama, Hiroshi; Shimizu, Toru; Shinomiya, Nariyoshi

2016-05-16

Gout is a common disease resulting from hyperuricemia. Recently, a genome-wide association study identified an association between gout and a single nucleotide polymorphism (SNP) rs2188380, located on an intergenic region between MYL2 and CUX2 on chromosome 12. However, other genes around rs2188380 could possibly be gout susceptibility genes. Therefore, we performed a fine-mapping study of the MYL2-CUX2 region. From 8,595 SNPs in the MYL2-CUX2 region, 9 tag SNPs were selected, and genotyping of 1,048 male gout patients and 1,334 male controls was performed by TaqMan method. Eight SNPs showed significant associations with gout after Bonferroni correction. rs671 (Glu504Lys) of ALDH2 had the most significant association with gout (P = 1.7 × 10(-18), odds ratio = 0.53). After adjustment for rs671, the other 8 SNPs no longer showed a significant association with gout, while the significant association of rs671 remained. rs671 has been reportedly associated with alcohol drinking behavior, and it is well-known that alcohol drinking elevates serum uric acid levels. These data suggest that rs671, a common functional SNP of ALDH2, is a genuine gout-associated SNP in the MYL2-CUX2 locus and that "A" allele (Lys) of rs671 plays a protective role in the development of gout.

SparkRS - Spark for Remote Sensing, Phase I

Data.gov (United States)

National Aeronautics and Space Administration — The proposed innovation is Spark-RS, an open source software project that enables GPU-accelerated remote sensing workflows in an Apache Spark distributed computing...

TSHR intronic polymorphisms (rs179247 and rs12885526) and their role in the susceptibility of the Brazilian population to Graves' disease and Graves' ophthalmopathy.

Science.gov (United States)

Bufalo, N E; Dos Santos, R B; Marcello, M A; Piai, R P; Secolin, R; Romaldini, J H; Ward, L S

2015-05-01

Intronic thyroid-stimulating hormone receptor polymorphisms have been associated with the risk for both Graves' disease and Graves' ophthalmopathy, but results have been inconsistent among different populations. We aimed to investigate the influence of thyroid-stimulating hormone receptor intronic polymorphisms in a large well-characterized population of GD patients. We studied 279 Graves' disease patients (231 females and 48 males, 39.80 ± 11.69 years old), including 144 with Graves' ophthalmopathy, matched to 296 healthy control individuals. Thyroid-stimulating hormone receptor genotypes of rs179247 and rs12885526 were determined by Real Time PCR TaqMan(®) SNP Genotyping. A multivariate analysis showed that the inheritance of the thyroid-stimulating hormone receptor AA genotype for rs179247 increased the risk for Graves' disease (OR = 2.821; 95 % CI 1.595-4.990; p = 0.0004), whereas the thyroid-stimulating hormone receptor GG genotype for rs12885526 increased the risk for Graves' ophthalmopathy (OR = 2.940; 95 % CI 1.320-6.548; p = 0.0083). Individuals with Graves' ophthalmopathy also presented lower mean thyrotropin receptor antibodies levels (96.3 ± 143.9 U/L) than individuals without Graves' ophthalmopathy (98.3 ± 201.9 U/L). We did not find any association between the investigated polymorphisms and patients clinical features or outcome. We demonstrate that thyroid-stimulating hormone receptor intronic polymorphisms are associated with the susceptibility to Graves' disease and Graves' ophthalmopathy in the Brazilian population, but do not appear to influence the disease course.

RS Ophiuchi: The Gift that Keeps on Giving

Science.gov (United States)

Starrfield, S.

2008-12-01

RS Oph experienced its sixth recorded outburst in 2006 and was observed in virtually every wavelength region from hard X-rays to the radio. Each observation, especially those with instruments that have come online since its last outburst in 1985, provided new and exciting information about the explosion. As a result, some of us organized a second workshop on the RS Oph outburst and it was held in June 2007 at Keele University. I gave the lead off talk in which I presented a number of questions to be discussed during the workshop, a brief summary of what had been discovered in previous outbursts concentrating on the ultraviolet studies with IUE, and a few observations of the 2006 outburst concentrating on the results from Swift and HST.

Lack of association between KCNJ11 (rs5219 and ABCC8 (rs757110 polymorphisms and sulphonylurea treatment response in type 2 diabetes patients in Novosibirsk region

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Irina Arkad'evna Bondar

2015-03-01

Full Text Available Aim. Sulfonylureas (SU are widely used in everyday clinical practice in treatment of patients with type 2 diabetes mellitus (T2DM. There is a considerable variability in SU effects, which may be caused by psychological, social, biological and genetic factors. The aim of the study was to investigate the association between rs5219 KCNJ11 gene and rs757110 ABCC8 gene polymorphism and long-term response to SU-drugs of second and third generation in the Novosibirsk region. Materials and Methods. 326 patients with type 2 diabetes in the Novosibirsk region were examined. Patients were divided into 2 groups, depending on HbA1c level. The first group included patients with target HbA1c levels on SU monotherapy. The second group included patients who did not reach target HbA1c levels on the highest dose of SU. Genotyping of KCNJ11 (rs5219 and ABCC8 (rs757110 was performed by TaqMan real-time PCR (ICBFM SB RAS, Novosibirsk, Russia. Results. Patients with type 2 diabetes with a good response to SU-therapy compared to the group of patients with a poor response to SU-therapy were older (65.8?9.1 years vs. 61.6?7.9 years, p

Preparation and characterization of ketoprofen loaded eudragit RS polymeric nanoparticles for controlled release

International Nuclear Information System (INIS)

Tuan Anh, Nguyen; Tuyen Dao, T P; Nhan Le, N T; Mau Chien, Dang; To Hoai, Nguyen; T Chi, Nguyen; Tran, T Khai

2012-01-01

Nanospheres containing ketoprofen (Keto) and polymer eudragit RS were prepared using an emulsion solvent evaporation method. The ultrasonic probe (VCX500, vibracell) was used as a tool to disperse oil phase into aqueous phase leading to water/oil emulsion. Nanoparticles were successfully prepared and their morphologies and diameters were confirmed by transmission electron microscope (TEM) and dynamic light scattering (DLS), respectively. The result showed that particles were spherical with submicron size. The particle size was dependent on the RS concentration, emulsification tools and the types of organic solvents. For the encapsulation ability, Keto-loaded RS nanoparticle showed 9.8% of Keto in nanoparticle, which was evaluated by high-performance liquid chromatography (HPLC). Moreover, the drug release behavior of Keto-loaded eudragit RS nanoparticle was also investigated in vitro at pH 7.4 and compared to referential profenid. (paper)

Transplante da educação européia no Brasil

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Casemiro dos Reis Filho

2012-02-01

Full Text Available O Brasil surge para a história em pleno Renascimento. Resultado da expansão da civilização ocidental, o descobrimento do Brasil é significativo incidente da aventura marítima do Atlântico no século XV. Este momento de expansão européia é de extrema importância para a análise das raízes de nossas origens como nacionalidade. O seu estudo nos interessa na medida em que o primeiro projeto de Brasil, elaborado e executado a partir do Descobrimento pelo colonizador português, estabeleceu linhas históricas determinantes de nossa evolução como povo ligado, embora perifericamente, à civilização ocidental [...].

Solvation quantities from a COSMO-RS equation of state

International Nuclear Information System (INIS)

Panayiotou, C.; Tsivintzelis, I.; Aslanidou, D.; Hatzimanikatis, V.

2015-01-01

Highlights: • Extension of the successful COSMO-RS model to an equation-of-state model. • Two scaling constants, obtained from atom-specific contributions. • Overall estimation of the solvation quantities and contributions. - Abstract: This work focuses on the extension of the successful COSMO-RS model of mixtures into an equation-of-state model of fluids and its application for the estimation of solvation/hydration quantities of a variety of chemical substances. These quantities include free-energies, enthalpies and entropies of hydration as well as the separate contributions to each of them. Emphasis is given on the estimation of contributions from the conformational changes of solutes upon solvation and the associated restructuring of solvent in its immediate neighborhood. COSMO-RS is a quantum-mechanics based group/segment contribution model in which the Quasi-Chemical (QC) approach is used for the description of the non-random distribution of interacting segments in the system. Thus, the equation-of-state development is done through such a QC framework. The new model will not need any adjustable parameters for the strong specific interactions, such as hydrogen bonds, since they will be provided by the quantum-mechanics based cosmo-files – a key feature of COSMO-RS model. It will need, however, one volumetric and one energy parameter per fluid, which are scaling constants or molecular descriptors of the fluid and are obtained from rather easily available data such as densities, boiling points, vapor pressures, heats of vaporization or second virial coefficients. The performance and the potential of the new equation-of-state model to become a fully predictive model are critically discussed

Para decifrar o Brasil (ou) a formação do estadista

OpenAIRE

Mota, Carlos Guilherme

2014-01-01

[ES]El autor analiza el libro Pensadores que inventaram o Brasil, de Fernando Henrique Cardoso, en lo cual se exponen, en diez ensayos, visiones e interpretaciones sobre la cultura, la sociedad y la política de Brasil contemporáneo.

Estudo geoeconômico do setor cervejeiro no Brasil

OpenAIRE

Limberger, Silvia Cristina

2016-01-01

Tese (doutorado) - Universidade Federal de Santa Catarina, Centro de Filosofia e Ciências Humanas, Programa de Pós-Graduação em Geografia, Florianópolis, 2016. Esta tese tratou de estudar o desenvolvimento da indústria cervejeira no Brasil, tendo como ponto central as diferentes estratégias competitivas elaboradas pelas empresas líderes e marginais, especialmente, no segmento de cervejas de alto valor agregado. O trabalho demonstra a evolução da produção cervejeira no mundo e no Brasil ass...

Standard mapping of the environment sensibility of oil to Lagoa dos Patos, Rio Grande do Sul, Brazil; Padronizacao do mapeamento da sensibilidade ambiental a derramamento de oleo para a Lagoa dos Patos, Rio Grande do Sul, Brasil

Energy Technology Data Exchange (ETDEWEB)

Dias, Felipe C; Griep, Gilberto H [Fundacao Universidade do Rio Grande (FURG), RS (Brazil)

2008-07-01

The intense flow of fossil fuels in the inland waters of Patos Lagoon (LP) - Rio Grande do Sul, justifies the importance of preventive actions to claims by oil and derivatives within the lagoon. The mapping and classification of coastline environmental sensitivity for oil spills (Cartas SAO) is fundamental tool for this type of action. Therefore, since 2001, the Laboratory of Geological Oceanography (LOG) of Federal University of Rio Grande (FURG) has developed the mapping SAO for the LP. In this work, through review of raw data from the database of LOG, and taking into account the methodology proposed by the Ministry of Environment (MMA, 2004), gave up a strategic projection of standardized environmental sensitivity of the oil spill to Patos Lagoon. This new account also enable a better understanding of the lagoon ecosystem, enables comparisons between its different areas, facilitating the planning and decision-making, allowing the management for faster action-in response. Like, highlights the regions of the estuary of the LP, the delta of the Camaqua River and Casamento Lagoon as the areas of greater sensitivity to environmental spillage of oil from Patos Lagoon. (author)

RACISMO CIENTÍFICO NO BRASIL PÓS-ESCRAVATURA

OpenAIRE

RAQUEL AMORIM DOS SANTOS; ROSÂNGELA MARIA DE NAZARÉ BARBOSA E SILVA

2017-01-01

Este estudo analisa a difusão do racismo cientifico no Brasil, reconhecendo seu caráter estrutural. Reconhecê-lo desta forma significa perceber que Cor, raça e preconceito no Brasil compõe o plexo de concepções para o enfrentamento das questões raciais e de seus desdobramentos nocivos na formação de crianças e adolescentes, por meio da construção de uma nova forma de se pensar a formação da nação e da nacionalidade. O estudo é de abordagem qualitativa com aplicação da pesquisa bibliográfica ...

PREVALÊNCIA DE SALMONELLA EM PRODUTOS DE FRANGOS E OVOS DE GALINHA COMERCIALIZADOS EM PELOTAS, RS, BRASIL PREVALENCE OF SALMONELLA IN CHICKEN PRODUCTS AND HEN'S EGGS FROM PELOTAS, RS, BRAZIL

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Ana Cristina Baú

2001-04-01

Full Text Available A prevalência de Salmonella em produtos de frangos e ovos de galinhas, os sorovares mais freqüentes e sua sensibilidadea a antimicrobianos, foram investigados em Pelotas, Brasil, no período de maio de 1997 a outubro de 1998. Um total de 124 amostras de produtos de frangos obtidas em supermercados e açougues e 94 amostras de 6 unidades de ovos de galinhas obtidas em supermercados e feiras-livres foram analisadas através do método convencional de cultivo. Entre as amostras de produtos de frangos analisadas, 13 (10,48% continham salmonelas. Os 13 isolamentos de salmonelas realizados foram sorotipificados como S. enteritidis (10, S. anatum (1 e S. enterica subespécie enterica sorovar 3,10:e,h:- (2. Todas as cepas isoladas foram resistentes à penicilina G e sensíveis aos demais antimicrobianos testados. Em amostras de ovos, não foram detectadas salmonelas.The prevalence of Salmonella in chicken products and hen's eggs, the most frequent serovars and their antimicrobial sensitivity, were investigated in the city of Pelotas, Brazil from May 1997 through October 1998. A total of 124 samples of chicken products obtained from local supermarkets and butcher shops, and 94 samples of eggs (6 units each obtained from supermarkets and street vendors, were examined through standard cultivation procedures. Salmonella were detected in 13 (10,48% samples of chicken products. Among the 13 strains of salmonellae isolated, 10 were serotyped as S. enteritidis, 1 was S. anatum and 2 were S. enterica subsp. enterica sorovar 3,10:e,h:-. All strains isolated were resistant to penicillin G and susceptible to the others antimicrobial drugs tested. Hen's eggs were not found contaminated with salmonellae.

Raca e mortalidade cerebrovascular no Brasil

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Paulo Andrade Lotufo

2013-12-01

Full Text Available Sendo desconhecidas as taxas de mortalidade cerebrovascular segundo raça no Brasil, foram coletadas informações de óbitos de 2010 do Sistema de Informação de Mortalidade do Ministério da Saúde. Foram calculadas as taxas de mortalidade cerebrovascular, ajustadas por idade (por 100 mil, com intervalo de confiança de 95%, por sexo e raça/cor de pele. A diferença entre brancos, pardos e negros foi significativa para homens, com taxas, respectivamente, de 44,4 (43,5;45,3, 48,2 (47,1;49,3 e 63,3 (60.6;66,6; e para mulheres, com taxa, respectivamente, de 29,0 (28,3;29,7, 33,7 (32,8;34,6 e 51,0 (48,6;53,4. Em conclusão, a mortalidade cerebrovascular no Brasil é maior entre negros.

Thomas Mann e a cena intelectual no Brasil: encontros e desencontros

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Sibele Paulino

2009-12-01

Full Text Available A origem brasileira de Thomas Mann, por parte de sua mãe, Julia da Silva Bruhns, deu ocasião, na maturidade do escritor, a seu contato com intelectuais brasileiros ou estrangeiros ligados à cena cultural do Brasil. No primeiro grupo, tem-se Gilberto Freyre, Sérgio Buarque de Holanda e Erico Verissimo. Residentes no Brasil, Karl Lustig-Prean, que posteriormente retornará à Europa, e o tradutor Herbert Caro, que se radica em definitivo no Brasil. Também o contato direto ou indireto com pensadores e escritores como Karl Loewenstein, Heinrich Eduard Jacob, Marte Brill e Stefan Zweig colaboraram para a aproximação de Thomas Mann ao universo brasileiro. Estes e outros pontos de contato são descritos no presente artigo, que pretende difundir dados e documentos há muito inacessíveis ou inéditos, no sentido de contribuir com abordagens atualizadas da obra de Thomas Mann e oferecer à pesquisa especializada a indicação de dados biográficos e documentais relacionados ao escritor, no que concerne à sua relação com o Brasil.

Characterization of novel RS1 exonic deletions in juvenile X-linked retinoschisis.

Science.gov (United States)

D'Souza, Leera; Cukras, Catherine; Antolik, Christian; Craig, Candice; Lee, Ji-Yun; He, Hong; Li, Shibo; Smaoui, Nizar; Hejtmancik, James F; Sieving, Paul A; Wang, Xinjing

2013-01-01

X-linked juvenile retinoschisis (XLRS) is a vitreoretinal dystrophy characterized by schisis (splitting) of the inner layers of the neuroretina. Mutations within the retinoschisis (RS1) gene are responsible for this disease. The mutation spectrum consists of amino acid substitutions, splice site variations, small indels, and larger genomic deletions. Clinically, genomic deletions are rarely reported. Here, we characterize two novel full exonic deletions: one encompassing exon 1 and the other spanning exons 4-5 of the RS1 gene. We also report the clinical findings in these patients with XLRS with two different exonic deletions. Unrelated XLRS men and boys and their mothers (if available) were enrolled for molecular genetics evaluation. The patients also underwent ophthalmologic examination and in some cases electroretinogram (ERG) recording. All the exons and the flanking intronic regions of the RS1 gene were analyzed with direct sequencing. Two patients with exonic deletions were further evaluated with array comparative genomic hybridization to define the scope of the genomic aberrations. After the deleted genomic region was identified, primer walking followed by direct sequencing was used to determine the exact breakpoints. Two novel exonic deletions of the RS1 gene were identified: one including exon 1 and the other spanning exons 4 and 5. The exon 1 deletion extends from the 5' region of the RS1 gene (including the promoter) through intron 1 (c.(-35)-1723_c.51+2664del4472). The exon 4-5 deletion spans introns 3 to intron 5 (c.185-1020_c.522+1844del5764). Here we report two novel exonic deletions within the RS1 gene locus. We have also described the clinical presentations and hypothesized the genomic mechanisms underlying these schisis phenotypes.

Ordenamento Territorial Ambiental Sustentável no Bioma Pampa: Estudo de Caso, São Francisco de Assis – RS, Brasil.

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Mg. Arq. Amélia Simões Schwertner

2013-04-01

Full Text Available O Bioma Pampa, tombado pela UNESCO (2008 se estende desde o Sul do Brasil aos países vizinhos Uruguai e Argentina. São Francisco de Assis, município da Metade Sul do Rio Grande do Sul, possui em seu território uma área de importante fragilidade ambiental: a zona de amortecimento entre a Mata Atlântica e o Bioma Pampa. Na sede urbana de São Francisco de Assis aconteceu um caso inusitado: um bando de bugios fez da sua praça central seu habitat. Adotados, a população urbana tomou para si a identidade «Querência do Bugio». Este fato levou os Planejadores Urbanos a questionar-se do por que estes animais não permaneciam nas matas, seu local de origem -o desmatamento a degradação ambiental. Ao redor do sítio urbano, ao longo de três mananciais hídricos foi criado o Parque Municipal do Bugio e por prolongamentos destes mananciais aos bosques mais distantes na zona rural, corredores ecológicos. Propostas de ordenamento territorial determinaram diretrizes para reposição florestal, recuperação das matas ciliares e de inúmeras voçorocas que provocavam degradação do solo e um crescente processo de arenização. A presença de bugios na praça desencadeou um processo de recuperação e consciência ambiental na preservação do Bioma Pampa e identidade local

Association between the rs7574865 polymorphism of STAT4 and rheumatoid arthritis: a meta-analysis.

Science.gov (United States)

Lee, Young Ho; Woo, Jin-Hyun; Choi, Seong Jae; Ji, Jong Dae; Song, Gwan Gyu

2010-03-01

The aim of this study was to determine whether the rs7574865 polymorphism of STAT4 (signal transducers and activators of transcription 4) confers susceptibility to rheumatoid arthritis (RA) in populations with different ethnicities. A meta-analysis was conducted on the T allele of the STAT4 rs7574865 polymorphism in 15 studies containing 16,088 RA patients and 16,509 normal control subjects. Meta-analysis revealed an association between RA and the STAT4 rs7574865 T allele in all subjects (OR = 1.271, 95% CI = 1.197-1.350, P rs7574865 T allele was found to be significantly associated with RA in Europeans and Asians (OR = 1.300, 95% CI = 1.195-1.414, P rs7574865 polymorphism is associated with RA susceptibility in different ethnic groups, and that its prevalence is ethnicity dependent.

A Psicologia no Brasil: um ensaio sobre suas contradições

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Mitsuko Aparecida Makino Antunes

Full Text Available Este artigo tem a finalidade de expor o percurso histórico da Psicologia no Brasil na perspectiva da tridimensionalidade do tempo, entendendo que a apreensão de sua concreticidade implica a compreensão do passado, que estrutura o presente e se projeta para o futuro. A compreensão da historicidade da Psicologia no Brasil como construção social, neste texto, tem como foco a análise das contradições que estiveram presentes nos diversos períodos, como condição para a compreensão das possibilidades de superação que permitiram saltos de qualidade no desenvolvimento da Psicologia, quer como conhecimento, quer como prática. Serão apresentadas, para cada período da história da Psicologia no Brasil, uma breve descrição de suas características e a análise de algumas produções, sejam elas teóricas, sejam práticas, que revelam suas contradições, sobretudo o confronto das concepções coexistentes em um mesmo tempo histórico, que demonstram o processo constitutivo dos saberes psicológicos e da Psicologia no Brasil a partir de distintos posicionamentos sociopolíticos e epistemológicos. Busca-se contribuir para a compreensão da constituição da Psicologia no Brasil a partir da dinâmica engendrada pelas e nas contradições históricas dessa área do saber, entendida como construção eminentemente social.

ApoE rs429358 and rs7412 Polymorphism and Gender Differences of Serum Lipid Profile and Cognition in Aging Chinese Population.

Science.gov (United States)

Zhen, Jie; Huang, Xiaochen; Van Halm-Lutterodt, Nicholas; Dong, Shengqi; Ma, Weiwei; Xiao, Rong; Yuan, Linhong

2017-01-01

ApoE gene polymorphism has been reportedly associated with serum lipids and cognition. However, very few studies have explored the combined effects of ApoE gene polymorphism and gender on serum lipid profile with subsequent impacts on cognition in Chinese population. A total of 1,000 Chinese community dwellers aged 55 years and above were recruited in this cross-sectional study. Demographic information of the participants was collected using well designed self-administered questionnaires. The Montreal Cognitive Assessment (MoCA) test was employed to evaluate the cognitive status of the participants. Semi-quantitative food frequency questionnaire (FFQ) was used to obtain the dietary intake information. Fasting venous blood samples were taken for ApoE genotyping and serum lipid measurements. Significant gender differences in cognition, serum lipid profile and dietary fat-rich foods consumption were observed ( p < 0.05). Cognition of the subjects was found to be associated with ApoE genotypes ( p < 0.05). ApoE rs429358 and rs7412 variants demonstrated a significant effect on cognitive performance in the male subjects; especially within the attention and language cognitive domains as well as the total MoCA score ( p < 0.05), respectively. Serum lipid profile and cognition of Chinese adults are significantly linked with gender and ApoE genetic polymorphism. The ApoE variant rs429358 is found to be notably associated with cognition in aging male Chinese population.

The RNA-binding protein HOS5 and serine/arginine-rich proteins RS40 and RS41 participate in miRNA biogenesis in Arabidopsis

KAUST Repository

Chen, Tao

2015-07-30

MicroRNAs are a class of small regulatory RNAs that are generated from primary miRNA (pri-miRNA) transcripts with a stem-loop structure. Accuracy of the processing of pri-miRNA into mature miRNA in plants can be enhanced by SERRATE (SE) and HYPONASTIC LEAVES 1 (HYL1). HYL1 activity is regulated by the FIERY2 (FRY2)/RNA polymerase II C-terminal domain phosphatase-like 1 (CPL1). Here, we discover that HIGH OSMOTIC STRESS GENE EXPRESSION 5 (HOS5) and two serine/arginine-rich splicing factors RS40 and RS41, previously shown to be involved in pre-mRNA splicing, affect the biogenesis of a subset of miRNA. These proteins are required for correct miRNA strand selection and the maintenance of miRNA levels. FRY2 dephosphorylates HOS5 whose phosphorylation status affects its subnuclear localization. HOS5 and the RS proteins bind both intronless and intron-containing pri-miRNAs. Importantly, all of these splicing-related factors directly interact with both HYL1 and SE in nuclear splicing speckles. Our results indicate that these splicing factors are directly involved in the biogenesis of a group of miRNA.

Thorium, UNFC (3,3,3) In Brasil

International Nuclear Information System (INIS)

Villas-Bôas, Roberto C.

2014-01-01

Types of thorium UNFC (3,3,3) in Brasil: • Placer, shoreline; • Placer, alluvial; • Carbonatite with residual enrichment (Barreiro,Catalao); • Carbonatite (Salitre, MG); • Pitinga granites (AM); • Alkalic Igneous

SHBG gene polymorphism (rs1799941 associates with metabolic syndrome in children and adolescents.

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Marquitta J White

Full Text Available Metabolic syndrome (MetS is a complex disorder characterized by coexistence of several cardiometabolic (CM factors, i.e. hyperlipidemia, obesity, high blood pressure and insulin resistance. The presence of MetS is strongly associated with increased risk of cardiovascular disease (CVD. The syndrome was originally defined as an adult disorder, but MetS has become increasingly recognized in children and adolescents.Genetic variants influence biological components common to the CM factors that comprise MetS. We investigated single locus associations between six single nucleotide polymorphisms (SNPs, previously shown to modulate lipid or sex hormone binding globulin (SHBG levels, with MetS in a Turkish pediatric cohort (37 cases, 323 controls.Logistic regression analysis revealed a significant association between rs1799941, located in SHBG, and MetS (OR = 3.09, p-value = 0.006. The association with MetS remained after sequential adjustment for each CM factor included in the syndrome definition, indicating that the identified association is not being driven by any single trait. A relationship between rs1799941 and SHBG levels, was also discovered, but it was dependent on MetS status. In control subjects, the A allele of rs1799941 associated with a significant increase in SHBG levels (p = 0.012, while in cases there was no association between rs1799941 and SHBG levels (p = 0.963.The significant association between rs1799941 and MetS in children is not contingent on any single CM trait. Additionally, the presence of MetS may abrogate effect of rs1799941 polymorphism on SHBG levels in children.

UNIDADES DE CONSERVAÇÃO E SUSTENTABILIDADE: Plano de manejo e aplicação da capacidade de carga no Parque Nacional da Lagoa do Peixe (RS

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Rodrigo Hakira Minohara

2016-12-01

Full Text Available É crescente a busca do homem pelo contato com o meio ambiente, sobre tudo por meio do turismo. Na década de 1960, houve uma mobilização mundial focada na preservação da natureza e o Brasil seguindo o exemplo, começou a estruturar políticas que garantissem a preservação dos seus ecossistemas. Esse processo acarretou na criação do Sistema Nacional de Unidades de Conservação (SNUC, que veio a regulamentar a visitação desses espaços e a sustentabilidade dos ambientes naturais, por meio de planos de manejo e da adoção de modelos de gestão que respeitem sua capacidade de carga. Considerando tais pressupostos, este artigo visa a composição de uma análise tendo como base o planejamento adotado pela Unidade de Conservação - Parque Nacional da Lagoa do Peixe (RS, local onde foram tratadas as questões de manejo e de capacidade de carga para viabilizar o recebimento de visitantes e da promoção da sensibilização para a conservação da biodiversidade. Para desenvolvimento de estudos posteriores, fica a sugestão de realização de pesquisa que englobe todos os parques pertencentes à Região Sul do Brasil, para um possível comparativo em relação ao uso público e à atividade turística.  Palavras-chave: Turismo. Unidades de Conservação. Plano de Manejo.

Design of Bus Protocol Intelligent Initiation System Based On RS485

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Li Liming

2017-01-01

Full Text Available In order to design an effective and reliable RS485 bus protocol based on RS485 bus, this paper introduces the structure and transmission mode of the command frame and the response frame, and also introduce four control measures and the communication in order to process quality of this system. The communication protocol is open, tolerant, reliable and fast, and can realize ignition more reliable and accurate in the intelligent initiation system.

Fat phenotype, associated factors and rs9939609 polymorphism of the FTO gene

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William Alves Lima

2010-02-01

Full Text Available The purpose of this work was to review the main results of studies that have analysed the relationship between the rs9939609 single nucleotide polymorphism (SNP of the FTO gene and the manifestation of overweight/obesity with its associated co-morbidity, and to discuss the interaction of this polymorphism with the other factors which cause obesity. The search was performed using the MEDLINE, Highwire, Science Direct and SciELO databases, applying the following key words: FTO rs9939609, obesity genetic, gene associated obesity, FTO contributes obesity. Inclusion criteria were: original articles where the search was performed in humans and including the rs9939609. Articles that analysed the FTO gene associated with preinstalled hormonal diseases were excluded. Of the several SNP associated with the FTO gene, rs9939609 has been the most researched (studied. This SNP comprises the A and T alleles, with the A homozygote being most susceptible to the development of overweight/obesity in all age ranges, especially in the caucasian population. In this situation, the control of environmental factors (alimentation and physical activity can prevent the excessive build up of fats. Obesity is related to the development of non-transmissible chronic illnesses. Association of rs9939609 polymorphism with the lipidic profile and glycemia were observed. The practicing of physical exercise and feeding habits seem to be the main contributors in the development of overweight/obesity and its resulting co-morbidity.

Familjearbetaren hos en ensamförsörjare : en kvalitativ studie om ensamförsörjarens livssituation och hur familjearbetet påverkas

OpenAIRE

Sjöblom, Mikaela; Azimi, Diana

2013-01-01

Syftet med vårt lärdomsprov är att redogöra för familjearbetarnas åsikter om familjearbetet har specifika drag i utförandet av det hos familjer med en försörjare. I teoridelen tas det upp om familjepolitiken i Finland, familjearbete samt om hur en ensamförsörjares livssituation kan se ut. I undersökningen använde vi oss av kvalitativa forskningsintervjuer. Undersökningspersonerna bestod av åtta familjearbetare från fyra olika kommuner. Intervjuerna gjordes både i grupper och som individue...

Brasil – México: trayectorias estructurales diferenciadas

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Clemente Ruiz Durán

2013-02-01

Full Text Available Na última década, o crescimento permitiu ao Brasil se tornar a sexta economia do mundo, enquanto o México ficou para trás, mesmo que, em meados da primeira década do século XXI, as duas economias estivessem emparelhadas. As raízes dessa diferença podem ser encontradas nas políticas governamentais que no Brasil fortaleceram mercado interno, enquanto o México buscou por estabilidade e a globalização dificultou o potencial do mercado interno e reduziu o efeito das cadeias de valor globais. A análise comparativa das economias latino-americanas confirma a abordagem teórica da teoria do desenvolvimento, que o fortalecimento do mercado interno é a melhor maneira de aproximar economias de escala na economia global.

A Nematode Calreticulin, Rs-CRT, Is a Key Effector in Reproduction and Pathogenicity of Radopholus similis.

Science.gov (United States)

Li, Yu; Wang, Ke; Xie, Hui; Wang, Yan-Tao; Wang, Dong-Wei; Xu, Chun-Lin; Huang, Xin; Wang, De-Sen

2015-01-01

Radopholus similis is a migratory plant-parasitic nematode that causes severe damage to many agricultural and horticultural crops. Calreticulin (CRT) is a Ca2+-binding multifunctional protein that plays key roles in the parasitism, immune evasion, reproduction and pathogenesis of many animal parasites and plant nematodes. Therefore, CRT is a promising target for controlling R. similis. In this study, we obtained the full-length sequence of the CRT gene from R. similis (Rs-crt), which is 1,527-bp long and includes a 1,206-bp ORF that encodes 401 amino acids. Rs-CRT and Mi-CRT from Meloidogyne incognita showed the highest similarity and were grouped on the same branch of the phylogenetic tree. Rs-crt is a multi-copy gene that is expressed in the oesophageal glands and gonads of females, the gonads of males, the intestines of juveniles and the eggs of R. similis. The highest Rs-crt expression was detected in females, followed by juveniles, eggs and males. The reproductive capability and pathogenicity of R. similis were significantly reduced after treatment with Rs-crt dsRNA for 36 h. Using plant-mediated RNAi, we confirmed that Rs-crt expression was significantly inhibited in the nematodes, and resistance to R. similis was significantly improved in transgenic tomato plants. Plant-mediated RNAi-induced silencing of Rs-crt could be effectively transmitted to the F2 generation of R. similis; however, the silencing effect of Rs-crt induced by in vitro RNAi was no longer detectable in F1 and F2 nematodes. Thus, Rs-crt is essential for the reproduction and pathogenicity of R. similis.

A Nematode Calreticulin, Rs-CRT, Is a Key Effector in Reproduction and Pathogenicity of Radopholus similis.

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Yu Li

Full Text Available Radopholus similis is a migratory plant-parasitic nematode that causes severe damage to many agricultural and horticultural crops. Calreticulin (CRT is a Ca2+-binding multifunctional protein that plays key roles in the parasitism, immune evasion, reproduction and pathogenesis of many animal parasites and plant nematodes. Therefore, CRT is a promising target for controlling R. similis. In this study, we obtained the full-length sequence of the CRT gene from R. similis (Rs-crt, which is 1,527-bp long and includes a 1,206-bp ORF that encodes 401 amino acids. Rs-CRT and Mi-CRT from Meloidogyne incognita showed the highest similarity and were grouped on the same branch of the phylogenetic tree. Rs-crt is a multi-copy gene that is expressed in the oesophageal glands and gonads of females, the gonads of males, the intestines of juveniles and the eggs of R. similis. The highest Rs-crt expression was detected in females, followed by juveniles, eggs and males. The reproductive capability and pathogenicity of R. similis were significantly reduced after treatment with Rs-crt dsRNA for 36 h. Using plant-mediated RNAi, we confirmed that Rs-crt expression was significantly inhibited in the nematodes, and resistance to R. similis was significantly improved in transgenic tomato plants. Plant-mediated RNAi-induced silencing of Rs-crt could be effectively transmitted to the F2 generation of R. similis; however, the silencing effect of Rs-crt induced by in vitro RNAi was no longer detectable in F1 and F2 nematodes. Thus, Rs-crt is essential for the reproduction and pathogenicity of R. similis.

DeAnnIso: a tool for online detection and annotation of isomiRs from small RNA sequencing data.

Science.gov (United States)

Zhang, Yuanwei; Zang, Qiguang; Zhang, Huan; Ban, Rongjun; Yang, Yifan; Iqbal, Furhan; Li, Ao; Shi, Qinghua

2016-07-08

Small RNA (sRNA) Sequencing technology has revealed that microRNAs (miRNAs) are capable of exhibiting frequent variations from their canonical sequences, generating multiple variants: the isoforms of miRNAs (isomiRs). However, integrated tool to precisely detect and systematically annotate isomiRs from sRNA sequencing data is still in great demand. Here, we present an online tool, DeAnnIso (Detection and Annotation of IsomiRs from sRNA sequencing data). DeAnnIso can detect all the isomiRs in an uploaded sample, and can extract the differentially expressing isomiRs from paired or multiple samples. Once the isomiRs detection is accomplished, detailed annotation information, including isomiRs expression, isomiRs classification, SNPs in miRNAs and tissue specific isomiR expression are provided to users. Furthermore, DeAnnIso provides a comprehensive module of target analysis and enrichment analysis for the selected isomiRs. Taken together, DeAnnIso is convenient for users to screen for isomiRs of their interest and useful for further functional studies. The server is implemented in PHP + Perl + R and available to all users for free at: http://mcg.ustc.edu.cn/bsc/deanniso/ and http://mcg2.ustc.edu.cn/bsc/deanniso/. © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research.

8q24 rs6983267G variant is associated with increased thyroid cancer risk

Science.gov (United States)

Sahasrabudhe, Ruta; Estrada, Ana; Lott, Paul; Martin, Lynn; Echeverry, Guadalupe Polanco; Velez, Alejandro; Neta, Gila; Takahasi, Meiko; Saenko, Vladimir; Mitsutake, Norisato; Jaeguer, Emma; Duque, Carlos Simon; Rios, Alejandro; Bohorquez, Mabel; Prieto, Rodrigo; Criollo, Angel; Echeverry, Magdalena; Tomlinson, Ian; Carvajal Carmona, Luis G.

2015-01-01

The G allele of the rs6983267 single nucleotide polymorphism, located on chromosome 8q24, has been associated with increased risk of several cancer types. The association between rs6983267G and thyroid cancer has been tested in different populations, mostly of European ancestry, and has led to inconclusive results. While significant associations have been reported in the British and Polish populations, no association has been detected in populations from Spain, Italy and the USA. To further investigate the role of rs6983267G in thyroid cancer susceptibility, we evaluated rs6983267 genotypes in three populations of different continental ancestry (British Isles, Colombia and Japan), providing a total of 3,067 cases and 8,575 controls. We detected significant associations between rs6983267G and thyroid cancer in the British Isles (Odds Ratio, OR= 1.19, 95% confidence interval, CI: 1.11–1.27, P= 4.03 × 10−7), Japan (OR= 1.20, 95% CI: 1.03–1.41, P= 0.022) and a borderline significant association of similar effect direction and size in Colombia (OR= 1.19, 95% CI: 0.99–1.44, P= 0.069). A meta-analysis of our multi-ethnic study and previously published non-overlapping datasets, which included a total of 5,484 cases and 12,594 controls, confirmed the association between rs6983267G and thyroid cancer (P= 1.23 × 10−7, OR= 1.13, 95% CI: 1.07–1.18). Our results therefore support the notion that rs6983267G is a bona fide thyroid cancer risk variant that increases the risk of disease by ~13%. PMID:26290501

Blending the most fundamental Remote-Sensing principles (RS ...

African Journals Online (AJOL)

Blending the most fundamental Remote-Sensing principles (RS) with the most functional spatial knowledge (GIS) with the objective of the determination of the accident-prone palms and points (case study: Tehran-Hamadan Highway on Saveh Superhighway)

RESENHA CRÍTICA - O BRASIL AFRICANO

OpenAIRE

Nery, Valéria

2017-01-01

Três mapas que proporcionam compreensões múltiplas e informações que transcendem tempo e espaço, que reúnem vidas, tradições e memórias, que nos levam a repensar os nossos conhecimentos sobre o Brasil e a África.

Composição de Heteroptera aquáticos e semi-aquáticos na área de abrangência da U.H.E. Dona Francisca, RS, Brasil: fase de pré-enchimento Composition of aquatic and semi-aquatic Heteroptera at the Hydroelectric Power Station of Dona Francisca region, RS, Brazil: before dam construction

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Damaris B. Neri

2005-12-01

Full Text Available Neste estudo, foi analisada a composição dos Heteroptera do curso médio da bacia do rio Jacuí, RS, Brasil, previamente à construção da U.H.E. Dona Francisca, bem como alguns fatores abióticos que poderiam afetar a distribuição e a abundância destes organismos. Nos ambientes lênticos, amostragens quantitativas foram realizadas utilizando-se peneiras, em seis localidades (janeiro 2000. Nos ambientes lóticos, as coletas foram feitas através de amostrador de Surber (de maio a outubro de 2000, privilegiando-se a captura de espécies tipicamente bentônicas. Em cada estação, pH, oxigênio dissolvido, precipitação mensal, temperatura do ar e da água e profundidade foram medidos. Nos rios e riachos, a velocidade da corrente também foi registrada. Quinze espécies foram registradas nos ambientes lênticos, sendo Belostoma sp. e Notonecta sp. as dominantes (70%. A abundância, a riqueza e os índices de diversidade foram mais altos nos locais com maiores dimensões. Nos ambientes lóticos, foram assinaladas duas espécies de Naucoridae, Ambrysus teutonius La Rivers, 1951 e Cryphocricus vianai De Carlo, 1951, sendo a primeira dominante (65%. A abundância foi maior nos pontos com maior sombreamento, presença de árvores e/ou com detritos vegetais, ou com a macrófita Podostemum sp. (Podostemaceae no fundo, e mais baixa em locais com curso semi-regulado. Possivelmente, fatores como temperatura e precipitação acumulada estejam relacionados com a abundância mensal dos Naucoridae. Os resultados deste estudo servirão de subsídio para futuros estudos de impacto ambiental após o enchimento do reservatório da U.H.E. Dona Francisca.The Heteroptera composition in the middle course of the Jacuí River basin, RS, Brazil, and some abiotic factors that might affect their distribution and abundance were studied previously to the Dona Francisca dam construction. The insects were quantitatively sampled in six sites, in lentic environments, with

IL-1B rs16944 polymorphism is related to septic shock and death.

Science.gov (United States)

Jiménez-Sousa, María Ángeles; Medrano, Luz M; Liu, Pilar; Almansa, Raquel; Fernández-Rodríguez, Amanda; Gómez-Sánchez, Esther; Rico, Lucía; Heredia-Rodríguez, María; Gómez-Pesquera, Estefanía; Tamayo, Eduardo; Resino, Salvador

2017-01-01

IL-1β is a primary mediator of systemic inflammatory response syndrome (SIRS) and it may lead to shock septic. Our aim was to analyse whether IL-1B rs16944 polymorphism is associated with the onset of septic shock and death after major surgery. We performed a case-control study on 467 patients who underwent major cardiac or abdominal surgery. Of them, 205 patients developed septic shock (cases, SS group) and 262 patients developed SIRS (controls, SIRS group). The primary outcome variables were the development of septic shock and death within 90 days after diagnosis of septic shock. The IL-1B rs16944 polymorphism was genotyped by Sequenom's MassARRAY platform. The association analysis was performed under a recessive genetic model (AA vs. GG/GC). The frequency of septic shock was higher in patients with IL-1B rs16944 AA genotype than in patients with IL-1B rs16944 GG/AG genotype when all patients were taken into account (63·6% vs. 41·8%; P = 0·006), cardiac surgery (52·2% vs. 33·3%; P = 0·072) and abdominal surgery (76·2% vs. 50·2%; P = 0·023). However, the IL-1B rs16944 AA genotype was only associated with higher likelihood of septic shock in the analysis of all population [adjusted odds ratio (aOR) = 2·26 (95%CI = 1·03; 4·97; P = 0·042], but not when it was stratified by cardiac surgery (P = 0·175) or abdominal surgery (P = 0·467). Similarly, IL-1B rs16944 AA genotype was also associated with higher likelihood of septic shock-related death in all population [aOR = 2·67 (95%CI = 1·07; 4·97); P = 0·035]. IL-1B rs16944 AA genotype seems to be related to the onset of septic shock and death in patients who underwent major surgery. © 2016 Stichting European Society for Clinical Investigation Journal Foundation.

SINAIS DOS TEMPOS: IGREJA E SEITAS NO BRASIL

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Paulo Fermando Carneiro de Andrade

1991-01-01

Full Text Available Entre os anos 1986-1987, o Instituto de Estudos da Religião (ISER, a pedido do Conselho Nacional de Igrejas Cristãs, desenvolveu um longo estudo acerca da Diversidade Religiosa no Brasil, com base num programa coordenado pela antropóloga Leilah Landim. As preocupações centrais que uniam os pesquisadores diziam respeito ao conhecimento do diversificado campo religioso brasileiro com especial ênfase às suas transformações recentes. Resumimos aqui o fruto dos diversos debates travados em torno a questões tais como: "como podem ser inventariadas e classificadas as diversas Igrejas, grupos, movimentos religiosos que compõem esse universo no Brasil hoje? Onde

P-bRS: A Physarum-Based Routing Scheme for Wireless Sensor Networks

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Mingchuan Zhang

2014-01-01

Full Text Available Routing in wireless sensor networks (WSNs is an extremely challenging issue due to the features of WSNs. Inspired by the large and single-celled amoeboid organism, slime mold Physarum polycephalum, we establish a novel selecting next hop model (SNH. Based on this model, we present a novel Physarum-based routing scheme (P-bRS for WSNs to balance routing efficiency and energy equilibrium. In P-bRS, a sensor node can choose the proper next hop by using SNH which comprehensively considers the distance, energy residue, and location of the next hop. The simulation results show how P-bRS can achieve the effective trade-off between routing efficiency and energy equilibrium compared to two famous algorithms.

Segurança alimentar de suplementos comercializados no Brasil

OpenAIRE

Silva,Luiz Fernando Miranda da; Ferreira,Karla Silva

2014-01-01

INTRODUÇÃO: A ingestão de suplementos deve ser seguro à saúde.OBJETIVO: Avaliar a segurança alimentar de suplementos dietéticos no Brasil.MÉTODOS: Os produtos foram pesquisados em 36 websites dos mais relevantes em venda de suplementos no Brasil. Para a verificação da situação legal dos produtos e seus fabricantes, consultou-se a legislação brasileira e o banco de dados do Ministério da Saúde.RESULTADOS: Identificou-se 3526 suplementos, sendo 63% comercializados para fins de emagrecimento e h...

Crime e desorganização familiar no Brasil

OpenAIRE

Costa, Daniel Souza

2012-01-01

O objetivo do trabalho é verificar empiricamente a influência da desorganização familiar nas taxas de homicídios dos municípios do Brasil. Com base na literatura clássica da economia do crime, a melhora no cenário econômico e social promoveria desincentivos à pratica de atividades ilícitas, reduzindo assim o crime. No entanto, o que se verificou na última década no Brasil foi o efeito inverso, devido ao aumento da criminalidade em várias regiões do país. Esse fenômeno abriu uma...

O retrato do Brasil no jornal The New York Times

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Karina Fensterseifer

2015-03-01

Full Text Available A forma como um país é retratado pelos meios de comunicação pode afetar a imagem do mesmo internacionalmente. Estereótipos podem ser formados e reforçados dependendo de como informações sobre o país são enquadradas pela mídia. Uma análise de conteúdo revelou que, em 2013, ao retratar o Brasil, o The New York Times cobriu temas como futebol e Copa do Mundo, política e governo, instabilidade social, crime e violência, economia e cultura. Os resultados deste estudo mostram que o Brasil foi retratado como o país do futebol, apaixonado por seus jogadores, mas violento e com grandes contrastes sociais. Ao cobrir apenas um número limitado de temas, ignorando outros, o The New York Times reforça antigos estereótipos e restringe as possibilidades do Brasil se apresentar ao mundo de forma diferente.

Associations of the FTO rs9939609 and the MC4R rs17782313 polymorphisms with type 2 diabetes are modulated by diet, being higher when adherence to the Mediterranean diet pattern is low

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Ortega-Azorín Carolina

2012-11-01

Full Text Available Abstract Background Although the Fat Mass and Obesity (FTO and Melanocortin-4 Receptor (MC4R genes have been consistently associated with obesity risk, the association between the obesity-risk alleles with type 2 diabetes is still controversial. In some recent meta-analyses in which significant results have been reported, the associations disappeared after adjustment for body mass index (BMI. However gene-diet interactions with dietary patterns have not been investigated. Our main aim was to analyze whether these associations are modulated by the level of adherence to the Mediterranean Diet (MedDiet. Methods Case-control study in 7,052 high cardiovascular risk subjects (3,430 type 2 diabetes cases and 3,622 non-diabetic subjects with no differences in BMI. Diet was assessed by validated questionnaires. FTO-rs9939609 and MC4R-rs17782313 were determined. An aggregate genetic score was calculated to test additive effects. Gene-diet interactions were analyzed. Results Neither of the polymorphisms was associated with type 2 diabetes in the whole population. However, we found consistent gene-diet interactions with adherence to the MedDiet both for the FTO-rs9939609 (P-interaction=0.039, the MC4R-rs17782313 (P-interaction=0.009 and for their aggregate score (P-interaction=0.006. When adherence to the MedDiet was low, carriers of the variant alleles had higher type 2 diabetes risk (OR=1.21, 95%CI: 1.03-1.40; P=0.019 for FTO-rs9939609 and OR=1.17, 95%CI:1.01-1.36; P=0.035 for MC4R-rs17782313 than wild-type subjects. However, when adherence to the MedDiet was high, these associations disappeared (OR=0.97, 95%CI: 0.85-1.16; P=0.673 for FTO-rs9939609 and OR=0.89, 95%CI:0.78-1.02; P=0.097 for MC4R-rs17782313. These gene-diet interactions remained significant even after adjustment for BMI. As MedDiet is rich in folate, we also specifically examined folate intake and detected statistically significant interaction effects on fasting plasma glucose

DISCUSSÕES SOBRE O CONCEITO DE ESCALA E OS MAPEAMENTOS DE SOLOS NO BRASIL

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Joildes Brasil dos Santos

2012-11-01

Full Text Available Os primeiros levantamentos de solos do Brasil datam da década de 50 até meados dos anos 80, graças às expedições lideradas projeto RadamBrasil o que cominou na carta de solos do Brasil. Posteriormente, estudos da Empresa Brasileira de Pesquisa Agropecuária (EMBRAPA e do Instituto Brasileiro de Geografia e Estatística (IBGE incrementaram novas informações a esse mapeamento, e mais recentemente classificaram os solos nacionais segundo o Sistema Brasileiro de Classificação de Solos (SiBCS, 2009, na escala de 1:5.000.000. Haja vista as dimensões continentais do Brasil, essas representações, em pequenas escalas da distribuição dos solos, engendram num problema de generalização excessiva, que não contempla a realidade local. Neste sentido, este artigo terá como objetivo discutir questões referentes à escala e suas ambíguas conceituações, no tocante a abordagem escalar na Ciência Geográfica. Relacionado a isso, perscrutar a certa dos mapeamentos de solos atuais do Brasil, e como estes, a depender da escala, se apresentam de formas distintas.

The miR-449b polymorphism, rs10061133 A>G, is associated with premature ovarian insufficiency.

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Pan, Hong; Chen, Beili; Wang, Jing; Wang, Xi; Hu, Ping; Wu, Shinan; Liu, Yunyun; Xu, Zuying; Zhang, Wei; Wang, Binbin; Cao, Yunxia

2016-09-01

To determine if the miR-449b polymorphism, rs10061133 A>G, is associated with premature ovarian insufficiency (POI) pathogenesis. From January 2011 to December 2014, a total of 148 individuals with POI and 225 age-matched controls were collected from the Center for Reproductive Medicine, 1st Affiliated Hospital of Anhui Medical University (Hefei, China). Genotyping of miR-449b rs1006113 was performed using matrix-assisted laser desorption ionization time-of-flight-based mass spectrometry. Rs10061133 A>G is a highly conserved SNP locus in the mature area of miR-449b. Association analysis shows that the rs10061133 AA genotype is a risk factor for POI. Our study provides the first evidence that the miR-449b rs10061133 AA genotype is associated with POI risk.

Propagation of ELF Radiation from RS-LC System and Red Sprites in Earth-Ionosphere Waveguide

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M. K. Paras

2012-10-01

Full Text Available In this paper, two different mechanisms return stroke-lateral corona (RS-LC system and red sprites which excite Earth-ionosphere waveguide have been discussed. The electric and magnetic fields from RS-LC system and red spites in the Earth-ionosphere waveguide have been calculated. It has been found that red sprites contribute to the Schumann resonances (SR greatly as compared to the RS-LC system.

Carotid intima-media thickness in the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil): a narrative review.

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Santos, Eduardo Henrique Sena; Santos Neto, Pedro José Dos; Santos, Itamar de Souza

2018-01-01

Carotid intima-media thickness (CIMT), as measured by ultrasound, has been used in large studies as a non-invasive marker for subclinical atherosclerosis. The Brazilian Longitudinal Study of Adult Health (ELSA-Brasil) is a cohort of 15,105 civil servants in six Brazilian cities that included CIMT evaluation in its baseline assessment. The aim of the present narrative review was to provide an overview of ELSA-Brasil CIMT articles published up to July 31, 2017. Narrative review of ELSA-Brasil CIMT studies using baseline assessment data. We searched PubMed for the terms "ELSA-Brasil" and "intima-media". This search yielded 21 published articles using CIMT data from the ELSA-Brasil baseline assessment, which were included in this review. We also present information about intima-media thickness assessment from ongoing onsite reevaluations of the study participants. Most published studies focused on the association with traditional and novel cardiovascular risk factors. Studies also presented information about the ELSA-Brasil CIMT protocol at baseline and CIMT value distribution in this large sample. Analyses on the ELSA-Brasil data led to important insights on CIMT interpretation and physiology. Besides the highlighted contributions which have already been made in this field, new data gathered during the ongoing third onsite assessment will enable investigation of substantially new research questions.

IkappaBalpha polymorphism at promoter region (rs2233408) influences the susceptibility of gastric cancer in Chinese.

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Wang, Shiyan; Tian, Linwei; Zeng, Zhirong; Zhang, Mingdong; Wu, Kaichun; Chen, Minhu; Fan, Daiming; Hu, Pinjin; Sung, Joseph J Y; Yu, Jun

2010-02-05

Nuclear factor of kappa B inhibitor alpha (I kappaB alpha) protein is implicated in regulating a variety of cellular process from inflammation to tumorigenesis. The objective of this study was to investigate the susceptibility of rs2233408 T/C genotype in the promoter region of I kappaB alpha to gastric cancer and the association of this polymorphism with clinicopathologic variables in gastric cancer patients. A population-based case-control study was conducted between 1999 and 2006 in Guangdong Province, China. A total of 564 gastric cancer patients and 566 healthy controls were enrolled in this study. rs2233408 genotypes in I kappaB alpha were analyzed by TaqMan SNP genotyping assay. Both rs2233408 T homozygote (TT) and T heterozygotes (TC and TT) had significantly reduced gastric cancer risk (TT: OR = 0.250, 95% CI = 0.069-0.909, P = 0.035; TC and TT: OR = 0.721, 95% CI = 0.530-0.981, P = 0.037), compared with rs2233408 C homozygote (CC). rs2233408 T heterozygotes were significantly associated with reduced risk of intestinal-type gastric cancer with ORs of 0.648 (95% CI = 0.459-0.916, P = 0.014), but not with the diffuse or mix type of gastric cancer. The association between rs2233408 T heterozygotes and gastric cancer appeared more apparent in the older patients (age>40) (OR = 0.674, 95% CI = 0.484-0.939, P = 0.02). rs2233408 T heterozygotes was associated with non-cardiac gastric cancer (OR = 0.594, 95% CI = 0.411-0.859, P = 0.006), but not with cardiac gastric cancer. However, rs2233408 polymorphism was not associated with the prognosis of gastric cancer patients. I kappaB alpha rs2233408 T heterozygotes were associated with reduced risk of gastric cancer, especially for the development of certain subtypes of gastric cancer in Chinese population.

IκBα polymorphism at promoter region (rs2233408 influences the susceptibility of gastric cancer in Chinese

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Sung Joseph JY

2010-02-01

Full Text Available Abstract Background Nuclear factor of kappa B inhibitor alpha (IκBα protein is implicated in regulating a variety of cellular process from inflammation to tumorigenesis. The objective of this study was to investigate the susceptibility of rs2233408 T/C genotype in the promoter region of IκBα to gastric cancer and the association of this polymorphism with clinicopathologic variables in gastric cancer patients. Methods A population-based case-control study was conducted between 1999 and 2006 in Guangdong Province, China. A total of 564 gastric cancer patients and 566 healthy controls were enrolled in this study. rs2233408 genotypes in IκBα were analyzed by TaqMan SNP genotyping assay. Results Both rs2233408 T homozygote (TT and T heterozygotes (TC and TT had significantly reduced gastric cancer risk (TT: OR = 0.250, 95% CI = 0.069-0.909, P = 0.035; TC and TT: OR = 0.721, 95% CI = 0.530-0.981, P = 0.037, compared with rs2233408 C homozygote (CC. rs2233408 T heterozygotes were significantly associated with reduced risk of intestinal-type gastric cancer with ORs of 0.648 (95% CI = 0.459-0.916, P = 0.014, but not with the diffuse or mix type of gastric cancer. The association between rs2233408 T heterozygotes and gastric cancer appeared more apparent in the older patients (age>40 (OR = 0.674, 95% CI = 0.484-0.939, P = 0.02. rs2233408 T heterozygotes was associated with non-cardiac gastric cancer (OR = 0.594, 95% CI = 0.411-0.859, P = 0.006, but not with cardiac gastric cancer. However, rs2233408 polymorphism was not associated with the prognosis of gastric cancer patients. Conclusions IκBα rs2233408 T heterozygotes were associated with reduced risk of gastric cancer, especially for the development of certain subtypes of gastric cancer in Chinese population.

The CHRNA3 rs578776 variant is associated with an intrinsic reward sensitivity deficit in smokers

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Jason D. Robinson

2013-09-01

Full Text Available A compromised brain reward system has been postulated as a key feature of drug dependence. We examined whether several polymorphisms of genes found to regulate nicotinic acetylcholine receptor (nAChR and dopamine (DA expression were related to an intrinsic reward sensitivity (IRS deficit we previously identified among a subgroup of smokers using event-related potentials (ERPs. We examined genetic polymorphisms within the CHRNA5-A3-B4 gene cluster (CHRNA3 rs578776, CHRNA5 rs16969968, LOC123688 rs8034191, and CHRNA3 rs1051730, the ANKK1 gene (rs1800497, and the D2 receptor gene (DRD2 rs1079597, DRD2 rs1799732 from 104 smokers of European ancestry in a smoking cessation trial. Prior to treatment, we recorded ERPs evoked by emotional (both pleasant and unpleasant, neutral, and cigarette-related pictures. Smokers were assigned to two groups (IRS+/IRS- based on the amplitude of the late positive potential (LPP component to the pictures, a neural marker of motivational salience. Smokers (n = 42 with blunted brain responses to intrinsically rewarding (pleasant pictures and enhanced responses to cigarette pictures were assigned to the IRS- group, while smokers (n = 62 with the opposite pattern of LPP responding were assigned to the IRS+ group. Carriers of the protective minor T allele (T/T, C/T of the CHRNA3 rs578776 were less likely to be members of the IRS- group than those homozygous for the at-risk C allele (C/C. The CHRNA3 rs578776 polymorphism did not differ on questionnaires of nicotine dependence, depressed mood, or trait affective disposition and did not predict abstinence at 6 months after the quit date. These results suggest that polymorphisms of genes influencing nAChR expression are related to an endophenotype of reward sensitivity in smokers.

The CHRNA3 rs578776 Variant is Associated with an Intrinsic Reward Sensitivity Deficit in Smokers.

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Robinson, Jason D; Versace, Francesco; Lam, Cho Y; Minnix, Jennifer A; Engelmann, Jeffrey M; Cui, Yong; Karam-Hage, Maher; Shete, Sanjay S; Tomlinson, Gail E; Chen, Tina T-L; Wetter, David W; Green, Charles E; Cinciripini, Paul M

2013-01-01

A compromised brain reward system has been postulated as a key feature of drug dependence. We examined whether several polymorphisms of genes found to regulate nicotinic acetylcholine receptor (nAChR) and dopamine expression were related to an intrinsic reward sensitivity (IRS) deficit we previously identified among a subgroup of smokers using event-related potentials (ERPs). We examined genetic polymorphisms within the CHRNA5-A3-B4 gene cluster (CHRNA3 rs578776, CHRNA5 rs16969968, LOC123688 rs8034191, and CHRNA3 rs1051730), the ANKK1 gene (rs1800497), and the D2 dopamine receptor gene (DRD2 rs1079597, DRD2 rs1799732) from 104 smokers of European ancestry in a smoking cessation trial. Prior to treatment, we recorded ERPs evoked by emotional (both pleasant and unpleasant), neutral, and cigarette-related pictures. Smokers were assigned to two groups (IRS+/IRS-) based on the amplitude of the late positive potential (LPP) component to the pictures, a neural marker of motivational salience. Smokers (n = 42) with blunted brain responses to intrinsically rewarding (pleasant) pictures and enhanced responses to cigarette pictures were assigned to the IRS- group, while smokers (n = 62) with the opposite pattern of LPP responding were assigned to the IRS+ group. Carriers of the protective minor T allele (T/T, C/T) of the CHRNA3 rs578776 were less likely to be members of the IRS- group than those homozygous for the at-risk C allele (C/C). The CHRNA3 rs578776 polymorphism did not differ on questionnaires of nicotine dependence, depressed mood, or trait affective disposition and did not predict abstinence at 6 months after the quit date. These results suggest that polymorphisms of genes influencing nAChR expression are related to an endophenotype of reward sensitivity in smokers.

Estados Unidos: do Iraque ao Brasil

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Virgílio Caixeta Arraes

2010-12-01

Full Text Available O presente artigo busca analisar os recentes temas recorrentes na política externa norte-americana, caracterizada pela “guerra contra o terror”, e seus impactos para a agenda a ser discutida na vindoura visita do presidente dos Estados Unidos, Geoge W. Bush, ao Brasil.

ASPECTOS FÍSICO-QUÍMICOS DE AZEITES DE OLIVA E DE FOLHAS DE OLIVEIRA PROVENIENTES DE CULTIVARES DO RS, BRASIL

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Lucilene Dornelles MELLO

2012-12-01

Full Text Available Este trabalho teve por objetivo apresentar os resultados da caracterização físico-química de azeites de oliva e folhas de oliveira da variedade Arbequina, cultivadas no estado do Rio Grande do Sul, Brasil, e determinar o potencial antioxidante pelo ensaio do DPPH na atividade sequestrante de radicais livres (ASRL %, atividade quelante (% AQ e poder redutor de extratos aquosos de folhas de oliveira in natura, folhas processadas para chás (comercial 1 e comercial 2 e azeites de oliva provenientes de olivais dos municípios de Caçapava do Sul (azeite 1 e Cachoeira do Sul (azeite 2. Os azeites de oliva também foram avaliados quanto aos índices de iodo, saponificação, peróxidos, refração absoluto a 20ºC e determinação da acidez, densidade, medida da absorbância no ultravioleta a 270nm/232nm e determinação do perfil de ácidos graxos. Os estudos com os derivados de oliveira para a fração fenólica e a atividade antioxidante elevaram-se concomitantemente. Os extratos de folhas processadas e os azeites de oliva foram às amostras que apresentaram teores mais altos de fenóis totais e as melhores respostas de ASRL (> 80%. Todas as amostras apresentaram baixos valores percentuais de AQ (< 30% e poder redutor (entre 20 – 50%. Pela análise dos parâmetros físico-químicos e perfil de ácidos graxos, os azeites de oliva podem ser classificados como azeite virgem extra.

ApoE rs429358 and rs7412 Polymorphism and Gender Differences of Serum Lipid Profile and Cognition in Aging Chinese Population

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Jie Zhen

2017-08-01

Full Text Available ApoE gene polymorphism has been reportedly associated with serum lipids and cognition. However, very few studies have explored the combined effects of ApoE gene polymorphism and gender on serum lipid profile with subsequent impacts on cognition in Chinese population. A total of 1,000 Chinese community dwellers aged 55 years and above were recruited in this cross-sectional study. Demographic information of the participants was collected using well designed self-administered questionnaires. The Montreal Cognitive Assessment (MoCA test was employed to evaluate the cognitive status of the participants. Semi-quantitative food frequency questionnaire (FFQ was used to obtain the dietary intake information. Fasting venous blood samples were taken for ApoE genotyping and serum lipid measurements. Significant gender differences in cognition, serum lipid profile and dietary fat-rich foods consumption were observed (p < 0.05. Cognition of the subjects was found to be associated with ApoE genotypes (p < 0.05. ApoE rs429358 and rs7412 variants demonstrated a significant effect on cognitive performance in the male subjects; especially within the attention and language cognitive domains as well as the total MoCA score (p < 0.05, respectively. Serum lipid profile and cognition of Chinese adults are significantly linked with gender and ApoE genetic polymorphism. The ApoE variant rs429358 is found to be notably associated with cognition in aging male Chinese population.

Aspectos do realismo-naturalismo no Brasil

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José Aderaldo Castello

1953-06-01

Full Text Available (Primeiro Parágrafo do Artigo Silvio Romero, no opúsculo O naturalismo em literatura, publicado em 1882, um ano depois de O mulato de Aluísio Azevedo, reivindica, para si a glória de ter sido o introdutor das idéias naturalistas no Brasil.

Atuação do Nutricionista no Programa Nacional de Alimentação Escolar na Região Sul do Brasil

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Rafaela da Silveira Corrêa

Full Text Available Resumo O objetivo deste estudo foi verificar a adequação dos parâmetros numéricos mínimos de referência com relação às atribuições obrigatórias do nutricionista da região Sul do Brasil de acordo com a Resolução do CFN 465/2010. Estudo transversal com amostra representativa de Responsáveis Técnicos do PNAE que atuam na alimentação escolar na região Sul do Brasil (PR, SC e RS. Os questionários foram encaminhados por meio eletrônico. Comparou-se o resultado obtido com o preconizado pela Resolução CFN 465/2010, quanto à realização das atribuições obrigatórias e adequação aos parâmetros numéricos mínimos definidos por esta legislação. Os resultados apontam para a não conformidade de 71,6% dos municípios da Região Sul no que tange o quantitativo de nutricionistas definido pelos parâmetros numéricos mínimos de referência. Esta inadequação se reflete no cumprimento das atribuições do nutricionista no PNAE. Essas inadequações reforçam a necessidade de formação de parcerias e do trabalho intersetorial para o fortalecimento da execução do PNAE, além de ratificarem a necessidade de se garantir condições de trabalho para que o profissional possa exercer suas atividades conforme planejado.

Levantamento soroepidemiológico de leptospirose em trabalhadores do serviço de saneamento ambiental em localidade urbana da região sul do Brasil

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Almeida Laerte Pereira de

1994-01-01

Full Text Available A pesquisa de aglutininas anti-Leptospira, pela técnica de soroaglutinação microscópica, em soros de trabalhadores dos serviços de águas, bueiros e galerias, esgotos, coleta de lixo e limpeza pública, do Município de Pelotas, RS, Brasil, revelou 10,4% de reagentes a um ou mais sorovares; não houve diferenças significantes entre as proporções de reagentes de cada um dos setores de trabalho. Foram identificados 12 sorovares diferentes; castelonis e australis, apesar de mais freqüentes, não apresentaram diferenças estatisticamente significantes com os demais. Constatou-se que 86,9% das amostras apresentavam títulos aglutinantes compreendidos entre 100 e 400; as proporções de soros com títulos iguais a 100 e 400 foram superiores às dos títulos 800, 1.600 e 3.200 (p < 0,05.

Validation of the Persian version of the Schizophrenia Cognition Rating Scale (SCoRS) in patients with schizophrenia.

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Mazhari, Shahrzad; Ghafaree-Nejad, Ali R; Soleymani-Zade, Somayeh; Keefe, Richard S E

2017-06-01

The Schizophrenia Cognition Rating Scale (SCoRS) is an interview-based assessment of cognition that involves interviews with patients and informants. The SCoRS has shown good reliability, validity, and sensitivity to cognitive impairment in schizophrenia, with the advantage of brief administration and scoring time. The present study aimed to test the concurrent validity of the Persian version of the SCoRS. A group of 35 patients with schizophrenia and a group of 35 healthy controls received the Persian-SCoRS in the first session, and a standardized performance-based cognitive battery, the Brief Assessment of Cognition in Schizophrenia (BACS), in the second session.Our results indicated that the Persian version of the SCoRS was sensitive to cognitive impairment in the patients. The Persian SCoRS global rating was significantly associated with the composite score generated from the Persian version of the BACS and predicted functional outcomes as measured by Global Assessment of Functioning (GAF) and World Health Organization Quality of Life (WHO QOL). A Persian version of the SCoRS, an interview based measure of cognition that included informants, is related to cognitive performance and global functioning. Copyright © 2017 Elsevier B.V. All rights reserved.

Association of the GRIN2B rs2284411 polymorphism with methylphenidate response in attention-deficit/hyperactivity disorder.

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Kim, Johanna I; Kim, Jae-Won; Park, Jong-Eun; Park, Subin; Hong, Soon-Beom; Han, Doug Hyun; Cheong, Jae Hoon; Choi, Jae-Won; Lee, Sumin; Kim, Bung-Nyun

2017-08-01

We investigated the possible association between two NMDA subunit gene polymorphisms (GRIN2B rs2284411 and GRIN2A rs2229193) and treatment response to methylphenidate (MPH) in attention-deficit/hyperactivity disorder (ADHD). A total of 75 ADHD patients aged 6-17 years underwent 6 months of MPH administration. Treatment response was defined by changes in scores of the ADHD-IV Rating Scale (ADHD-RS), clinician-rated Clinical Global Impression-Improvement (CGI-I), and Continuous Performance Test (CPT). The association of the GRIN2B and GRIN2A polymorphisms with treatment response was analyzed using logistic regression analyses. The GRIN2B rs2284411 C/C genotype showed significantly better treatment response as assessed by ADHD-RS inattention ( p=0.009) and CGI-I scores ( p=0.009), and there was a nominally significant association in regard to ADHD-RS hyperactivity-impulsivity ( p=0.028) and total ( p=0.023) scores, after adjusting for age, sex, IQ, baseline Clinical Global Impression-Severity (CGI-S) score, baseline ADHD-RS total score, and final MPH dose. The GRIN2B C/C genotype also showed greater improvement at the CPT response time variability ( pADHD.

A editora portuguesa Livros do Brasil e suas obras eróticas na ditadura militar brasileira

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Sandra Reimao

2018-03-01

Full Text Available Há no Arquivo Nacional cinco pareceres, datados de 1977, do Serviço de Censura de Diversões Públicas, orgão do Ministério da Justiça do Brasil, indicando o veto a cinco livros eróticos publicados pela editora portuguesa Livros do Brasil. Visando elaborar uma compreensãso contextualizada destes pareceres, esse estudo aborda inicialmente a história da editora Livros do Brasil e seu perfil editorial; a seguir, busca caracterizar as edições eróticas desta editora vetadas no Brasil, e, por fim, discute e analisa especificidades dos pareceres censórios brasileiros e de suas articulações argumentativas.

Logística reversa dos pneus usados no Brasil

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Lagarinhos,Carlos A. F.; Tenório,Jorge A. S.

2013-01-01

Após a aprovação da Resolução CONAMA (Conselho Nacional do Meio Ambiente) nº 258/99, ocorreu um avanço significativo na reciclagem de pneus no Brasil, com o desenvolvimento de tecnologias para reutilização, reciclagem e valorização energética. Em 2009, foi aprovada a Resolução CONAMA nº 416/09 que muda a forma de cálculo para a reciclagem, de pneus produzidos para venda no mercado de reposição. O objetivo principal deste trabalho é apresentar a logística reversa dos pneus usados no Brasil e c...

Cuerpas Gordas: Gordofobia, Feminismo y Activismo de la Gordura en Brasil

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Luna Montalbetti, Cynthia Jazmin

2017-01-01

Metadados do Trabalho de Conclusão de Curso: CUERPAS GORDAS: Gordofobia, Feminismo y Activismo de la Gordura en Brasil, pela/o discente: Cynthia Jazmin Luna Montalbetti do Centro de Integração e Relações Internacionais, curso de Ciência Política - Sociologia da Universidade Federal da Integração Latino-Americana (UNILA), no Repositório Institucional da UNILA (RI-UNILA) Cuerpas Gordas: Gordofobia, Feminismo y Activismo de la Gordura en Brasil

Association of calcium sensing receptor polymorphisms at rs1801725 with circulating calcium in breast cancer patients.

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Wang, Li; Widatalla, Sarrah E; Whalen, Diva S; Ochieng, Josiah; Sakwe, Amos M

2017-08-02

Breast cancer (BC) patients with late-stage and/or rapidly growing tumors are prone to develop high serum calcium levels which have been shown to be associated with larger and aggressive breast tumors in post and premenopausal women respectively. Given the pivotal role of the calcium sensing receptor (CaSR) in calcium homeostasis, we evaluated whether polymorphisms of the CASR gene at rs1801725 and rs1801726 SNPs in exon 7, are associated with circulating calcium levels in African American and Caucasian control subjects and BC cases. In this retrospective case-control study, we assessed the mean circulating calcium levels, the distribution of two inactivating CaSR SNPs at rs1801725 and rs1801726 in 199 cases and 384 age-matched controls, and used multivariable regression analysis to determine whether these SNPs are associated with circulating calcium in control subjects and BC cases. We found that the mean circulating calcium levels in African American subjects were higher than those in Caucasian subjects (p calcium levels were higher in BC cases compared to control subjects (p calcium levels in BC patients were independent of race. We also show that in BC cases and control subjects, the major alleles at rs1801725 (G/T, A986S) and at rs1801726 (C/G, Q1011E) were common among Caucasians and African Americans respectively. Compared to the wild type alleles, polymorphisms at the rs1801725 SNP were associated with higher calcium levels (p = 0.006) while those at rs1801726 were not. Using multivariable linear mixed-effects models and adjusting for age and race, we show that circulating calcium levels in BC cases were associated with tumor grade (p = 0.009), clinical stage (p = 0.003) and more importantly, with inactivating mutations of the CASR at the rs1801725 SNP (p = 0.038). These data suggest that decreased sensitivity of the CaSR to calcium due to inactivating polymorphisms at rs1801725, may predispose up to 20% of BC cases to high circulating calcium

ChemiRs: a web application for microRNAs and chemicals.

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Su, Emily Chia-Yu; Chen, Yu-Sing; Tien, Yun-Cheng; Liu, Jeff; Ho, Bing-Ching; Yu, Sung-Liang; Singh, Sher

2016-04-18

MicroRNAs (miRNAs) are about 22 nucleotides, non-coding RNAs that affect various cellular functions, and play a regulatory role in different organisms including human. Until now, more than 2500 mature miRNAs in human have been discovered and registered, but still lack of information or algorithms to reveal the relations among miRNAs, environmental chemicals and human health. Chemicals in environment affect our health and daily life, and some of them can lead to diseases by inferring biological pathways. We develop a creditable online web server, ChemiRs, for predicting interactions and relations among miRNAs, chemicals and pathways. The database not only compares gene lists affected by chemicals and miRNAs, but also incorporates curated pathways to identify possible interactions. Here, we manually retrieved associations of miRNAs and chemicals from biomedical literature. We developed an online system, ChemiRs, which contains miRNAs, diseases, Medical Subject Heading (MeSH) terms, chemicals, genes, pathways and PubMed IDs. We connected each miRNA to miRBase, and every current gene symbol to HUGO Gene Nomenclature Committee (HGNC) for genome annotation. Human pathway information is also provided from KEGG and REACTOME databases. Information about Gene Ontology (GO) is queried from GO Online SQL Environment (GOOSE). With a user-friendly interface, the web application is easy to use. Multiple query results can be easily integrated and exported as report documents in PDF format. Association analysis of miRNAs and chemicals can help us understand the pathogenesis of chemical components. ChemiRs is freely available for public use at http://omics.biol.ntnu.edu.tw/ChemiRs .

Effects of VRK2 (rs2312147 on white matter connectivity in patients with schizophrenia.

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Hoyoung Sohn

Full Text Available Recent genome-wide association studies of schizophrenia reported a novel risk variant, rs2312147 at vaccinia-related kinase 2 gene (VRK2, in multiple Asian and European samples. However, its effect on the brain structure in schizophrenia is little known. We analyzed the brain structure of 36 schizophrenia patients and 18 healthy subjects with regard to rs2312147 genotype groups. Brain magnetic resonance scans for gray matter (GM and white matter (WM analysis, and genotype analysis for VRK2 rs2312147, were conducted. The Positive and Negative Syndrome Scale and the Digit Symbol Test were assessed for schizophrenia patients. There was no significant difference in either GM volume or WM connectivity with regard to rs2312147 genotype in healthy subjects. In contrast, we found significant differences in the WM connectivity between rs2312147 CC and CT/TT genotype groups of schizophrenia patients. The related brain areas included the splenium of corpus callosum, the left occipital lobe WM, the internal capsule (left anterior limb and right retrolenticular part, the bilateral temporal lobe WM, the left fornix/stria terminalis, the left cingulate gyrus WM, and the left parietal lobe WM. Voxelwise correlation analysis revealed that the Digit Symbol Test scores (age corrected correlated with the fractional anisotropy in WM tracts that previously showed significant group differences between the CT/TT and CC genotypes in the rs2312147 CT/TT genotype group, while no significant correlation was found in the CC genotype group. Our data may provide evidence for the effect of VRK2 on WM connectivity in patients with schizophrenia.

LINC00673 rs11655237 C>T confers neuroblastoma susceptibility in Chinese population.

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Zhang, Zhuorong; Chang, Yitian; Jia, Wei; Zhang, Jiao; Zhang, Ruizhong; Zhu, Jinhong; Yang, Tianyou; Xia, Huimin; Zou, Yan; He, Jing

2018-02-28

Neuroblastoma, which accounts for approximately 10% of all pediatric cancer-related deaths, has become a therapeutic challenge and global burden attributed to poor outcomes and mortality rates of its high-risk form. Previous genome-wide association studies (GWASs) identified the LINC00673 rs11655237 C>T polymorphism to be associated with the susceptibility of several malignant tumors. However, the association between this polymorphism and neuroblastoma susceptibility is not clear. We genotyped LINC00673 rs11655237 C>T in 393 neuroblastoma patients in comparison with 812 age-, gender-, and ethnicity-matched healthy controls. We found a significant association between the LINC00673 rs11655237 C>T polymorphism and neuroblastoma risk (TT compared with CC: adjusted odds ratio (OR) =1.80, 95% confidence interval (CI) =1.06-3.06, P =0.029; TT/CT compared with CC: adjusted OR =1.31, 95% CI =1.02-1.67, P =0.033; and T compared with C: adjusted OR =1.29, 95% CI =1.06-1.58, P =0.013). Furthermore, stratified analysis indicated that the rs11655237 T allele carriers were associated with increased neuroblastoma risk for patients with tumor originating from the adrenal gland (adjusted OR =1.51, 95% CI =1.06-2.14, P =0.021) and International Neuroblastoma Staging System (INSS) stage IV disease (adjusted OR =1.60, 95% CI =1.12-2.30, P =0.011). In conclusion, we verified that the LINC00673 rs11655237 C>T polymorphism might be associated with neuroblastoma susceptibility. Prospective studies with a large sample size and different ethnicities are needed to validate our findings. © 2018 The Author(s).

A imagem do Brasil no discurso do New York Times. Aspectos sociais

Directory of Open Access Journals (Sweden)

Maria Inez Mateus Dota

2010-01-01

Full Text Available Este texto presenta un análisis de las noticias publicadas en el periódico The New York Times, versión digital, entre los meses de enero y junio de 2004. Al relacionarlas con los aspectos sociales del Brasil se intenta ver cuál es la imagen que ese periódico muestra del Brasil. El artículo adopta como fundamentos teóricos y metodológicos el análisis del discurso, principalmente las contribuiciones de Bell (1991, Fairclough (1995 y 2001, Fowler (1991 y Sousa (2004, discute las estrategias discursivas usadas para representar al Brasil y examina qué elementos escoge y los recursos de lenguaje que son empleados para la producción de los textos analizados.

The 8q24 rs6983267G variant is associated with increased thyroid cancer risk.

Science.gov (United States)

Sahasrabudhe, Ruta; Estrada, Ana; Lott, Paul; Martin, Lynn; Polanco Echeverry, Guadalupe; Velez, Alejandro; Neta, Gila; Takahasi, Meiko; Saenko, Vladimir; Mitsutake, Norisato; Jaeguer, Emma; Duque, Carlos Simon; Rios, Alejandro; Bohorquez, Mabel; Prieto, Rodrigo; Criollo, Angel; Echeverry, Magdalena; Tomlinson, Ian; Carmona, Luis G Carvajal

2015-10-01

The G allele of the rs6983267 single-nucleotide polymorphism, located on chromosome 8q24, has been associated with increased risk of several cancer types. The association between rs6983267G and thyroid cancer (TC) has been tested in different populations, mostly of European ancestry, and has led to inconclusive results. While significant associations have been reported in the British and Polish populations, no association has been detected in populations from Spain, Italy and the USA. To further investigate the role of rs6983267G in TC susceptibility, we evaluated rs6983267 genotypes in three populations of different continental ancestry (British Isles, Colombia and Japan), providing a total of 3067 cases and 8575 controls. We detected significant associations between rs6983267G and TC in the British Isles (odds ratio (OR)=1.19, 95% CI: 1.11-1.27, P=4.03×10(-7)), Japan (OR=1.20, 95% CI: 1.03-1.41, P=0.022) and a borderline significant association of similar effect direction and size in Colombia (OR=1.19, 95% CI: 0.99-1.44, P=0.069). A meta-analysis of our multi-ethnic study and previously published non-overlapping datasets, which included a total of 5484 cases and 12 594 controls, confirmed the association between rs6983267G and TC (P=1.23×10(-7), OR=1.13, 95% CI: 1.08-1.18). Our results therefore support the notion that rs6983267G is a bona fide TC risk variant that increases the risk of disease by ∼13%. © 2015 Society for Endocrinology.

Chemical chaperones exceed the chaperone effects of RIC-3 in promoting assembly of functional α7 AChRs.

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Alexander Kuryatov

Full Text Available Functional α7 nicotinic acetylcholine receptors (AChRs do not assemble efficiently in cells transfected with α7 subunits unless the cells are also transfected with the chaperone protein RIC-3. Despite the presence of RIC-3, large amounts of these subunits remain improperly assembled. Thus, additional chaperone proteins are probably required for efficient assembly of α7 AChRs. Cholinergic ligands can act as pharmacological chaperones to promote assembly of mature AChRs and upregulate the amount of functional AChRs. In addition, we have found that the chemical chaperones 4-phenylbutyric acid (PBA and valproic acid (VPA greatly increase the amount of functional α7 AChRs produced in a cell line expressing both α7 and RIC-3. Increased α7 AChR expression allows assay of drug action using a membrane potential-sensitive fluorescent indicator. Both PBA and VPA also increase α7 expression in the SH-SY5Y neuroblastoma cell line that endogenously expresses α7 AChRs. VPA increases expression of endogenous α7 AChRs in hippocampal neurons but PBA does not. RIC-3 is insufficient for optimal assembly of α7 AChRs, but provides assay conditions for detecting additional chaperones. Chemical chaperones are a useful pragmatic approach to express high levels of human α7 AChRs for drug selection and characterization and possibly to increase α7 expression in vivo.

A Polymorphism in Hepatocyte Nuclear Factor 1 Alpha, rs7310409, Is Associated with Left Main Coronary Artery Disease

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Rui Liu

2014-01-01

Full Text Available Coronary artery disease is the leading cause of mortality and morbidity in the world. Left main coronary artery disease (LMCAD is a particularly severe phenotypic form of CAD and has a genetic basis. We hypothesized that some inflammation- and hyperhomocysteinemia-related gene polymorphisms may contribute to LMCAD susceptibility in a Chinese population. We studied the association between polymorphisms in the genes hepatocyte nuclear factor 1 alpha (HNF1A; rs7310409, G/A, C-reactive protein (rs1800947 and rs3093059 T/C, methylenetetrahydrofolate reductase (rs1801133, C/T, and methylenetetrahydrofolate dehydrogenase (rs1076991, A/G in 402 LMCAD and 804 more peripheral CAD patients in a Chinese population. Genotyping was performed using the matrix-assisted laser desorption/ionization time-of-flight mass spectrometry method. When the HNF1A rs7310409 GG homozygote genotype was used as the reference group, both the individual, GA and AA, and combined GA/AA genotypes were associated with an increased risk of LMCAD. This single nucleotide polymorphism (rs7310409 is strongly associated with plasma CRP levels. In conclusion, the present study provides evidence that the HNF1A rs7310409 G/A functional polymorphism may contribute to the risk of LMCAD.

ANIMAL WELFARE FROM MOUSE TO MOOSE--IMPLEMENTING THE PRINCIPLES OF THE 3RS IN WILDLIFE RESEARCH.

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Lindsjö, Johan; Fahlman, Åsa; Törnqvist, Elin

2016-04-01

The concept of the 3Rs (replacement, reduction, and refinement) was originally developed for improving laboratory animal welfare and is well known in biomedical and toxicologic research. The 3Rs have so far gained little attention in wildlife research, and there could be several reasons for this. First, researchers may prioritize the welfare of populations and ecosystems over the welfare of individual animals. The effects of research on individual animals can, however, impact welfare and research quality at group and population levels. Second, researchers may find it difficult to apply the 3Rs to studies of free-living wildlife because of the differences between laboratory and wild animals, species, research environment, and purpose and design of the studies. There are, however, several areas where it is possible to transfer the 3R principles to wildlife research, including replacement with noninvasive research techniques, reduction with optimized experimental design, and refinement with better methods of capture, anesthesia, and handling. Third, researchers may not have been trained in applying the 3Rs in wildlife research. This training is needed since ethics committees, employers, journal publishers, and funding agencies increasingly require researchers to consider the welfare implications of their research. In this paper, we compare the principles of the 3Rs in various research areas to better understand the possibilities and challenges of the 3Rs in wildlife research. We emphasize the importance of applying the 3Rs systematically throughout the research process. Based on experiences from laboratory research, we suggest three key factors to enhance implementation of the 3Rs in wildlife research: 1) organizational structure and management, 2) 3R awareness, and 3) research innovation, validation, and implementation. Finally, we encourage an interdisciplinary approach to incorporate the 3R principles in wildlife research. For improved animal welfare and increased

FIRE, A Test Bed for ARIES-RS/AT Advanced Physics and Plasma Technology

International Nuclear Information System (INIS)

Meade, Dale M.

2004-01-01

The overall vision for FIRE [Fusion Ignition Research Experiment] is to develop and test the fusion plasma physics and plasma technologies needed to realize capabilities of the ARIES-RS/AT power plant designs. The mission of FIRE is to attain, explore, understand and optimize a fusion dominated plasma which would be satisfied by producing D-T [deuterium-tritium] fusion plasmas with nominal fusion gains ∼10, self-driven currents of ∼80%, fusion power ∼150-300 MW, and pulse lengths up to 40 s. Achieving these goals will require the deployment of several key fusion technologies under conditions approaching those of ARIES-RS/AT. The FIRE plasma configuration with strong plasma shaping, a double null pumped divertor and all metal plasma-facing components is a 40% scale model of the ARIES-RS/AT plasma configuration. ''Steady-state'' advanced tokamak modes in FIRE with high beta, high bootstrap fraction, and 100% noninductive current drive are suitable for testing the physics of the ARIES-RS/A T operating modes. The development of techniques to handle power plant relevant exhaust power while maintaining low tritium inventory is a major objective for a burning plasma experiment. The FIRE high-confinement modes and AT-modes result in fusion power densities from 3-10 MWm -3 and neutron wall loading from 2-4 MWm -2 which are at the levels expected from the ARIES-RS/AT design studies

Diversidad de macroalgas asociada con un manto de rodolitos tropical de Brasil

OpenAIRE

Amado-Filho, GM; Maneveldt, GW; Pereira-Filho, GH; Manso, RCC; Bahia, RG.; Barros-Barreto, MB; Guimarães, SMPB

2010-01-01

Se describen las poblaciones de las macroalgas submareales predominantemente tropicales que crecen sobre rodolitos entre 4 y 18 m de profundidad en la parte sur del estado de Espirito Santo (Brasil). Muestreos cualitativos y cuantitativos revelaron comunidades ricas en especies de algas, incluyendo 167 especies. Tres especies de rodofitas son nuevas adiciones a la flora marina de Brasil (Lithothamnion muelleri, Scinaia aborealis y Mesophyllum engelhartii). Las marcadas diferencias estacionale...

RS-SNP: a random-set method for genome-wide association studies

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Mukherjee Sayan

2011-03-01

Full Text Available Abstract Background The typical objective of Genome-wide association (GWA studies is to identify single-nucleotide polymorphisms (SNPs and corresponding genes with the strongest evidence of association (the 'most-significant SNPs/genes' approach. Borrowing ideas from micro-array data analysis, we propose a new method, named RS-SNP, for detecting sets of genes enriched in SNPs moderately associated to the phenotype. RS-SNP assesses whether the number of significant SNPs, with p-value P ≤ α, belonging to a given SNP set is statistically significant. The rationale of proposed method is that two kinds of null hypotheses are taken into account simultaneously. In the first null model the genotype and the phenotype are assumed to be independent random variables and the null distribution is the probability of the number of significant SNPs in greater than observed by chance. The second null model assumes the number of significant SNPs in depends on the size of and not on the identity of the SNPs in . Statistical significance is assessed using non-parametric permutation tests. Results We applied RS-SNP to the Crohn's disease (CD data set collected by the Wellcome Trust Case Control Consortium (WTCCC and compared the results with GENGEN, an approach recently proposed in literature. The enrichment analysis using RS-SNP and the set of pathways contained in the MSigDB C2 CP pathway collection highlighted 86 pathways rich in SNPs weakly associated to CD. Of these, 47 were also indicated to be significant by GENGEN. Similar results were obtained using the MSigDB C5 pathway collection. Many of the pathways found to be enriched by RS-SNP have a well-known connection to CD and often with inflammatory diseases. Conclusions The proposed method is a valuable alternative to other techniques for enrichment analysis of SNP sets. It is well founded from a theoretical and statistical perspective. Moreover, the experimental comparison with GENGEN highlights that it is

Fatty acid translocase gene CD36 rs1527483 variant influences oral fat perception in Malaysian subjects.

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Ong, Hing-Huat; Tan, Yen-Nee; Say, Yee-How

2017-01-01

We determined whether single nucleotide polymorphisms (SNPs; rs1761667 and rs1527483) in the fatty acid translocase CD36 gene - a receptor for fatty acids - is associated with oral fat perception (OFP) of different fat contents in custards and commercially-available foods, and obesity measures in Malaysian subjects (n=313; 118 males, 293 ethnic Chinese; 20 ethnic Indians). A 170-mm visual analogue scale was used to assess the ratings of perceived fat content, oiliness and creaminess of 0%, 2%, 6% and 10% fat content-by-weight custards and low-fat/regular versions of commercially-available milk, mayonnaise and cream crackers. Overall, the subjects managed to significantly discriminate the fat content, oiliness and creaminess between low-fat/regular versions of milk and mayonnaise. Females rated the perception of fat content and oiliness of both milks higher, but ethnicity, obesity and adiposity status did not seem to play a role in influencing most of OFP. The overall minor allele frequencies for rs1761667 and rs1527483 were 0.30 and 0.26, respectively. Females and individuals with rs1527483 TT genotype significantly perceived greater creaminess of 10% fat-by-weight custard. Also, individuals with rs1527483 TT genotype and T allele significantly perceived greater fat content of cream crackers, independent of fat concentration. rs1761667 SNP did not significantly affect OFP, except for cream crackers. Both gene variants were also not associated with obesity measures. Taken together, this study supports the notion that CD36 - specifically rs1527483, plays a role in OFP, but not in influencing obesity in Malaysian subjects. Besides, gender is an important factor for OFP, where females had higher sensitivity. Copyright © 2016 Elsevier Inc. All rights reserved.

(Re)Descobrimento do Brasil

OpenAIRE

Gatti, José; Universidade Federal de Santa Catarina

2008-01-01

Como todos aprendemos nas escolas brasileiras, os navegadores portugueses chegaram ao Brasil em 1500. Desde então, esse evento tem sido objeto de controvérsias (casualidade? intencionalidade dos navegadores?) e disputas (quem os teria precedido? espanhóis? franceses? africanos?). Acima das polêmicas, o que continua sendo ensinado é que a frota comandada por Pedro Álvares Cabral realizou o primeiro contato oficial de Portugal com a nova terra a 16° Sul e a identificou como possessão Del Rey, c...

Can rs3767140 SNP of the perlecan (HSPG2) gene affect the diabetes mellitus through the dyslipidemia?

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Kurnaz-Gömleksiz, Ö; Tokat, B; Aslan, E I; Yanar, F; Ermiş-Karaali, Z; Öztürk, O; Yilmaz-Aydoğan, H

2016-07-31

Perlecan (HSPG2) play an important role in the lipoprotein metabolisms. The G allele of the HSPG2-rs3767140 may affect the binding of heparan sulfate (HS) chains and hence cause loss of HS from the basement membrane. HSPG2-rs3767140 was studied in 60 T2DM patients and 109 healthy controls. In diabetic patients HSPG2-rs3767140 T variant allele carriers (TT+GT) have decreased fasting plasma glucose (FPG) and serum LDL-C levels (p=0.071 and p=0.060, respectively) versus GG genotype carriers. Moreover, in both of the two groups in which the T allele carriers HDL-cholesterol levels tend to be high. We investigated that the HSPG2-rs3767140 promoted to the dyslipidemic phenotype in the type 2 diabetes mellitus (T2DM) patients. We suggest that the HSPG2-rs3767140 might be associated with the decreased FPG and LDL-C and with the increased HDL-C in diabetics. Therefore, the HSPG2-rs3767140 might be a protective for the diabetes mellitus due to its ameliorating effect on the dyslipidemic phenotype.

Calcium-sensing receptor gene polymorphism (rs7652589) is associated with calcium nephrolithiasis in the population of Yi nationality in Southwestern China.

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Li, Hao; Zhang, Jianhua; Long, Jiang; Shi, Jiarun; Luo, Yuhui

2018-04-16

The calcium-sensing receptor (CaSR) gene plays an important role in regulating the Ca 2+ balance and reducing the risk for calcium stones. In this study, we evaluated the association of CaSR polymorphisms with calcium nephrolithiasis in the population of Yi nationality in Southwestern China. Biochemical variables were evaluated in 624 calcium nephrolithiasis patients and 470 age-matched healthy controls without a history of nephrolithiasis. CaSR polymorphisms rs7652589, rs1501899, rs1801725 (Ala986Ser), rs1042636 (Arg990Gly) and rs1801726 (Gln1011Glu) were investigated between the calcium nephrolithiasis patients and healthy controls, using direct sequencing. Compared with the healthy controls, serum creatinine and 24-hour urine calcium levels were significantly higher in calcium nephrolithiasis patients. Among these five polymorphisms, the genotypic and allelic frequency distributions of rs7652589 SNP was significantly associated with the risk of calcium nephrolithiasis. However, there were no genotypic or allelic distribution differences for rs1501899, rs1801725, rs1042636, and rs1801726 polymorphisms between calcium nephrolithiasis patients and healthy controls. Moreover, the association between rs7652589 SNP genotypes and the biochemical variables was not found. Our study showed that CaSR rs7652589 polymorphism had a significant effect on the risk of developing calcium nephrolithiasis in the population of Yi nationality in Southwestern China. © 2018 John Wiley & Sons Ltd/University College London.

La confianza interpersonal brasileña en perspectiva comparada

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Timothy Joseph POWER

2009-11-01

Full Text Available RESUMEN: Uno de los aspectos menos estudiados de la cultura política del Brasil es su tasa extraordinariamente baja de confianza interpersonal. Después de revisar la literatura sobre confianza interpersonal, el presente artículo examina el nivel brasileño de confianza social en perspectiva regional y global. Analiza datos de sondeos recientes y demuestra que el mejor predictor de confianza es la educación, una área en que Brasil presenta un desarrollo inferior al de sus vecinos. El artículo también sugiere una agenda de investigación futura para estudiar este aspecto singular de la cultura política brasileña, dentro de la cual las variables de desigualdad social y de exposición a la televisión tendrían papeles importantes. Tal agenda de investigación es de gran consecuencia dado el papel importante de la confianza interpersonal, tanto para el desarrollo económico como para la consolidación democrática.ABSTRACT: One of the most understudied aspects of Brazilian political culture is the country’s extraordinarily low rates of interpersonal trust. After reviewing the literature on interpersonal trust, this paper provides regional and global perspective on Brazil’s level of social trust. It examines data from recent public opinion surveys in Brazil and demonstrates that the strongest predictor of trust is education, an area in which Brazil lags behind its neighbors. The paper also suggests a future research agenda for investigating this unique aspect of Brazilian political culture, in which the variables of inequality and television exposure would play important roles. Such a research agenda is critical given the important role played by trust in both economic development and democratic consolidation.

Jornalismo, literatura e urbanização no Brasil

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Roberto Nicolato

2013-12-01

Full Text Available RESUMOEste artigo temcomo objetivo revelar as relações existentes entre jornalismo, literatura eurbanização no Brasil, no período compreendido entre o descobrimento e o iníciodas duas primeiras décadas do século XX. Em termos historiográficos, sãoanalisadas a Carta de Pero Vaz de Caminha, as Cartas Chilenas, a chegada e aconsolidação da imprensa no Brasil. Neste último, a análise é feita a partirdas reflexões sobre a identidade nacional nas figuras de Lima Barreto, João doRio e Euclides da Cunha.Palavras-chave: Jornalismo. Literatura. História. ABSTRACTThis article aims to reveal the existingrelations among journalism, literature and urbanization in Brazil, in theperiod between the discovery and the beginning of the first two decades of the20th century. In historiographical terms, the Letter of Pero Vaz de Caminha,the Chilean Letters, the arrival and the consolidation of the press in Brazilare analyzed. In the latter, the analysis is conducted from the reflections ofLima Barreto, João do Rio and Euclides da Cunha as pictures of nationalidentity.Key words: Journalism. Literature.History RESUMENEste artículo tiene comoobjetivo mostrar las relaciones existentes entre el periodismo, la literatura yla urbanización en Brasil, en el período transcurrido entre el descubrimiento yel inicio de las dos primeras décadas del siglo 20. Desde el punto de vistahistoriográfico, se analizan la Carta de Pero Vaz de Caminha, las CartasChilenas, la llegada y la consolidación de la prensa en Brasil. En este últimocaso, el análisis se lleva a cabo desde las reflexiones sobre la identidadnacional en las figuras de Lima Barreto, João do Rio y Euclides da Cunha.Palabras-clave: Periodismo. Literatura. Historia.

MicroRNAs (MiRs) Precisely Regulate Immune System Development and Function in Immunosenescence Process.

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Aalaei-Andabili, Seyed Hossein; Rezaei, Nima

2016-01-01

Human aging is a complex process with pivotal changes in gene expression of biological pathways. Immune system dysfunction has been recognized as one of the most important abnormalities induced by senescent names immunosenescence. Emerging evidences suggest miR role in immunosenescence. We aimed to systemically review all relevant reports to clearly state miR effects on immunosenescence process. Sensitive electronic searches carried out. Quality assessment has been performed. Since majority of the included studies were laboratory works, and therefore heterogen, we discussed miR effects on immunological aging process nonstatically. Forty-six articles were found in the initial search. After exclusion of 34 articles, 12 studies enrolled to the final stage. We found that miRs have crucial roles in exact function of immune system. MiRs are involved in the regulation of the aging process in the immune system components and target certain genes, promoting or inhibiting immune system reaction to invasion. Also, miRs control life span of the immune system members by regulation of the genes involved in the apoptosis. Interestingly, we found that immunosenescence is controllable by proper manipulation of the various miRs expression. DNA methylation and histone acetylation have been discovered as novel strategies, altering NF-κB binding ability to the miR promoter sites. Effect of miRs on impairment of immune system function due to the aging is emerging. Although it has been accepted that miRs have determinant roles in the regulation of the immunosenescence; however, most of the reports are concluded from animal/laboratory works, suggesting the necessity of more investigations in human.

O Rugby, identidade e processos econômicos no Brasil

OpenAIRE

Diego Monteiro Gutierrez

2016-01-01

A dissertação cria um panorama amplo da prática do rugby no Brasil abordando aspectos sociológicos e históricos da modalidade em território nacional com o objetivo de compreender a sua prática, características e dinâmicas na atualidade. A partir do referencial teórico de Bourdieu e Mauss, entre outros, o trabalho constrói uma história do rugby no Brasil, utilizando como base documentos e entrevistas. A dissertação procura demonstrar que o rugby, inicialmente praticado quase que só por jogador...

Mercado de água (envasada) no Brasil e no mundo

OpenAIRE

Gorini, Ana Paula Fontenelle

2000-01-01

Este artigo traça o panorama do setor de água engarrafada no Brasil e no mundo, que representa a quinta maior categoria de bebidas (em volume) no país, vindo atrás de refrigerantes, leite, cerveja e café solúvel e à frente de sucos e vinhos. Ao longo da década de 90, o segmento vem apresentando as maiores taxas de crescimento entre todas as categorias mencionadas. Comparado com países como Itália, França, Estados Unidos, entre outros, o Brasil apresenta ainda um baixo consumo per capita e exc...

VfrB Is a Key Activator of the Staphylococcus aureus SaeRS Two-Component System.

Science.gov (United States)

Krute, Christina N; Rice, Kelly C; Bose, Jeffrey L

2017-03-01

In previous studies, we identified the fatty acid kinase virulence factor regulator B (VfrB) as a potent regulator of α-hemolysin and other virulence factors in Staphylococcus aureus In this study, we demonstrated that VfrB is a positive activator of the SaeRS two-component regulatory system. Analysis of vfrB , saeR , and saeS mutant strains revealed that VfrB functions in the same pathway as SaeRS. At the transcriptional level, the promoter activities of SaeRS class I ( coa ) and class II ( hla ) target genes were downregulated during the exponential growth phase in the vfrB mutant, compared to the wild-type strain. In addition, saePQRS expression was decreased in the vfrB mutant strain, demonstrating a need for this protein in the autoregulation of SaeRS. The requirement for VfrB-mediated activation was circumvented when SaeS was constitutively active due to an SaeS (L18P) substitution. Furthermore, activation of SaeS via human neutrophil peptide 1 (HNP-1) overcame the dependence on VfrB for transcription from class I Sae promoters. Consistent with the role of VfrB in fatty acid metabolism, hla expression was decreased in the vfrB mutant with the addition of exogenous myristic acid. Lastly, we determined that aspartic acid residues D38 and D40, which are predicted to be key to VfrB enzymatic activity, were required for VfrB-mediated α-hemolysin production. Collectively, this study implicates VfrB as a novel accessory protein needed for the activation of SaeRS in S. aureus IMPORTANCE The SaeRS two-component system is a key regulator of virulence determinant production in Staphylococcus aureus Although the regulon of this two-component system is well characterized, the activation mechanisms, including the specific signaling molecules, remain elusive. Elucidating the complex regulatory circuit of SaeRS regulation is important for understanding how the system contributes to disease causation by this pathogen. To this end, we have identified the fatty acid kinase

[Wetland landscape pattern change based on GIS and RS: a review].

Science.gov (United States)

Kong, Fan-Ting; Xi, Min; Li, Yue; Kong, Fan-Long; Chen, Wan

2013-04-01

Wetland is an ecological landscape with most biodiversity in nature, which has unique ecological structure and function, and contains abundant natural resources to provide material guarantee for human's living and development. Wetland landscape pattern is the comprehensive result of various ecological processes, and has become a hot issue in wetland ecological study. At present, the combination of geographic information system (GIS) and remote sensing (RS) technologies is an important way to study the wetland landscape pattern change. This paper reviewed the research progress in the wetland landscape change based on GIS and RS from the aspects of the research methods of wetland landscape pattern, index of wetland landscape pattern, and driving forces of wetland landscape pattern evolution, and discussed the applications of the combination of GIS and RS in monitoring the wetland landscape pattern change, the index selection of wetland landscape pattern, and the driving mechanisms of the combined action of human and nature. Some deficiencies in the current studies were put forward, and the directions of the future-studies were prospected.

Synchronization, TIGoRS, and Information Flow in Complex Systems: Dispositional Cellular Automata.

Science.gov (United States)

Sulis, William H

2016-04-01

Synchronization has a long history in physics where it refers to the phase matching of two identical oscillators. This notion has been extensively studied in physics as well as in biology, where it has been applied to such widely varying phenomena as the flashing of fireflies and firing of neurons in the brain. Human behavior, however, may be recurrent but it is not oscillatory even though many physiological systems do exhibit oscillatory tendencies. Moreover, much of human behaviour is collaborative and cooperative, where the individual behaviours may be distinct yet contemporaneous (if not simultaneous) and taken collectively express some functionality. In the context of behaviour, the important aspect is the repeated co-occurrence in time of behaviours that facilitate the propagation of information or of functionality, regardless of whether or not these behaviours are similar or identical. An example of this weaker notion of synchronization is transient induced global response synchronization (TIGoRS). Previous work has shown that TIGoRS is a ubiquitous phenomenon among complex systems, enabling them to stably parse environmental transients into salient units to which they stably respond. This leads to the notion of Sulis machines, which emergently generate a primitive linguistic structure through their dynamics. This article reviews the notion of TIGoRS and its expression in several complex systems models including tempered neural networks, driven cellular automata and cocktail party automata. The emergent linguistics of Sulis machines are discussed. A new class of complex systems model, the dispositional cellular automaton is introduced. A new metric for TIGoRS, the excess synchronization, is introduced and applied to the study of TIGoRS in dispositional cellular automata. It is shown that these automata exhibit a nonlinear synchronization response to certain perturbing transients.

Expanding the three Rs to meet new challenges in humane animal experimentation.

Science.gov (United States)

Schuppli, Catherine A; Fraser, David; McDonald, Michael

2004-11-01

The Three Rs are the main principles used by Animal Ethics Committees in the governance of animal experimentation, but they appear not to cover some ethical issues that arise today. These include: a) claims that certain species should be exempted on principle from harmful research; b) increased emphasis on enhancing quality of life of research animals; c) research involving genetically modified (GM) animals; and d) animals bred as models of disease. In some cases, the Three Rs can be extended to cover these developments. The burgeoning use of GM animals in science calls for new forms of reduction through improved genetic modification technology, plus continued attention to alternative approaches and cost-benefit analyses that include the large numbers of animals involved indirectly. The adoption of more expanded definitions of refinement that go beyond minimising distress will capture concerns for enhancing the quality of life of animals through improved husbandry and handling. Targeting refinement to the unpredictable effects of gene modification may be difficult; in these cases, careful attention to monitoring and endpoints are the obvious options. Refinement can also include sharing data about the welfare impacts of gene modifications, and modelling earlier stages of disease, in order to reduce the potential suffering caused to disease models. Other issues may require a move beyond the Three Rs. Certain levels of harm, or numbers and use of certain species, may be unacceptable, regardless of potential benefits. This can be addressed by supplementing the utilitarian basis of the Three Rs with principles based on deontological and relational ethics. The Three Rs remain very useful, but they require thoughtful interpretation and expansion in order for Animal Ethics Committees to address the full range of issues in animal-based research.

PDYN rs2281285 variant association with drinking to avoid emotional or somatic discomfort.

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Ulrich W Preuss

Full Text Available One of the proposed psychobiological pathways of craving attributes the desire for drinking in the context of tension, discomfort or unpleasant emotions, to "negative" (or "relief" craving. The aim of this study was to replicate a previously reported association of the PDYN rs2281285 variant with negative craving using a different phenotyping approach.The TaqMan® Genotyping Assay was used to genotype the rs2281285 variant in 417 German alcohol-dependent subjects. The presence of negative/relief craving was assessed by asking if participants ever ingested alcohol to avoid unwanted emotional or somatic discomfort.The minor allele of rs2281285 was associated with an increased risk of drinking to avoid/escape unwanted emotional or somatic events (OR=2.29, 95% CI=1.08-4.85, p=0.0298.Despite the use of a different phenotyping approach to the measurement of negative craving, our results confirm the association between negative craving and PDYN rs2281285. Genetic markers of negative craving may help to identify subgroups of alcohol-dependent individuals vulnerable to relapse in the context of negative emotions or somatic discomfort, leading to the development of specifically tailored treatment strategies.

Association between BDNF-rs6265 and obesity in the Boston Puerto Rican Health Study

Science.gov (United States)

The objective of this study is to examine a functional variant (rs6265) in the BDNF gene interacting with dietary intake modulate obesity traits in the Boston Puerto Rican Health Study population. BDNF rs6265 was genotyped in 1147 Puerto Ricans (aged 45-75 years), and examined for association with o...

FLUXOS DE CAPITAL NO BRASIL PÃS-PLANO REAL

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Horst Dieter Möller

2004-12-01

Full Text Available O trabalho focaliza os fluxos de capital no Brasil pós-Plano Real sob os problemas da globalização financeira para mercados emergentes. A volatilidade dos fluxos de capital no Brasil sob crises cambiais e bancárias em mercados emergentes, começando com a crise mexicana em 1994/95, é analisada sob as perspectivas de ocorrências de reversões expressivas em tempos de crise e da influência das reversões sobre a eclosão das crises no Brasil. A análise econométrica mostra que a volatilidade dos fluxos de capital é diferente em seus segmentos, maior no segmento dos outros investimentos e nos investimentos em carteira do que nos investimentos diretos. Houve também reversões significativas em todos os segmentos em conseqüência das crises. Nesse sentido, os fluxos de capital trazem, em geral, benefícios para a economia nacional, mas podem também piorar expressivamente a situação econômica do país em tempos de crise.

El refugio de las masas: recepción de la obra de Lavive D’Epinay en Brasil

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Ricardo Mariano

2008-12-01

Full Text Available El Refugio de las Masas, publicada en Brasil por la editora Paz e Terra en 1970, se le considera una obra clásica por investigadores brasileños, definió las grandes líneas que hasta hoy inspiran el debate sobre el protestantismo latinoamericano como un problema sociológico.Aunque inspiró varios investigadores brasileños, el trabajo de D’Epinay repercutió, en especial,sobre las discusiones de tres temas: 1 el crecimiento pentecostal en Brasil; 2 la función del protestantismo en fase de la transición de la sociedad tradicional para la moderna; 3 la alienación política del pentecostalismo.

Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.

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Jürgen Glas

Full Text Available BACKGROUND: Recent studies demonstrated an association of STAT4 variants with systemic lupus erythematosus (SLE and rheumatoid arthritis (RA, indicating that multiple autoimmune diseases share common susceptibility genes. We therefore investigated the influence of STAT4 variants on the susceptibility and phenotype of inflammatory bowel diseases (IBD in a large patient and control cohort. METHODOLOGY/PRINCIPAL FINDINGS: Genomic DNA from 2704 individuals of Caucasian origin including 857 patients with Crohn's disease (CD, 464 patients with ulcerative colitis (UC, and 1383 healthy, unrelated controls was analyzed for seven SNPs in the STAT4 gene (rs11889341, rs7574865, rs7568275, rs8179673, rs10181656, rs7582694, rs10174238. In addition, a detailed genotype-phenotype analysis was performed. Our analysis revealed an association of the STAT4 SNP rs7574865 with overall decreased susceptibility to CD (p = 0.047, OR 0.86 [95% CI 0.74-0.99]. However, compared to CD patients carrying the wild type genotype, the STAT4 SNP rs7574865 was significantly associated with early CD onset (p = 0.021 and colonic CD (p = 0.008; OR = 4.60, 95% CI 1.63-12.96. For two other STAT4 variants, there was a trend towards protection against CD susceptibility (rs7568275, p = 0.058, OR 0.86 [95% CI 0.74-1.00]; rs10174238, p = 0.057, OR 0.86 [95% CI 0.75-1.00]. In contrast, we did not observe any association with UC susceptibility. Evidence for weak gene-gene interaction of STAT4 with the IL23R SNP rs11209026 was lost after Bonferroni correction. CONCLUSIONS/SIGNIFICANCE: Our results identified the STAT4 SNP rs7574865 as a disease-modifying gene variant in colonic CD. However, in contrast to SLE and RA, the effect of rs7574865 on CD susceptibility is only weak.

Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.

Science.gov (United States)

Glas, Jürgen; Seiderer, Julia; Nagy, Melinda; Fries, Christoph; Beigel, Florian; Weidinger, Maria; Pfennig, Simone; Klein, Wolfram; Epplen, Jörg T; Lohse, Peter; Folwaczny, Matthias; Göke, Burkhard; Ochsenkühn, Thomas; Diegelmann, Julia; Müller-Myhsok, Bertram; Roeske, Darina; Brand, Stephan

2010-04-29

Recent studies demonstrated an association of STAT4 variants with systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA), indicating that multiple autoimmune diseases share common susceptibility genes. We therefore investigated the influence of STAT4 variants on the susceptibility and phenotype of inflammatory bowel diseases (IBD) in a large patient and control cohort. Genomic DNA from 2704 individuals of Caucasian origin including 857 patients with Crohn's disease (CD), 464 patients with ulcerative colitis (UC), and 1383 healthy, unrelated controls was analyzed for seven SNPs in the STAT4 gene (rs11889341, rs7574865, rs7568275, rs8179673, rs10181656, rs7582694, rs10174238). In addition, a detailed genotype-phenotype analysis was performed. Our analysis revealed an association of the STAT4 SNP rs7574865 with overall decreased susceptibility to CD (p = 0.047, OR 0.86 [95% CI 0.74-0.99]). However, compared to CD patients carrying the wild type genotype, the STAT4 SNP rs7574865 was significantly associated with early CD onset (p = 0.021) and colonic CD (p = 0.008; OR = 4.60, 95% CI 1.63-12.96). For two other STAT4 variants, there was a trend towards protection against CD susceptibility (rs7568275, p = 0.058, OR 0.86 [95% CI 0.74-1.00]; rs10174238, p = 0.057, OR 0.86 [95% CI 0.75-1.00]). In contrast, we did not observe any association with UC susceptibility. Evidence for weak gene-gene interaction of STAT4 with the IL23R SNP rs11209026 was lost after Bonferroni correction. Our results identified the STAT4 SNP rs7574865 as a disease-modifying gene variant in colonic CD. However, in contrast to SLE and RA, the effect of rs7574865 on CD susceptibility is only weak.

Insect nicotinic acetylcholine receptors (nAChRs): Important amino ...

African Journals Online (AJOL)

STORAGESEVER

2008-12-29

Dec 29, 2008 ... nAChRs within the insect central nervous system has led to the development of insecticides targeting .... binding protein (AChBP), a homopentameric structural and functional homolog of ..... of the honey bee, Apis mellifera.

The RS-485 communication system design of the waste steel radioactivity detector system

International Nuclear Information System (INIS)

Zhang Yongli

2014-01-01

The importance and schematic structure of the waste steel radioactivity detector system is given firstly in this paper, and then the RS-485 communication system design including the circuit and program of the waste steel radioactivity detector system is provided. The test result of RS-485 communication system is also introduced, that shows the design completely meets the requirements of the waste steel radioactivity detector system. (author)

NACIONAL DE TURISMO NO BRASIL (1934-2014

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Gisélia Lima Carvalho

2016-01-01

Full Text Available Este artículo tiene como objetivo analizar el proceso de institucionalización del turismo en Brasil a través de la identificación de las medidas relacionadas con el turismo que ayudaron a formar la Política Nacional de Turismo (PNT. Se parte del principio de que las acciones, ubicadas en diferentes momentos históricos, formaron la estructura de la política nacional, siendo relevante durante toda la investigación, lo que contrar - resta a las tesis de algunos investigadores en Brasil que sostienen que sólo hubo política de facto después de 1990. Por lo tanto, la estrategia se basó en lo enfoque crítico de la literatura sobre la política de turismo y en el esfuerzo de investigación documental, a través de un estudio de la legislación pertinente del período entre 1934 y 2014.

Percepção das paisagens da Floresta Nacional de Canela (RS pelos turistas / Landscapes perception of the of the National Forest of Canela (RS

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Nara Rejane Zamberlan dos Santos

2012-04-01

Full Text Available ResumoUm estudo foi realizado com os turistas da cidade de Canela (RS, em quatro períodos do ano (julho-outubro, dezembro e fevereiro, com o objetivo de valorar 22 fotos (substitutos da paisagem da Floresta Nacional de Canela (RS, cuja escala de ponderação era variável de 1 a 5, correspondendo a classes de qualidade da paisagem de muito baixa a muito alta, respectivamente. Os resultados mostram que as mulheres são mais perceptivas do que os homens na análise de paisagens. Os menores valores médios valorados correspondem aos substitutos da classe baixa (2,74 e os mais altos, à classe alta de qualidade da paisagem (4,61. Por meio da Análise de Agrupamento Hierárquico, são observados dois grupos, sendo o primeiro, formado por mulheres de 15 a mais de 70 anos e jovens de 15 a 20 anos, do sexo masculino; e o segundo grupo, pelos demais homens.AbstractA study was carried out with the tourists of the city of Canela (RS, in four periods of the year (July, October, December and February, in order to value 22 photographs (landscape substitutes of the National Forest of Canela (RS, which weighting scale varied from 1 to 5. it was corresponding to very low to very high landscape classifications. The results show that women are more perceptive than men in landscape analysis. The lowest average values given correspond with low –class substitutes (2.74 and the highest with high quality landscapes (4.61. Through hierarchical group analysis were shown two groups, the first formed by women from 15 to over 70 years of age and young men of 15 to 20 years of age and second group by older men.

Simplified Antenna Group Determination of RS Overhead Reduced Massive MIMO for Wireless Sensor Networks

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Byung Moo Lee

2017-12-01

Full Text Available Massive multiple-input multiple-output (MIMO systems can be applied to support numerous internet of things (IoT devices using its excessive amount of transmitter (TX antennas. However, one of the big obstacles for the realization of the massive MIMO system is the overhead of reference signal (RS, because the number of RS is proportional to the number of TX antennas and/or related user equipments (UEs. It has been already reported that antenna group-based RS overhead reduction can be very effective to the efficient operation of massive MIMO, but the method of deciding the number of antennas needed in each group is at question. In this paper, we propose a simplified determination scheme of the number of antennas needed in each group for RS overhead reduced massive MIMO to support many IoT devices. Supporting many distributed IoT devices is a framework to configure wireless sensor networks. Our contribution can be divided into two parts. First, we derive simple closed-form approximations of the achievable spectral efficiency (SE by using zero-forcing (ZF and matched filtering (MF precoding for the RS overhead reduced massive MIMO systems with channel estimation error. The closed-form approximations include a channel error factor that can be adjusted according to the method of the channel estimation. Second, based on the closed-form approximation, we present an efficient algorithm determining the number of antennas needed in each group for the group-based RS overhead reduction scheme. The algorithm depends on the exact inverse functions of the derived closed-form approximations of SE. It is verified with theoretical analysis and simulation that the proposed algorithm works well, and thus can be used as an important tool for massive MIMO systems to support many distributed IoT devices.

O programa Estúdio Móvel da TV Brasil no Facebook

OpenAIRE

Rozados, Helen Beatriz Frota; Corrêa, Rochele Tonello Zago

2013-01-01

Este artigo trata do uso do Facebook por programa de televisão pública. O objetivo geral é compreender com que finalidade o Estúdio Móvel da TV Brasil utiliza a rede social virtual Facebook, contextualizando a TV Pública Brasileira, a TV Brasil, o Núcleo Multimídia (NUMID) e o programa Estúdio Móvel. Apresenta o conceito de TV Social, convergência transmídia de conteúdos e o Estúdio Móvel no Facebook. Discute a metodologia aplicada e os resultados da pesquisa. Considera que os conteúdos compa...

El perfil del consumidor de hostel en Brasil y sus motivaciones

OpenAIRE

Mané, Alexandra; Ferreira, Lissa

2017-01-01

El creciente número de hostels en Brasil ha atraído cada vez más brasileños que buscan este tipo de establecimiento para hospedarse. No obstante, vale destacar que deben realizarse más estudios que aborden la importancia de los hostels y sus consumidores en el mercado de turismo. Podrán contribuir al conocimiento teórico y práctico posibilitando un mejor entendimiento sobre este segmento. El objetivo de este artículo es identificar y describir el perfil del consumidor de hostel, sus motivacio...

Cesariana no Brasil: uma análise epidemiológica

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Jefferson Carlos Tolentino Rodrigues

2016-09-01

Full Text Available É comumente afirmado que o Brasil lidera o número de cesáreas no mundo. Desta forma, estetrabalho busca entender se o parto cesáreo é o principal procedimento cirúrgico eleito e sefatores socioeconômicos podem ser norteadores dessa escolha utilizando para tanto pesquisaevolutiva e comparação entre estados brasileiros. Analisou-se para tanto, a evolução durante osúltimos três anos do número de cesáreas no Brasil e comparou-se essa evolução tomando comobase os três estados mais pobres do Brasil com os três estados mais ricos. Assim, foi realizadoum estudo descritivo de corte transversal, em que se avaliou o número de cesarianas realizadasentre os anos de 2009 e 2011, contrapondo-os com o número de partos naturais, e como essenúmero foi modificado durante esse período. Verificou-se que o número de partos cesáreos emtodos os estados analisados é maior do que o de partos normais. Observou-se ainda que essenúmero é crescente e maior em estados com maior IDH. Conforme o presente estudo, o Brasilefetivamente continua tendo altos índices de partos por cesárea, sendo que mais da metadedos nascimentos ocorrem através do procedimento cirúrgico. Desta forma, a realidade brasileiracontrapõe aquilo que é recomendado pela OMS. Verificou-se também que o procedimentocesáreo vai sendo eleito paulatinamente como principal forma de parto no Brasil, mesmo entreestados menos desenvolvidos e, portanto, sem todos os recursos capazes a garantir o sucessodessa escolha.

The Use of Systematic Reviews and Reporting Guidelines to Advance the Implementation of the 3Rs

Science.gov (United States)

Avey, Marc T; Fenwick, Nicole; Griffin, Gilly

2015-01-01

In 1959, Russell and Burch published The Principles of Humane Experimental Technique, which included concrete advice on factors that they considered would govern progress in the implementation of these principles (enunciated as the 3Rs [Replacement, Reduction, and Refinement in animal-based studies]). One challenge to the implementation of the 3Rs was identified as information retrieval. Here, we further explore this challenge—the need for ‘research on research’—and the role that systematic reviews and reporting guidelines can play in implementation of the 3Rs. First, we examine the 2-fold nature of the challenge of information retrieval: 1) the identification of relevant publications spread throughout a large population of nonrelevant publications and 2) the incomplete reporting of relevant details within those publications. Second, we evaluate how systematic reviews and reporting guidelines can be used generally to address this challenge. Third, we assess the explicit reporting of the 3Rs in a cohort of preclinical animal systematic reviews. Our results show that Reduction methods are the most commonly reported by authors of systematic reviews but that, in general, reporting on how findings relate to the 3Rs is limited at best. Although systematic reviews are excellent tools for resolving the challenge of information retrieval, their utility for making progress in implementation of the 3Rs may be limited unless authors improve their reporting of these principles. PMID:25836961

A systems immunology approach identifies the collective impact of 5 miRs in Th2 inflammation.

Science.gov (United States)

Kılıç, Ayşe; Santolini, Marc; Nakano, Taiji; Schiller, Matthias; Teranishi, Mizue; Gellert, Pascal; Ponomareva, Yuliya; Braun, Thomas; Uchida, Shizuka; Weiss, Scott T; Sharma, Amitabh; Renz, Harald

2018-06-07

Allergic asthma is a chronic inflammatory disease dominated by a CD4+ T helper 2 (Th2) cell signature. The immune response amplifies in self-enforcing loops, promoting Th2-driven cellular immunity and leaving the host unable to terminate inflammation. Posttranscriptional mechanisms, including microRNAs (miRs), are pivotal in maintaining immune homeostasis. Since an altered expression of various miRs has been associated with T cell-driven diseases, including asthma, we hypothesized that miRs control mechanisms ensuring Th2 stability and maintenance in the lung. We isolated murine CD4+ Th2 cells from allergic inflamed lungs and profiled gene and miR expression. Instead of focusing on the magnitude of miR differential expression, here we addressed the secondary consequences for the set of molecular interactions in the cell, the interactome. We developed the Impact of Differential Expression Across Layers, a network-based algorithm to prioritize disease-relevant miRs based on the central role of their targets in the molecular interactome. This method identified 5 Th2-related miRs (mir27b, mir206, mir106b, mir203, and mir23b) whose antagonization led to a sharp reduction of the Th2 phenotype. Overall, a systems biology tool was developed and validated, highlighting the role of miRs in Th2-driven immune response. This result offers potentially novel approaches for therapeutic interventions.

Interleukin-21 gene polymorphism rs2221903 is associated with disease activity in patients with rheumatoid arthritis.

Science.gov (United States)

Malinowski, Damian; Paradowska-Gorycka, Agnieszka; Safranow, Krzysztof; Pawlik, Andrzej

2017-08-01

Interleukin-21 (IL-21) is a cytokine which plays a significant role in the pathogenesis and disease activity of rheumatoid arthritis (RA). Genetic polymorphisms in the IL-21 gene may alter the synthesis of IL-21. The aim of this study was to examine IL-21 and IL-21R polymorphisms in patients with RA. We examined 422 patients with RA and 338 healthy controls. Single nucleotide polymorphisms (SNPs) within the IL-21 (rs6822844 G>T, rs6840978 C>T, rs2221903 T>C) and IL-21R (rs2285452 G>A) genes were genotyped using TaqMan genotyping assays. There were no statistically significant differences in the distribution of studied genotypes and alleles between RA patients and the control group. To examine whether IL-21 polymorphisms affect disease activity in RA patients, we compared the distribution of IL-21 genotypes between patients with DAS28 ≤ 2.5 (patients with remission of disease symptoms) and patients with DAS28 > 2.5 (patients with active RA). Among patients with DAS28 > 2.5, increased prevalence of rs2221903 CT and CC genotypes was observed (OR = 1.54; 95% CI: 1.04-2.28; p = 0.035). The results of this study suggest that IL-21 and IL-21R gene polymorphisms are not risk loci for RA susceptibility, whereas the IL-21 rs2221903 polymorphism is associated with disease activity.

The rs1527483, but not rs3212018, CD36 polymorphism associates with linoleic acid detection and obesity in Czech young adults

Czech Academy of Sciences Publication Activity Database

Plesník, J.; Šerý, Omar; Khan, A. S.; Bielik, P.; Khan, N. A.

2018-01-01

Roč. 119, č. 4 (2018), s. 472-478 ISSN 0007-1145 R&D Projects: GA MZd(CZ) NV16-29900A Institutional support: RVO:67985904 Keywords : CD36 * fat taste * genetic polymorphism * rs1527483 Subject RIV: ED - Physiology OBOR OECD: Physiology (including cytology) Impact factor: 3.706, year: 2016

El Control Policial-Medico-Securitario Brasileño

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Thayara Silva Castelo Branco

2016-10-01

Full Text Available El artículo trata de los contornos del nuevo modelo de gobierno medico-policial, introducido en Brasil a finales del siglo XIX , en los cuales tenía como objetivo promover la salud básica a través de la vía policialesca conectada al control y normalización de los peligrosos e indeseables. Así, cuestiona la medicalización y policialización de las acciones del gobierno que empiezó a conectar el concepto de "enfermedad" a la lógica de la anticipación del peligro, la delincuencia, el control, la exclusión e inocuização, cumpliendo así, la política de seguridad que allí sobresalía y que dejó graves consecuencias en el Brasil.

Novos registros em Tillandsia L. (Bromeliaceae, Tillandsioideae) para o Rio Grande do Sul, Brasil

OpenAIRE

Büneker,Henrique Mallmann; Pontes,Rodrigo Corrêa; Witeck-Neto,Leopoldo

2015-01-01

Resumo São registradas pela primeira vez para a flora do estado do Rio Grande do Sul (Brasil) Tillandsia loliacea Mart. ex Schult.f. e Tillandsia pohliana Mez, sendo também redescoberta Tillandsia bandensis Baker neste estado e Brasil. São fornecidas descrições, fotografias e dados de suas distribuições geográficas.

Beta cell 5'-shifted isomiRs are candidate regulatory hubs in type 2 diabetes.

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Jeanette Baran-Gale

Full Text Available Next-generation deep sequencing of small RNAs has unveiled the complexity of the microRNA (miRNA transcriptome, which is in large part due to the diversity of miRNA sequence variants ("isomiRs". Changes to a miRNA's seed sequence (nucleotides 2-8, including shifted start positions, can redirect targeting to a dramatically different set of RNAs and alter biological function. We performed deep sequencing of small RNA from mouse insulinoma (MIN6 cells (widely used as a surrogate for the study of pancreatic beta cells and developed a bioinformatic analysis pipeline to profile isomiR diversity. Additionally, we applied the pipeline to recently published small RNA-seq data from primary human beta cells and whole islets and compared the miRNA profiles with that of MIN6. We found that: (1 the miRNA expression profile in MIN6 cells is highly correlated with those of primary human beta cells and whole islets; (2 miRNA loci can generate multiple highly expressed isomiRs with different 5'-start positions (5'-isomiRs; (3 isomiRs with shifted start positions (5'-shifted isomiRs are highly expressed, and can be as abundant as their unshifted counterparts (5'-reference miRNAs. Finally, we identified 10 beta cell miRNA families as candidate regulatory hubs in a type 2 diabetes (T2D gene network. The most significant candidate hub was miR-29, which we demonstrated regulates the mRNA levels of several genes critical to beta cell function and implicated in T2D. Three of the candidate miRNA hubs were novel 5'-shifted isomiRs: miR-375+1, miR-375-1 and miR-183-5p+1. We showed by in silico target prediction and in vitro transfection studies that both miR-375+1 and miR-375-1 are likely to target an overlapping, but distinct suite of beta cell genes compared to canonical miR-375. In summary, this study characterizes the isomiR profile in beta cells for the first time, and also highlights the potential functional relevance of 5'-shifted isomiRs to T2D.

A meta-analysis of adiponectin gene rs22411766 T>G polymorphism and ischemic stroke susceptibility

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Xiuju Chen

2016-01-01

Full Text Available Several studies have investigated the correlation between adiponectin gene rs22411766 T>G polymorphism and ischemic stroke risk. However, the results were not conclusive with each other. Therefore, to overcome this obstacle, we performed this meta-analysis to further explicate the adiponectin gene rs22411766 T>G polymorphism and ischemic stroke susceptibility. Case-control or cohort studies focused on adiponectin gene rs22411766 T>G polymorphism and ischemic stroke risk were electronic searched in the databases of Medline, Pubmed, Cochrane library, Excerpta Medica database(EMBASE and China National Knowledge Infrastructure (CNKI. All the potentially relevant studies were included in this meta-analysis. The association between adiponectin gene rs22411766 T>G polymorphism and ischemic stroke was expressed by odds ratio with its confidence interval. Publication bias has been assessed by begg’s funnel plot. All the analyses have been performed by Revman 5.1 statistical software. Finally, a total of six studies with 1,345 cases and 1,421 controls were included in this meta-analysis. Our results demonstrated that there was a significant association between adiponectin gene rs22411766 T>G polymorphism and ischemic stroke risk (p<0.05. People with G single nucleotide of adiponectin gene have the increased risk of developing ischemic stroke compared to T single nucleotide.

Annual report - Industrias Nucleares do Brasil S A - 1998; Relatorio anual - Industrias Nucleares do Brasil S A - 1998

Energy Technology Data Exchange (ETDEWEB)

NONE

1999-07-01

The annual report of 1998 of Industrias Nucleares do Brasil S A - Brazilian company responsible for the industrial activities of the nuclear fuel cycle - introduces the next main topics: mineral resource directory main actions; industrial directory main actions; finance and administration directory main actions; transparency; environment, safety and quality; the company; and financial statements.

A bebida de Ninkasi em terras tupiniquins: O mercado da cerveja e o Turismo Cervejeiro no Brasil

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Ewerton Reubens Coelho-Costa

2015-08-01

Full Text Available O artigo versa sobre o mercado de cervejas e o turismo cervejeiro no Brasil. Apresenta considerações sobre a origem da cerveja no mundo, a chegada da bebida ao Brasil e o panorama de produção e consumo da bebida no país, na contemporaneidade. Trata-se de um estudo exploratório com base na revisão bibliográfica, que tem como objetivo averiguar o potencial da cerveja artesanal para o desenvolvimento do turismo cervejeiro brasileiro. Dentre os resultados obtidos, destaca-se que o número de cervejaria artesanais no Brasil é incerto pela falta de dados oficiais; o turismo cervejeiro no Brasil tem maior expressividade a partir da existência de eventos ligados à cerveja; o Brasil dispões de roteiros turísticos para este nicho do mercado onde um dos principais atrativos está na visitação às fabricas de cerveja para entender o processo de fabricação e degustar diferentes tipos da bebida.  Palavras-chave: Cerveja, turismo cervejeiro, mercado.

Contaminação por compostos organoclorados em salsichas hot-dog comercializadas na cidade de Santa Maria (RS, Brasil Contamination for organochlorine compounds in hot-dog sausages, commercialized in the city of Santa Maria (RS, Brazil

Directory of Open Access Journals (Sweden)

Stanislau Bogusz Junior

2004-10-01

Full Text Available Com o objetivo de monitorar os resíduos de compostos tóxicos em alimentos, verificou-se a freqüência e os níveis de praguicidas organoclorados (OC e bifenilas policloradas (PCBs em amostras de salsichas Hot-Dog, comercializadas na Cidade de Santa Maria, Estado do Rio Grande do Sul (RS e, compararam-se os valores com aqueles estabelecidos pela Legislação. Para as análises, procedeu-se a extração da gordura das amostras. A partir da purificação desta, obteve-se um extrato do qual se determinaram os resíduos organoclorados por cromatografia gasosa com detector de captura eletrônica (CG - µECD63Ni. Verificou-se que o lindano e o HCB foram os pesticidas que apresentaram as maiores concentrações médias (0,001798ppm e 0,001652ppm, respectivamente. O somatório dos níveis médios dos pesticidas organoclorados detectados foi de 0,015783ppm, sendo que deste total 0,011165ppm pertencia aos metabólitos do DDT. Quanto as bifenilas policloradas, as maiores concentrações médias corresponderam às PCBs 10 (0,001817ppm e 28 (0,000317ppm. O somatório das PCBs foi de 0,002172ppm. As concentrações de praguicidas organoclorados e PCBs encontradas nas amostras analisadas estavam abaixo dos limites máximos permitidos pela legislação.With the objective of monitoring toxic compounds residues in food, the frequency and levels of organochlorine pesticides and polychlorinated biphenyls were verified in sausage samples, hot dog type, commercialized in the city of Santa Maria (RS, Brazil. Values were compared with the ones established by Brazilian legislation. For the analyses the extraction of fat from the samples was done. From the purification of the fat, there was acquisition of an extract in which was determined the organochlorine contaminants residues by gas chromatography with electronic capture detector (CG - µECD63Ni. It was learned that the lindane and HCB were the pesticides that presented the biggest concentration averages (0

PDYN rs2281285 Variant Association with Drinking to Avoid Emotional or Somatic Discomfort

Science.gov (United States)

Preuss, Ulrich W.; Winham, Stacey J.; Biernacka, Joanna M.; Geske, Jennifer R.; Bakalkin, Georgy; Koller, Gabriele; Zill, Peter; Soyka, Michael; Karpyak, Victor M.

2013-01-01

Introduction One of the proposed psychobiological pathways of craving attributes the desire for drinking in the context of tension, discomfort or unpleasant emotions, to “negative” (or “relief”) craving. The aim of this study was to replicate a previously reported association of the PDYN rs2281285 variant with negative craving using a different phenotyping approach. Methods The TaqMan® Genotyping Assay was used to genotype the rs2281285 variant in 417 German alcohol-dependent subjects. The presence of negative/relief craving was assessed by asking if participants ever ingested alcohol to avoid unwanted emotional or somatic discomfort. Results The minor allele of rs2281285 was associated with an increased risk of drinking to avoid/escape unwanted emotional or somatic events (OR = 2.29, 95% CI = 1.08–4.85, p = 0.0298). Discussion Despite the use of a different phenotyping approach to the measurement of negative craving, our results confirm the association between negative craving and PDYN rs2281285. Genetic markers of negative craving may help to identify subgroups of alcohol-dependent individuals vulnerable to relapse in the context of negative emotions or somatic discomfort, leading to the development of specifically tailored treatment strategies. PMID:24223163

Aligning the 3Rs with new paradigms in the safety assessment of chemicals.

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Burden, Natalie; Mahony, Catherine; Müller, Boris P; Terry, Claire; Westmoreland, Carl; Kimber, Ian

2015-04-01

There are currently several factors driving a move away from the reliance on in vivo toxicity testing for the purposes of chemical safety assessment. Progress has started to be made in the development and validation of non-animal methods. However, recent advances in the biosciences provide exciting opportunities to accelerate this process and to ensure that the alternative paradigms for hazard identification and risk assessment deliver lasting 3Rs benefits, whilst improving the quality and relevance of safety assessment. The NC3Rs, a UK-based scientific organisation which supports the development and application of novel 3Rs techniques and approaches, held a workshop recently which brought together over 20 international experts in the field of chemical safety assessment. The aim of this workshop was to review the current scientific, technical and regulatory landscapes, and to identify key opportunities towards reaching these goals. Here, we consider areas where further strategic investment will need to be focused if significant impact on 3Rs is to be matched with improved safety science, and why the timing is right for the field to work together towards an environment where we no longer rely on whole animal data for the accurate safety assessment of chemicals.

Association of rs662799 in APOA5 with CAD in Chinese Han population.

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Chen, Hua; Ding, Shifang; Zhou, Mi; Wu, Xiayin; Liu, Xi; Wu, Yun; Liu, Dechao

2018-01-08

CAD (Coronary Artery Disease) is a complex disease that influenced by various environmental and genetic factors. Previous studies have found many single nucleotide polymorphisms (SNPs) associated with the risk of CAD occurrence. However, the results are inconsistent. In this study, we aim to investigate genetic etiology in Chinese Han population by analysis of 7 SNPs in lipid metabolism pathway that previously has been reported to be associated with CAD. A total of 631 samples were used in this study, including 435 CAD cases and 196 normal healthy controls. SNP genotyping were conducted via multiplex PCR amplifying followed by NGS (next-generation sequencing). Rs662799 in APOA5 (Apolipoprotein A5) gene was associated with CAD in Chinese Han population (Odds-ratio = 1.374, P-value = 0.03). No significant association was observed between the rest of SNPs and CAD. Stratified association analysis revealed rs5882 was associated with CAD in non-hypertension group (Odds-ratio = 1.593, P-value = 0.023). Rs1800588 was associated with CAD in smoking group (Odds-ratio = 1.603, P-value = 0.035). The minor allele of rs662799 was the risk factor of CAD occurrences in Chinese Han population.

Replication study of STAT4 rs7574865 G/T polymorphism and risk of rheumatoid arthritis in a Chinese population.

Science.gov (United States)

Shen, Li; Liu, Ruiping; Zhang, Hui; Huang, Yong; Sun, Rongbin; Tang, Peifu

2013-09-10

Rheumatoid arthritis (RA) and ankylosing spondylitis (AS) are common systemic autoimmune diseases with genetic and environmental predisposing factors. Signal transducer and activator of transcription 4 (STAT4) transmits signals induced by interleukin-12, interleukin-23 and interferon-γ, which are key cytokines and play important roles in the development of autoimmune diseases. Previous studies confirmed the STAT4 rs7574865 G/T locus to be associated with RA. Thus we conducted a replication study to investigate STAT4 rs7574865 G/T polymorphism and RA/AS susceptibility in a Chinese population. We studied STAT4 rs7574865 G/T gene polymorphism in 520 patients with RA, 100 AS patients and 520 controls in a Chinese population. Genotyping was done using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). When the STAT4 rs7574865 GG homozygote genotype was used as the reference group, the GT or GT/TT genotypes were associated with the risk for RA. After stratification analyses, a significantly increased risk for RA associated with the STAT4 rs7574865 GT genotype was evident among the rheumatoid factor (RF)-positive patients, patients with higher erythrocyte sedimentation rate (ESR) level and patients with higher RA disease activity score (DAS28) compared with the STAT4 rs7574865 GG genotype. A significantly increased risk for RA associated with the STAT4 rs7574865 TT genotype was evident among older patients and RF-negative patients compared with the STAT4 rs7574865 GG genotype. STAT4 rs7574865 G/T was not associated with susceptibility to AS. This replication study confirmed that STAT4 rs7574865 G/T polymorphism was associated with the risk of RA. STAT4 polymorphisms are associated with rheumatoid arthritis risk. Copyright © 2013 Elsevier B.V. All rights reserved.

Polymorphism of MDM2 promoter 309 (rs 2279744) and the risk of PCOS.

Science.gov (United States)

Chan, Ying; Jiang, Hongguo; Yang, Xiaoling; Li, Dongya; Ma, Lan; Luo, Ying; Tang, Wenru

2016-01-01

This study aimed at evaluating possible association between MDM2 SNP309 polymorphism (rs 2279744) and polycystic ovary syndrome (PCOS). One hundred and twenty-five women with PCOS and two hundred and fifty women without PCOS were collected from the department of reproductive medicine of college hospital in this case-control study. Peripheral blood samples were collected from all participants and DNA was extracted, MDM2 SNP309 polymorphism (rs 2279744) was determined from the 125 cases and 250 controls. Women were grouped into PCOS (n = 125) group and control group (n = 250). Odds ratios (OR) and 95% confidence intervals (CI) were used to evaluate the association between MDM2 SNP309 polymorphism (rs 2279744) and PCOS. The distribution of T allele was significant higher in PCOS cases than controls. MDM2 SNP 309 T allele is associated with PCOS.

Lack of association between PKLR rs3020781 and NOS1AP rs7538490 and type 2 diabetes, overweight, obesity and related metabolic phenotypes in a Danish large-scale study: case-control studies and analyses of quantitative traits

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Almind Katrine

2008-12-01

Full Text Available Abstract Background Several studies in multiple ethnicities have reported linkage to type 2 diabetes on chromosome 1q21-25. Both PKLR encoding the liver pyruvate kinase and NOS1AP encoding the nitric oxide synthase 1 (neuronal adaptor protein (CAPON are positioned within this chromosomal region and are thus positional candidates for the observed linkage peak. The C-allele of PKLR rs3020781 and the T-allele of NOS1AP rs7538490 are reported to strongly associate with type 2 diabetes in various European-descent populations comprising a total of 2,198 individuals with a combined odds ratio (OR of 1.33 [1.16–1.54] and 1.53 [1.28–1.81], respectively. Our aim was to validate these findings by investigating the impact of the two variants on type 2 diabetes and related quantitative metabolic phenotypes in a large study sample of Danes. Further, we intended to expand the analyses by examining the effect of the variants in relation to overweight and obesity. Methods PKLR rs3020781 and NOS1AP rs7538490 were genotyped, using TaqMan allelic discrimination, in a combined study sample comprising a total of 16,801 and 16,913 individuals, respectively. The participants were ascertained from four different study groups; the population-based Inter99 cohort (nPKLR = 5,962, nNOS1AP = 6,008, a type 2 diabetic patient group (nPKLR = 1,873, nNOS1AP = 1,874 from Steno Diabetes Center, a population-based study sample (nPKLR = 599, nNOS1AP = 596 from Steno Diabetes Center and the ADDITION Denmark screening study cohort (nPKLR = 8,367, nNOS1AP = 8,435. Results In case-control studies we evaluated the potential association between rs3020781 and rs7538490 and type 2 diabetes and obesity. No significant associations were observed for type 2 diabetes (rs3020781: pAF = 0.49, OR = 1.02 [0.96–1.10]; rs7538490: pAF = 0.84, OR = 0.99 [0.93–1.06]. Neither did we show association with overweight or obesity. Additionally, the PKLR and the NOS1AP genotypes were demonstrated not

Effect of Tryptophan Hydroxylase-2 rs7305115 SNP on suicide attempts risk in major depression

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Zhang Yuqi

2010-08-01

Full Text Available Abstract Background Suicide and major depressive disorders (MDD are strongly associated, and genetic factors are responsible for at least part of the variability in suicide risk. We investigated whether variation at the tryptophan hydroxylase-2 (TPH2 gene rs7305115 SNP may predispose to suicide attempts in MDD. Methods We genotyped TPH2 gene rs7305115 SNP in 215 MDD patients with suicide and matched MDD patients without suicide. Differences in behavioral and personality traits according to genotypic variation were investigated by logistic regression analysis. Results There were no significant differences between MDD patients with suicide and controls in genotypic (AG and GG frequencies for rs7305115 SNP, but the distribution of AA genotype differed significantly (14.4% vs. 29.3%, p p p Conclusions The study suggested that hopelessness, negative life events and family history of suicide were risk factors of attempted suicide in MDD while the TPH2 rs7305115A remained a significant protective predictor of suicide attempts.

Adidos Trabalhistas e lideres sindicais norteamericanos no Brasil 1943 – 1952

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Eduardo José Afonso

2014-12-01

Full Text Available Este trabalho analisa documentos restritos e secretos do Departamento de Estado norte-americano, principalmente os Relatórios “Mensais do Trabalho”, relatórios do FBI, da CIA e do Departamento do Trabalho dos Estados Unidos, e procura descrever a ação dos Adidos Trabalhistas Americanos e Ingleses no Brasil, no período de 1943 a 1952, como elementos-chave na política externa dos Estados Unidos, direcionada à possível intervenção em assuntos internos brasileiros. O presente estudo destaca, igualmente, a tarefa de líderes sindicais norte-americanos, ligados à Federação Americana do Trabalho e ao Departamento de Estado - em visita ao Brasil no período descrito, no intento de obter a cooptação de líderes sindicais brasileiros para a associação na formação de uma grande Central Sindical Mundial, cujo intuito era o controle do movimento operário do Brasil e de outros países sob sua influência.

Association of OPN rs11730582 polymorphism with cancer risk: a meta-analysis

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He LL

2016-03-01

Full Text Available Lanlan He,1,* Yong Wang2,* 1Emergency Department, Zhenjiang First People’s Hospital, Zhenjiang, People’s Republic of China; 2Department of Interventional Radiology and Vascular Surgery, Zhongda Hospital, Southeast University, Nanjing, Jiangsu, People’s Republic of China *Both authors contributed equally to this work Purpose: Several molecular epidemiological studies have investigated the association between OPN rs11730582 C>T polymorphism and cancer risk, but the results are inconsistent. Hence, a meta-analysis was conducted to determine the association of this polymorphism with cancer risk. Materials and methods: The related articles were searched in PubMed, Embase, and Chinese National Knowledge Infrastructure databases. Pooled odds ratios and 95% confidence intervals were calculated to evaluate the strength of the associations. A random-effects model or fixed-effects model was employed depending on the heterogeneity. Results: A total of ten case-control studies involving 2,749 cancer cases and 3,398 controls were included in the meta-analysis. In overall analysis, OPN rs11730582 C>T polymorphism was not associated with cancer risk. In a stratified analysis by cancer type, no significant association was found between OPN rs11730582 C>T polymorphism and the risk of glioma, gastric cancer, and other cancers. Conclusion: This meta-analysis suggests that OPN rs11730582 C>T polymorphism is not associated with cancer susceptibility. Keywords: osteopontin, polymorphism, cancer, risk 

Activation of anthocyanin biosynthesis by expression of the radish R2R3-MYB transcription factor gene RsMYB1.

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Lim, Sun-Hyung; Song, Ji-Hye; Kim, Da-Hye; Kim, Jae Kwang; Lee, Jong-Yeol; Kim, Young-Mi; Ha, Sun-Hwa

2016-03-01

RsMYB1, a MYB TF of red radish origin, was characterized as a positive regulator to transcriptionally activate the anthocyanin biosynthetic machinery by itself in Arabidopsis and tobacco plants. Anthocyanins, providing the bright red-orange to blue-violet colors, are flavonoid-derived pigments with strong antioxidant activity that have benefits for human health. We isolated RsMYB1, which encodes an R2R3-MYB transcription factor (TF), from red radish plants (Raphanus sativus L.) that accumulate high levels of anthocyanins. RsMYB1 shows higher expression in red radish than in common white radish, in both leaves and roots, at different growth stages. Consistent with RsMYB1 function as an anthocyanin-promoting TF, red radishes showed higher expression of all six anthocyanin biosynthetic and two anthocyanin regulatory genes. Transient expression of RsMYB1 in tobacco showed that RsMYB1 is a positive regulator of anthocyanin production with better efficiency than the basic helix-loop-helix (bHLH) TF gene B-Peru. Also, the synergistic effect of RsMYB1 with B-Peru was larger than the effect of the MYB TF gene mPAP1D with B-peru. Arabidopsis plants stably expressing RsMYB1 produced red pigmentation throughout the plant, accompanied by up-regulation of the six structural and two regulatory genes for anthocyanin production. This broad transcriptional activation of anthocyanin biosynthetic machinery in Arabidopsis included up-regulation of TRANSPARENT TESTA8, which encodes a bHLH TF. These results suggest that overexpression of RsMYB1 promotes anthocyanin production by triggering the expression of endogenous bHLH genes as potential binding partners for RsMYB1. In addition, RsMYB1-overexpressing Arabidopsis plants had a higher antioxidant capacity than did non-transgenic control plants. Taken together, RsMYB1 is an actively positive regulator for anthocyanins biosynthesis in radish plants and it might be one of the best targets for anthocyanin production by single gene

Associations of rs3918242 and rs2285053 MMP-9 and MMP-2 polymorphisms with the risk, severity, and short- and long-term complications of degenerative mitral valve diseases: a 4.8-year prospective cohort study.

Science.gov (United States)

Balistreri, Carmela Rita; Allegra, Alberto; Crapanzano, Floriana; Pisano, Calogera; Triolo, Oreste Fabio; Argano, Vincenzo; Candore, Giuseppina; Lio, Domenico; Ruvolo, Giovanni

2016-01-01

Degenerative forms of mitral valve diseases (MVDs) are very complex pathologies. Thus, it is difficult to make generalizations about the disease pathways or genetic risk factors contributing to these diseases. However, a key role of metalloproteinases (MMPs) in their pathophysiology is emerging. Thus, we performed for the first time a perspective study to assess eventual associations of some functional single nucleotide polymorphisms (SNPs) in MMP-2 and MMP-9 genes with the MVD risk, symptom severity, and short- and long-term (4.8 years) complications. For this purpose, 90 patients and two control groups were genotyped for rs3918242, rs243865, and rs2285053 MMP-2 and MMP-9 gene SNPs, and systemic levels of pro-atrial natriuretic peptide (pro-ANP) and two enzymes were quantified and correlated to genotypes of MMP-2 and MMP-9 SNPs studied. In addition, associations between these SNPs and symptom severity and short- and long-term (4.8 years) complications were evaluated. Interestingly, rs3918242 MMP-9 and rs2285053 MMP-2 SNPs were significantly represented in cases than two control groups and were associated with a higher MVD risk, as demonstrated using dominant/recessive models. Cases stratified for NYHA symptoms and particularly those NYHA III+IV with rs3918242 CT+TT MMP-9 and rs2285053CT+TT genotypes also showed higher severity related to significant higher systemic levels of MMP enzymes and pro-ANP at enrolment and 4.8 follow-up times. In addition, cases with these genotypes and particularly those NYHA III+IV had a very significant percentage of complications, particularly at the 4.8 follow-up. Surprisingly, 20% of patient controls developed MVD at 4.8-year follow-up and were carriers of these genotypes. Thus, the associations observed seem to suggest that the two SNPs might represent useful biomarkers and targets for preventing and monitoring MVDs and developing personalized treatments, consenting a more appropriate management and outcome. Copyright © 2016

The joint effect of the endothelin receptor B gene (EDNRB polymorphism rs10507875 and nitric oxide synthase 3 gene (NOS3 polymorphism rs869109213 in Slovenian patients with type 2 diabetes mellitus and diabetic retinopathy

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Dejan Bregar

2018-02-01

Full Text Available Increasing evidence suggests that endothelin and nitric oxide synthase genes and their products exert biological effects on the vasculature via the nitric oxide or endothelin pathway. The aim of the study was to evaluate the association of rs10507875 and rs869109213 (alone or in interaction with diabetic retinopathy (DR in subjects with type 2 diabetes mellitus (T2DM. We genotyped the single nucleotide polymorphism rs10507875 of the endothelin receptor B gene (EDNRB and variable number tandem repeats rs869109213 of the nitric oxide synthase 3 gene (NOS3 in 270 Slovenian patients with DR and T2DM and 256 controls with T2DM without clinical signs of DR. The genotyping was performed using either real-time polymerase chain reaction (PCR or standard PCR. We found a significant association between the genotypes of NOS3 rs869109213 polymorphism and the risk of DR in the co-dominant model (4a4b genotype; 1.99-fold increased risk [1.09-3.65]; 95% confidence interval [CI]; p = 0.02, co-dominant model (4a4a genotype; 4.16-fold increased risk [1.03-16.74]; 95% CI; p = 0.04, and dominant model (4a4a and 4a4b genotypes; 2.22-fold increased risk [1.26-3.92]; 95% CI; p = 0.01 compared to the 4b4b genotype. Moreover, the joint effect of the two polymorphisms on DR risk was greater than the individual effect of each polymorphism in the analyzed genetic models. Additionally, adjusted odds ratio showed an increased risk in dominant × dominant (4.15-fold [1.40-12.26]; 95% CI; p = 0.01 and recessive × dominant (2.24-fold [1.25-4.01]; 95% CI; p = 0.02 genotype combinations of the two polymorphisms. In conclusion, our results indicate that NOS3 rs869109213 polymorphism alone or in a combination with EDNRB rs10507875 polymorphism may be associated with DR in Slovenian patients with T2DM.

Estudo fenológico em três fases sucessionais de uma floresta estacional decidual no município de Santa Tereza, RS, Brasil Phenology study in three successional stages of a seasonal deciduous forest in Santa Tereza, RS, Brazil

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Cáren Andreis

2005-02-01

Full Text Available O presente estudo foi realizado em 40 parcelas de área fixa pertencentes a três estágios sucessionais, denominados: Capoeirão, Floresta Secundária e Floresta Madura, em uma Floresta Estacional Decidual no município de Santa Tereza, RS. Foram realizadas observações fenológicas quinzenais em 53 espécies arbóreas, numa média de 8,4 indivíduos por espécie, durante o período de 16 de novembro de 2001 a 10 de novembro de 2002. As fenofases observadas foram floração, frutificação e mudança foliar. Os resultados indicaram que a atividade reprodutiva manteve uma porcentagem relativamente baixa nos três estágios sucessionais durante o período observado, com tendências em ser menor durante a estação de inverno. A quantidade total de folhas na árvore, não se distinguindo estágio sucessional, diminuiu de aproximadamente 85% no período de maior atividade vegetativa para até 35% no inverno, período de repouso, sendo a Floresta Madura a subsere, que manteve os maiores porcentuais de folhas durante o período estudado.The present study was accomplished in forty permanent plots belonging to three forest successional stages, denominated: Brush Forest, Secondary Forest and Mature Forest, in a seasonal deciduous forest in the municipal district of Santa Tereza, RS, Brazil. Phenologic observations were accomplished fortnightly for 53 arboreal species, in an average of 8,4 individuals per species, during the period of November 2001 to November 2002. The stages observed were flowering, fruiting and foliage change. The results indicate that the reproductive activity remained relatively low for three successional stages during the observed period, with a tendency to be even lower during winter. The total amount of leaves on the trees, regardless of the successional stage, decreased from approximately 85%, in the period of higher vegetative activity, to 35% in the winter, resting season. The Mature Forest maintained the largest percentage

OS BRASILEIROS E O BRASIL DE AQUILINO: O MINEIRO CARIOCA E OS OUTROS

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Francisco Topa (Univ. Porto

2015-03-01

Full Text Available O artigo estuda a representação do brasileiro – o português que emigrou para o Brasil e regressa rico à terra natal – e do Brasil na obra de um dos grandes romancistas portugueses, Aquilino Ribeiro (1885-1963, mostrando como estamos já longe do estereótipo caricatural promovido por Camilo Castelo Branco e outros autores oitocentistas.PALAVRAS-CHAVE: Aquilino Ribeiro; brasileiro de torna-viagem; Brasil Abstract The article analyzes the representation of the brasileiro – the Portuguese who emigrated to Brazil and rich returns to his homeland – and Brazil in the work of one of the great Portuguese novelists, Aquilino Ribeiro (1885-1963, showing how we are past the cartoonish stereotype promoted by Camilo Castelo Branco and other nineteenth-century authors.KEYWORDS: Aquilino Ribeiro; brasileiro; Brazil

Validity and clinical feasibility of the ADHD rating scale (ADHD-RS) A Danish Nationwide Multicenter Study

DEFF Research Database (Denmark)

Szomlaiski, N; Dyrborg, J; Rasmussen, H

2008-01-01

Aim: To establish the validity of a Danish version of the Attention Deficit Hyperactivity Disorder Rating Scale (ADHD-RS), secondly to present national norm scores compared to that of United States and other European data and thirdly to evaluate ADHD-RS when used for monitoring treatment...... effectiveness. Methods: A Danish translation of the ADHD-RS was used on a normative sample of 837 children. Two clinical samples, 138 hyperkinetic disorder (HKD) cases and 110 clinical controls were recruited from eleven Danish Child and Adolescent Mental Health (CAMH) centres and assessed according to usual...... clinical standards. The HKD children were rated by parents and teachers at baseline and at follow-up 3 months later. Results: Internal validity of ADHD-RS was high and the factor structure supported the diagnostic classification system ICD-10. The questionnaire discriminated HKD patients in a mixed...

Assessment of river plan changes in Terengganu River using RS ...

African Journals Online (AJOL)

Journal of Fundamental and Applied Sciences ... The database can help in the appropriate understanding of river plan change and know ... The data collected from Geographic Information System (GIS) and Remote Sensing (RS) database.

Caminhos comoventes: Concretismo, neoconcretismo e arte contemporânea no Brasil

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Otavio Leonidio

2013-10-01

Full Text Available O artigo problematiza os nexos existentes entre modernismo, concretismo, neoconcretismo e arte contemporânea no Brasil, abordados aqui a partir da análise de uma obra específica – a performance Symbebeko, da artista Juliana Notari, ocorrida em março de 2011 no vão-livre do Museu de Arte Moderna do Rio de Janeiro/MAM. Defende-se a tese de que, em contraste com narrativas mais ou menos canônicas, a passagem do moderno ao contemporâneo é marcada, no Brasil, por compromissos e contradições inusitadas e por vezes surpreendentes.

Reis do Congo no Brasil, séculos XVIII e XIX

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Marina de Mello e Souza

2005-06-01

Full Text Available Esse artigo busca explicar a presença de reinados negros, depois chamados de congadas, em quase todas as regiões do Brasil que receberam escravos africanos, do século XVI ao XIX. O enfoque adotado abarca Portugal, África Central e Brasil como partes integrantes de um mesmo sistema econômico, social e cultural, tecido em torno do Atlântico. A esfera da cultura e as relações de poder são os centros focais da análise, que se preocupa acima de tudo com a formação de identidades.

Sex differences in microRNA regulation of gene expression: no smoke, just miRs

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Morgan Christopher P

2012-09-01

Full Text Available Abstract Males and females differ widely in morphology, physiology, and behavior leading to disparities in many health outcomes, including sex biases in the prevalence of many neurodevelopmental disorders. However, with the exception of a relatively small number of genes on the Y chromosome, males and females share a common genome. Therefore, sexual differentiation must in large part be a product of the sex biased expression of this shared genetic substrate. microRNAs (miRs are small non-coding RNAs involved in the post-transcriptional regulation of up to 70% of protein-coding genes. The ability of miRs to regulate such a vast amount of the genome with a high degree of specificity makes them perfectly poised to play a critical role in programming of the sexually dimorphic brain. This review describes those characteristics of miRs that make them particularly amenable to this task, and examines the influences of both the sex chromosome complement as well as gonadal hormones on their regulation. Exploring miRs in the context of sex differences in disease, particularly in sex-biased neurodevelopmental disorders, may provide novel insight into the pathophysiology and potential therapeutic targets in disease treatment and prevention.

Description of the Implementation of Home Care Servicer at RS Murni Teguh, Medan

OpenAIRE

Manalu, Ayu P Sary

2014-01-01

Home care service constitutes providing service and nurses’ equipment for patients and their families at home in order to keep their health, education, prevention from diseases, palliative therapy, and rehabilitation. Home care service at RS Murni Teguh, Medan, has its specification in management, compared with home care service in other places. The objective of the research was to find out the description of the implementation of home care service at RS Murni Teguh, Medan. The research used ...

Blaise Cendrars e o Brasil: "Brésil, des hommes sont venus"

OpenAIRE

Wimmer, Norma [UNESP

2013-01-01

The paper intitled Blaise Cendrars and Brazil: Brésil, des hommes sont venus discusses the way Cendrars portrays Brazil, and also debates his influence on the artists of the Semana de Arte Moderna (Modern Art Week) in 1922. O texto intitulado Blaise Cendrars e o Brasil: Brésil, des hommes sont venus tece considerações acerca da perspectiva sob a qual Cendrars vê o Brasil, bem como de sua relação com os artistas da Semana de Arte Moderna de 1922.

Diptera, Muscidae, Cariocamyia maculosa Snyder: Primeiro Registro para o Nordeste do Brasil

OpenAIRE

Thayana Monteiro; Freddy Ruben Bravo

2011-01-01

Cariocamyia maculosa Snyder, é um Muscidae com registros para a Colômbia e Brasil (regiões Sul, Sudeste e Centro-Oeste). Em um levantamento de dípteros saprófagos na cidade de Feira de Santana no estado da Bahia com iscas de origem orgânico animal em putrefação, foram coletados 46 espécimes de C. maculosa. Esse é o primeiro registro da espécie para a Bahia e Nordeste do Brasil. Apesar de C. maculosa ter sido encontrada...

9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer

DEFF Research Database (Denmark)

Warren, Helen; Dudbridge, Frank; Fletcher, Olivia

2012-01-01

Our recent genome-wide association study identified a novel breast cancer susceptibility locus at 9q31.2 (rs865686).......Our recent genome-wide association study identified a novel breast cancer susceptibility locus at 9q31.2 (rs865686)....

Lack of association between miR-218 rs11134527 A>G and Kawasaki disease susceptibility.

Science.gov (United States)

Pi, Lei; Fu, Lanyan; Xu, Yufen; Che, Di; Deng, Qiulian; Huang, Xijing; Li, Meiai; Zhang, Li; Huang, Ping; Gu, Xiaoqiong

2018-05-01

Abstract Kawasaki disease (KD) is a type of disease that includes the development of a fever that lasts at least five days and involves the clinical manifestation of multicellular vasculitis. KD has become one of the most common pediatric cardiovascular diseases. Previous studies have reported that miR-218 rs11134527 A>G is associated with susceptibility to various cancer risks. However, there is a lack of evidence regarding the relationship between this polymorphism and KD risk. This study explored the correlation between the miR-218 rs11134527 A>G polymorphism and the risk of KD. We recruited 532 patients with KD and 623 controls to genotype the miR-218 rs11134527 A>G polymorphism with a TaqMan allelic discrimination assay. Our results illustrated that the miR-218 rs11134527 A>G polymorphism was not associated with KD risk. In an analysis stratified by age, sex, and coronary artery lesions, we found only that the risk of KD was significantly decreased for children older than 5 years (GG vs. AA/AG: adjusted OR=0.26, 95% CI=0.07-0.94, P =0.041). This study demonstrated that the miR-218 rs1113452 A>G polymorphism may have an age-related relationship with KD susceptibility that has not previously been revealed. ©2018 The Author(s).

Prediction of solubilities for ginger bioactive compounds in hot water by the COSMO-RS method

Science.gov (United States)

Zaimah Syed Jaapar, Syaripah; Azian Morad, Noor; Iwai, Yoshio

2013-04-01

The solubilities in water of four main ginger bioactives, 6-gingerol, 6-shogaol, 8-gingerol and 10-gingerol, were predicted using a conductor-like screening model for real solvent (COSMO-RS) calculations. This study was conducted since no experimental data are available for ginger bioactive solubilities in hot water. The σ-profiles of these selected molecules were calculated using Gaussian software and the solubilities were calculated using the COSMO-RS method. The solubilities of these ginger bioactives were calculated at 50 to 200 °C. In order to validate the accuracy of the COSMO-RS method, the solubilities of five hydrocarbon molecules were calculated using the COSMO-RS method and compared with the experimental data in the literature. The selected hydrocarbon molecules were 3-pentanone, 1-hexanol, benzene, 3-methylphenol and 2-hydroxy-5-methylbenzaldehyde. The calculated results of the hydrocarbon molecules are in good agreement with the data in the literature. These results confirm that the solubilities of ginger bioactives can be predicted using the COSMO-RS method. The solubilities of the ginger bioactives are lower than 0.0001 at temperatures lower than 130 °C. At 130 to 200 °C, the solubilities increase dramatically with the highest being 6-shogaol, which is 0.00037 mole fraction, and the lowest is 10-gingerol, which is 0.000039 mole fraction at 200 °C.

Prediction of solubilities for ginger bioactive compounds in hot water by the COSMO-RS method

International Nuclear Information System (INIS)

Jaapar, Syaripah Zaimah Syed; Iwai, Yoshio; Morad, Noor Azian

2013-01-01

The solubilities in water of four main ginger bioactives, 6-gingerol, 6-shogaol, 8-gingerol and 10-gingerol, were predicted using a conductor-like screening model for real solvent (COSMO-RS) calculations. This study was conducted since no experimental data are available for ginger bioactive solubilities in hot water. The σ-profiles of these selected molecules were calculated using Gaussian software and the solubilities were calculated using the COSMO-RS method. The solubilities of these ginger bioactives were calculated at 50 to 200 °C. In order to validate the accuracy of the COSMO-RS method, the solubilities of five hydrocarbon molecules were calculated using the COSMO-RS method and compared with the experimental data in the literature. The selected hydrocarbon molecules were 3-pentanone, 1-hexanol, benzene, 3-methylphenol and 2-hydroxy-5-methylbenzaldehyde. The calculated results of the hydrocarbon molecules are in good agreement with the data in the literature. These results confirm that the solubilities of ginger bioactives can be predicted using the COSMO-RS method. The solubilities of the ginger bioactives are lower than 0.0001 at temperatures lower than 130 °C. At 130 to 200 °C, the solubilities increase dramatically with the highest being 6-shogaol, which is 0.00037 mole fraction, and the lowest is 10-gingerol, which is 0.000039 mole fraction at 200 °C.

Association of STAT4 rs7574865 with susceptibility to systemic lupus erythematosus in Iranian population.

Science.gov (United States)

Mirkazemi, Sedigheh; Akbarian, Mahmoud; Jamshidi, Ahmad Reza; Mansouri, Reza; Ghoroghi, Shima; Salimi, Yahya; Tahmasebi, Zahra; Mahmoudi, Mahdi

2013-12-01

Systemic lupus erythematosus (SLE) is a multifactorial autoimmune disease with complex genetic inheritance that affecting different organs and systems. STAT4 has been newly identified as a susceptible gene in the development of SLE. According to recent studies, STAT4 has been associated with SLE in various populations. We investigated whether STAT4 single nucleotide polymorphisms (SNPs) were associated with susceptibility and clinical features of SLE in Iranian patients. The study group comprised 280 patients with SLE and 281 sex-, age-, and ethnicity-matched healthy controls of Iranian ancestry. Two SNPs (rs7574865 and rs7601754) were genotyped using the TaqMan MGB Allelic Discrimination method. Our results showed a significant association between rs7574865 T allele (odds ratio (OR) = 1.50, 95 % CI = 1.18-1.92, P = 0.002) and susceptibility to SLE. The rs7574865TT genotype (P = 0.02, OR = 1.94, 95 % CI = 1.74-3.19) and GT genotype (P = 0.008, OR = 1.71, 95 % CI = 1.19-2.45) showed a significant association with the risk of SLE in the Iranian population. We concluded that STAT4 rs7574865 is associated with SLE susceptibility in the Iranian population and this SNP might be a factor in the pathogenesis of SLE. However, further studies are required to investigate the mechanism by which polymorphisms in this gene lead to SLE.

Empolgação com Copa freia protestos nas redes sociais no Brasil e no mundo

OpenAIRE

Zarko, Raphael

2014-01-01

Depois da Copa das Confederações de 2013 serem marcadas pelas manifestações contrárias à realização e gastos excessivos para o Mundial do Brasil – tanto nas ruas quanto na internet -, a impressão de que houve uma queda nos protestos da Copa do Mundo do Brasil se confirma com uma ampla pesquisa nas redes sociais. Em monitoramento de mais de 11 milhões de mensagens de Twitter no Brasil e no mundo, o número de menções a protestos é de apenas 17 mil – percentualmente, significa dizer que apenas 0...

BRASIL BAJO INFLUENCIA NAPOLEÓNICA Y FRANCESA: LOS MENSAJEROS DE LA INDEPENDENCIA: MILITARES, LIBREROS Y PERIODISTAS

OpenAIRE

PUIGMAL, PATRICK

2013-01-01

La historiografía clásica presenta la independencia de Brasil como un evento particular, generalmente aislado del acontecer continental y sin hacer referencia a la influencia militar y política napoleónica. Este artículo tiene como propósito principal entender la emancipación brasileña en un contexto mucho más amplio y demostrar la amplia presencia e influencia napoleónica en el marco de la lucha militar y de la construcción del Estado nuevo, permitiendo así integrar a Brasil en un movimiento...

Association Between rs1344706 of ZNF804A and Schizophrenia: A Meta-analysis

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Meiyan Zhu

2014-12-01

Full Text Available Schizophrenia is one of the most serious mental diseases found in humans. Previous studies indicated that the single nucleotide polymorphism (SNP rs1344706 in the gene ZNF804A encoding zinc finger protein 804A was associated with schizophrenia in Caucasian population but not in Chinese Han population. However, current results are conflicting in Asian population. In the present study, a meta-analysis was performed to revisit the association between rs1344706 and the risk of schizophrenia in Asian, Caucasian and other populations. Electronic search of PubMed database identified 25 case–control studies with available genotype frequencies of rs1344706 for the meta-analysis, involving a total of 15,788 cases and 22,654 controls. A pooled odds ratio (OR with 95% confidence interval (CI was used to assess the association. The current meta-analysis showed an association between rs1344706 and schizophrenia in Caucasian populations (P = 0.028, OR = 1.138, 95% CI: 1.014–1.278; P = 0.004 for heterogeneity and Asian populations (P = 0.008, OR = 1.092, 95% CI: 1.023–1.165; P = 0.001 for heterogeneity, but not in other populations (P = 0.286, OR = 1.209, 95% CI: 0.853–1.714, P = 0.120 for heterogeneity. Egger’s test (P > 0.05 and Begg’s test (P > 0.05 are both suggestive of the lack of publication bias for the included studies. Thus, the absence of association in other populations suggests a genetic heterogeneity in the susceptibility of schizophrenia and demonstrates the difficulties in replicating genome-wide association study findings regarding schizophrenia across different ethnic populations. To validate the association between rs1344706 and schizophrenia, further studies with larger participant populations worldwide are needed.

[Association between rs10938397 polymorphism in GNPDA2 and obesity in children at different stages of development].

Science.gov (United States)

Gao, L W; Zhang, M X; Wu, L J; Fu, L W; Zhao, X Y; Mi, J

2018-01-10

Objective: To examine the association between rs10938397 polymorphism in glucosamine-6-phosphate deaminase 2 ( GNPDA2 ) and risk of obesity in children at different stages of development and analyze the differences in the association. Methods: A total of 3 503 school-aged children were selected from the Beijing Child and Adolescent Metabolic Syndrome (BCAMS) study in Beijing and their complete anthropometry weight, height, fat mass percentage (FMP), fat mass index (FMI) and free fat mass index (FFMI) and sexual maturation (SM) data were used. The developmental stages were evaluated using male testicular volume and female breast Tanner staging. FMP, FM and FFM were measured by bioelectrical impedance analysis. General obesity and adiposity were respectively defined according to Chinese sex-age-specific body mass index (BMI) cutoffs and sex-age-specific FMP cutoffs. The SNP rs10938397 were genotyped by the TaqMan Allelic Discrimination Assay with the GeneAmp 7900 sequence detection system (Applied Biosystems, Foster city, CA, USA). Relationships between rs10938397 polymorphism and BMI, FMP, FMI and FFMI and different types of obesity were tested using multivariate linear regression and logistic regression models. Results: After age adjustment and correction for multiple testing, the rs10938397-G was associated with BMI and risk of general obesity in boys in early puberty ( β =0.328, P =0.001; OR =1.420, 95% CI : 1.126-1.790), and the rs10938397-G was associated with BMI in girls in late puberty ( β =0.266, P =0.001). The associations of GNPDA2 rs10938397-G with FFMI and FMI were observed in boys in early puberty ( β =0.137, P =0.016; β =0.202, P =0.007) and the associations of rs10938397-G with FMP and FMI were observed in girls in late puberty ( β =0.153, P =0.002; β =0.168, P =0.001). The rs10938397-G was also associated with adiposity in girls in late puberty ( OR =1.339, 95% CI : 1.093-1.637). Conclusion: The rs10938397 polymorphism in GNPDA2 is associated

Sphincterodiplostomum musculosum (Digenea, Diplostomidae infecting Steindachnerina insculpta (Characiformes, Curimatidae in the Chavantes Reservoir, Southeastern Brazil Sphincterodiplostomum musculosum (Digenea, Diplostomidae infectando Steindachnerina insculpta (Characiformes, Curimatidae no reservatório de Chavantes, Sudeste do Brasil

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Aline Cristina Zago

2013-03-01

Full Text Available This study aimed to report the infection by Sphincterodiplostomum musculosum metacercariae in Steindachnerina insculpta from the Chavantes Reservoir, medium Paranapanema River, municipality of Ipaussu, State of São Paulo, Brazil. Thirty specimens of S. insculpta were collected and 29 were infected with S. musculosum metacercariae (prevalence = 96.67% in the eyes and visceral cavity. The mean intensity of infection and abundance were 96.6 ± 29.41 (7-846 and 93.3 ± 28.6 (0-846, respectively. Positive correlation was observed between parasite abundance in the eyes and standard length (rs = 0.5, p = 0.005, total weight (rs = 0.649, p = 0.0001, and condition factor (rs = 0.439, p = 0.0154. The high parasitism rates by S. musculosum metacercariae in S. insculpta can be an indicative that this fish species is highly susceptible to infection by this diplostomid, and even reflect the presence of a large abundance of the intermediate host. Moreover, S. musculosum metacercariae are reported for the first time in S. insculpta.O presente estudo tem como objetivo relatar a infecção por metacercárias de Sphincterodiplostomum musculosum em Steindachnerina insculpta provenientes do Reservatório de Chavantes, médio Paranapanema, município de Ipaussu, Estado de São Paulo, Brasil. Foram coletados 30 espécimes de S. insculpta, sendo que 29 estavam infectados por metacercárias de S. musculosum (prevalência = 96,67% nos olhos e na cavidade visceral. A intensidade média de infecção e abundância apresentaram valores de 96,6 ± 29,41 (7-846 e 93,3 ± 28,6 (0-846, respectivamente. Foi observada correlação positiva entre a abundância dos parasitas presentes nos olhos com relação ao comprimento padrão (rs = 0.5, p = 0.005, peso (rs = 0.649, p = 0.0001 e fator de condição (rs = 0.439, p = 0.0154. As altas taxas de parasitismo de metacercárias de S. musculosum em S. insculpta podem ser um indicativo de que esta espécie de peixe é altamente suscept

Para quem ler?: os números do analfabetismo no Brasil

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Paloma Cristina de Souza

2014-07-01

Full Text Available O presente artigo traz um compilado de dados estatísticos sobre o analfabetismo no Brasil, possíveis causas e justificativas, e sua relação com outros aspectos socioeconômicos do país. Com base na observação e análise dos números fornecidos pelo Governo Federal, por meio do IBGE (PNAD e Censo 2010, procuramos demonstrar a influência das políticas públicas nos dados e, sobretudo de que forma esses números refletem (se é que refletem a realidade do país. Palavras-chave: analfabetismo estatísticas; Brasil; regiões; políticas públicas.

À PARTE - Pensamento Autoritário e Modernidade no Brasil

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Silene de Moraes Freire

2010-05-01

Full Text Available

Effect of Bcl-2 rs956572 polymorphism on age-related gray matter volume changes.

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Mu-En Liu

Full Text Available The anti-apoptotic protein B-cell CLL/lymphoma 2 (Bcl-2 gene is a major regulator of neural plasticity and cellular resilience. Recently, the Bcl-2 rs956572 single nucleotide polymorphism was proposed to be a functional allelic variant that modulates cellular vulnerability to apoptosis. Our cross-sectional study investigated the genetic effect of this Bcl-2 polymorphism on age-related decreases in gray matter (GM volume across the adult lifespan. Our sample comprised 330 healthy volunteers (191 male, 139 female with a mean age of 56.2±22.0 years (range: 21-92. Magnetic resonance imaging and genotyping of the Bcl-2 rs956572 were performed for each participant. The differences in regional GM volumes between G homozygotes and A-allele carriers were tested using optimized voxel-based morphometry. The association between the Bcl-2 rs956572 polymorphism and age was a predictor of regional GM volumes in the right cerebellum, bilateral lingual gyrus, right middle temporal gyrus, and right parahippocampal gyrus. We found that the volume of these five regions decreased with increasing age (all P<.001. Moreover, the downward slope was steeper among the Bcl-2 rs956572 A-allele carriers than in the G-homozygous participants. Our data provide convergent evidence for the genetic effect of the Bcl-2 functional allelic variant in brain aging. The rs956572 G-allele, which is associated with significantly higher Bcl-2 protein expression and diminished cellular sensitivity to stress-induced apoptosis, conferred a protective effect against age-related changes in brain GM volume, particularly in the cerebellum.

Aspectos florísticos e fitossociológicos da reserva Capão de Tupanciretã, Tupanciretã, RS, Brasil.

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Suzana Ferreira da Rosa

2008-01-01

Full Text Available Este trabalho foi realizado na Reserva Capão de Tupanciretã, município de Tupanciretã (RS, em uma área com 8 hectares pertencente à Fundação de Pesquisa Agropecuária do Rio Grande do Sul (FEPAGRO. O objetivo do trabalho foi avaliar a composição florística e estrutura fitossociológica da floresta. Utilizaram-se dez parcelas de tamanho 10 x 20 m distribuídas sistematicamente na área. Nessas parcelas, foram medidos e identificados todos os indivíduos com DAP maior ou igual a 5 cm. Dentro das parcelas principais, alocaram-se subunidades de 5 x 5 m para avaliar o componente arbustivo (DAP entre 1 e 5 cm e de 2 x 2 m para a regeneração natural (DAP menor que 1 cm e altura superior a 30 cm. Os resultados foram analisados usando o programa FITOANALISE, calculando-se os parâmetros fitossociológicos tradicionais de densidade, dominância, freqüência, valor de importância, valor de cobertura e índice de diversidade. As espécies com maior representatividade no componente arbóreo da floresta foram Camboatá-vermelho (Cupania vernalis Cambess. e o Branquilho (Sebastiania commersoniana (Baill. L. B. Sm. & Downs. No componente arbustivo e na regeneração, as espécies que apresentaram o maior número de indivíduos foram Camboatá-vermelho (Cupania vernalis Cambess., Primavera (Brunfelsia australis Benth., Chal-chal (Allophylus edulis (A. St.–Hil, Cambess. & A. Juss. e Canela-amarela (Nectandra lanceolata Nees

Faktor-Faktor Yang Mempengaruhi Kejadian Insomnia di Poliklinik Saraf RS DR. M. Djamil Padang

OpenAIRE

Lydia Susanti

2015-01-01

Abstrak Faktor risiko seperti usia lanjut, jenis kelamin wanita, penyakit penyerta (depresi dan penyakit lain), status sosial ekonomi rendah menyebabkan insomnia. Penelitian mengenai prevalensi dan faktor-faktor yang mempengaruhi kejadian insomnia di Poliklinik Saraf RS DR. M. Djamil Padang belum pernah dilakukan. Tujuan penelitian ini adalah menentukan faktor-faktor yang mempengaruhi terjadinya insomnia di poliklinik saraf RS DR. M. Djamil Padang. Penelitian ini merupakan penelitian cross se...

The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing

DEFF Research Database (Denmark)

Pharoah, Paul D P; Palmieri, Rachel T; Ramus, Susan J

2011-01-01

PURPOSE: An assay for the single nucleotide polymorphism (SNP) rs61764370 has recently been commercially marketed as a clinical test to aid ovarian cancer risk evaluation in women with family histories of the disease. rs67164370 is in a 3'UTR miRNA binding site of the KRAS oncogene, and is a cand...

7q21-rs6964587 and breast cancer risk

DEFF Research Database (Denmark)

Milne, Roger L; Lorenzo-Bermejo, Justo; Burwinkel, Barbara

2011-01-01

Using the Breast Cancer Association Consortium, the authors previously reported that the single nucleotide polymorphism 7q21-rs6964587 (AKAP9-M463I) is associated with breast cancer risk. The authors have now assessed this association more comprehensively using 16 independent case-control studies....

Desviación positiva y responsabilidad social empresarial (RSE. La experiencia de Ethos en Brasil

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Alam Aguilar-Platas

2010-08-01

Full Text Available El presente artículo de investigación analiza la fundación y la expansión del Instituto Ethos, una organización sin ánimo de lucro que ha contribuido a crear y desarrollar la infraestructura necesaria para fomentar la responsabilidad social empresarial (RSE en Brasil. Entre 1998 y 2008, el Instituto Ethos reunió a más de 1200 pequeñas, medianas y grandes empresas con el fin de ayudarles a administrar sus negocios de una manera socialmente responsable en Brasil. Estas empresas en la actualidad representan aproximadamente un 35% del PIB en Brasil y emplean alrededor de 2 millones de personas. Los resultados de esta investigación sugieren que Ethos ha logrado difundir la RSE aplicando una perspectiva basada en el uso de la desviación positiva en el mundo de los negocios en Brasil. El artículo contribuye a los debates sobre RSE a partir de la identificación de un mecanismo de difusión de la RSE utilizando un modelo de desviación positiva.

Overview of the ARIES-RS reversed-shear tokamak power plant study

International Nuclear Information System (INIS)

Najmabadi, F.; Billone, M.C.

1997-01-01

The ARIES-RS tokamak is a conceptual, D-T-burning 1000 MWe power plant. As with earlier ARIES design studies, the final design of ARIES-RS was obtained in a self-consistent manner using the best available physics and engineering models. Detailed analyses of individual systems together with system interfaces and interactions were incorporated into the ARIES systems code in order to assure self-consistency and to optimize towards the lowest cost system. The ARIES-RS design operates with a reversed-shear plasma and employs a moderate aspect ratio (A=4.0). The plasma current is relatively low (I p =11.32 MA) and bootstrap current fraction is high (f BC =0.88). Consequently, the auxiliary power required for RF current drive is relatively low (∝80 MW). At the same time, the average toroidal beta is high (β=5%), providing power densities near practical engineering limits (the peak neutron wall loading is 5.7 MW m -2 ). The toroidal-field (TF) coil system is designed with relatively 'conventional' materials (Nb 3 Sn and NbTi conductor with 316SS structures), and is operated at a design limit of ∝16 T at the coil in order to optimize the design point. The ARIES-RS design uses a self-cooled lithium blanket with vanadium alloy as the structural material. The V-alloy has low activation, low afterheat, high temperature capability and can handle high heat flux. A self-cooled liquid lithium blanket is simple, and with the development of an insulating coating, has low operating pressure. Also, this blanket gives excellent neutronics performance. Detailed analysis has been performed to minimize the cost and maximize the performance of the blanket and shield. (orig.)

Quantification of porosity evolution from unaltered to propylitic-altered granites: the 14C-PMMA method applied on the hydrothermal system of Lavras do Sul, Brazil

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Everton M. Bongiolo

2007-09-01

Full Text Available This work is an application of the 14C-Polymethylmethacrylate method to compare the porosity evolution between unaltered and propylitic-altered granites, using samples from Lavras do Sul region, Brazil. This method, when coupled with optical and electronic petrography has the advantage over other methods to provide the quantification and identification of total and local porosity of rocks. From petrographic observations, different kinds of porous zones were identified and quantified (microfractures, grain boundaries, alteration of minerals, etc. Results show that unaltered granites have 0.5 to 0.6% porosity and propylitic-altered ones have 1.7 to 1.8% porosity, even between samples with different textures. Porosity of altered rocks increases mainly due to higher porosity of neoformed chlorite, calcite, sericite and microfractures. Field observations show that later phyllic alteration halos are wider in equigranular than in porphyritic granites, which could not be explained by different original porosity between those rocks. The observed differences of phyllic halos diffusion were controlled by structural and fluid/rock ratio variations between the equigranular and porphyritic granitic facies during the later hydrothermal stage.Este trabalho é uma aplicação do método 14C-polimetilmetacrilato na comparação da evolução da porosidade entre granitos não alterados e propilitizados, utilizando amostras da região de Lavras do Sul, Brasil. Este método, quando associado a análises por petrografia ótica, eletrônica e processamento digital de imagens tem a vantagem de fornecer, além da porosidade total, a quantificação e identificação da porosidade em locais específicos das rochas. A partir da petrografia foi possível identificar e quantificar os diferentes tipos de poros presentes nas rochas (microfraturas, limites de grãos, alteração de minerais, etc. Os resultados mostram que granitos não alterados têm porosidade de 0,5 a 0,6% e

nos anos 40 e 50 no Brasil, no século XX

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Tatiana de Oliveira Gomes

2005-01-01

Full Text Available RESUMEN: Estudio de cuño histórico–social, tiene como objeto: las luchas de las enfermeras católicas por mejores posiciones en el campo de la educación y de la práctica de enfermería en el Brasil. Tuvo como objetivos; describir las circunstancias que llevaron a las enfermeras católicas a organizarse políticamente; analizar la creación de la Unión Católica de las Enfermeras del Brasil como una estrategia de lucha de las enfermeras católicas y, comentar la importancia de la Unión para el realineamiento del campo de la educación y de la práctica de la enfermería en el Brasil. Fuentes primarias; los documentos escritos y testimonios orales. Se utilizaron como fuentes secundaras; libros, artículos, disertaciones y tesis que tratan sobre el tema. La Unión fue creada con la finalidad de congregar en una única asociación de clase, enfermeras-religiosas y enfermeras católicas laicas. Así contribuyó para asegurar el fortalecimiento de la enfermería de carácter católico en el campo de la educación y de la práctica, lo que instituyó un nuevo modelo de enfermería en la sociedad brasileña.

[Design and implementation of the ELSA-Brasil biobank: a prospective study in a Brazilian population].

Science.gov (United States)

Pereira, Alexandre C; Bensenor, Isabela M; Fedeli, Ligia M; Castilhos, Cristina; Vidigal, Pedro G; Maniero, Viviane; Leite, Claudia M; Pimentel, Robercia A; Duncan, Bruce B; Mill, Jose Geraldo; Lotufo, Paulo A

2013-06-01

The Brazilian Longitudinal Study for Adult Health (ELSA-Brasil) is a multicenter prospective cohort of civil servants designed to assess the determinants of chronic diseases, especially cardiovascular diseases and type 2 diabetes. The present article describes the main design and implementation points of the ELSA-Brasil biobank project. Economic, political, logistical and technological aspects of this study are characterized. Additionally, it discusses the final biorepository protocol and the facilities implemented to achieve this objective. The design and implementation process of the ELSA-Brasil biobank took three years to be performed. Both the central and local biobanks were built according to the best biorepository techniques, using different technological solutions for the distinct needs expected in this study.

Intenções versus desempenho: o Brasil na política externa portuguesa (1976-2007

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Carmen Sofia Fonseca

2010-01-01

Full Text Available Partindo dos eixos orientadores da política externa portuguesa no pós-25 de Abril de 1974, o artigo visa compreender o enquadramento do Brasil nas opções da política externa portuguesa, centrando-se na análise dos programas dos Governos Constitucionais, nas visitas oficiais, no investimento português no Brasil e na influência da imigração brasileira na política externa. Pretendemos mostrar que, apesar das alterações exigidas pela democratização portuguesa, a relação com o Brasil subsistiu embora tenha prevalecido a retórica e o simbolismo sobre as concretizações práticas.

A putative gene sbe3-rs for resistant starch mutated from SBE3 for starch branching enzyme in rice (Oryza sativa L..

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Ruifang Yang

Full Text Available Foods high in resistant starch (RS are beneficial to prevent various diseases including diabetes, colon cancers, diarrhea and chronic renal or hepatic diseases. Elevated RS in rice is important for public health since rice is a staple food for half of the world population. A japonica mutant 'Jiangtangdao 1' (RS = 11.67% was crossed with an indica cultivar 'Miyang 23' (RS = 0.41%. The mutant sbe3-rs that explained 60.4% of RS variation was mapped between RM6611 and RM13366 on chromosome 2 (LOD = 36 using 178 F(2 plants genotyped with 106 genome-wide polymorphic SSR markers. Using 656 plants from four F(3:4 families, sbe3-rs was fine mapped to a 573.3 Kb region between InDel 2 and InDel 6 using one STS, five SSRs and seven InDel markers. SBE3 which codes for starch branching enzyme was identified as a candidate gene within the putative region. Nine pairs of primers covering 22 exons were designed to sequence genomic DNA of the wild type for SBE3 and the mutant for sbe3-rs comparatively. Sequence analysis identified a missense mutation site where Leu-599 of the wild was changed to Pro-599 of the mutant in the SBE3 coding region. Because the point mutation resulted in the loss of a restriction enzyme site, sbe3-rs was not digested by a CAPS marker for SpeI site while SBE3 was. Co-segregation of the digestion pattern with RS content among 178 F(2 plants further supported sbe3-rs responsible for RS in rice. As a result, the CAPS marker could be used in marker-assisted breeding to develop rice cultivars with elevated RS which is otherwise difficult to accurately assess in crops. Transgenic technology should be employed for a definitive conclusion of the sbe3-rs.

A review of research on ecosystem of arid area using RS-GIS in China

Science.gov (United States)

Han, Hongling

2007-06-01

Arid area is classical mountain-oasis-desert ecosystem in North-west China. As the ecosystem has its nature geography character obviously, it has superior to research with remote-sensing and geography information system. The study on arid ecosystem in RS-GIS' way is focused on that the landscape spatial pattern of complex MODS ecosystem, the dynamic development of Land use/land cover, the security of ecological environment of eco-tone and so on. At the same time, the research on the single system is more and more, which has provided more ways and deeper fields of arid area using RS-GIS. Through the use of RS-GIS, desertification, oasis' development, urbanization etc. can be known, which would provide precaution for human-being and suitable ways to adjust the problems.

Synthesis of (R,S)-[2,3-13C2]-1-(1'-methyl-2'-pyrrolidinyl)propan-2-one; {(R,S)-[2',3'-13C2]hygrinePound right bracePound

International Nuclear Information System (INIS)

Abraham, T.W.; Leete, Edward

1996-01-01

2-Ethoxy-1-methyl-5-pyrrolidinone (1) was reacted with ethyl [3,4- 13 C 2 ]-acetoacetate (2) in the presence of TiCl 4 to give ethyl [3,4- 13 C 2 ]-2-(1'-methyl-5'-oxo-2'-pyrrolidinyl)-3-oxobutanoate (3) in 85% yield. Decarboethoxylation of ethyl [3,4- 13 C 2 ]-2-(1'-methyl-5'-oxo-2'-pyrrolidinyl)-3-oxobutan-oate (3) was accomplished using NaCl and H 2 O in DMSO to give (R,S)-[2,3- 13 C 2 ]-1-(1'-methyl-5'-oxo-2'-pyrrolidinyl)propan-2-o ne (4) in 91% yield. Protection of the ketone as a ketal (ethylene glycol, H + ), followed by reduction of the amide to the amine using LiAlH 4 and subsequent deprotection of the ketal gave (R,S)-[2,3- 13 C 2 ]-1-(1'-methyl-2'-pyrrolidinyl)propan-2-one ((R,s)-[2', 3'- 13 C 2 ]Hygrine) (8) in 78% yield. (61% overall yield from ethyl [3,4- 13 C 2 ]acetoacetate). (Author)

TERT-CLPTM1 locus polymorphism (rs401681 is associated with the prognosis of hepatocellular carcinoma

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Lee HW

2017-10-01

Full Text Available Hye Won Lee,1,* Won-Jin Park,2,* Yu-Ran Heo,2 Tae In Park,3 Soo Young Park,4 Jae-Ho Lee2,* 1Department of Pathology, Keimyung University School of Medicine, Daegu, Republic of Korea; 2Department of Anatomy, Keimyung University School of Medicine, Daegu, Republic of Korea; 3Department of Pathology, Kyungpook National University School of Medicine, Daegu, Republic of Korea; 4Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Republic of Korea *These authors contributed equally to this work Abstract: Telomere length is associated with the development of hepatocellular carcinoma (HCC, and recent studies have focused on the genetic alteration or polymorphism in telomere-maintaining genes. We examined the clinicopathologic and prognostic value of rs401681 polymorphism, located in the TERT-CLPTM1L locus, in HCC. The relationship between rs401681 variants and telomere length was also analyzed in 156 HCC patients. The rs401681 polymorphism had the following genotype frequencies: C/C in 51.3% of the samples, C/T in 39.7%, and T/T in 9.0%. Telomeres in the tumor samples were 4.04-fold longer, on average, than the telomeres in matched normal samples (SD =1.32, and there were no differences in telomere length according to rs401681 polymorphism (p=0.802. Our results indicate that the rs401681 C allele was significantly associated with increased T and International Union for Cancer Control stages (p<0.01. Univariate and multivariate survival analyses showed that HCC with C allele had poorer prognosis (p<0.01. In conclusion, our findings suggest that rs401681 is a possible prognostic biomarker for HCC patients. Keywords: CLPTM1L polymorphism, hepatocellular carcinoma, TERT-CLPTM1L locus, telomere length

Unilateral RS3PE in a Patient of Seronegative Rheumatoid Arthritis

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Ankur Nandan Varshney

2013-01-01

Full Text Available Remitting seronegative symmetrical synovitis with pitting edema (RS3PE is a rare but well-reported clinical entity. It is classically described as symmetrical involvement of both upper extremities. Asymmetrical involvement had also been reported, but unilateral presentation is very rare. We hereby report a case of unilateral RS3PE in a patient of seronegative rheumatoid arthritis which was initially misdiagnosed as cellulitis and was given high dose antibiotics without any significant improvement. Later a rheumatologic consultation leads to a prompt diagnosis, and treatment with steroids leads to dramatic reversal of symptoms. This case demonstrates the rare presentation of this rare clinical entity and highlights the necessity of awareness regarding unilateral disease to clinicians.

SaeRS Is Responsive to Cellular Respiratory Status and Regulates Fermentative Biofilm Formation in Staphylococcus aureus.

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Mashruwala, Ameya A; Gries, Casey M; Scherr, Tyler D; Kielian, Tammy; Boyd, Jeffrey M

2017-08-01

Biofilms are multicellular communities of microorganisms living as a quorum rather than as individual cells. The bacterial human pathogen Staphylococcus aureus uses oxygen as a terminal electron acceptor during respiration. Infected human tissues are hypoxic or anoxic. We recently reported that impaired respiration elicits a p rogrammed c ell l ysis (PCL) phenomenon in S. aureus leading to the release of cellular polymers that are utilized to form biofilms. PCL is dependent upon the AtlA murein hydrolase and is regulated, in part, by the SrrAB two-component regulatory system (TCRS). In the current study, we report that the SaeRS TCRS also governs fermentative biofilm formation by positively influencing AtlA activity. The SaeRS-modulated factor fibronectin-binding protein A (FnBPA) also contributed to the fermentative biofilm formation phenotype. SaeRS-dependent biofilm formation occurred in response to changes in cellular respiratory status. Genetic evidence presented suggests that a high cellular titer of phosphorylated SaeR is required for biofilm formation. Epistasis analyses found that SaeRS and SrrAB influence biofilm formation independently of one another. Analyses using a mouse model of orthopedic implant-associated biofilm formation found that both SaeRS and SrrAB govern host colonization. Of these two TCRSs, SrrAB was the dominant system driving biofilm formation in vivo We propose a model wherein impaired cellular respiration stimulates SaeRS via an as yet undefined signal molecule(s), resulting in increasing expression of AtlA and FnBPA and biofilm formation. Copyright © 2017 American Society for Microbiology.

Pharmacological and immunochemical characterization of α2* nicotinic acetylcholine receptors (nAChRs) in mouse brain

Science.gov (United States)

Whiteaker, Paul; Wilking, Jennifer A; Brown, Robert WB; Brennan, Robert J; Collins, Allan C; Lindstrom, Jon M; Boulter, Jim

2009-01-01

Aim: α2 nAChR subunit mRNA expression in mice is most intense in the olfactory bulbs and interpeduncular nucleus. We aimed to investigate the properties of α2* nAChRs in these mouse brain regions. Methods: α2 nAChR subunit-null mutant mice were engineered. Pharmacological and immunoprecipitation studies were used to determine the composition of α2 subunit-containing (α2*) nAChRs in these two regions. Results: [125I]Epibatidine (200 pmol/L) autoradiography and saturation binding demonstrated that α2 deletion reduces nAChR expression in both olfactory bulbs and interpeduncular nucleus (by 4.8±1.7 and 92±26 fmol̇mg-1 protein, respectively). Pharmacological characterization using the β2-selective drug A85380 to inhibit [125I]epibatidine binding proved inconclusive, so immunoprecipitation methods were used to further characterize α2* nAChRs. Protocols were established to immunoprecipitate β2 and β4 nAChRs. Immunoprecipitation specificity was ascertained using tissue from β2- and β4-null mutant mice, and efficacy was good (>90% of β2* and >80% of β4* nAChRs were routinely recovered). Conclusion: Immunoprecipitation experiments indicated that interpeduncular nucleus α2* nAChRs predominantly contain β2 subunits, while those in olfactory bulbs contain mainly β4 subunits. In addition, the immunoprecipitation evidence indicated that both nuclei, but especially the interpeduncular nucleus, express nAChR complexes containing both β2 and β4 subunits. PMID:19498420

Historiografía didáctica brasileñaen el siglo XIX: Joaquim Manuel de Macedo y sus Lecciones

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Ana Paula Squinelo

2015-12-01

Full Text Available El Proceso de Independencia brasileño ocurrido en 1822 ha impuesto a la intelectualidad de la Nación recién Formada la Necesidad de Pensar y Construir su Historia Relación pecado con los designios de Portugal. Dos Espacios concibieron e irradiaron los Conocimientos Acerca de la Historia brasileña: el Colegio de Pedro II (1837 y el Instituto Histórico y Geográfico Brasileño (1838. En ESE contexto Joaquim Manuel de Macedo escribio la obra Lições de Historia do Brasil (1861 Presentando ONU Método para Enseñar y estudiar la Historia Nacional. Propongo En Esta Reflexión ONU Diálogo con la historiografía didáctica brasileña en el siglo XIX desde la Obra Lições de Macedo y Tomando Como directriz los Contenidos Relacionados a la Guerra del Paraguay.

No correlation between PNPLA3 rs738409 genotype and fatty liver and hepatic cirrhosis in Japanese patients with HCV.

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Masato Nakamura

Full Text Available BACKGROUND: Hepatitis C virus (HCV infection is associated with the development of cirrhosis and hepatocellular carcinoma and is also related to fatty change of the liver. Variation in patatin-like phospholipase domain-containing 3 (PNPLA3 gene is associated with disease progression in nonalcoholic fatty liver disease (NAFLD. Recent reports have suggested that PNPLA3, IL28B and TLR4-associated single nucleotide polymorphisms (SNPs may have an impact on hepatic steatosis or fibrosis in patients with chronic HCV infection. METHODS AND FINDINGS: Four SNPs (PNPLA3 rs738409, TLR4 rs4986790, TLR4 rs4986791, IL28B rs8099917 were identified in Japanese patients infected with HCV. We examined the association between the distribution of these SNP alleles and fatty change of the liver or existence of hepatic cirrhosis diagnosed by ultrasonography, one of the widely accessible and easy-to-use methods. PNPLA3 rs738409 G-allele and IL28B rs 8099917 minor allele were found in 70.0% and 31.1%, respectively. These two TLR4 SNPs were uniform in Japanese. Fatty change of the liver developed independent of the abscence of hepatic cirrhosis on sonographic findings and younger age. Hepatic cirrhosis was associated with a higher aspartate aminotransferase/platelet ratio index (APRI, no fatty change of the liver, higher BMI and higher AFP levels. No association between PNPLA3 rs738409/IL28B rs8099917 genotypes and hepatic steatosis or liver fibrosis was observed. CONCLUSIONS: According to ultrasound examinations, no association between PNPLA3 rs738409 genotype and fatty change of the liver or hepatic cirrhosis was found in Japanese patients infected with HCV. Together, our results suggested that the mechanism of hepatic steatosis underlying HCV infection might differ from that of NAFLD and should be explored.

Developing RESTful services with JAX-RS 2.0, WebSockets, and JSON

CERN Document Server

Kalali, Masoud

2013-01-01

Written as an easy and practical guide, this book is a crash course on using JAX-RS 2.0, JSON, and WebSockets to develop RESTful services.Getting Started with Developing RESTful Web Services using JAX-RS 2.0, JSON, and WebSockets is a perfect reading source for application developers who are familiar with Java EE and are keen to understand the new HTML5-related functionality introduced in Java EE 7 to improve productivity. To take full advantage of this book, you need to be familiar with Java EE and have some basic understanding of using the GlassFish application server.

ARIES-RS safety design and analysis

International Nuclear Information System (INIS)

Steiner, D.; El-Guebaly, L.; Herring, S.; Khater, H.; Mogahed, E.; Thayer, R.; Tillack, M.S.

1997-01-01

The ARIES-RS safety design and analysis focused on achieving two objectives: (1) The avoidance of sheltering or evacuation in the event of an accident; and (2) the generation of only low-level waste, no greater than Class C. The ARIES-RS baseline design employs V-4Cr-4Ti as the blanket structural material and a low activation ferritic steel in the reflector and shield. In the event of a LOCA, the baseline design first wall maximum temperature falls in the range of 1100-1200 C. For this temperature range, the hazard assessment indicates that the dose at the site boundary will be less than 1 rem per year. Thus, no sheltering or evacuation would be required in the event of a LOCA. Although the baseline design satisfies the first safety objective noted above, a first wall maximum temperature of ∝1100-1200 C would likely compromise the integrity of the vanadium blanket structure and would require blanket replacement following such a temperature excursion. To avoid this situation, a modified blanket design incorporating supplemental heat removal is also proposed. Preliminary analysis of this modified design suggests that the first wall maximum temperature can be kept below the temperature range of concern, ∝1000-1100 C, in the event of a LOCA. When the ferritic steel used in the reflector and shield is one reduced in Ir and Ag impurities, all in-vessel components qualify for near-surface shallow land burial as Class C low-level waste. (orig.)

Solubility of water in fluorocarbons: Experimental and COSMO-RS prediction results

International Nuclear Information System (INIS)

Freire, Mara G.; Carvalho, Pedro J.; Santos, Luis M.N.B.F.; Gomes, Ligia R.; Marrucho, Isabel M.; Coutinho, Joao A.P.

2010-01-01

This work aims at providing experimental and theoretical information about the water-perfluorocarbon molecular interactions. For that purpose, experimental solubility results for water in cyclic and aromatic perfluorocarbons (PFCs), over the temperature range between (288.15 and 318.15) K, and at atmospheric pressure, were obtained and are presented. From the experimental solubility dependence on temperature, the partial molar solution and solvation thermodynamic functions such as Gibbs free energy, enthalpy and entropy were determined and are discussed. The process of dissolution of water in PFCs is shown to be spontaneous for cyclic and aromatic compounds. It is demonstrated that the interactions between the non-aromatic PFCs and water are negligible while those between aromatic PFCs and water are favourable. The COSMO-RS predictive capability was explored for the description of the water solubility in PFCs and others substituted fluorocompounds. The COSMO-RS is shown to be a useful model to provide reasonable predictions of the solubility values, as well as to describe their temperature and structural modifications dependence. Moreover, the molar Gibbs free energy and molar enthalpy of solution of water are predicted remarkably well by COSMO-RS while the main deviations appear for the prediction of the molar entropy of solution.

ESTUDOS ESTILÍSTICOS NO BRASIL

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Carlos Eduardo Falcão Uchôa

2013-06-01

Full Text Available Este artigo objetiva mostrar os inícios e a progressão dos estudos estilísticos no Brasil. Após uma introdução sobre o surgimento, na Europa, da Estilística como disciplina de pesquisa no campo da linguagem, detém-se, sucessivamente, nas contribuições de filólogos, linguistas, teóricos da literatura e gramáticos para o estudo dos mais variados recursos estilísticos ocorrentes sobretudo em autores brasileiros.

RACISMO CIENTÍFICO NO BRASIL PÓS-ESCRAVATURA

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RAQUEL AMORIM DOS SANTOS

2017-12-01

Full Text Available Este estudo analisa a difusão do racismo cientifico no Brasil, reconhecendo seu caráter estrutural. Reconhecê-lo desta forma significa perceber que Cor, raça e preconceito no Brasil compõe o plexo de concepções para o enfrentamento das questões raciais e de seus desdobramentos nocivos na formação de crianças e adolescentes, por meio da construção de uma nova forma de se pensar a formação da nação e da nacionalidade. O estudo é de abordagem qualitativa com aplicação da pesquisa bibliográfica com base em Skidmore (2012, Schwarcz (1993, Guimarães (1999, Ianni (1962, 1978, Hasenbalg (2005, Munanga (2004, Hofbauer (2006, Costa (2006, entre outros. A análise aponta que o mestiço era admitido como elemento transitório que levaria a constituição de uma nação de brancos.

Risco crescente de melanoma de pele no Brasil

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Guinar Azevedo e Silva Mendonça

1992-08-01

Full Text Available A ocorrência de melonoma maligno de pele no Brasil é analisada a partir dos dados de mortalidade disponíveis no Ministério da Saúde e dos dados de incidência dos seis Registros de Câncer de Base Populacional, localizados em seis capitais brasileiras. Os coeficientes de incidência nessas capitais situam-se em padrões intermediários se comparadas às cifras mundiais. Para o Município de Porto Alegre, uma das capitais estudas, que apresentou os maiores coeficientes de incidência, é feita comparação entre os dados relativos ao período 1979-1982 e 1987, constatando-se que houve aumento relativo de 38% entre homens e de 11% entre mulheres. Concluiu-se pela necessidade de se conduzir estudos no Brasil entre comunidades de indivíduos de pele clara, os quais apresentam risco potencializado para o desenvolvimento de melanoma, para que sejam definidas medidas específicas e eficazes de controle.

Combatendo o racismo: Brasil, África do Sul e Estados Unidos

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Guimarães Antonio Sérgio Alfredo

1999-01-01

Full Text Available O autor identifica o que se pode chamar hoje de "racismo", tomando como referência empírica o debate político e intelectual corrente na África do Sul, no Brasil e nos Estados Unidos. Com base neste debate, sugere uma agenda internacional mínima de combate ao racismo. O texto é estruturado sob a forma de notas. A primeira nota demarca um terreno axiológico comum ao anti-racismo; a segunda esclarece o significado do termo "racismo"; a terceira procura situar sociologicamente o racismo nos três países tomados como referência, fazendo um esforço para situar a relação entre a definição dos direitos da cidadania e a definição da nacionalidade; a quarta explora os tipos de mecanismos que produzem e reproduzem desigualdades sociais relevantes na distribuição de recursos e honra sociais; a quinta define melhor a especificidade do racismo no Brasil, enquanto a sexta, a sétima e a oitava notas discutem o movimento anti-racista hoje em dia no Brasil, Estados Unidos e África do Sul, respectivamente.

CABOTAGEM UMA ALTERNATIVA ECONÔMICA DE TRANSPORTE EFICAZ PARA O BRASIL

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Leandra Machado Gonçalves

2011-06-01

Full Text Available O presente artigo apresenta o panorama atual do transporte marítimo por Cabotagem no Brasil. Fez-se um breve descritivo do contexto em que se situa a Cabotagem no segmento do transporte marítimo no Brasil destacando suas vantagens, avaliando as condições para sua viabilidade, apontando os principais entraves e reformas necessárias para o desenvolvimento do setor portuário Destacou-se as políticas de estímulo ao transporte aquaviário e de infra-estrutura que estão sendo implantadas assim como as medidas implementadas para minimizar as limitações a Cabotagem e sugeridas novas medidas. Foi enfatizada a vocação marítima do Brasil, o cenário atual da economia que favorecem o crescimento da Cabotagem, o crescimento do transporte multimodal e principalmente a mobilização de portos e armadores para mostrar a via marítima como diferencial competitivo e vantagens comerciais assim como de que forma o crescimento da navegação de Cabotagem poderá contribuir para a mudança da Matriz de Transporte Brasileira. .

FLORÍSTICA E ESTRUTURA EM ÁREA DE FLORESTA ESTACIONAL DECIDUAL NA REGIÃO DO ALTO URUGUAI, RS / FLORISTIC AND STRUCTURE IN AREA OF SEASONAL DECIDUOUS FOREST IN THE REGION OF THE ALTO URUGUAI, RS

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F. R. Lambrecht

2016-06-01

Full Text Available           O trabalho teve como objetivos realizar a análise florística das estruturas horizontal e vertical em um fragmento de Floresta Estacional Decidual (FED na região do Alto Uruguai, em Frederico Westphalen, RS, Brasil. Foi realizado um censo em uma área amostral de 10.000 m², subdividida em 100 subparcelas de 10x10 m. Realizou-se a mensuração e a identificação de todos os indivíduos de espécies arbóreas com circunferência a altura do peito (CAP≥ 31,4cm. Com os dados obtidos, foram realizados cálculos de densidade (D, frequência (F, dominância (Do, índice de valor de importância (IVI, índice de valor de cobertura (IVC e a estratificação dos indivíduos. O maior número de espécies concentrou-se na família Fabaceae (10 e o maior número de indivíduos na família Meliaceae (147 ou 25,3%. Trichilia claussenii C. DC. Nectandra megapotamica (Spreng. Mez, Achatocarpus praecox Griseb. e Eugenia rostrifolia D. Legrand representaram 38,28% da densidade relativa e Holocalyx balansae Micheli, Trichilia claussenii, Nectandra megapotamica, Cordia americana (L. Gottshling & J.E.Mill., Phytolacca dioica  L., Achatocarpus praecox, e Eugenia rostrifolia representaram 50,5% da dominância relativa. Considerando a estrutura vertical, as sete espécies mais frequentes apresentaram uma maior quantidade de indivíduos no estrato médio. Conclui-se que a área florestal encontra-se em estágio intermediário de sucessão.

Mortalidade por acidentes de motocicleta no Brasil: analise de tendencia temporal, 1996-2009

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Evandro Tostes Martins

2013-10-01

Full Text Available OBJETIVO Analisar a tendência da mortalidade por acidentes de motocicleta no Brasil. MÉTODOS Estudo descritivo de séries temporais sobre a taxa de mortalidade de acidentes de motocicleta no Brasil, segundo unidades federativas e faixas etárias entre 1996 e 2009. Os dados de óbitos foram obtidos no Sistema de Informação sobre Mortalidade do Ministério da Saúde e da população no Instituto Brasileiro de Geografia Estatística. Taxas de mortalidade padronizadas foram calculadas no período para o Brasil como um todo e Unidades Federativas. Variações anuais das taxas de mortalidade foram estimadas pelo método de Prais-Winsten de regressão linear. RESULTADOS A taxa de mortalidade por acidentes de motocicleta aumentou de 0,5 para 4,5/100.000 habitantes de 1996 a 2009 (aumento de 800% no período e 19% ao ano. Estados com maiores taxas em 2009 foram: Piauí, Tocantins, Sergipe e Mato Grosso. As maiores taxas de crescimento foram observadas nos Estados das regiões Norte, Nordeste e Centro-Oeste. CONCLUSÕES Houve grande aumento das taxas de mortalidade por acidente de motocicleta em todo o Brasil no período, principalmente nos Estados do Nordeste.

Formação da comunidade científica de enfermagem no Brasil

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Eliane Brandão Salles

2010-01-01

Full Text Available Estudio del proceso de ciencia de la enfermería brasileña que abarca la formación de grupos generacionales portadores del habitus científico y la construcción del campo científico de la enfermería. Tuvo por objetivos caracterizar las generaciones de enfermeras investigadoras en Brasil y discutir la dinámica del campo científico de enfermería. Referencia teórico: concepto de generación de Karl Mannhein y Sirinelli, del habitus y de campo, de Pierre Bourdieu.. Investigacion com abordaje socio-historico. Como resultados se clasificaron cinco generaciones de enfermeras investigadoras brasileñas: las "pioneras", de los años 50; las "autodidactas", de los años 60; las "académicas", de los años 70 y 80; la generación de la "producción sistemática y colectiva", iniciada en la media de los años 80/90; la generación de las "investigadoras con producción científica internacional", surgida en mediados de la década de 90. Se concluyó que el proceso de ciencia ocurrió según las características generacionales de la comunidad científica y las luchas simbólicas ocurridas en el campo de la enfermería brasileña.

La emoción, la sociedad y la cultura en la sociabilidad urbana brasileña

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Jainara Gomes de Oliveira

2016-09-01

Full Text Available Esta reseña analiza el libro "Da Subjetividades às Emoções", publicado en Brasil en 2015 y organizado por investigadores Mauro Guilherme Pinheiro Koury y Raoni Borges. El libro, en este sentido, explora el lugar de las emociones como el objeto de análisis de las ciencias sociales, en particular la antropología y la sociología de las emociones en Brasil, a partir de una lectura de las principales obras de dos intelectuales, a saber, Gilberto Velho y Mauro Koury, pioneros en el proceso de construcción de estos campos emergentes de estudios en la academia brasileña. 

[ELSA-Brasil strategies for outcome identification, investigation and ascertainment].

Science.gov (United States)

Barreto, Sandhi Maria; Ladeira, Roberto Marini; Bastos, Maria do Socorro Castelo Branco de Oliveira; Diniz, Maria de Fátima Haueisen Sander; Jesus, Elcimara Amorim de; Kelles, Silvana Márcia Bruschi; Luft, Vivian Cristine; Melo, Enirtes Caetano Prates; Oliveira, Elizabete Regina Araújo de

2013-06-01

The article describes the strategies adopted by the Brazilian Longitudinal Study for Adult Health (ELSA-Brasil) for participation and retention of subjects. This is key to ensure internal validity of longitudinal studies, and to identify, investigate, and ascertain outcomes of interest. The follow-up strategies include annual telephone contacts with new assessments and interviews every three to four years this approach aims to identify transient outcomes (reversible or not), permanent outcomes as well as complications related to the progression of major diseases--cardiovascular diseases and diabetes--to be studied. Telephone interviews are designed to monitor subjects' health status and to identify potential health-related events such as hospital admissions, medical visits or pre-selected medical procedures. Subjects are also encouraged to report to the ELSA-Brasil team any new health-related events. When a potential event is identified, a thorough investigation is carried out to collect relevant information about that event from medical records. All data are blinded and reviewed and analyzed by a medical expert committee. Incident outcome ascertainment follows well-established international criteria to ensure data comparability and avoid misclassification. In addition to these strategies, the occurrence of health-related events is also investigated through linkage of secondary databases, such as national mortality and hospital admission databases. Accurate identification of outcomes will allow to estimating their incidence in the study cohort and to investigate the effect of the exposures studied in the ELSA-Brasil at baseline and at its subsequent waves.

Association of polycystic ovary syndrome susceptibility single nucleotide polymorphism rs2479106 and PCOS in Caucasian patients with PCOS or hirsutism as referral diagnosis.

Science.gov (United States)

Eriksen, Mette B; Brusgaard, Klaus; Andersen, Marianne; Tan, Qihua; Altinok, Magda L; Gaster, Michael; Glintborg, Dorte

2012-07-01

Polycystic ovary syndrome (PCOS) is the most common endocrine disease among premenopausal women. A recent study found association between three single nucleotide polymorphisms (SNPs) and PCOS in a cohort of Han Chinese women. To investigate the association between rs13405728 (LHCGR gene), rs13429458 (THADA gene) and rs2479106 (DENND1A gene), PCOS, hirsutism and metabolic and hormonal parameters in a well characterized cohort of Caucasian patients of Danish descendant with PCOS or hirsutism. Patients underwent clinical examination, hormone analyses, oral glucose tolerance test and transvaginal ultrasound. Genetic variation was tested using allelic discrimination by real-time PCR. 268 patients referred to The Department of Endocrinology, Odense University Hospital, Denmark with PCOS or hirsutism between 1997 and 2011. Two hundred and forty-eight healthy females were included as controls. Genotype distributions and allele frequencies of rs13405728, rs13429458, and rs2479106 were comparable in patients and controls. The rs2479106 G allele was associated with a decreased PCOS susceptibility. None of the SNPs were associated with hirsutism or increased metabolic parameters. The rs2479106 G allele was associated with decreased PCOS susceptibility, thus confirming previously reported findings of association between rs2479106 and PCOS. Metabolic and hormonal parameters were comparable between genotypes of rs13405728 and rs2479106. Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.

Avaliação da qualidade das águas subterrâneas em áreas de preservação permanente (sistema aquífero guarani – sag, bacia hidrográfica do Rio Pardo, RS, Brasil

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Adilson Ben da Costa

2010-01-01

Full Text Available O objetivo principal deste estudo foi avaliar a qualidade das águas subterrâneas em áreas de preservação permanente (SistemaAqüífero Guarani – SAG da Bacia Hidrográfica do Rio Pardo, RS, Brasil, através de variáveis físicas, químicas emicrobiológicas, tendo como base a resolução nº 396 do Conselho Nacional do Meio Ambiente – CONAMA. Nove pontos decoleta foram distribuídos ao longo da bacia, nos quais as águas subterrâneas foram classificadas quanto aos íons de maiorocorrência quantitativa através do diagrama de Piper. Os resultados indicaram que a maioria dos poços avaliados enquadraram-sena Classe 4 de usos da água, correspondendo a águas de usos menos restritivos. Entretanto, deve-se considerar que os aquíferos seapresentam em diferentes contextos geológicos, e que possuem características físicas, químicas e biológicas intrínsecas, comvariações hidrogeoquímicas, sendo necessário que as suas classes de qualidade sejam pautadas nessas especificidades, como seobservou no diagrama de Piper, onde as amostras P1, P2, P3, P5 e P9 classificaram-se como bicarbonatadas cálcicas, as águas dospontos P4, P6, P7 como bicarbonatadas sódicas e P8 se classificou como sulfatada. Verificou-se que a qualidade das águas depoços com profundidade inferior a 6 m está mais vulnerável devido a alterações antrópicas em função da concentração de nitrato,coliformes totais e termotolerantes, enquanto que a qualidade das águas de poços mais profundos depende basicamente de suascaracterísticas hidrogeológicas e hidrogeoquímicas naturais, em função das variáveis sulfato e sódio. Contudo, tambémapresentaram contaminação por atividade antrópica, principalmente pela variável nitrato.Abstract The aim of this research was to evaluate thequality of groundwater in areas of permanent preservation(Guarani Aquifer System – GAS in the Rio PardoHydrographical Basin, RS, Brazil, using physical, chemicaland

Cloning of radiation-induced new gene RS1 expressed in mouse intestinal epithelium by enhanced RACE

International Nuclear Information System (INIS)

Wang Fengchao; Wang Junping; Su Yongping; Gao Jinsheng; Lou Shufen; Liu Xiaohong; Ren Jiong; Zhang Bo

2003-01-01

Objective: To obtain full-length cDNA of radiation-induced new gene RS1 expressed in mouse intestinal epithelium. Methods: The tissue expression profile of RS1 was analyzed by semi-quantitative RT-PCR to find the target tissue which highly expresses RS1. The total RNA extracted from the corresponding tissue was taken as the template for reverse-transcription. Enhanced RACE PCR was used to clone the full-length cDNA of RS1, including enrichment of the target gene through biotin-labeled probe for magnetic bead purification and nested PCR. Results: About a 2 kb long 3' end was successfully cloned and cloning of the 5' end proceeded well. Conclusion: The result is consistent with our experiment design. The set of combined techniques has been identified with the cloning of full-length cDNA from EST sequence especially when the optimal gene-specific primers are not available or the expression level of target gene is low

Brasil alfabetizado e misión robinson : um estudo comparativo acerca das políticas de alfabetização no Brasil e na Venezuela – 2003-2013

OpenAIRE

Jaira Coelho Moraes

2015-01-01

Esta pesquisa é um estudo comparado entre dois programas de alfabetização de jovens e adultos que tiveram início no ano de 2003: o PBA – Programa Brasil Alfabetizado, desenvolvido no Brasil, e a Misión Robinson, na Venezuela. A análise destas políticas nos dois países em relação ao momento particular do capitalismo é objetivo principal, e em específico, buscou-se conhecer como se formam os alfabetizadores. O tema aborda a questão do alfabetismo/analfabetismo como um dos problemas sociais que ...

Work in Progress: The Seven Rs of Team Building

Science.gov (United States)

Brunelli, Jean; Schneider, Elaine Fogel

2004-01-01

This article argues that supportive teams--including professionals, paraprofessionals, and parents--can teach staff members how to identify and implement best practices in early intervention settings. The authors describe "the seven Rs of team building" distilled from their many years of team building and maintenance: 1) Reading cues; 2) Regular…

Esporte e TV pública no Brasil: a TV Brasil, a audiência e as transmissões do campeonato brasileiro de futebol da série C

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Priscila Eugênia Trevisan Cestari

2017-12-01

Full Text Available A TV Brasil é uma emissora pública que pertence à Empresa Brasil de Comunicação (EBC. Foi criada para implantar o Sistema Público de Comunicação no país. Desde 2013 a emissora transmite partidas do Campeonato Brasileiro de Futebol da Série C. O objetivo deste artigo é discutir, à luz de conceitos como audiência, cultura de mídia e valor-notícia, se a emissora cumpre, através do esporte, o papel para o qual foi criada. Para isso, realizamos uma pesquisa qualitativa, exploratória e descritiva, com a análise de documentos internos da emissora e a realização de entrevistas. O estudo pretende contribuir com reflexões a respeito dos processos existentes entre a gestão do esporte e a comunicação pública no Brasil. Assim, procuramos verificar se a emissora cumpre sua missão de formação e fortalecimento da cidadania e da identidade nacional ou se é apenas regida, em seu relacionamento com o esporte, pela ótica comercial da audiência.

[Association of IL-1β-511T gene rs16944 polymorphism with febrile seizures].

Science.gov (United States)

Ren, Xiao-Tun; Sun, Su-Zhen; Liu, Fang; Wang, Xiao-Ming

2014-02-01

Despite substantial research efforts worldwide, the role of inflammatory cytokine IL-1β in the onset of febrile seizures (FS) remains controversial. The aim of this study was to assess the relationship between rs16944 polymorphism of the IL-1β-511T gene and occurrence of simple FS in a sample of Han children in northern China. The IL-1β-511T gene rs16944 was genotyped by SNaPshot SNP technique in 141 FS children and 130 healthy control subjects. The genotypic and allelic frequencies in the two groups were comparatively analyzed. There were no significant differences in genotypic and allelic frequencies of rs16944 polymorphism of the IL-1β-511T gene between FS patients and control subjects (P>0.05).When the clinical data on A/A, A/G and G/G genotypes of the rs16944 polymorphism in FS patients, there was statistically significant difference in age of first onset (χ(2)=19.491, Prs16944 polymorphism of the IL-1β-511T gene and the incidence of FS in Han children in Northern China. However, the differences in genotypes of this polymorphism might be associated with pathogenesis and prognosis of simple FS in the population studied.

A politica nuclear da Argentina e do Brasil : Desenvolvimento, nao-proliferacao e democratizacao

OpenAIRE

澤田, 眞治

1994-01-01

Este artigo e uma tentativa de analisar o desenvolvimento da politica da energia nuclear da Argentina e do Brasil, com relacao ao regime internacional de naoproliferacao das armas nucleares. Dado o fato de que ambos os paises da America do Sul recusaram a assinatura do TNP(Tratad0 sobre Nao-Proliferacao das Armas Nucleares), em razao do carater discriminatorio de inspecao, a Argentina e o Brasil estavam sendo considerado os estados duvidossos que potencialmente teriam a bomba atomica. A despe...

Association of a single-nucleotide polymorphism (rs6180) in GHR ...

Indian Academy of Sciences (India)

in the GHR gene and investigated an effect of SNP rs6180 on human organ weight ... and approved by the Human Ethics Committee of Shimane. University School of ..... This work was supported by JSPS KAKENHI grant number. 26713025 ...

POLÍTICAS Y SUJETOS DEL SIDA en Brasil y Colombia

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César Ernesto Abadía-Barrero

2004-01-01

Full Text Available BASADO EN DATOS HISTÓRICOS Y DE INVESTIGACIONES ETNOGRÁFICAS, Y EN UNA SERIE de entrevistas a profundidad, este artículo analiza las respuestas exitosas de Brasil y muy deficientes de Colombia frente a la epidemia del sida, y propone vínculos entre estas respuestas, los sujetos que las han liderado y las reformas en salud en marcha en los dos países. Los datos sugieren que existe retroalimentación entre las políticas en salud, las respuestas frente al sida y lo que piensan los actores involucrados en los procesos, y que ésta se relaciona con el momento histórico de ideologías de izquierda en Brasil y de derecha en Colombia.

Políticas migratórias no Brasil, abrindo espaço para a polifonia

OpenAIRE

Santos, Sandro M. Almeida

2015-01-01

O seguinte texto trata sobre as políticas migratórias no Brasil. Abordando sobre a discussão dos desafios impostos pelo crescimento da imigração no país que ocorreu no seminário “Migração Laboral no Brasil: desafios para construção de políticas”.

Brasil Mulher e Nós Mulheres: origens da imprensa feminista brasileira Brasil Mulher e Nós Mulheres: origins of the feminist press in Brazil

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Rosalina de Santa Cruz Leite

2003-06-01

Full Text Available Este artigo apresenta algumas reflexões sobre a imprensa feminista alternativa que surgiu no Estado de São Paulo, Brasil, na segunda metade dos anos 1970. Essa imprensa se tornou um espaço de expressão de uma linha política intimamente vinculada ao despertar das mulheres para as idéias feministas do período posterior à luta armada contra a ditadura no Brasil. Os jornais Brasil Mulher e Nós Mulheres retrataram, em seus artigos e editoriais, a luta pela anistia, pelas creches e pelas liberdades democráticas - todos símbolos da oposição contra o regime no período da ditadura militar. Além disso, eles incluíam matérias específicas, tais como violência doméstica, condições de trabalho das mulheres, direitos reprodutivos, aborto e sexualidade. Do ponto de vista do movimento popular e das organizações de mulheres, essa imprensa constitui, sem sombra de dúvida, uma fonte importante e ainda inexplorada para compreender o período considerado.This article presents some reflections about the feminist alternative press that appeared in the state of São Paulo, Brazil, in the second half of the 70's. The press was a space for expression of a special breed of politics that was closely linked to the awakening of women to feminist ideas in the period after the armed struggle against the Brazilian dictatorship. The journals Brasil Mulher and Nós Mulheres portray, in their articles and editorials, the fight for amnesty, for day nurseries, for democratic freedoms - all symbols of opposition against the regime in the era of military dictatorship. In addition they report on specific matters, such as, domestic violence, women's working-conditions, reproductive rights, abortion and sexuality. From the point of view of the popular movement and the women's organizations, the alternative press of women is without any doubt an important source, and still under-explored, for understanding the period considered.

Hematopoietically expressed homeobox (HHEX) gene polymorphism (rs5015480) is associated with increased risk of gestational diabetes mellitus.

Science.gov (United States)

Tarnowski, M; Malinowski, D; Safranow, K; Dziedziejko, V; Czerewaty, M; Pawlik, A

2017-06-01

Gestational diabetes mellitus (GDM) is a metabolic disorder that occurs during pregnancy. HHEX and PROX1 are genetic loci associated with diabetes mellitus type 2. HHEX and PROX1 play significant roles in carbohydrate intolerance and diabetes because these transcription factors may be involved in the regulation of insulin secretion and in glucose and lipid metabolism. The aim of this study was to examine the association between HHEX (rs5015480) and PROX1 (rs340874) gene polymorphisms and GDM. This study included 204 pregnant women with GDM and 207 pregnant women with the normal glucose tolerance (NGT). The diagnosis of GDM was based on a 75-g oral glucose tolerance test at 24-28 weeks' gestation. There was a statistically significant prevalence of the HHEX rs5015480 CC genotype and C allele among women with GDM (C vs T allele, p = 0.021, odds ratio OR = 1.40, 95% CI: 1.05-1.87). Statistically significant higher increase of body mass and BMI during pregnancy was found in women with the HHEX rs5015480 CC genotype. The results of our study suggest an association between the HHEX gene rs5015480 polymorphism and risk of GDM. The HHEX gene rs5015480 C allele may be a risk allele of GDM that is associated with increased BMI during pregnancy. © 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

El uso de placebo en ensayos clínicos de fase III en Brasil

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Gustavo Butzge Rubenich

2015-01-01

Full Text Available El Consejo Federal de Medicina de Brasil (CFM –órgano normativo y fiscalizador del ejercicio ético de la medicina– prohibió, en 2008, la participación de médicos brasileños en investigaciones que utilizaran placebo para enfermedades con tratamiento eficaz y efectivo, en contraposición a la Declaración de Helsinki, que permite su uso en condiciones metodológicamente justificadas. Con el objetivo de verificar si la normativa ética del CFM modificó el uso de placebo en ensayos clínicos de fase III en Brasil, se analizaron varias características de sus registros en el ClinicalTrials.gov, en los períodos de 2003 a 2007 y de 2009 a 2013. Se concluye que: a la normativa promulgada por el CFM en 2008 fue ineficaz y prevaleció la posición adoptada por la Declaración de Helsinki; b el patrocinio de ensayos con placebo por parte de la industria farmacéutica multinacional fue significativo; c predominaron las investigaciones de fármacos para enfermedades crónicas, y fueron poco significativas para las enfermedades postergadas, de importancia para Brasil.

El Mercosur como una prioridad de la política exterior brasileña

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Miriam GOMES SARAIVA

2009-11-01

Full Text Available RESUMEN: En este artículo se presentan los antecedentes, constitución y primeros momentos del proceso de integración emprendido por Brasil, Argentina, Paraguay y Uruguay. Desde una perspectiva brasileña, la autora señala de qué manera una historia caracterizada por las tensiones diplomáticas fue convirtiéndose en un presente definido por metas comunes. También analiza los factores externos e internos que impulsaron a Brasil a la estrategia de la integración. Finalmente resume algunos de los avances económicos e institucionales conseguidos a lo largo del proceso y que definen el modelo de inserción de la economía brasileña en la mundial.ABSTRACT: In this article there are displayed the antecedents, constitution and first moments of the process of integration undetaken by Brazil, Argentina, Paraguay and Uruguay. From a brazilean perspective, the author specifies the way in which a history of diplomacy tensions ends with common goals. There are also described the external and internal factors which impulsed Brazil into the strategy of integration. Finally, the author resumes some of the economic and institutional advances got during the process which define the model of insertion of brazilean economy in the world market.

Association of STAT4 rs7574865 polymorphism with autoimmune diseases: a meta-analysis.

Science.gov (United States)

Liang, Ya-Ling; Wu, Hua; Shen, Xi; Li, Pei-Qiang; Yang, Xiao-Qing; Liang, Li; Tian, Wei-Hua; Zhang, Li-Feng; Xie, Xiao-Dong

2012-09-01

The association between the signal transducer and activator of transcription 4 (STAT4) gene rs7574865 single nucleotide polymorphism and different autoimmune diseases remains controversial and ambiguous. We conducted this study to investigate whether combined evidence shows the association between STAT4 rs7574865 polymorphism and autoimmune diseases. Comprehensive Medline search and review of the references were used to get the relevant reports published before September 2011. Meta-analysis was conducted for genotype T/T (recessive effect), T/T + G/T (dominant effect) and T allele in random effects models. 40 studies with 90 comparisons including 32 systemic lupus erythematosus (SLE), 19 rheumatoid arthritis (RA), 3 type 1 diabetes (T1D), 11 Systemeric Sclerosis (SSc), 4 inflammatory bowed diseases (IBD), 3 Primary Sjogren's syndrome (pSS), 4 juvenile idiopathic arthritis (JIA), 2 Primary antiphospholipid syndrome (APS), 1 Autoimmune thyroid diseases, 1 multiple sclerosis, 1 Psoriasis, 1 Wegener's granulomatosis, 1 Type 2 diabetes, and 1 giant cell arteritis disease were available for this meta-analysis. The overall odds ratios for rs7574865 T-allele significantly increased in SLE, RA, T1D, SSc, JIA, and APS (OR = 1.56, 1.25, 1.13, 1.34, 1.25, and 2.15, respectively, P rs7574865 T allele confers susceptibility to SLE, RA, T1D, SSc, JIA, APS, IBD-UC, and pSS patients, supporting the hypothesis of association between STAT4 gene polymorphism and subgroup of autoimmune diseases.

MeQTL analysis of childhood obesity links epigenetics with a risk SNP rs17782313 near MC4R from meta-analysis.

Science.gov (United States)

Tang, Yuping; Jin, Bo; Zhou, Lingling; Lu, Weifeng

2017-01-10

Earlier GWAS has identified that rs17782313 near MC4R was associated with obesity. However, subsequent studies showed conflicting results, especially among childhood. Besides, the mechanisms underlying the association between rs17782313 and childhood obesity remain largely unexplored, and genetic and epigenetic may interact and together affect the development of childhood obesity. We conducted a comprehensive meta-analysis to assess the association between rs17782313 and childhood obesity. MeQTL and eQTL analysis was applied to explore the effect of rs17782313 on DNA methylation and MC4R expression. We found that rs17782313 near MC4R was associated with increased childhood obesity risk and BMI z-score in several inheritable models (P obesity. Furthermore, rs17782313 T allele was correlated with promoter hypermethylation and decreased expression of MC4R, thus involved in the development of childhood obesity.

Percepción del estrés competitivo y cultura en futbolistas profesionales de Brasil y Portugal

Directory of Open Access Journals (Sweden)

M. Regina F. Brand\\u00E3o

2006-01-01

Full Text Available El objetivo del presente estudio fue comparar jugadores de fútbol con diferentes perspectivas culturales y similar nivel de experiencia, en la percepción del estrés. Fueron evaluados 18 jugadores Brasileños de la Selección Nacional Brasileña, y 20 jugadores Portugueses de la Selección Nacional Portuguesa, con una media de edad de 26,69 + 4,1 y 26,05 + 2,3 años respectivamente, mediante el Inventario de Estrés en Fútbol. Aparece una tendencia resulta muy marcada, los ítems que son evaluados como positivos por los dos grupos, los Brasileños tienden a evaluarlos significativamente más positivos que los Portugueses y en los evaluados como negativos por las dos nacionalidades, los Brasileños tienden a evaluarlos como más negativos. Quizás más interesante aún resulta la gran cantidad de ítems que son evaluados como influyentes en tendencias totalmente inversas, lo que los Brasileños consideran negativo es considerado por los Portugueses como positivo o neutro. Muy probablemente la variable cultural puede explicar la variabilidad de percepción del estrés.

Pensamento social, ciência e imagens do Brasil: tradições revisitadas pelos educadores brasileiros

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Marcos Freitas Cezar de

2000-01-01

Full Text Available Este artigo analisa dois momentos decisivos no âmbito da história das idéias no Brasil. Imagens e sínteses do Brasil tornaram-se referências fundamentais na história da cultura brasileira, especialmente aquelas produzidas por uma “tradição realista”, que vem desde o século XIX, por intermédio dos escritos do Visconde do Uruguai, e prossegue com Silvio Romero, com Alberto Torres, com Oliveira Vianna e com Alberto Guerreiro Ramos. Tais autores deram vida à imagem do Brasil cindido em dois brasis: o país legal e o país real. A partir de 1902, o marco fundamental dessa tradição passará a ser Euclides da Cunha, autor que projetou o sertão como “metáfora para a nação”. Nos anos cinqüentas, ao redor de Anísio Teixeira, intelectuais como Antonio Candido, Florestan Fernandes, Luiz Pereira, Fernando de Azevedo e muitos antropólogos mergulharam novamente nas metáforas euclidianas e compuseram novas imagens sobre a cultura regional no Brasil que se modernizava

Lidt om DØRS' selvforståelse: om lønrelationerne i SMEC

DEFF Research Database (Denmark)

Harck, Søren H.

1997-01-01

at all: if the wage-to-price elasticity is taken to be equal to one (as stipulated by DØRS), the model turns out to imply, even in the long run, an old-fashioned, stable Phillips curve; and if, more realistically, this elasticity is taken to be smaller than one, the error-correction specification by DØRS...... does in fact entail a horizontal Phillips curve, the level of which is determined by the exchange rate adjusted foreign inflation rate. Evidently, the policy implications of getting the interpretation right are, potentially, huge....

AS FRONTEIRAS DO NORTE DO BRASIL E O ACESSO AOS DIREITOS SOCIAIS

OpenAIRE

Silva, João Carlos Jarochinski; Universidade Federal de Roraima; Jubilut, Liliana Lyra; Universidade Católica de Santos

2015-01-01

Fruto das percepções e análises obtidas durante a pesquisa de campo para o projeto “Pensando o Direito: Desafios à efetividade dos direitos fundamentais” – “Mapeamento institucional, normativo e estrutural e análise dos obstáculos para efetivação do atendimento e acesso dos migrantes, apátridas e refugiados aos serviços públicos no Brasil: subsídios para o aperfeiçoamento de políticas públicas” em algumas áreas de fronteira da Região Norte do Brasil, o texto procura refletir sobre a realidade...

Fútbol y violencia en Brasil. Propuesta comunicativa para el estado de Pernambuco

OpenAIRE

Pereira de Lima, José Leandro

2017-01-01

El presente trabajo tenía como principal objetivo de la investigación, profundizar en la representación mediática de la violencia en el fútbol brasileño, a través de un análisis del contenido de las noticias publicadas en medios digitales de Brasil, entre 2015 y 2016, teniendo así un marco conceptual del análisis del problema y una estrategia de comunicación frente a ello. Este trabajo se completa con la propuesta comunicativa, donde se creó una campaña de publicidad con fines sociales,...

Lack of association between PKLR rs3020781 and NOS1AP rs7538490 and type 2 diabetes, overweight, obesity and related metabolic phenotypes in a Danish large-scale study: case-control studies and analyses of quantitative traits

DEFF Research Database (Denmark)

Andreasen, Camilla Helene; Mogensen, Mette S.; Borch-Johnsen, Knut

2008-01-01

of the variants in relation to overweight and obesity. METHODS: PKLR rs3020781 and NOS1AP rs7538490 were genotyped, using TaqMan allelic discrimination, in a combined study sample comprising a total of 16,801 and 16,913 individuals, respectively. The participants were ascertained from four different study groups...

Data integration from gamma radiation decay from uranium: a case-study in the region of Santa Maria, Rio Grande do Sul-Brazil;Integracao de dados de decaimento radiometrico de uranio: estudo de caso na regiao de Santa Maria (RS)

Energy Technology Data Exchange (ETDEWEB)

Pereira, Joao Eduardo; Silva, Jose Luiz Silverio da; Pires, Carlos Alberto, E-mail: jesp61@gmail.co, E-mail: silverio@smail.ufsm.b, E-mail: calpires@base.ufsm.b [Universidade Federal de Santa Maria (CCNE/UFSM), RS (Brazil). Centro de Ciencias Naturais e Exatas. Dept. de Geociencias; Strieder, Adelir Jose, E-mail: adelir@ufrgs.b [Universidade Federal do Rio Grande do Sul (DEM/UFRGS), Porto Alegre, RS (Brazil). Dept. de Engenharia de Minas

2008-09-15

This work consists of data integration of uranium concentrations, parts per million (ppm), associated to the different rock formations belonging to Parana Basin in the region of Santa Maria, in the Rio Grande do Sul state southern Brazil. This study was developed from primary data generated by the Companhia de Pesquisas de Recursos Minerais as part of the AERO/Camaqua; Project, 1010 code series, digitalized in the 1997 Geosoft XYZ format. Through an irregular net of values of uranium concentration, with 25806 observations were spatially oriented by Universal Transverse Mercator/ UTM coordinates. Which were varied from west to east 206190 to 276813 E, and from north to south 6670888 to 6735665 N, totalizing an area of 4574.75 km{sup 2}. Using Statistica 7.1 software licensed to the Department of Statistics at the Federal University of Santa Maria, the mean values of and the confidence limits with alpha = 0.05, the standard deviations of uranium concentrations for each rock formation. The comparisons between the mean values were made through the Tuckey's Test and the spatial variation of the concentrations in relation to the geographical coordinates were adjusted to a polynomial model. The results obtained showed that the uranium concentrations occur in a distinct way in the different geological formations studied (aluvionar unconsolidated sediments, sandstones and igneous volcanic acid and basic rocks). The uranium variable, when spatialized in relation to the geographical coordinates UTM were adjusted to a second order polynomial model. (author)

Principais Acervos de Paleontologia do Brasil

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Eloisa Magalhães Pássaro

2014-07-01

Full Text Available O presente trabalho apresenta uma súmula dos principais acervos paleontológicos no Brasil, sem considerar instituições que por ora se encontram fechadas para reforma, com coleções predominantemente didáticas ou acadêmicas e acervos com menos de uma centena de exemplares catalogados. Das trinta instituições listadas, doze deles estão situadas no sudeste (Rio de Janeiro, Belo Horizonte, Peirópolis, Ouro Preto, São Paulo, Rio Claro, Taubaté e Monte Alto, dez no nordeste (Ceará, Rio Grande do Norte, Pernambuco, Sergipe e Bahia, cinco na região sul (Mafra, Porto Alegre, São Leopoldo e Santa Maria, duas na região norte (Acre e Pará e uma na região centro-oeste. Os maiores acervos de fósseis no Brasil se encontram no Museu de Ciências da Terra do DNPM e no Museu Nacional, ambos no Rio de Janeiro, que reúnem cerca de 260.000 exemplares, ainda que em Aracaju, Sergipe, esteja a terceira maior coleção paleontológica brasileira, com aproximadamente 38.000 fósseis pertencentes à Fundação Paleontológica Phoenix. A maioria dos acervos temáticos está relacionada a fósseis cretáceos, o que é concordante com a abundância de fósseis brasileiros desta idade: no nordeste, os acervos se destacam pelo grande número de invertebrados e peixes, e em Minas Gerais e São Paulo, pelos seus répteis. Outros acervos temáticos encontram-se no Rio Grande do Sul (répteis triássicos, São Paulo (icnofósseis mesozóicos, Santa Catarina (invertebrados paleozoicos, Ceará e Pernambuco (icnofósseis siluro-devonianos e Ceará, Bahia, Minas Gerais e Acre (megafauna cenozoica. Os museus mais antigos do Brasil com acervos paleontológicos são o Museu Nacional, criado em 1818 no Rio de Janeiro, o Museu Paraense Emílio Goeldi, aberto em 1866 em Belém, e o Museu de Ciência e Técnica da Escola de Minas de Ouro Preto, criado em 1884, todos centenários.

CAT bags orders worth Rs 90 Crore from EU

CERN Multimedia

2002-01-01

"Orders to the tune of Rs 90 crore have been received by Indore-based Centre for Advanced Technology (CAT) from laboratories in the European Union (EU) and more orders are likely to follow in the near future, according to Pune-based Patel Analog and Digital Measurement Company (PADMCO) director Madhu Patel" (1/2 page).

A Constitucionalidade do Projeto Mais Médicos para o Brasil

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Janaina Pontes Cerqueira

2016-05-01

Full Text Available A escassez de profissionais médicos em determinadas áreas no Brasil é tema que sempre mereceu atenção especial do Estado. O Projeto Mais Médicos para o Brasil, implementado por meio da Medida Provisória nº 621, de 8 de julho de 2013, autoriza a atuação de médicos estrangeiros sob regime especial de aperfeiçoamento profissional no Sistema Único de Saúde (SUS, na Atenção Básica, possibilitando a cobertura médica assistencial em  regiões prioritárias e vulneráveis do país, e foi fruto de questionamento judicial junto ao Supremo Tribunal Federal, por meio de ação direta de inconstitucionalidade, que colocou em confronto os limites constitucionais de autorização para essa forma de atuação profissional. O estudo objetivou identificar os argumentos jurídicos utilizados pelos diversos atores que atuaram nas ADINs 5035-DF e 5037-DF, notadamente no que se refere ao Projeto Mais Médicos para o Brasil, ajuizadas no Supremo Tribunal Federal e analisá-los à luz da Teoria dos Direitos Fundamentais de Robert Alexy. Os resultados apontam que o Projeto, na sua estruturação legal, encontra legitimidade na medida em que não se confunde com a abertura de mercado de trabalho, institui regime específico de atuação profissional, com garantias essenciais dos indivíduos, atenta para diretrizes de cooperação internacional em saúde da Organização Mundial de Saúde (OMS e demonstra eficácia social com a concreta ampliação de acesso da população na cobertura assistencial até que medidas conjunturais e estruturantes da formação médica no Brasil sejam implementadas e alcancem resultados diretos à população usuária do SUS.

[RS-1 enhanced the efficiency of CRISPR-Cas9 mediated knock-in of human lactoferrin].

Science.gov (United States)

Zhou, Wenjun; Guo, Rihong; Deng, Mingtian; Wang, Feng; Zhang, Yanli

2017-08-25

This study aims to knock out the goat β-lactoglobulin (BLG) gene using CRISPR-Cas9 system and knock in human lactoferrin (hLF) at the BLG locus, and further study the effect of RAD51 stimulatory compound (RS-1) on homologous recombination efficiency. First, we designed an sgRNA targeting the first exon of goat BLG gene and constructed a co-expression vector pCas9-sgBLG. This sgRNA vector was then transfected into goat ear fibroblasts (GEFs), and the target region was examined by T7EN1 assay and sequencing. Second, we constructed a targeting vector pBHA-hLF-NIE including NEO and EGFP genes based on BLG gene locus. This targeting vector together with pCas9-sgBLG expression vector was co-transfected into GEFs. Transfected cells were then treated with 0, 5, 10 and 20 μmol/L RS-1 for 72 h to analyse the EGFP expression efficiency. Next, we used 800 μg/mL G418 to screen G418-resistent cell clones, and studied hLF site-specific knock-in cell clones by PCR and sequencing. The editing efficiency of sgBLG was between 25% and 31%. The EGFP expression efficiency indicated that the gene knock-in efficiency was improved by RS-1 in a dose-dependent manner, which could reach 3.5-fold compared to the control group. The percentage of positive cells with hLF knock-in was increased to 32.61% when 10 μmol/L RS-1 was used. However, when the concentration of RS-1 increased to 20 μmol/L, the percentage of positive cells decreased to 22.22% and resulted in an increase of senescent cell clone number. These results suggested that hLF knock-in and BLG knock-out in GEFs were achieved by using CRISPR/Cas9 system, and optimum concentration of RS-1 could improve knock-in efficiency, which provides a reference for efficiently obtaining gene knock-in cells using CRISPR/Cas9 in the future.

Cuotas raciales, identidad negra y derechos en el Brasil

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Gislene Aparecida

2008-09-01

Full Text Available La implementación de políticas públicas basadas en criterios raciales para el acceso de estudiantes negros a las universidades en el Brasil divide a intelectuales respecto a la viabilidad de esta forma de acción afirmativa. Sin embargo, esta discusión ha considerado muy poco las perspectivas de los propios estudiantes. En este artículo se presentan datos sobre cómo los jóvenes, futuros beneficiarios del actual proyecto de ley, re p resentan la política de cuotas y muestra cómo este tema revela la complejidad de la sociedad brasileña. Se sugiere por lo tanto, que esta cuestión sea abordada desde una perspectiva múltiple que nos permita reflexionar sobre los pro blemas que las sociedades multiculturales presentan a las teorías clásicas del derecho y la justicia.

In Silico Identification of OncomiRs in Different Cancer Types

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Bhattacharyya, Malay; Bandyopadhyay, Sanghamitra

2012-03-01

The diagnosis, prognosis and therapeutics of various kinds of cancers are challenging domains of research. Current landmark of cancer research at the molecular level mainly focuses on the regulation of genes for studying cancer pathways. Recent investigations highlight that there is a significant association of a class of short RNAs in the progression of different types of cancer. In this paper, the involvement of microRNAs (miRNAs), a type of small endogenous RNAs, is explored in two categories of cancers in human, one tumor-based and another non-tumorous. A new approach of in silico identification of the miRNAs that might be associated with these cancer types is proposed. The oncomiRs, miRNAs associated with cancer, are identified by analyzing the differentially co-expressed miRNAs and further exploring how they cooperate with each other. Extensive computational analysis on miRNA expression profiles for the discovery of novel oncomiRs is pursued. The results are found to be promising by going deep into the regulatory information available on oncogenes from the up-to-date literature. Some of the miRNAs as oncogenic are identified by the approach like hsa-miR-186 and hsa-miR-154 for leukemia and prostate cancer, respectively, which are not included in standard databases. However, some of the emerging studies give evidences to these findings. Statistical and biological studies, on the other hand, strengthen the effectiveness of the proposed method in futuristic investigations for the exploration of undiscovered oncomiRs. On the whole, these analyses provide insight into the discovery of miRNA markers.

A RESPONSABILIDADE DO BRASIL PELOS CRIMES CONTRA HUMANIDADE: ANÁLISE DO JULGAMENTO «GOMES LUND E OUTROS»

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José Carlos Macedo de Pinto Ferreira Júnior

2013-01-01

Full Text Available Esta investigación tiene como objetivo analizar el juicio del caso conocido como “Guerrilla de Araguaia” y la responsabilidad internacional del Estado brasileño. Brasil había sido declarado culpable de graves violaciones de los derechos humanos, al exigir el cumplimiento de la sen- tencia la Corte Interamericana de Derechos Humanos (CIDH y el castigo de los culpables. El caso se vuelve relevante en el escenario legal en el mundo, debido que la principal institu- ción de la justicia brasileña, la Corte Suprema de Justicia, celebró una ley constitucional que indultó a todos los acusados de asesinatos de esa guerrilla. Surge, por lo tanto, un conflicto ​​ entre el Tribunal Internacional y la jurisdicción brasileña. Para el desarrollo de este trabajo, la investigación se realizó sobre la base de la jurisprudencia brasileña, la legislación nacional e internacional y las decisiones de la Corte Suprema de Justicia y el Tribunal de Derechos Humanos. El método aplicado fue deductivo y se llegó a la conclusión de que en el citado caso hasta ahora nadie ha sido castigado por los crímenes crueles contra la dignidad humana. Brasil es signatario de varios tratados y transnacionales que buscan una protección eficaz de los derechos humanos. La auto-amnistía a los torturadores y asesinos traerá un enorme des- crédito y, probablemente, nuevos cargos en el ámbito internacional. Palabras clave Derechos Humanos, Jurisdicción Nacional, Tortura, Juzgamiento, Condena, Responsabilidad del Estado brasilero, Guerrilla de Araguaia.

Interleukin 1 gene cluster SNPs (rs1800587, rs1143634) influences post-orthodontic root resorption in endodontic and their contralateral vital control teeth differently.

Science.gov (United States)

Iglesias-Linares, A; Yañez-Vico, R M; Ballesta, S; Ortiz-Ariza, E; Mendoza-Mendoza, A; Perea, E; Solano-Reina, E

2012-11-01

To investigate whether the genetic variants of the interleukin-1 gene cluster (IL1) are associated with a possible genetically induced variability in post-orthodontic external apical root resorption (EARR) in root filled teeth and their control counterparts with vital pulps. One hundred and forty-six maxillary premolars were evaluated radiographically following orthodontic treatment. Genetic screening was performed on orthodontic patients for two single-nucleotide polymorphisms (SNPs: rs1800587 and rs1143634) in the IL1 gene cluster. Subjects were divided into two groups according to the presence or absence of radiographic post-orthodontic EARR (>2 mm) in root filled teeth and their controls with vital pulps. Logistic regression analysis was performed to obtain an adjusted estimation between EARR and IL1 polymorphisms. Allelic frequencies, genotype distributions, and adjusted odds ratio (OR), at 95% confidence interval, were also calculated. Whilst no clear statistical association was found for gene variations in IL1A, a sound association was found in the comparative analysis of subjects homozygous [2/2(TT)] for the IL1B gene, which resulted in a two times increased risk of suffering post-orthodontic EARR in root filled teeth [OR, 2.032 (P = 0.031); CI,1.99-14.77] when compared with their controls with vital pulps. There was, however, a shared predisposition to EARR in controls with vital pulps and root filled teeth of subjects homozygous for allele 1 [OR, 5.05 (P = 0.002)] and [OR, 2.77 (P = 0.037)], respectively. Genetic variations in the interleukin-1β gene (rs1143634) predispose root filled teeth to EARR for matched pairs secondary to orthodontic treatment in a different way from their control teeth with vital pulps in subjects homozygous for allele 2 [2/2(TT)]. © 2012 International Endodontic Journal.

The haptoglobin promoter polymorphism rs5471 is the most definitive genetic determinant of serum haptoglobin level in a Ghanaian population.

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Soejima, Mikiko; Teye, Kwesi; Koda, Yoshiro

2018-08-01

The serum haptoglobin (HP) level varies in various clinical conditions and among individuals. Recently, the common HP alleles, rs5472, and rs2000999 have been reported to associate with serum HP level, but no studies have been done on Africans. Here, we explored the relationship of not only these polymorphisms but also rs5470 and rs5471 to the serum HP level in 121 Ghanaians. Genotyping of rs2000999 was performed by PCR using hydrolysis probes, while the other polymorphisms have been already genotyped. Serum HP level was measured by a sandwich ELISA. We observed a significant association between rs5471 and the serum HP level (p = 0.026). It was also observed within the subgroups of HP 2 /HP 2 and HP 2 /HP 1 . In addition, we detected a trend toward lower HP levels for individuals with the A allele of rs2000999 than those without A, but it was not statistically significant (p = 0.156). However, we did not observe the clear associations between other polymorphisms and serum HP level that were observed for Europeans and Asians because of the small sample size and the complexity of SNPs affecting the HP level. We suggest that rs5471 is a strong genetic determinant of HP levels in Ghanaians, and this seems to be characteristic of Africans. Further investigation using large scale samples will help in understanding the genetic background of individual variability of the serum HP level. Copyright © 2018 Elsevier B.V. All rights reserved.

Face and emotion expression processing and the serotonin transporter polymorphism 5-HTTLPR/rs22531.

Science.gov (United States)

Hildebrandt, A; Kiy, A; Reuter, M; Sommer, W; Wilhelm, O

2016-06-01

Face cognition, including face identity and facial expression processing, is a crucial component of socio-emotional abilities, characterizing humans as highest developed social beings. However, for these trait domains molecular genetic studies investigating gene-behavior associations based on well-founded phenotype definitions are still rare. We examined the relationship between 5-HTTLPR/rs25531 polymorphisms - related to serotonin-reuptake - and the ability to perceive and recognize faces and emotional expressions in human faces. For this aim we conducted structural equation modeling on data from 230 young adults, obtained by using a comprehensive, multivariate task battery with maximal effort tasks. By additionally modeling fluid intelligence and immediate and delayed memory factors, we aimed to address the discriminant relationships of the 5-HTTLPR/rs25531 polymorphisms with socio-emotional abilities. We found a robust association between the 5-HTTLPR/rs25531 polymorphism and facial emotion perception. Carriers of two long (L) alleles outperformed carriers of one or two S alleles. Weaker associations were present for face identity perception and memory for emotional facial expressions. There was no association between the 5-HTTLPR/rs25531 polymorphism and non-social abilities, demonstrating discriminant validity of the relationships. We discuss the implications and possible neural mechanisms underlying these novel findings. © 2016 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society.

Association of Lin-28A rs3811464 Variant with Susceptibility to Type 2 Diabetes

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Mona Khodabandeh

2017-11-01

Full Text Available Introduction: It has been suggested that Lin-28A and the let-7 microRNA family (Lin-28/let-7 axis play a critical role in the control of glucose metabolism, insulin sensitivity and resistance to diabetes. Aim: This case-control study aimed at evaluating the association between Lin-28 rs3811464 polymorphism and the susceptibility to Type 2 Diabetes (T2D in a sample of Iranian population. Materials and Methods: This study involved 172 T2D patients and 160 non-diabetic age and gender-matched controls. Lin 28A rs3811464 genotypes were determined by Polymerase Chain Reaction–Restriction Fragment Length Polymorphism (PCR-RFLP technique. Results: The results showed that the frequency of the AA genotype was significantly higher in control subjects than in diabetic patients (13.12% vs. 4.65%. In addition, binary logistic regression analysis revealed that rs3811464-AA genotype was significantly associated to T2D after adjustment for BMI, age and lipid profiles. Indeed, subjects with AA genotype were less likely to develop T2D than GG and AG subjects (OR of 0.26, 95% CI 0.10-0.66, p=0.005. Conclusion: The findings of our study suggest that the Lin 28A rs3811464 is associated with type 2 diabetes susceptibility and subjects with AA genotypes were less likely to develop T2D diabetes.

Predicting Hemorrhagic Transformation of Acute Ischemic Stroke: Prospective Validation of the HeRS Score.

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Marsh, Elisabeth B; Llinas, Rafael H; Schneider, Andrea L C; Hillis, Argye E; Lawrence, Erin; Dziedzic, Peter; Gottesman, Rebecca F

2016-01-01

Hemorrhagic transformation (HT) increases the morbidity and mortality of ischemic stroke. Anticoagulation is often indicated in patients with atrial fibrillation, low ejection fraction, or mechanical valves who are hospitalized with acute stroke, but increases the risk of HT. Risk quantification would be useful. Prior studies have investigated risk of systemic hemorrhage in anticoagulated patients, but none looked specifically at HT. In our previously published work, age, infarct volume, and estimated glomerular filtration rate (eGFR) significantly predicted HT. We created the hemorrhage risk stratification (HeRS) score based on regression coefficients in multivariable modeling and now determine its validity in a prospectively followed inpatient cohort.A total of 241 consecutive patients presenting to 2 academic stroke centers with acute ischemic stroke and an indication for anticoagulation over a 2.75-year period were included. Neuroimaging was evaluated for infarct volume and HT. Hemorrhages were classified as symptomatic versus asymptomatic, and by severity. HeRS scores were calculated for each patient and compared to actual hemorrhage status using receiver operating curve analysis.Area under the curve (AUC) comparing predicted odds of hemorrhage (HeRS score) to actual hemorrhage status was 0.701. Serum glucose (P hemorrhages were more likely to be symptomatic and more severe.The HeRS score is a valid predictor of HT in patients with ischemic stroke and indication for anticoagulation.

Ledelse på tværs i de danske sygehuse

DEFF Research Database (Denmark)

Plesner, Jeppe; Christensen, Anne Birgitte; Bech, Mickael

2012-01-01

behovet for bedre koordinering og samarbejde på tværs af organisatoriske grænser. I kontrast hertil var ledelsestænkningen baseret på hierarkiske, positionsorienterede ledelsesdiskurser, der ikke matcher de organisatoriske behov. Sygehuse er komplekse organisationer, men en rationalistisk styrings- og...

“Nervo deste Reyno” La red europea de agentes de la Companhia Geral de Comércio do Brasil

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Francisco Zamora Rodriguez

Full Text Available RESUMEN En 1649 fue creada la Companhia Geral de Comércio do Brasil por parte del gobierno portugués bajo los auspicios del rey João IV. La idea primigenia fue la de atraer a los comerciantes y hombres de negocios más activos del momento para que participaran del lucrativo comercio que ofrecía el Atlántico portugués, concretamente las tierras de Brasil. De esta manera, se fomentaría el comercio internacional de Portugal con Brasil utilizando los contactos de muchos cristianos nuevos y sus redes de naturaleza transnacional. Este artículo pretende analizar el funcionamiento de la red europea de la Companhia Geral de Comércio do Brasil así como las competencias, funciones y actividades de sus agentes.

O Enoturismo no Brasil: um estudo comparativo entre as regiões vinícolas do Vale dos Vinhedos (RS e do Vale do São Francisco (BA/PE

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Talise Valduga Zanini

2010-07-01

Full Text Available Resumo Este artigo tem como objetivo fazer uma análise comparativa entre duas das mais importantes regiões vinícolas brasileiras: o Vale dos Vinhedos (VV no Rio Grande do Sul e o Vale do São Francisco (VSF localizado entre os Estados da Bahia e Pernambuco. O objetivo é compreender se as motivações dos turistas que visitam as regiões estudadas se relacionam ao vinho e seu contexto ou possuem características similares a de outros eventos turísticos. Os resultados encontrados permitem inferir que no VV, as motivações dos turistas referem-se ao vinho, e essa região já pode ser considerada um destino enoturístico consolidado. Já no VSF, as motivações dos turistas relacionam-se a aspectos comuns a todos tipos de turismo. Conclui-se que a pluralidade destas duas regiões enoturísticas, desde que devidamente planejada no contexto regional específico, poderá constituir-se um fator de diferenciação para o Brasil no cenário mundial. Palavras-chave: turismo; enoturismo; Vale dos Vinhedos; Vale do São Francisco; Brasil. Abstract This article has as objective to do a comparative analysis among two of the most important Brazilian wine-producing areas: The Vale dos Vinhedos in Rio Grande do Sul and Vale do São Francisco (VSF located among Bahia e Pernambuco. The objective is to understand the tourists' motivations that visit the studied areas these they link to the wine and her context or they possess similar characteristics the one of other tourist events. The joined results allow to infer that in Vale dos Vinhedos, the motivation of tourists is related to wine and this region can already be considered a consolidated wine tourism destination. On the other hand, in Vale do São Francisco, the motivation of tourists is related to common aspects to all types of tourism, and in less intensity to the reasons regarding wine. It is ended that the plurality of these two wine regions, as long as properly managed, can be a factor of

Representatividade do gênero Lopesia Rübsaamen (Diptera, Cecidomyiidae no Brasil

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Valéria Cid Maia

2011-01-01

Full Text Available Vinte e três espécies de Lopesia Rübsaamen (Diptera, Cecidomyiidae são conhecidas, todas como indutoras de galhas. A maioria das espécies é Neotropical, também com distribuição Neártica, Afrotropical e Australasiana. A diversidade do gênero no Brasil é avaliada com base na literatura e dados da coleção de Cecidomyiidae do Museu Nacional, Rio de Janeiro. O gênero está representado no Brasil por 23 espécies (18 descritas e 5 não determinadas, o que corresponde a 78% do total de espécies descritas e 95% da fauna neotropical fauna. Estes dados mostram que o gênero é representado no Brasil. A maioria das espécies (78% induz galhas foliares. Gema e caule foram outros órgãos vegetais galhados. As espécies estão associadas a dez famílias botânicas, sendo mais comuns em Burseraceae, Clusiaceae e Fabaceae. A maior parte foi coletada em Mata Atlântica, principalmente em restinga, e o Rio de Janeiro suporta o maior número de espécies registradas. A distribuição geográfica de três espécies é ampliada.

The rs391957 variant cis-regulating oncogene GRP78 expression contributes to the risk of hepatocellular carcinoma.

Science.gov (United States)

Zhu, Xiao; Zhang, Jinfang; Fan, Wenguo; Wang, Fang; Yao, Hong; Wang, Zifeng; Hou, Shengping; Tian, Yinghong; Fu, Weiming; Xie, Dan; Zhu, Wei; Long, Jun; Wu, Leijie; Zheng, Xuebao; Kung, Hsiangfu; Zhou, Keyuan; Lin, Marie C M; Luo, Hui; Li, Dongpei

2013-06-01

Glucose-regulated protein 78 (GRP78) is one of the most important responders to disease-related stress. We assessed the association of the promoter polymorphisms of GRP78 with risk of hepatocellular carcinoma (HCC) and GRP78 expression in a Chinese population. We examined 1007 patients undergoing diagnostic HCC and 810 unrelated healthy controls. Mechanisms by which the GRP78 promoter polymorphism modulates HCC risk and GRP78 levels were analyzed. The promoter haplotype and diplotype carrying rs391957 (-415bp) allele G and genotype GG was strongly associated with HCC risk. Luciferase reporter assays indicated that the promoter carrying rs391957 allele G (haplotype GCCd) showed increased activity in HepG2 cells and Hela cells. rs391957 was also shown to increase the affinity of the transcriptional activator Ets-2, the resistance to apoptosis, as well as cell instability in stressful microenvironment. Furthermore, compared with allele A, rs391957 allele G was associated with higher levels of GRP78 mRNA and protein in HCC tissues. These findings provided new insights into the pathogenesis of HCC and an unexpected effect of the interaction between rs391957 and Ets-2 on hepatocarcinogenesis, and especially supported the hypothesis that stress-related and evolutionarily conserved genetic variant(s) influencing transcriptional regulation could predict susceptibilities.

La salud de las mujeres: la experiencia de Brasil: reflexiones y acciones internacionales

OpenAIRE

1985-01-01

Cuando Isis Internacional invitó al Colectivo Feminista Sexualidad y Salud de Sao Paulo a realizar conjuntamente este número de las Ediciones de Isis Internacional, se nos dio total libertad para seleccionar el material que informaría sobre la experiencia brasileña en el área de la salud de la mujer. Eran muchas las opciones y puntos de partida, porque sin duda en Brasil, el movimiento de las mujeres en esta área ha crecido y se ha diversificado bastante en estos últimos cinco años, tal como ...

The interaction effects of pri-let-7a-1 rs10739971 with PGC and ERCC6 gene polymorphisms in gastric cancer and atrophic gastritis.

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Qian Xu

Full Text Available BACKGROUND: The aim of this study was to investigate the interaction effects of pri-let-7a-1 rs10739971 with pepsinogen C (PGC and excision repair cross complementing group 6 (ERCC6 gene polymorphisms and its association with the risks of gastric cancer and atrophic gastritis. We hoped to identify miRNA polymorphism or a combination of several polymorphisms that could serve as biomarkers for predicting the risk of gastric cancer and its precancerous diseases. METHODS: Sequenom MassARRAY platform method was used to detect polymorphisms of pri-let-7a-1 rs10739971 G → A, PGC rs4711690 C → G, PGC rs6458238 G → A, PGC rs9471643 G → C, and ERCC6 rs1917799 in 471 gastric cancer patients, 645 atrophic gastritis patients and 717 controls. RESULTS: An interaction effect of pri-let-7a-1 rs10739971 polymorphism with ERCC6 rs1917799 polymorphism was observed for the risk of gastric cancer (P interaction = 0.026; and interaction effects of pri-let-7a-1 rs10739971 polymorphism with PGC rs6458238 polymorphism (P interaction = 0.012 and PGC rs9471643 polymorphism (P interaction = 0.039 were observed for the risk of atrophic gastritis. CONCLUSION: The combination of pri-let-7a-1 rs10739971 polymorphism and ERCC6 and PGC polymorphisms could provide a greater prediction potential than a single polymorphism on its own. Large-scale studies and molecular mechanism research are needed to confirm our findings.

El tratado secreto del Barón de Río Branco: la alianza entre Brasil y Ecuador, 1904

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Luís Cláudio Villafañe G. Santos

2016-06-01

Full Text Available Es casi desconocida en las historiografías de Brasil y Ecuador la existencia de un tratado militar secreto entre ambos países, rmado el 5 de mayo de 1904, dirigido contra las pretensiones territoriales de Perú. El artículo estudia una creciente tensión entre Brasil y Perú, que disputaban un área de 442 mil kilómetros cuadrados en la Amazonía. Por iniciativa del Barón de Río Branco, se rmó un tratado secreto de alianza militar entre Brasil y Ecuador. Si bien este acuerdo no fue raticado por los países rmantes, fue de suma importancia para forzar al gobierno peruano a iniciar negociaciones con Brasil, que años más tarde resultaron en el tratado de límites entre los dos países.

Pensamiento crítico e inflexión en el pensamiento social brasileño: las políticas de acción afirmativa en Brasil

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Paulo Alberto Dos Santos Vieira

2014-11-01

Full Text Available Se pretende hacer un acercamiento y analizar las convergencias y tensiones presentes en las relaciones entre los distintos grupos étnicos y raciales en el Brasil contemporáneo. El texto se basó en el análisis del pensamiento de Florestan Fernandes y del Movimiento Negro, así como en los acontecimientos de los años sesenta y setenta, cuya importancia radica en los nuevos abordajes teóricos para los temas de la emancipación, la desigualdad, la diferencia y la democracia. Tales perspec-tivas parecen estar enraizadas en las polémicas que han posibilitado la elaboración de críticas y la inžexión al interior del pensamiento social brasileño.

Statistical analysis of the potassium concentration obtained through; Analise estatistica da concentracao de potassio obtida por aerolevantamentos geofisicos em diferentes formacoes geologicas na regiao de Santa Maria, RS

Energy Technology Data Exchange (ETDEWEB)

Pereira, Joao Eduardo da Silva [Universidade Federal de Santa Maria (UFSM), RS (Brazil). Dept. de Estatistica]. E-mail: jesp61@gmail.com; Silva, Jose Luiz Silverio da; Pires, Carlos Alberto da Fonseca [Universidade Federal de Santa Maria (UFSM), RS (Brazil). Lab. de Hidrogeologia; Strieder, Adelir Jose [Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS (Brazil). Lab. de Modelagem Geologica e Ambiental

2007-07-01

The present work was developed in outcrops of Santa Maria region, southern Brazil, Rio Grande do Sul State. Statistic evaluations were applied in different rock types. The possibility to distinguish different geologic units, sedimentary and volcanic (acid and basic types) by means of the statistic analyses from the use of airborne gamma-ray spectrometry integrating potash radiation emissions data with geological and geochemistry data is discussed. This Project was carried out at 1973 by Geological Survey of Brazil/Companhia de Pesquisas de Recursos Minerais. The Camaqua Project evaluated the behavior of potash concentrations generating XYZ Geosof 1997 format, one grid, thematic map and digital thematic map files from this total area. Using these data base, the integration of statistics analyses in sedimentary formations which belong to the Depressao Central do Rio Grande do Sul and/or to volcanic rocks from Planalto da Serra Geral at the border of Parana Basin was tested. Univariate statistics model was used: the media, the standard media error, and the trust limits were estimated. The Tukey's Test was used in order to compare mean values. The results allowed to create criteria to distinguish geological formations based on their potash content. The back-calibration technique was employed to transform K radiation to percentage. Inside this context it was possible to define characteristic values from radioactive potash emissions and their trust ranges in relation to geologic formations. The potash variable when evaluated in relation to geographic Universal Transverse Mercator coordinates system showed a spatial relation following one polynomial model of second order, with one determination coefficient. The statistica 7.1 software Generalist Linear Models produced by Statistics Department of Federal University of Santa Maria/Brazil was used. (author)

Galectin-3 and Its Genetic Variation rs4644 Modulate Enterovirus 71 Infection.

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Wen-Chan Huang

Full Text Available Galectin-3, a chimeric type β-galactoside-binding protein, is known to modulate viral infection; however, its role in enterovirus 71 (EV71 infection has not been investigated. We generated galectin-3 null rhabdomyosarcoma (RD cells and evaluated whether EV71 infection would be affected. In galectin-3 null cells, the released and intracellular EV71 viral loads were suppressed after 24 h of infection, and cell death rates were significantly lower, while cell proliferation remained unaltered. In addition, RD cells expressing a nonsynonymous genetic variant of galectin-3, rs4644 (LGALS3 +191C/A, P64H, produced lower virus titers than those with wild-type galectin-3 (C allele. To clarify whether the in vitro viral load reduction correlates with clinical severity, we enrolled children with laboratory-confirmed EV71 infection. Since hyperglycemia is an indicator of severe EV71 infection in children, 152 of 401 enrolled children had glucose examinations at admission, and 59 subjects had serum glucose levels ≥ 150 mg/dL. In comparison to the rs4644 AA genotype (2.2 ± 0.06 log10 mg/dL, serum glucose levels during EV71 infection were higher in patients with CC (2.4 ± 0.17 log10 mg/dL, p = 0.03 and CA (2.4 ± 0.15 log10 mg/dL, p = 0.02 genotypes, respectively. These findings suggest that the rs4644 AA genotype of galectin-3 might exert a protective effect. In summary, galectin-3 affects EV71 replication in our cellular model and its variant, rs4644, is associated with hyperglycemia in the clinical setting. The underlying mechanism and its potential therapeutic application warrant further investigation.

Brasil, Argentina e América do Sul

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Paulo Nogueira Batista Jr.

2005-12-01

Full Text Available ESTE trabalho discute alguns aspectos da evolução econômica recente do Brasil, da Argentina e de outros países da América do Sul. Tendências econômicas e intelectuais perigosas, tais como a "globalização", o chamado Consenso de Washington, a dolarização e as negociações da Alca (Área de Livre Comércio das Américas, perderam ímpeto e a América do Sul está se movendo gradualmente na direção de um posicionamento mais independente na condução das suas política econômicas e internacionais. As mudanças foram muito mais significativas na Argentina do que no Brasil e isso se tornou fonte de alguma tensão entre os dois principais países sul-americanos. Não obstante, uma aliança estratégica entre Argentina e Brasil continua sendo a pedra angular da integração da América do Sul.THIS PAPER discusses some aspects of the recent economic evolution of Brazil, Argentina and other South American countries. Dangerous economic and intellectual trends, such as "globalization", the so-called Washington Consensus, dollarization, and FTAA (Free Trade Area of the Americas negotiations, have lost momentum and South America is moving gradually towards a more independent stance in the conduct of its economic and foreign policies. Changes have been much more significant in Argentina than in Brazil and this has become a source of some tension between the two major South American countries. Nevertheless, a strategic alliance between Argentina and Brazil remains the corner stone of South American integration.

URBANIDADE, PRODUÇÃO AGRÍCOLA E CONSERVAÇÃO AMBIENTAL – ESTUDO DE CASO NA REGIÃO DO VALE DO TAQUARI/RS/BRASIL

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Claudete Rempel

2015-02-01

Full Text Available O processo de urbanidade e a prática agrícola convencional ocorrem onstantemente, modificando as condições do ambiente natural e transformando áreas vegetadas contínuas em fragmentos florestais. O objetivo deste estudo foi verificar a existência de relação entre a densidade populacional, o uso e cobertura da terra e os hotspots e firepoints existentes na região do Vale do Taquari - RS. Para tanto, foram gerados mapas de densidade populacional e de zoneamento ecológico econômico com áreas indicadas para conservação. Por meio da análise dos resultados, discutiu-se a melhor forma de conservar e ao mesmo tempo produzir. Além das alternativas trazidas pela agroecologia, sugere-se que as áreas aptas para a produção sejam melhor exploradas, enquanto que as regiões com restrições mantenham áreas mais extensas e conservadas. Fragmentos diminutos, apesar de servirem como ilhas conectivas, não cumprem a mesma função ambiental que fragmentos extensos, principalmente devido à influência de borda que sofrem.

Esquistossomose no Brasil: ensinar versus educar

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Marcos Rogério Capello Sousa

Full Text Available Trata-se de um ensaio sobre a diferença entre ensinar e educar na área da saúde. A partir de alguns casos de esquistossomose em adolescentes de Campinas, assistidos pelo autor no próprio serviço em que desempenha tarefas de docente e assistente na área de Pediatria, discute-se o modo como esta doença vem sendo abordada nos últimos 50 anos, sempre numa perspectiva educacional, isto é, mais complexa e ampla. A partir deste debate, podem-se encaminhar reflexões e críticas sobre o modelo de ensino-assistência na área da saúde no Brasil nas últimas décadas, apesar das novas diretrizes curriculares. Questionam-se as diferenças entre a esquistossomose no Brasil na década de 1960 e no início do século 21, considerando, em cada período, a população, a migração, as condições de vida da população, as terapêuticas, etc. Também se interroga sobre qual tem sido o papel da educação multidisciplinar na mudança deste quadro. Apontam-se algumas direções, para discussão e reflexão, sobre estratégias de ensino na área da saúde.

Structures of Ionic Liquids Dictate the Conversion and Selectivity of Enzymatic Glycerolysis: Theoretical Characterization by COSMO-RS

DEFF Research Database (Denmark)

Guo, Zheng

2008-01-01

be quantitatively associated with the structural characteristics of the IL by means of quantum chemical and COSMO-RS calculation. Misfit interaction, Van der Waals interaction and chemical potential, etc. derived from COSMO-RS calculation are shown to be effective measures to delineate multiple interactions of ILs...

ANÁLISE FLORÍSTICA E ESTRUTURAL DE UM FRAGMENTO DE FLORESTA OMBRÓFILA MISTA MONTANA, SITUADO EM CRIÚVA, RS - BRASIL

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Rubens Marques Rondon Neto

2001-10-01

Full Text Available O presente trabalho teve como objetivo conhecer e analisar a composição florística e descrever a estrutura do componente arbóreo de um fragmento de Floresta Ombrófila Mista Montana, localizado no município de Criúva, RS. Em oito parcelas de 10 x 100 m foram inventariados 673 indivíduos com DAP  5 cm, distribuídos em 37 espécies, pertencentes a 32 gêneros e 22 famílias. O valor do índice de diversidade de Shannon foi de 2,768. As famílias que apresentaram maior número de indivíduos amostrados são: Araucariaceae, Myrsinaceae, Euphorbiaceae, Anacardiaceae e Rutaceae. O dossel dessa floresta é dominado pela Araucaria angustifolia e o sub-bosque por espécies das famílias Lauraceae e Myrtaceae. A densidade total encontrada foi de 841,25 indivíduos/ha, com DAP médio de 24,01 cm e altura média de 9,34 m. As cinco espécies que tiveram os maiores valores de importância, em ordem decrescente, foram: Araucaria angustifolia, Sebastiania commersoniana, Lithraea brasiliensis, Zanthoxylum rhoifolium e Myrcia sp.. O fragmento apresenta uma considerável diversidade florística de espécies, apesar das perturbações sofridas no passado. Para que a vegetação atinja as características florísticas e estruturais próximas às da vegetação original é preciso evitar a presença de bovinos e eqüinos na área e explorações da floresta.

Transgenic tobacco plants expressing BoRS1 gene from Brassica ...

Indian Academy of Sciences (India)

Water stress is by far the leading environmental stress limiting crop yields worldwide. Genetic engineering techniques hold great promise for developing crop cultivars with high tolerance to water stress. In this study, the Brassica oleracea var. acephala BoRS1 gene was transferred into tobacco through ...

Anos de vida perdidos por mortalidade: um dos componentes da carga de doenças Years of life lost by mortality: a component of the burden of disease

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Fúlvio B Nedel

1999-10-01

Full Text Available OBJETIVO: Calculou-se a carga de doença devida à mortalidade, os anos de vida perdidos por "morte prematura" (AVP, nos Estados do Rio Grande do Sul e Santa Catarina, comparando alguns resultados com o Brasil. MÉTODOS: Baseou-se nos anos de vida ajustados em função da incapacidade (AVAI, indicador que agrega mortalidade e morbidade em uma medida global. As populações de estudo foram os óbitos de residentes nos Estados em 1994 e no Brasil em 1993. RESULTADOS: Embora a maior carga por mortalidade seja imposta por causas ligadas a um estágio mais avançado da transição epidemiológica, tanto o Rio Grande do Sul como Santa Catarina, mas principalmente o Brasil, sofrem importante carga por doenças do subdesenvolvimento. As lesões representam o segundo grupo nos Estados e terceiro no Brasil. CONCLUSÃO: O indicador permite comparar agravos de alta e baixa letalidade, sendo instrumento útil na gestão e controle social das políticas e ações de saúde.INTRODUCTION: The register of death by cause, sex and age groups of residents in 1994 in Rio Grande do Sul (RS and Santa Catarina (SC, two Brazilian southern states, were studied to calculate the years of life lost (YLL, one of the two components that summarize disability adjusted life years (DALY, in RS, SC and Brazil. METHODS: The methodology employed is the same used in the Global Burden of Disease study to quantify the mortality component (YLL of DALY in the world. RESULTS: The results show that the greatest proportion and rates caused by Group II (Noncommunicable diseases, linked with more advanced stages of the epidemiological transition, in RS, SC and Brazil. But in both states and especially in Brazil, Group I (Communicable, maternal, perinatal and nutritional conditions causes an important proportion of YLL. The Group III (Injuries was the second more important group in RS and SC and the third in Brazil. Road traffic accidents are particularly important in SC, where the intentional

A functional TNFAIP2 3'-UTR rs8126 genetic polymorphism contributes to risk of esophageal squamous cell carcinoma.

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Jian Zhang

Full Text Available BACKGROUND: Accumulated evidences demonstrated that single nucleotide polymorphisms (SNPs in mRNA 3'-untranslated region (3'-UTR may impact microRNAs (miRNAs-mediated expression regulation of oncogenes and tumor suppressors. There is a TNFAIP2 3'-UTR rs8126 T>C genetic variant which has been proved to be associated with head and neck cancer susceptibility. This SNP could disturb binding of miR-184 with TNFAIP2 mRNA and influence TNFAIP2 regulation. However, it is still unclear how this polymorphism is involved in development of esophageal squamous cell carcinoma (ESCC. Therefore, we hypothesized that the functional TNFAIP2 rs8126 SNP may affect TNFAIP2 expression and, thus, ESCC risk. METHODS: We investigated the association between the TNFAIP2 rs8126 variant and ESCC risk as well as the functional relevance on TNFAIP2 expression in vivo. Genotypes were determined in a case-control set consisted of 588 ESCC patients and 600 controls. The allele-specific regulation on TNFAIP2 expression by the rs8126 SNP was examined in normal and cancerous tissue specimens of esophagus. RESULTS: We found that individuals carrying the rs8126 CC or CT genotype had an OR of 1.89 (95%CI  = 1.23-2.85, P = 0.003 or 1.38 (95%CI  = 1.05-1.73, P = 0.017 for developing ESCC in Chinese compared with individual carrying the TT genotype. Carriers of the rs8126 CC and CT genotypes had significantly lower TNFAIP2 mRNA levels than those with the TT genotypes in normal esophagus tissues (P<0.05. CONCLUSIONS: Our data demonstrate that functional TNFAIP2 rs8126 genetic variant is a ESCC susceptibility SNP. These results support the hypothesis that genetic variants interrupting miRNA-mediated gene regulation might be important genetic modifiers of cancer risk.

Alimentação nos primeiros três meses de vida dos bebês de uma coorte na cidade de Pelotas, Rio Grande do Sul Alimentación en los primeros tres meses de vida de los bebés de una coorte en la ciudad de Pelotas, Rio Grande do Sul (Brasil Feeding during the first three months of life for infants of a cohort in Pelotas, Rio Grande do Sul, Brazil

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Cristina Corrêa Kaufmann

2012-06-01

Full Text Available OBJETIVO: Estudar o padrão alimentar nos primeiros três meses de vida de crianças nascidas na cidade de Pelotas (RS. MÉTODOS: Estudo de coorte prospectivo com os bebês nascidos entre setembro de 2002 e maio de 2003, na cidade de Pelotas (RS. Incluíram-se 2.741 bebês nas maternidades e uma amostra aleatória de 30% acompanhada no primeiro e terceiro meses de vida. Foram realizadas análises uni, bi e multivariada. Somente as variáveis com pOBJETIVO: Estudiar el estándar alimentar en los primeros tres meses de vida de niños nascidos en la ciudad de Pelotas (RS, Brasil. MÉTODOS: Estudio de coorte prospectivo con bebés nascidos entre septiembre de 2002 y mayo de 2003, en la ciudad de Pelotas (RS, Brasil. Se incluyó a 2.741 bebés en las maternidades y una muestra aleatoria de 30%, seguida en el primero y el tercero meses de vida. Se realizaron análisis uni, bi y multivariados, y solamente las variables con pOBJECTIVE: To study the feeding pattern in the first three months of babies born in the Pelotas city, in Sothern Brazil. METHODS: Prospective cohort study, with babies born between september 2002 and may 2003. Among 2,741 babies whose mothers were interviewed at the maternity ward, a random sample of 30% was followed up on the first and third months of age. Univariate, bivariate and multivariate analyses were applied. Variables with a p<0.05 were considered as associated. RESULTS: 951 babies were followed up on the first month, 60% were under exclusive maternal breastfeeding, and 10% were already weaned. Smoking during pregnancy, father's educational level lower than four years and the use of a pacifier were associated to weaning. On the third month, 29% had been weaned, 39% received maternal milk exclusively, and 59% were bottle fed. Smoking during pregnancy, father schooling and the use of a pacifier were associated with weaning. There was an increase in the pacifier use - from 56 to 66% between the first and the third month of

Mastite em pequenos ruminantes no Brasil

OpenAIRE

Peixoto,Rodolfo de M.; Mota,Rinaldo Aparecido; Costa,Mateus M. da

2010-01-01

Este artigo objetivou revisar as informações recentes sobre mastite em pequenos ruminantes, abrangendo etiologia, epidemiologia, aspectos de controle e profilaxia. Houve a preocupação em reunir resultados de estudos desenvolvidos no Brasil, uma vez que a mastite tem a interferência de uma série de fatores, como fatores ambientais e outros decorrentes dos sistemas de manejo empregados, condições essas determinantes para etiologia e epidemiologia da enfermidade. A prevalência da mastite em capr...

Memoria y territorio quilombola en Brasil

OpenAIRE

Larrea Killinger, Cristina; Ruíz-Peinado, José Luis

2004-01-01

El proceso de legalización del territorio qilombola ha abierto un debate político y social que parte del reconocimiento de la deuda histórica que el estado brasileño ha tenido con los descendientes de esclavos. Este nuevo derecho ha potenciado la definición y redefinición de conceptos de identificación de las comunidades mocambeiras, tales como "quilombolas", "comunidades de remanentes quilombolas", "comunidades negras rurales", "terras de pretos", etc. Distintos actores sociales han pa...

ESR1 single nucleotide polymorphism rs1062577 (c.*3804T>A) alters the susceptibility of breast cancer risk in Iranian population.

Science.gov (United States)

Dehghan, Zahra; Sadeghi, Samira; Tabatabaeian, Hossein; Ghaedi, Kamran; Azadeh, Mansoureh; Fazilati, Mohammad; Bagheri, Fatemeh

2017-05-05

Albeit single nucleotide polymorphisms related to ESR1 gene have been studied, only a number of them have been reported to be associated with breast cancer risk. rs1062577 is one of the most recent microRNA-related ESR1 SNPs; however, no study has been conducted to investigate the significance this polymorphism in Iranian population. In this study, we aimed to investigate the frequency and also the association between rs1062577 and breast cancer. rs1062577 position was genotyped by Tetra-primer ARMS-PCR in totally 182 blood specimens obtained from breast cancer patients (n=86), and healthy blood donors (n=96). The distribution of different genotypes was statistically analyzed in terms of the potential association between rs1062577 different alleles, breast cancer risk and clinicopathological criteria of breast cancer patients. The statistical analyses confidently indicated that rs1062577 A allele is associated with the increased breast cancer risk in both univariate and multivariate regression models (Odds Ratio=8.403 and 32.602 respectively). rs1062577 T allele was statistically associated with stage I of breast cancer patients (p-value=0.025). In silico studies implied that rs1062577 A allele can alter the binding capacity of ESR1 mRNA and miRNAs via either breakage or formation of hydrogen bonds. rs1062577 A allele is significantly and dramatically associated with the elevated risk and greater stages of breast cancer. Copyright © 2017 Elsevier B.V. All rights reserved.

Going up in Smoke? A Review of nAChRs-based Treatment Strategies for Improving Cognition in Schizophrenia

Science.gov (United States)

Boggs, Douglas L.; Carlson, Jon; Cortes-Briones, Jose; Krystal, John H.; D’Souza, D. Cyril

2015-01-01

Cognitive impairment is known to be a core deficit in schizophrenia. Existing treatments for schizophrenia have limited efficacy against cognitive impairment. The ubiquitous use of nicotine in this population is thought to reflect an attempt by patients to self-medicate certain symptoms associated with the illness. Concurrently there is evidence that nicotinic receptors that have lower affinity for nicotine are more important in cognition. Therefore, a number of medications that target nicotinic acetylcholine receptors (nAChRs) have been tested or are in development. In this article we summarize the clinical evidence of nAChRs dysfunction in schizophrenia and review clinical studies testing either nicotine or nicotinic medications for the treatment of cognitive impairment in schizophrenia. Some evidence suggests beneficial effects of nAChRs based treatments for the attentional deficits associated with schizophrenia. Standardized cognitive test batteries have failed to capture consistent improvements from drugs acting at nAChRs. However, more proximal measures of brain function, such as ERPs relevant to information processing impairments in schizophrenia, have shown some benefit. Further work is necessary to conclude that nAChRs based treatments are of clinical utility in the treatment of cognitive deficits of schizophrenia. PMID:24345265

Monitoramento do desenvolvimento infantil realizado no Brasil La monitoración del desarrollo infantil realizada en Brasil Monitoring of child development held in Brazil

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Silvio Cesar Zeppone

2012-12-01

Full Text Available OBJETIVO: Revisar a literatura científica para verificar como a vigilância do desenvolvimento infantil vem sendo realizada no Brasil. FONTES DE DADOS: Pesquisa em bases de dados (PubMed, Medline, SciELO e Banco de Teses da Coordenação de Aperfeiçoamento de Pessoal de Nível Superior sobre estudos das práticas médicas em relação à vigilância e ao monitoramento do desenvolvimento infantil no Brasil, de 2000 a 2011. Os termos usados para pesquisa foram: vigilância de desenvolvimento infantil, intervenção precoce, triagem de desenvolvimento e testes de triagem de desenvolvimento. Foram encontrados dez textos referentes ao tema em estudo. Artigos originais, de revisão e teses foram revisados, bem como as listas de referências das publicações sobre o assunto. SÍNTESE DOS DADOS: Os estudos sobre a prática do monitoramento do desenvolvimento infantil no Brasil apontam uma importante falha, desde a formação do médico pediatra até a prática clínica, em relação a este tema. CONCLUSÕES: Há necessidade urgente, principalmente frente a uma população emergente de prematuros, que os pediatras façam uma reciclagem do conhecimento sobre o desenvolvimento infantil.OBJETIVO: Revisar la literatura científica para verificar cómo la vigilancia del desarrollo infantil viene siendo realizada en Brasil. FUENTES DE DATOS: Investigación en las bases de datos (Pubmed, Medline, SciELO y Base de Tesis CAPES sobre estudios de las prácticas médicas respecto a la vigilancia y monitoración del desarrollo infantil en Brasil de 2000 a 2011. Los términos usados para la investigación fueron: vigilancia de desarrollo infantil, intervención temprana, screening de desarrollo y pruebas de screening de desarrollo. Se encontraron 10 textos relativos al tema en estudio. Artículos originales, de revisión y tesis fueron revisados, así como las listas de referencias de las publicaciones sobre el tema. SÍNTESIS DE LOS DATOS: Los estudios sobre la pr

rs657075 (CSF2 Is Associated with the Disease Phenotype (BAS-G of Ankylosing Spondylitis

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Wei-Chiao Chen

2017-01-01

Full Text Available Ankylosing spondylitis (AS is a systemic autoimmune disease mainly affecting the lumbar spine and sacroiliac joints, and exhibits peripheral inflammatory arthropathy. More than 25 loci have been identified as associated with AS. Because both AS and rheumatoid arthritis (RA are autoimmune diseases that may share some common genetic factors, we therefore examined if the newly identified RA genetic polymorphisms were associated with AS in a Taiwanese population. In this study, we enrolled 475 AS patients and 11,301 healthy subjects from a Taiwanese biobank as controls. Although none of single-nucleotide polymorphisms (SNPs were associated with the susceptibility to AS, the AS disease index Bath AS Global (BAS-G clinical phenotype was observed as significantly correlated to the AA genotype of rs657075 (CSF2. The significance remains after gender/age/disease duration adjustment and after group categorization by human leukocyte antigen-B 27 (HLA-B27 genotype. We further investigated the possible functions of rs657075 through bioinformatics approaches. Results revealed that polymorphism of rs657075 is able to influence the expression of acyl-CoA synthetase long-chain family member 6 (ACSL6. In conclusion, our study indicated that rs657075 (CSF2 is strongly associated with the AS disease index Bath AS Global (BAS-G clinical phenotype.

O descobrimento do Brasil (1937)

OpenAIRE

Jacques, Tatyana de Alencar

2014-01-01

Tese (doutorado) - Universidade Federal de Santa Catarina, Centro de Filosofia e Ciências Humanas, Programa de Pós-Graduação em Antropologia Social, Florianópolis, 2014. Esta é uma etnografia de Descobrimento do Brasil (1937), de Humberto Mauro, um filme em preto e branco, de uma hora de duração, com poucos diálogos e percorrido de seu início ao fim por música de Villa-Lobos. Organiza-se a partir de dois principais eixos de investigação, quais sejam as técnicas de reprodução constituintes ...

Las manifestaciones sociales en Brasil

OpenAIRE

Gonçalves Chaves, Mariluci

2013-01-01

El país del fútbol se ha convertido en el país de las protestas y manifestaciones. Manifestaciones que han sido pacíficas algunas veces y violenta otras, surgió inicialmente como respuesta a los aumentos en las tarifas de transporte público, con convocatorias a través de redes sociales, obtuvo un fuerte apoyo popular después de la violenta y desproporcionada represión de la policía , convirtiéndose en uno de los mayores movimientos sociales en la historia de Brasil, comparable sólo con los mo...

O Brasil e as negociações multilaterais

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Shiguenoli Miyamoto

2000-06-01

Full Text Available O artigo procura demonstrar que o Brasil sempre favoreceu a participação em fóruns multilaterais e que esta tendência tem se acentuado na década de 1990.The article seeks to show that Brazil has favored multilateral instances throughout its history. In the nineties, this trend has increased.

Tratamento em saúde mental: estudo documental da legislação federal do surgimento do Brasil até 1934

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Danielly de Souza Canabrava

2010-03-01

Full Text Available Os modos de tratamento em saúde mental e os estigmas a que os portadores de transtorno mental são submetidos constituem questões de reflexão e discussão na área da saúde. Com o intuito de se aprofundar nesta temática desenvolveu-se uma pesquisa documental com o objetivo de analisar os modos de tratamento na legislação federal de saúde mental surgida no Brasil do seu descobrimento até 1934. Obteve-se 16 Decretos, que constituíram as fontes primárias deste estudo, mediante busca no acervo de Leis da Biblioteca Pública do Paraná e no site do Ministério da Saúde. As fontes foram discutidas em três eixos temporais da história do Brasil: Brasil Colonial, Brasil Imperial e Brasil República: a partir de 1889. Conclui-se que o período estudado constituiu uma trajetória de tratamentos marcada por isolamentos, terapêuticas repressoras e desumanas à pessoa com transtorno mental.

Hans Kelsen, estado de exceção e Copa do Mundo no Brasil || Hans Kelsen, State of Emergency and World Cup in Brasil

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Andityas Soares de Moura Costa Matos

2014-06-01

Full Text Available RESUMEN. Este trabajo presenta la situación de excepción económica creada en Brasil al hilo de la realización de los llamados “grandes eventos”, en particular la Copa del Mundo de 2014, que ha registrado la suspensión de diversos derechos y garantías fundamentales del derecho brasileño con objeto de garantizar la explotación económica monopólica del evento por la FIFA. El marco teórico del artículo se basa en la Teoría Pura del Derecho de Kelsen, que al ejemplificar una teoría del derecho de la normalidad, en la que la excepción no tiene espacio, sirve perfectamente de contra-paradigma para analizar el escenario político-legal autoritario que se ha introducido en Brasil, el cual se aborda brevemente a través del análisis de parte de la legislación de excepción que actúa como garante de la Copa del Mundo.. ABSTRACT. This article intends to analyze the situation of economic exception established in Brazil for the accomplishment of the so-called “mega events”, specially the 2014 World Cup, when many rights and guarantees foreseen in the Brazilian legal system were suspended with the purpose of guaranteeing FIFA’s monopolistic economic exploitation at the event. The work’s theoretical framework has its basis in Kelsen’s Pure Theory of Law, which, as an example of a legal theory of normality, where the exception has no room, perfectly suits as an inverted paradigm for the authoritarian political-legal scenario established in Brazil, the latter being briefly presented through the analysis of part of the exceptional legislation approved to ensure the World Cup. RESUMO. O presente artigo pretende analisar a situação de exceção econômica instaurada no Brasil para a realização dos chamados “megaeventos”, em especial a Copa do Mundo de 2014, quando diversos direitos e garantias fundamentais do ordenamento jurídico brasileiro foram suspensos com o objetivo de garantir a exploração econômica monopolística do

A multi-institutional outcome and prognostic factor analysis of radiosurgery (RS) for resectable single brain metastasis

Energy Technology Data Exchange (ETDEWEB)

Auchter, RM; Lamond, JP; Alexander, E; Buatti, JM; Chappell, RJ; Friedman, W; Kinsella, TJ; Levin, AB; Noyes, WR; Schultz, C; Loeffler, JS; Mehta, MP

1995-07-01

PURPOSE: Recent randomized trials comparing resection of single brain metastasis (BM) in selected patients (pts) followed by whole brain radiotherapy (WBRT) to WBRT alone demonstrated statistically significant survival advantage for surgery (Patchell, 1990 and Noordijk, 1994). This multi-institutional retrospective study was performed in similar pts who were treated with RS and WBRT to provide a baseline for comparison for a future randomized trial. MATERIALS AND METHODS: The RS databases of four institutions were reviewed to identify all pts who met the following criteria: single BM; age > 18; surgically resectable lesion; independently functional (KPS {>=} 70); non-radiosensitive histology (small cell, lymphoma, myeloma, germ cell excluded); no prior cranial surgery or WBRT. 122 of 533 pts with BM treated with RS met these criteria. Pts were categorized by: (a) status of the primary: 'absent' = complete resection, 26 pts; 'controlled' locally controlled with radiotherapy or chemotherapy, 70 pts; 'under treatment' = undergoing radiotherapy, 15 pts; 'active' = no definitive or successful treatment of the primary, 11 pts; (b) status of non-CNS metastasis: present=64 pts, absent=58 pts; (c) age: median=61, range 23-83; (d) KPS : KPS 70/80/90/100=20/26/44/32 pts; (e) histology: lung=58, melanoma=16, breast=13, renal=12,colon=9, other=10, unknown primary=4; (f) time from primary to BM: median=12 months, range=1-252 months; (g) gender: male=64, female=58; (h) tumor volume: median=2.68 cc, range=0.13-27.2 cc. RS was performed with a linear accelerator based technique (peripheral dose 10-27 Gy, median 17 Gy). WBRT was performed in all but 5 pts who refused it (range 25 - 40 Gy, median 37.5 Gy). RESULTS: The potential median follow-up for all pts is 123 weeks (wks). The overall local response rate is 59% (complete response = 25%, partial response = 34%). In field progression occurred in 17 patients (14%), with overall local control of 86%. Local control was highest for

A caracterização dos agricultores familiares que cultivam tabaco no Território Centro-Sul/RS

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Décio Souza Cotrim

2016-10-01

Full Text Available O cultivo de tabaco no Brasil está centrado na Região Sul e em sua ampla maioria assentado na categoria da Agricultura Familiar. Esse fato traz um conjunto de características típicas desse grupo social que ao mesmo tempo os diferencia e os aproxima. O presente artigo tem como objetivo apresentar e analisar algumas dessas características focando em agricultores do território Centro-Sul do Rio Grande do Sul - RS. O método utilizado foi a construção e análise de um banco de dados baseado em entrevistas primárias realizadas pela equipe de profissionais da extensão rural. Como resultado, foi possível constatar que esses agricultores, em sua maioria, possuem uma educação formal no nível fundamental, sendo que o ensino superior e técnico não se configura como uma realidade atual. Eles estão envolvidos com o cultivo do tabaco entre 20 a 30 anos, o que produz um alto grau de conhecimento sobre o tema e um grupo de estruturas dentro da propriedade. Eles plantam, em média, trinta mil pés de fumo por safra, mas muitos utilizam a estratégia de ampliação dessa área cultivada voltando a comercialização para o mercado de “atravessadores”. As famílias apresentaram de alta a altíssima dependência econômica do tabaco, porém 65% demonstraram interesse em sair da atividade.

Violência sexual e sua prevalência em adolescentes de Porto Alegre, Brasil

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Polanczyk Guilherme Vanoni

2003-01-01

Full Text Available OBJETIVO: Verificar a prevalência da exposição à violência sexual entre adolescentes estudantes de escolas estaduais. MÉTODOS: Foram selecionadas 52 escolas estaduais de Porto Alegre, RS, Brasil, com ensino fundamental completo, por meio de um processo de amostragem aleatória, estratificada de acordo com o tamanho das escolas. Foi selecionada, em cada escola, uma turma de oitava série por sorteio aleatório e foram incluídos todos os adolescentes presentes nas salas de aula que consentiram em participar do estudo. Foi utilizado o instrumento Triagem da Exposição de Crianças à Violência na Comunidade para identificar jovens que foram vítimas, testemunhas ou que conheciam vítimas de atos de violência sexual. RESULTADOS: Foram incluídos 1.193 adolescentes, representando 10,3% dos alunos matriculados na oitava série da rede estadual da cidade. Vinte e sete (2,3% adolescentes relataram ter sido vítimas de violência sexual, 54 (4,5% ter sido testemunhas de algum tipo de violência sexual e 332 (27,9% relataram conhecer alguém que tenha sido vítima de violência sexual. CONCLUSÕES: A exposição à violência sexual pelas três formas de contato relatadas mostrou-se freqüente entre os adolescentes estudados. São necessários estudos que abordem a violência sexual como um fenômeno social amplo, com múltiplos fatores associados, amparando estratégias comunitárias de prevenção e de tratamento.

Desenvolvimento dos biocombustíveis no Brasil e no Leste Asiático: experiências e desafios

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Gilmar Masiero

2011-01-01

Full Text Available Este artigo resume o papel que as novas tecnologias e as políticas governamentais têm desempenhado na evolução da indústria dos biocombustíveis no Brasil e no Leste Asiático. Ele documenta os fatores que contribuíram para que o Brasil, China, Japão e Coreia do Sul se tornassem produtores e consumidores de biocombustíveis, bem como a extensão em que essa fonte de energia tem sido efetivamente adotada em cada uma dessas economias. Em seguida, avalia a extensão do comércio e da cooperação em biocombustíveis entre os três países do Leste Asiático e o Brasil. Argumenta que o Japão é muito mais avançado em sua cooperação sobre biocombustíveis com o Brasil e que nas demais economias asiáticas existe grande potencial para maior cooperação.

ANÁLISE DO DIAGNÓSTICO DO DESEMPENHO EM LEITURA: PROVINHA BRASIL vs. FLUÊNCIA EM LEITURA ORAL

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Ayane Nararela Santos Almeida

2013-01-01

Full Text Available Analisamos, por meio dos resultados obtidos na aplicação do Teste 2 da Provinha Brasil 2011 e de uma matriz de competência de fluência em leitura oral, o desempenho dos alfabetizandos na fluência em leitura oral e sua convergência com o desempenho na Provinha Brasil. Como corpus, tomamos quatro histórias sem imagens para que alunos, do 2º ano do ensino fundamental de uma escola municipal de Aracaju, fizessem a leitura oral. Durante a análise, correlacionamos a competência de fluência em leitura oral desenvolvida pelos alunos, e verificada por meio da matriz proposta neste estudo, com os resultados obtidos no Teste 2 da Provinha Brasil 2011. Concluímos que a articulação entre a matriz de competência de fluência em leitura oral em conjunto com a matriz de referência da Provinha Brasil 2011 permite contribuir significativamente para o aprimoramento da competência comunicativa e letramento do aluno alfabetizando.

[Association Between SNP rs6007897 of CELSR1 and Acute Ischemic Stroke in Western China Han Population: a Case-control Study].

Science.gov (United States)

Qin, Feng-qin; Yu, Li-hua; Hu, Wen-ting; Guo, Jian; Chen, Ning; Guo, Jiang; Fang, Jing-huan; He, Li

2015-07-01

To investigate the relationship between single nucleotide polymorphism (SNP) rs6007897 of CELSR1 and acute ischemic stroke in Western China Han population. All subjects (759 acute ischemic stroke patients and 786 controls) were genotyped using ligation detection reaction (LDR). We analyzed the differences between SNP rs6007897 genotypes and allele frequencies between two groups. Two genotypes (AA, AG) of rs6007897 were found in both stroke and control group. There was no statistically significance between two groups about genotype and allele frequency. After adjusting for risk factors, we found there was no significant association between rs6007897 and ischemic stroke CP = 0.797, odds ratio (OR) = 0.886, 95% confidence interval (CI) = 0.352-2.227). SNP rs6007897 of CELSR1 was not significantly associated with ischemic stroke in Western China Han population.

Polyvalent cation receptor proteins (CaRs) are salinity sensors in fish.

Science.gov (United States)

Nearing, J; Betka, M; Quinn, S; Hentschel, H; Elger, M; Baum, M; Bai, M; Chattopadyhay, N; Brown, E M; Hebert, S C; Harris, H W

2002-07-09

To determine whether calcium polyvalent cation-sensing receptors (CaRs) are salinity sensors in fish, we used a homology-based cloning strategy to isolate a 4.1-kb cDNA encoding a 1,027-aa dogfish shark (Squalus acanthias) kidney CaR. Expression studies in human embryonic kidney cells reveal that shark kidney senses combinations of Ca(2+), Mg(2+), and Na(+) ions at concentrations present in seawater and kidney tubules. Shark kidney is expressed in multiple shark osmoregulatory organs, including specific tubules of the kidney, rectal gland, stomach, intestine, olfactory lamellae, gill, and brain. Reverse transcriptase-PCR amplification using specific primers in two teleost fish, winter flounder (Pleuronectes americanus) and Atlantic salmon (Salmo salar), reveals a similar pattern of CaR tissue expression. Exposure of the lumen of winter flounder urinary bladder to the CaR agonists, Gd(3+) and neomycin, reversibly inhibit volume transport, which is important for euryhaline teleost survival in seawater. Within 24-72 hr after transfer of freshwater-adapted Atlantic salmon to seawater, there are increases in their plasma Ca(2+), Mg(2+), and Na(+) that likely serve as a signal for internal CaRs, i.e., brain, to sense alterations in salinity in the surrounding water. We conclude that CaRs act as salinity sensors in both teleost and elasmobranch fish. Their tissue expression patterns in fish provide insights into CaR functions in terrestrial animals including humans.

Association of Calcium-Sensing Receptor (CASR rs 1801725 with Colorectal Cancer

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Fateme Rostami

2012-07-01

Full Text Available Background: Calcium induces apoptosis in intestinal epithelial cells and subsequently prevents colorectal cancer through ion calcium receptor. Calcium-sensing receptor mutation reduces the expression of this receptor, and subsequently in reduces calcium transportation. Many studies have shown that Calcium-sensing receptor gene polymorphism may increase the risk of colorectal cancer. The purpose of this study is to assess the prevalence of calcium-sensing receptor polymorphisms (rs 1801725 in Iran society and to examine the role of this polymorphism in the increased risk of colorectal cancer (CRC.Materials and Methods: The research was a case-control study. 105 patients with colorectal cancer and 105 controls were randomly studied using polymerase chain reaction and restriction fragment length polymorphism. χ2 test and software 16- SPSS were used for statistical analysis.Results: In patient samples, the frequency of the genotypes TT, GT, GG in gene CASR rs 1801725 was respectively 64.8, 32.4, and 2.9 and the frequency of this polymorphism in control samples was respectively 51.2, 45.7, and 2.9. Frequency of allele G in patient samples was 0/48 and frequency of allele T was 0.25. In addition, Frequency of allele G in control samples was 0.74 and Frequency of allele T was calculated 0.19.Conclusion: The results show that calcium-sensing receptor variant (1801725 rs is not associated with increased risk of colorectal cancer.

Evaluation of [O-methyl-11C]RS-15385-197 as a positron emission tomography radioligand for central α2-adrenoceptors

International Nuclear Information System (INIS)

Hume, S.P.; Hirani, E.; Opacka-Juffry, J.; Osman, S.; Myers, R.; Gunn, R.N.; McCarron, J.A.; Pike, V.W.; Clark, R.D.; Melichar, J.; Nutt, D.J.

2000-01-01

Carbon-11 labelled RS-15385-197 and its ethylsulphonyl analogue, RS-79948-197, were evaluated in rats as potential radioligands to image central α 2 -adrenoceptors in vivo. The biodistributions of both compounds were comparable with that obtained in an earlier study using tritiated RS-79948-197 and were consistent with the known localisation of α 2 -adrenoceptors. The maximal signals (total to non-specific binding) were, however, reduced, in the order [ 11 C]RS-79948-197 11 C]RS-15385-197 3 H]RS-79948-197, primarily due to the difference in radiolabel position (O-methyl for carbon-11 compared with S-ethyl for tritium). This resulted in the in-growth of radiolabelled metabolites in plasma, which, in turn, contributed to the non-specific component of brain radioactivity. Nonetheless, the signal ratio of ∝5 for a receptor-dense tissue compared with the receptor-sparse cerebellum, at 90-120 min after radioligand injection, encouraged the development of [O-methyl- 11 C]RS-15385-197 for human positron emission tomography (PET). Unfortunately, in two human PET scans (each of 90 min), brain extraction of the radioligand was minimal, with volumes of distribution more than an order of magnitude lower than that measured in rats. Following intravenous injection, radioactivity was retained in plasma and metabolism of the radiolabelled compound was very low. Retrospective measurements of in vitro plasma protein binding and in vivo brain uptake index (BUI) in rats demonstrated a higher protein binding of the radioligand in human compared with rat plasma and a lower BUI in the presence of human plasma. It is feasible that a higher affinity of RS-15385-197 for human plasma protein compared with receptor limited the transport of the radioligand. Although one of the PET scans showed a slight heterogeneity in biodistribution of radioactivity which was consistent with the known localisation of α 2 -adrenoceptors in human brain, it was concluded that [O-methyl- 11 C]RS-15385

Common variant in the glucokinase regulatory gene rs780094 and risk of nonalcoholic fatty liver disease: a meta-analysis.

Science.gov (United States)

Zain, Shamsul Mohd; Mohamed, Zahurin; Mohamed, Rosmawati

2015-01-01

Although studies have suggested that rs780094, a common variant in the glucokinase regulatory (GCKR) gene to be associated with type 2 diabetes, obesity, and their related traits, the genetic basis of the association between GCKR rs780094 and nonalcoholic fatty liver disease (NAFLD) is still being examined. This meta-analysis was performed to evaluate the effect strength caused by GCKR rs780094 on NAFLD. We searched Medline, PubMed, Scopus, and Embase for relevant articles published up to April 2014. Data were extracted, and summary estimates of the association between GCKR rs780094 and NAFLD were examined. Heterogeneity and publication bias were also examined. This meta-analysis incorporated a total of 2091 NAFLD cases and 3003 controls from five studies. Overall, the pooled result indicated that the GCKR rs780094 was significantly associated with increased risk of NAFLD (additive: odds ratio (OR) 1.25, 95% confidence interval (CI) 1.14-1.36, P risk of NAFLD. Similar effect size was demonstrated in both Asian and non-Asian populations. © 2014 Journal of Gastroenterology and Hepatology Foundation and Wiley Publishing Asia Pty Ltd.

Interleukin-6 Receptor rs7529229 T/C Polymorphism Is Associated with Left Main Coronary Artery Disease Phenotype in a Chinese Population

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Feng He

2014-04-01

Full Text Available Left main coronary artery disease (LMCAD is a particular severe phenotype of coronary artery disease (CAD and heritability. Interleukin (IL may play important roles in the pathogenesis of CAD. Although several single nucleotide polymorphisms (SNPs identified in IL related genes have been evaluated for their roles in inflammatory diseases and CAD predisposition, the investigations between genetic variants and CAD phenotype are limited. We hypothesized that some of these gene SNPs may contribute to LMCAD phenotype susceptibility compared with more peripheral coronary artery disease (MPCAD. In a hospital-based case-only study, we studied IL-1A rs1800587 C/T, IL-1B rs16944 G/A, IL-6 rs1800796 C/G, IL-6R rs7529229 T/C, IL-8 rs4073 T/A, IL-10 rs1800872 A/C, and IL-10 rs1800896 A/G SNPs in 402 LMCAD patients and 804 MPCAD patients in a Chinese population. Genotyping was done using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS and ligation detection reaction (LDR method. When the IL-6R rs7529229 TT homozygote genotype was used as the reference group, the CC or TC/CC genotypes were associated with the increased risk for LMCAD (CC vs. TT, adjusted odds ratio(OR = 1.46, 95% confidence interval (CI = 1.02–2.11, p = 0.042; CC + TC vs. TT, adjusted OR = 1.31, 95% CI = 1.02–1.69, p = 0.037. None of the other six SNPs achieved any significant differences between LMCAD and MPCAD. The present study suggests that IL-6R rs7529229 T/C functional SNP may contribute to the risk of LMCAD in a Chinese population. However, our results were limited. Validation by a larger study from a more diverse ethnic population is needed.

Effect of rs1344706 in the ZNF804A gene on the brain network

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Xiongying Chen

2018-01-01

Full Text Available ZNF804A rs1344706 (A/C was the first SNP that reached genome-wide significance for schizophrenia. Recent studies have linked rs1344706 to functional connectivity among specific brain regions. However, no study thus far has examined the role of this SNP in the entire functional connectome. In this study, we used degree centrality to test the role of rs1344706 in the whole-brain voxel-wise functional connectome during the resting state. 52 schizophrenia patients and 128 healthy controls were included in the final analysis. In our whole-brain analysis, we found a significant interaction effect of genotype × diagnosis at the precuneus (PCU (cluster size = 52 voxels, peak voxel MNI coordinates: x = 9, y = −69, z = 63, F = 32.57, FWE corrected P < 0.001. When we subdivided the degree centrality network according to anatomical distance, the whole-brain analysis also found a significant interaction effect of genotype × diagnosis at the PCU with the same peak in the short-range degree centrality network (cluster size = 72 voxels, F = 37.29, FWE corrected P < 0.001. No significant result was found in the long-range degree centrality network. Our results elucidated the contribution of rs1344706 to functional connectivity within the brain network, and may have important implications for our understanding of this risk gene's role in functional dysconnectivity in schizophrenia.

Controle alternativo da murcha bacteriana do pimentão utilizando óleos essenciais vegetais e silicato de cálcio.

OpenAIRE

Aldenir de Oliveira Alves

2012-01-01

A murcha bacteriana do pimentão, causada por Ralstonia solanacearum (Rs) raça 1, é uma fitobacteriose importante em Pernambuco e outros estados do Brasil. Este trabalho teve como objetivos testar o efeito de óleos vegetais e do silício (Si) no controle alternativo desta doença, seus efeitos diretos sobre Rs e verificar os possíveis mecanismos envolvidos nestes processos. Os óleos essenciais de bergamota, canela, capim limão, copaíba, eucalipto citriodora, eucalipto globulus, funcho, hortel...

Role of micro RNAs (miRs) involved in hemato lymphoid differentiation and malignancy: identification of novel miRs expressed in b-, t- lymphoid and hematopoietic cells

International Nuclear Information System (INIS)

Bronte, V.; Zanovello, P.; Dalla Favera, R.

2009-01-01

Total RNA from CD14+ cells (monocytes), CD15+ cells (polymorphonuclear cells), eosinophils, CD8+ T cells, resting and activated CD4+ T cells, two HTLV-1-infected cell lines (C91PL and MT-2), and different thymocyte populations was used as a source of small RNAs for the construction of miR cDNA libraries. In the initial phase of the study, sequences were identified after cloning cDNAs into a plasmid; to expedite this analysis, the cloning step has been replaced by direct 454 sequencing of uncloned cDNAs, carried out by Drs. G. DeBellis and A. Guffanti of the CNR, Istituto di Tecnologie Biomediche (Segrate-Milano). Resulting sequences are subjected to a series of bioinformatics analysis steps designed to identify known miRs (i.e., those catalogued in the Sanger miRBASE) and sequences that represent potential new miRs

Vozes femininas: trajetórias de sobreviventes do holocausto radicadas no Brasil (1933-1960)

OpenAIRE

Lilian Ferreira de Souza

2014-01-01

A partir do registro das narrativas orais sobre o Holocausto, pretendemos analisar um conjunto de testemunhos que expressem as trajetórias das mulheres judias sobreviventes do nazismo radicadas no Brasil entre 1933-1960. A historiografia sobre o tema revela que um grande número de mulheres judias foram perseguidas, torturadas e confinadas em guetos, campos de trabalho e de extermínio. No entanto, muito pouco se sabe sobre a trajetória daquelas que optaram por viver no Brasil. Suas histórias...

Desarrollo nuclear, condicionantes externos y acuerdos nucleares bilaterales: el caso de Argentina y Brasil

OpenAIRE

Quintanar, Silvia; Romegialli, Mónica

2007-01-01

Argentina y Brasil han sido países pioneros dentro del escenario latinoamericano en la investigación y desarrollo de tecnología nuclear. En el período anterior al advenimiento de las democracias, ambos países sostuvieron posiciones convergentes frente a los acuerdos mundiales, al mismo tiempo que rivalizaban en sus respectivos desarrollos en materia nuclear. Argentina era el país que tenía la vanguardia en el programa desarrollo nuclear. Las democracias reencontradas en Brasil y Argenti...

Spectrophotometry of RS Oph during the nebular phase

International Nuclear Information System (INIS)

Bohigas, J.; Echevarria, J.; Diego, F.; Sarmiento, J.A.

1989-01-01

Blue-wavelength spectroscopic observations of RS Oph, 201 day after the 1985 outburst are presented. An analysis of the TiO bands indicates a spectral type M4III for the secondary and a distance of 2 kpc to the system. The system of forbidden lines is excited by a shock wave, whereas Balmer emission is mainly produced by photoionization. The source of photons is probably residual thermonuclear burning occurring at the surface of the white dwarf. (author)

Dimensão verbo-visual de enunciados de Scientific American Brasil / Verbo-Visual Dimension in Utterances from Scientifc American Brasil

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Sheila Vieira de Camargo Grillo

2009-12-01

Full Text Available RESUMO: Os enunciados de divulgação científica caracterizam-se pelo diálogo de saberes da esfera científica com os de outras esferas. Entre as diferentes dimensões pertinentes à abordagem da divulgação científica, serão investigadas as relações entre as imagens e o texto, materializadas na parceria entre as ilustrações e o material verbal. O corpus da pesquisa é constituído por artigos da revista Scientific American Brasil no período entre 2002 e 2007. A análise focará os sentidos produzidos pela “ilustração síntese” de uma capa. ABSTRACT: The utterances of the scientific diffusion are characterized by the dialogue between the knowledge from the scientific sphere with the others spheres. It will be investigated the relationships between the images and the text, materialized in the partnership between illustrations and verbal material. The corpus of the research is formed by articles from the magazine Scientific American Brasil published from 2002 to 2007. The analyses willfocus the senses produced by the “synthetic illustration” in a cover.

Efisiensi Pendayagunaan Tempat Tidur dengan Metode Grafik BarberJohnson di Rs Lancang Kuning

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Edi Susilo

2012-05-01

Full Text Available Pendayagunaan tempat tidur di rumah sakit seharusnya efisien dari aspek ekonomi maupun aspek medis. Untuk menyatukan dua aspek tersebut maka diperlukan suatu parameter yang tepat, yaitu; BOR, AvLOS, TOI, dan BTO. Menyajikan keempat parameter tersebut dapat digunakan suatu metode yaitu grafik barber-johnson, dimana kita dapat melihat tingkat efisiensi pendayagunaan tempat tidur di rumah sakit dengan jelas dan keempat parameter dipertemukan dalam satu titik. Penelitian ini bertujuan untuk menilai tingkat efisiensi pendayagunaan tempat tidur di RS Lancang Kuning Pekanbaru tahun 2011. Penelitian ini menggunakan jenis penelitian deskriptif. Populasi penelitian ini adalah formulir (RP 1 dan RL 1 periode tahun 2011, pengambilan sampel dengan menggunakan teknik total sampling. Teknik pengumpulan data menggunakan observasi dan dokumentasi, analisis data dilakukan secara univariat. Dari hasil penelitian ditemukan bahwa pendayagunaan tempat tidur di RS Lancang Kuning Pekanbaru tahun 2011 dengan metode grafik BJ titik keempat parameter tidak bertemu pada satu titik melainkan terpisah 2 bagian, angka (AvLOS 8 hari dan TOI 11 hari sedangkan (BOR 50% dan BTO 15 kali. Hal ini kemungkinan disebabkan adanya kasalahan dalam sensus harian pasien rawat inap yang menjadi sumber data primer. Temuan ini diperkuat dengan tidak berjalannya sensus harian pasien rawat inap di RS Lancang Kuning Pekanbaru dengan baik. Selain itu, bila dilihat dari masing-masing titik parameter dalam grafik BJ berada di luar daerah efisien yang berarti menunjukan sistem yang berjalan kurang baik. Kesimpulan penelitian ini adalah bahwa pendayagunaan tempat tidur di RS Lancang Kuning Pekanbaru pada tahun 2011 masih kurang efisien. Disarankan agar pihak manajemen mengevaluasi akan kurangnya permintaan tempat tidur dan unit rekam medis agar menjalankan kegiatan sensus harian pasien rawat inap sesuai dengan ketentuan

(RS-Efonidipine acetone hemisolvate

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Yu-Heng Liu

2016-09-01

Full Text Available The asymmetric unit of the title compound, C34H38N3O7P·0.5C3H6O {systematic name: (RS-2-[phenyl(phenylmethylamino]ethyl 5-(5,5-dimethyl-2-oxo-1,3-dioxa-2λ5-phosphacyclohex-2-yl-2,6-dimethyl-4-(3-nitrophenyl-1,4-dihydropyridine-3-carboxylate acetone hemisolvate}, contains one R-efonidipine molecule, one S-efonidipine molecule and half of a solvate acetone molecule. In both efonidipine molecules, the six-membered rings of the dioxaphosphinanyl moieties display a chair conformation and the dihydropyridine rings display a flattened boat conformation. In the crystal, N—H...O, C—H...O hydrogen bonds and weak C—H...π interactions link the molecules into a three-dimensional supramolecular structure. A solvent-accessible void of 199 Å3 is found in the structure; the contribution of the heavily disordered solvate molecule was suppressed by use of the SQUEEZE routine in PLATON [Spek (2015. Acta Cryst. C71, 9–18].

Attention-deficit/hyperactivity disorder associated with KChIP1 rs1541665 in Kv channels accessory proteins.

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Fang-Fen Yuan

Full Text Available Attention-deficit/hyperactivity disorder (ADHD is an early onset childhood neurodevelopmental disorder with high heritability. A number of genetic risk factors and environment factors have been implicated in the pathogenesis of ADHD. Genes encoding for subtypes of voltage-dependent K channels (Kv and accessory proteins to these channels have been identified in genome-wide association studies (GWAS of ADHD. We conducted a two-stage case-control study to investigate the associations between five key genes (KChIP4, KChIP1, DPP10, FHIT, and KCNC1 and the risk of developing ADHD. In the discovery stage comprising 256 cases and 372 controls, KChIP1 rs1541665 and FHIT rs3772475 were identified; they were further genotyped in the validation stage containing 328cases and 431 controls.KChIP1 rs1541665 showed significant association with a risk of ADHD at both stages, with CC vs TT odds ratio (OR = 1.961, 95% confidence interval (CI = 1.366-2.497, in combined analyses (P-FDR = 0.007. Moreover, we also found rs1541665 involvement in ADHD-I subtype (OR (95% CI = 2.341(1.713, 3.282, and Hyperactive index score (P = 0.005 in combined samples.Intriguingly, gene-environmental interactions analysis consistently revealed the potential interactionsof rs1541665 collaboratingwith maternal stress pregnancy (Pmul = 0.021 and blood lead (Padd = 0.017 to modify ADHD risk. In conclusion, the current study provides evidence that genetic variants of Kv accessory proteins may contribute to the susceptibility of ADHD.Further studies with different ethnicitiesare warranted to produce definitive conclusions.

Association between SERPING1 rs2511989 polymorphism and age-related macular degeneration: Meta-analysis

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Yi Dong

2015-04-01

Full Text Available AIM: To investigate the association between SERPING1 rs2511989 (G>A polymorphism and age-related macular degeneration (AMD. METHODS: A number of electronic databases (up to July 15, 2014 were searched independently by two investigators. A Meta-analysis was performed on the association between SERPING1 rs2511989 polymorphism and AMD. Pooled odds ratios (ORs with 95% confidence intervals (CIs were estimated. RESULTS: Eight studies with 16 cohorts consisting of 9163 cases and 6813 controls were included in this Meta-analysis. There was no significant association between rs2511989 polymorphism and AMD under all genetic models in overall estimates (A vs G: OR= 0.938, 95%CI =0.858-1.025; AA vs GG:OR =0.871, 95%CI =0.719-1.056; AG vs GG: OR =0.944, 95%CI =0.845-1.054; AA+AG vs GG: OR =0.927, 95% CI =0.823-1.044; AA vs AG+GG: OR =0.890, 95%CI =0.780-1.034. Cumulative Meta-analyses also showed a trend of no association between rs2511989 polymorphism and AMD as information accumulated by year. Subgroup analysis and Meta-regression analysis indicated that age-matching status was the main source of heterogeneity. Sensitivity analysis found the results in overall comparisons and subgroup comparisons of white subjects under the allele model were found to have significantly statistical differences after studies deviating from Hardy-Weinberg equilibrium (HWE were excluded (overall: OR=0.918, 95%CI = 0.844-0.999, P =0.049; whites: OR =0.901, 95%CI = 0.817-0.994, P =0.038. However, the results were not sufficiently robust for further sensitivity analysis and statistical differences disappeared on applying Bonferroni correction (with a significance level set at 0.05/25. CONCLUSION: This Meta-analysis indicates that SERPING1 rs2511989 polymorphism and AMD tend to have no association with each other. Age matching status is a big confounding factor, and more studies with subtle designs are warranted in future.

Association of genetic polymorphisms CYP2A6*2 rs1801272 and CYP2A6*9 rs28399433 with tobacco-induced lung Cancer: case-control study in an Egyptian population.

Science.gov (United States)

Ezzeldin, Nada; El-Lebedy, Dalia; Darwish, Amira; El Bastawisy, Ahmed; Abd Elaziz, Shereen Hamdy; Hassan, Mirhane Mohamed; Saad-Hussein, Amal

2018-05-03

Several studies have reported the role of CYP2A6 genetic polymorphisms in smoking and lung cancer risk with some contradictory results in different populations. The purpose of the current study is to assess the contribution of the CYP2A6*2 rs1801272 and CYP2A6*9 rs28399433 gene polymorphisms and tobacco smoking in the risk of lung cancer in an Egyptian population. A case-control study was conducted on 150 lung cancer cases and 150 controls. All subjects were subjected to blood sampling for Extraction of genomic DNA and Genotyping of the CYP2A6 gene SNPs (CYP2A6*2 (1799 T > A) rs1801272 and CYP2A6*9 (- 48 T > G) rs28399433 by Real time PCR. AC and CC genotypes were detected in CYP2A6*9; and AT genotype in CYP2A6*2. The frequency of CYP2A6*2 and CYP2A6*9 were 0.7% and 3.7% respectively in the studied Egyptian population. All cancer cases with slow metabolizer variants were NSCLC. Non-smokers represented 71.4% of the CYP2A6 variants. There was no statistical significant association between risk of lung cancer, smoking habits, heaviness of smoking and the different polymorphisms of CYP2A6 genotypes. The frequency of slow metabolizers CYP2A6*2 and CYP2A6*9 are poor in the studied Egyptian population. Our findings did not suggest any association between CYP2A6 genotypes and risk of lung cancer.

FADS1 rs174549 Polymorphism May Predict a Favorable Response to Chemoradiotherapy in Oral Cancer Patients.

Science.gov (United States)

Chen, Fa; He, Baochang; Yan, Lingjun; Qiu, Yu; Lin, Lisong; Cai, Lin

2017-01-01

The fatty acid desaturase 1 (FADS1) gene variant is a novel susceptibility marker for laryngeal squamous cell carcinoma identified by a recent genome-wide association study, but it is still unclear whether this genetic variant continues to influence oral cancer recurrence or death. The purpose of this study was to evaluate the role of FADS1 rs174549 polymorphism and its interaction with postoperative chemoradiotherapy in the prognosis of oral cancer. A prospective cohort study involving 304 oral cancer patients with surgical resection was conducted in Fujian, China. Demographic and clinical data (adjuvant therapy types, histologic types, clinical stage, etc.) were extracted from medical records, and follow-up data were obtained by telephone interviews. We collected 5 to 8 mL of venous blood from all patients for DNA extraction, and rs174549 genotypes were determined by TaqMan assays (Life Technologies, Carlsbad, CA). A Cox proportional hazards model and Kaplan-Meier curve were used to assess the association between FADS1 rs174549 polymorphism and progression-free survival (PFS), as well as overall survival, in oral cancer. Carrying the AA genotype was significantly associated with a decreased risk of PFS: The hazard ratio was 0.52 (95% confidence interval, 0.29 to 0.93) for the codominant model and 0.54 (95% confidence interval, 0.31 to 0.94) for the recessive model. Moreover, better PFS was particularly obvious in patients who had received chemoradiotherapy. A positive multiplicative interaction between FADS1 rs174549 polymorphism and chemoradiotherapy was observed for PFS (P = .036). No significant association was found between FADS1 rs174549 polymorphism and overall survival. Our study suggests, for the first time, that FADS1 rs174549 polymorphism is a potentially independent and favorable factor in predicting oral cancer PFS especially for patients who undergo chemoradiotherapy, and it may serve as a potential target for individualized treatment in the future

Glypican-4 gene polymorphism (rs1048369) and susceptibility to Epstein-Barr virus-associated and -negative gastric carcinoma.

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Zhao, Danrui; Liu, Shuzhen; Sun, Lingling; Zhao, Zhenzhen; Liu, Song; Kuang, Xiaojing; Shu, Jun; Luo, Bing

2016-07-15

Gastric cancer (GC) is one of the most common malignant tumors in China and single nucleotide polymorphisms (SNPs) have been found to be highly related to GC carcinogenesis. Glypican-4 (GPC4), a member of the heparan sulphate proteoglycan family, plays an important role in the regulation of cell growth and differentiation. However, little is known about polymorphisms of GPC4 gene and their associated susceptibility to GC, especially to Epstein-Barr virus-associated GC (EBVaGC). Here we studied the GPC4 polymorphism (rs1048369) in GC individuals, especially those with EBVaGC, and we explored an association between the GPC4 gene polymorphism (rs1048369) and susceptibility to EBVaGC and Epstein-Barr virus-negative GC (EBVnGC) in a population from Northern China. The GPC4 gene polymorphism (rs1048369) was detected in 54 cases of EBVaGC and 73 cases of EBVnGC using polymerase chain reaction (PCR). One hundred and seven peripheral blood samples from healthy individuals were also measured as a control group. There were significant differences in both the genotype and allelic frequency of GPC4 gene (rs1048369) between the EBVaGC and EBVnGC patients. Meanwhile, the distribution of genotype and allelic frequency of GPC4 (rs1048369) differed between EBVaGC and control groups. Distribution of the GPC4 genotype also revealed differences between EBVnGC and control groups, no significant differences in the allelic frequency of the GPC4 gene (rs1048369) were observed. The frequency of the T allele in EBVaGC group was significantly higher than that in control and EBVnGC groups. The GPC4 gene polymorphism and the allele of GPC4 are both associated with susceptibility to EBVaGC. The T allele of GPC4 may represent a risk factor for EBVaGC. Copyright © 2016 Elsevier B.V. All rights reserved.

The association between the polymorphism rs2231142 in the ABCG2 gene and gout risk: a meta-analysis.

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Lv, Xiaofei; Zhang, Yuan; Zeng, Fangfang; Yin, Aihua; Ye, Ning; Ouyang, Haimei; Feng, Dan; Li, Dan; Ling, Wenhua; Zhang, Xiaozhuang

2014-12-01

Gout is a common metabolic disorder with high heritability. We tried to explore the association between rs2231142 and gout. We searched "rs2231142 or Q141K and gout" in four databases and scholar searching website until 1 June, 2013 and included data from 52,010 participants in meta-analysis and subgroup analysis. The T allele of rs2231142 was associated with increased gout susceptibility (odds ratio [OR] [95 % confidence interval (95 % CI)] = 1.73 [1.55-1.91], P gout risk in Caucasians with OR (95 % CI) = 1.68 (1.50-1.87), P gout.

Assessing the search for information on Three Rs methods, and their subsequent implementation: a national survey among scientists in the Netherlands.

Science.gov (United States)

van Luijk, Judith; Cuijpers, Yvonne; van der Vaart, Lilian; Leenaars, Marlies; Ritskes-Hoitinga, Merel

2011-10-01

A local survey conducted among scientists into the current practice of searching for information on Three Rs (i.e. Replacement, Reduction and Refinement) methods has highlighted the gap between the statutory requirement to apply Three Rs methods and the lack of criteria to search for them. To verify these findings on a national level, we conducted a survey among scientists throughout The Netherlands. Due to the low response rate, the results give an impression of opinions, rather than being representative of The Netherlands as a whole. The findings of both surveys complement each other, and indicate that there is room for improvement. Scientists perceive searching the literature for information on Three Rs methods to be a difficult task, and specific Three Rs search skills and knowledge of Three Rs databases are limited. Rather than using a literature search, many researchers obtain information on these methods through personal communication, which means that published information on possible Three Rs methods often remains unfound and unused. A solution might be to move beyond the direct search for information on Three Rs methods and choose another approach. One approach that seems rather appropriate is that of systematic review. This provides insight into the necessity for any new animal studies, as well as optimal implementation of available data and the prevention of unnecessary animal use in the future. 2011 FRAME.

Disentangling Gratitude: A Theoretical and Psychometric Examination of the Gratitude Resentment and Appreciation Test-Revised Short (GRAT-RS).

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Hammer, Joseph H; Brenner, Rachel E

2017-07-14

This study extended our theoretical and applied understanding of gratitude through a psychometric examination of the most popular multidimensional measure of gratitude, the Gratitude, Resentment, and Appreciation Test-Revised Short form (GRAT-RS). Namely, the dimensionality of the GRAT-RS, the model-based reliability of the GRAT-RS total score and 3 subscale scores, and the incremental evidence of validity for its latent factors were assessed. Dimensionality measures (e.g., explained common variance) and confirmatory factor analysis results with 426 community adults indicated that the GRAT-RS conformed to a multidimensional (bifactor) structure. Model-based reliability measures (e.g., omega hierarchical) provided support for the future use of the Lack of a Sense of Deprivation raw subscale score, but not for the raw GRAT-RS total score, Simple Appreciation subscale score, or Appreciation of Others subscale score. Structural equation modeling results indicated that only the general gratitude factor and the lack of a sense of deprivation specific factor accounted for significant variance in life satisfaction, positive affect, and distress. These findings support the 3 pillars of gratitude conceptualization of gratitude over competing conceptualizations, the position that the specific forms of gratitude are theoretically distinct, and the argument that appreciation is distinct from the superordinate construct of gratitude.

Revisiting the impact of OXTR rs53576 on empathy: A population-based study and a meta-analysis.

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Gong, Pingyuan; Fan, Huiyong; Liu, Jinting; Yang, Xing; Zhang, Kejin; Zhou, Xiaolin

2017-06-01

Oxytocin in the brain is related to empathy, which refers to the ability to understand and share others' internal states or responses. Previous studies have investigated the impact of OXTR rs53576, the most intensively examined polymorphism in the oxytocin receptor (OXTR) gene, on individual differences in empathy. However, these studies produced inconsistent results. In the current study, we reexamined the association of OXTR rs53576 with empathy in a relatively large population (N=1830) and also evaluated the association by a comprehensive meta-analysis (N=6631, 13 independent samples). The replication study indicated that OXTR rs53576 was indeed associated with individual differences in empathy. Individuals with a greater number of G alleles showed better empathic ability, particularly in fantasizing other's feelings and actions. The meta-analysis not only confirmed this association, but also indicated that the impact of this polymorphism was significant in both Europeans and Asians. These findings provide convincing evidence for the impact of OXTR rs53576 on empathy, highlighting the importance of OXTR gene in individuals' social cognition. Copyright © 2017. Published by Elsevier Ltd.

The rs3857059 variant of the SNCA gene is associated with Parkinson’s disease in Mexican Mestizos

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S. García

2016-06-01

Full Text Available ABSTRACT Among the candidate genes for Parkinson’s disease (PD, SNCA has replicated association in different populations. Besides other known mutations in the SNCA gene, the rs3857059 variant has also been linked to various neurodegenerative disorders. Therefore, the aim of the present study was to search for association of this variant and sporadic PD in Mexican Mestizo patients. A case-control study was performed including 241 individuals, 106 patients, and 135 healthy controls. Genotyping was performed using real-time PCR. The rs3857059 variant demonstrated an association with PD in Mexican Mestizos (OR = 2.40, CI, 1.1 to 5.1, p = 0.02 under the recessive model. In addition, a gender effect was found for the GG genotype in females (OR = 1.31, CI, 1.01 to 1.7, p = 0.037. This is the first study to confirm an association of the rs3857059 variant with PD and also to show a gender effect. Our data contribute to the elucidation of the link between rs3857059 and susceptibility to PD observed in the Mexican Mestizo population.

Proteomic analysis of a high aluminum tolerant yeast Rhodotorula taiwanensis RS1 in response to aluminum stress.

Science.gov (United States)

Wang, Chao; Wang, Chang Yi; Zhao, Xue Qiang; Chen, Rong Fu; Lan, Ping; Shen, Ren Fang

2013-10-01

Rhodotorula taiwanensis RS1 is a high-aluminum (Al)-tolerant yeast that can survive in Al concentrations up to 200mM. The mechanisms for the high Al tolerance of R. taiwanensis RS1 are not well understood. To investigate the molecular mechanisms underlying Al tolerance and toxicity in R. taiwanensis RS1, Al toxicity-induced changes in the total soluble protein profile were analyzed using two-dimensional gel electrophoresis (2-DE) coupled with mass spectrometry. A total of 33 differentially expressed proteins responding to Al stress were identified from approximately 850 reproducibly detected proteins. Among them, the abundance of 29 proteins decreased and 4 increased. In the presence of 100mM Al, the abundance of proteins involved in DNA transcription, protein translation, DNA defense, Golgi functions and glucose metabolism was decreased. By contrast, Al treatment led to increased abundance of malate dehydrogenase, which correlated with increased malate dehydrogenase activity and the accumulation of intracellular citrate, suggesting that Al-induced intracellular citrate could play an important role in detoxification of Al in R. taiwanensis RS1. © 2013.

Paleoparasitologia no Brasil

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Marcelo L. C. Gonçalves

Full Text Available Neste artigo faz-se uma revisão sobre o início da paleoparasitologia no Brasil e seu desenvolvimento. A pesquisa de parasitos em vestígios humanos pode trazer informações sobre questões tais como a origem e antiguidade da relação parasito-hospedeiro, distribuição de parasitos através do tempo e migrações humanas pré-históricas. O estudo de seqüências de ADN de parasitos encontrados em tecidos mumificados e coprólitos pode ser uma importante fonte de informação para filogenia e co-evolução parasito-hospedeiro. A análise de ácidos nucléicos de parasitos encontrados em material arqueológico (paleoparasitologia molecular abre novas perspectivas para estudos sobre evolução ao nível molecular.

LA TECNOLOGÍA DE LA INFORMACIÓN COMO FACTOR COMPETITIVO: UN ESTUDIO EN EL APL COSECHA METAL-MECÁNICO SANTA ROSA/HORIZONTINA, RS, BRASIL

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Graniel, Gilmar J.

2011-06-01

Full Text Available El presente artículo aborda la utilización de la Tecnología de la Información (TI como factor competitivo en un Arreglo Productivo Local (APL Cosecha Metal-Mecánica en el estado de Río Grande del Sur, Brasil y tiene como objetivo buscar la comprensión de como el uso de la TI contribuye al aumento de la competitividad. Para alcanzar este objetivo, fue realizada una investigación en las empresas que componen el APL. Los resultados de la investigación indicaron que las empresas perciben la importancia del uso de la TI, pero que, en la práctica, su utilización es limitada, sobre todo tratándose de la planificación de la TI. Otro de los resultados que se encontró es que las empresas, aunque formen parte del APL, aún no colaboran entre sí, ya sea a través del cambio de informaciones, o a través de Sistemas de Información. Las principales recomendaciones ante estos resultados es que las empresas traten de actuar activamente para el fortalecimiento del APL. En lo que se refiere al uso de la TI se hace necesaria la planificación y la inversión en la adquisición de sistemas integrados para la mejor gerencia de las informaciones, lo cual contribuirá al aumento de la competitividad de las empresas que pertenecen al arreglo.

The TT genotype of the rs6860 polymorphism of the charged multivesicular body protein 1A gene is associated with susceptibility to fibromyalgia in southern Spanish women

NARCIS (Netherlands)

Estévez-López, Fernando; Aparicio, Virginia A; Ruiz, Jonatan R; Martínez-González, Luis J; Delgado-Fernández, Manuel; Álvarez-Cubero, María J

In 2012, Barbosa et al. analysed the association between the genotype frequencies of the rs4680 and rs4818 polymorphisms of the catechol-O-methyltransferase (COMT) gene. Of note is that, in the abstract, they mentioned the rs6860 polymorphism when it should have been rs4680. Indeed, the rs6860

Repositórios institucionais de acesso livre no Brasil: estudo Delfos

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Ernani Rufino dos Santos Junior

2015-06-01

Full Text Available A filosofia do acesso livre ao conhecimento científico surgiu da dificuldade das bibliotecas universitárias de todo mundo em manter atualizadas as assinaturas das coleções de periódicos científicos. Os repositórios institucionais são uma das ferramentas que se mostram como alternativa para a comunicação da Ciência livre de barreiras de acesso. A pesquisa tem por objetivo verificar quais são as perspectivas futuras das atuais políticas de implementação de repositórios institucionais de acesso livre no Brasil na opinião de especialistas na área, tendo como base a análise do estado da arte das implementações de Repositórios Institucionais no Brasil. Neste trabalho, a pesquisa é dividida em três etapas: a primeira consiste na coleta de dados descritivos dos repositórios institucionais da Universidade de Brasília (RIUnB e do Superior Tribunal de Justiça (BDJur-STJ; já na segunda etapa de pesquisa, procede-se à consulta aos especialistas indagando-os acerca da situação atual das implementações de repositórios institucionais no Brasil; e, por fim, na terceira etapa de pesquisa consultamos estes mesmos especialistas sobre os desdobramentos futuros destas políticas no País. Utilizamos da técnica Delfos de pesquisa, onde os especialistas são consultados através de questionários constituídos de perguntas abertas, possibilitando assim chegar a um consenso das opiniões no final da pesquisa. Como resultado da pesquisa, é elaborado um quadro com a tabulação das respostas dos especialistas consultados revelando o panorama das perspectivas futuras das implementações de repositórios institucionais no Brasil na opinião dos especialistas que fazem parte da nossa amostra de pesquisa.

Universidade, sociedade e território no Brasil: Um estudo de caso na Bahia

OpenAIRE

da Silva Brito, Marialda

2013-01-01

Esta investigación aborda la relación de la universidad con la sociedad y el territorio en Brasil y, particularmente, en el estado de Bahía. Concretamente son estudiados algunos condicionantes socio-territoriales a fin de comprobar sus relaciones con el surgimiento de esas instituciones de enseñanza superior y, al mismo tiempo, también son observadas las influencias de ellas sobre el desarrollo territorial. La metodología para investigar esta realidad dirigida al Brasil y Bahía, ha seguido pr...

Genotyping Rs2274625 Marker in NPHS2 Gene Associated with Nephrotic Syndrome in Isfahan Population