How theories became knowledge: Morgan's chromosome theory of heredity in America and Britain.

Science.gov (United States)

Brush, Stephen G

2002-01-01

T. H. Morgan, A. H. Sturtevant, H. J. Muller and C. B. Bridges published their comprehensive treatise The Mechanism of Mendelian Heredity in 1915. By 1920 Morgan's "Chromosome Theory of Heredity" was generally accepted by geneticists in the United States, and by British geneticists by 1925. By 1930 it had been incorporated into most general biology, botany, and zoology textbooks as established knowledge. In this paper, I examine the reasons why it was accepted as part of a series of comparative studies of theory-acceptance in the sciences. In this context it is of interest to look at the persuasiveness of confirmed novel predictions, a factor often regarded by philosophers of science as the most important way to justify a theory. Here it turns out to play a role in the decision of some geneticists to accept the theory, but is generally less important than the CTH's ability to explain Mendelian inheritance, sex-linked inheritance, non-disjunction, and the connection between linkage groups and the number of chromosome pairs; in other words, to establish a firm connection between genetics and cytology. It is remarkable that geneticists were willing to accept the CTH as applicable to all organisms at a time when it had been confirmed only for Drosophila. The construction of maps showing the location on the chromosomes of genes for specific characters was especially convincing for non-geneticists.

Heredity of acne in Korean patients.

Science.gov (United States)

Cho, Eun Byul; Ha, Ji Min; Park, Eun Joo; Kim, Kwang Ho; Kim, Kwang Joong

2014-10-01

Acne is a chronic inflammatory disease of the pilocebaceous unit that presents with various spectrum and severity. Genetic backgrounds and environmental factors are also considered to be relevant, but few studies have focused on Korean patients. A cross-sectional epidemiologic study on family history of Korean acne patients was performed to analyze family history of acne, and to compare the severity and characteristics of acne in association with family history. A total of 221 patients were enrolled, 98 male (44.3%) and 123 female (55.7%). Patients were grouped as patients with (A+) or without (A-) family history of acne. In a second analysis, patients with any experience of acne treatment were evaluated. Severity of acne was measured with Burton's grading system and Korean Acne Grading System (KAGS). Female patients had a higher tendency to have family history than males (P = 0.002). Group A+ had statistically significant earlier onset of acne (P = 0.002). In inexperienced patients, patients with family history showed a relatively earlier onset (P = 0.084). This study confirmed the role of heredity in acne. Family history of acne is associated with earlier onset of the disease, and more non-inflammatory lesions. © 2014 Japanese Dermatological Association.

The history of genetics in Mexico in the light of A Cultural History of Heredity.

Science.gov (United States)

Barahona, Ana

2013-01-01

In this paper I analyze the conditions for scientific research and the social relationships that allowed the establishment of genetics in Mexico, in the laboratory, the clinic and in agronomy. I give three examples to illustrate how the cultural history of heredity has enlightened this work: the introduction and institutionalization of Mendelism in Mexico, the hereditarian ideas of medical doctors in the late nineteenth century, and the introduction of medical genetics in Mexico.

Structural heredity influence upon principles of strain wave hardening

Science.gov (United States)

Kiricheck, A. V.; Barinov, S. V.; Yashin, A. V.

2017-02-01

It was established experimentally that by penetration of a strain wave through material hardened not only the technological modes of processing, but also a technological heredity - the direction of the fibers of the original macrostructure have an influence upon the diagram of microhardness. By penetration of the strain wave along fibers, the degree of hardening the material is less, however, a product is hardened throughout its entire section mainly along fibers. In the direction of the strain waves across fibers of the original structure of material, the degree of material hardening is much higher, the depth of the hardened layer with the degree of hardening not less than 50% makes at least 3 mm. It was found that under certain conditions the strain wave can completely change the original structure of the material. Thus, a heterogeneously hardened structure characterized by the interchange of harder and more viscous areas is formed, which is beneficial for assurance of high operational properties of material.

Exploring podcasting in heredity and evolution teaching.

Science.gov (United States)

Almeida-Aguiar, Cristina; Carvalho, Ana Amélia

2016-09-10

Podcasts are digital files very popular in several and very distinct areas. In higher education, they have been explored in a multitude of ways mainly to support teaching and learning processes. The study here described focuses the integration of podcasts in Heredity and Evolution, a course from the Biology and Geology Degree Program at University of Minho, Portugal. It aimed to introduce podcasts in the teaching/learning context, to empirically study different dimensions of podcasting, and to evaluate students' acceptance and receptiveness to the pedagogical use of this technology. Five informative podcasts and three with feedback were produced and delivered. All the students listened to the audio files and considered the episodes audible and clear, their preference going to episodes of short or moderate length and containing summaries, study guidelines or syllabus contents. Students judged extremely valuable the integration of this technology in learning and showed receptiveness to podcasting in other courses. Curiously, in spite of owning mobile devices, students clearly favored the use of personal computers to listen to the podcasts. This student acceptance and openness to podcasting has been encouraging its pedagogical application in other teaching courses. The episodes produced often maintain the characteristics identified as the best by the students of this study but the pedagogical approach has been moving to a more student-centered learning situation, with students as podcasts producers. © 2016 by The International Union of Biochemistry and Molecular Biology, 44(5):429-432, 2016. © 2016 The International Union of Biochemistry and Molecular Biology.

Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphism

DEFF Research Database (Denmark)

Rao, Fangwen; Wessel, Jennifer; Wen, Gen

2007-01-01

biosynthesis (tyrosine hydroxylase), catabolism (monoamine oxidase A), storage/release (chromogranin A), receptor target (dopamine D1 receptor), and postreceptor signal transduction (sorting nexin 13 and rho kinase). Epistasis (gene-by-gene interaction) occurred between alleles at rho kinase, tyrosine...... hydroxylase, chromogranin A, and sorting nexin 13. Dopamine D1 receptor polymorphism showed pleiotropic effects on both albumin and dopamine excretion. These studies establish new roles for heredity and environment in albumin excretion. Urinary excretions of albumin and catecholamines are highly heritable......, and their parallel suggests adrenergic mediation of early glomerular permeability alterations. Albumin excretion is influenced by multiple adrenergic pathway genes and is, thus, polygenic. Such functional links between adrenergic activity and glomerular injury suggest novel approaches to its prediction, prevention...

Scaffolding as an effort for thinking process optimization on heredity

Science.gov (United States)

Azizah, N. R.; Masykuri, M.; Prayitno, B. A.

2018-04-01

Thinking is an activity and process of manipulating and transforming data or information into memory. Thinking process is different between one and other person. Thinking process can be developed by interaction between student and their environment, such as scaffolding. Given scaffolding is based on each student necessity. There are 2 level on scaffolding such as explaining, reviewing, and restructuring; and developing conceptual thinking. This research is aimed to describe student’s thinking process on heredity especially on inheritance that is before and after scaffolding. This research used descriptive qualitative method. There were three kinds of subject degree such as the students with high, middle, and low achieving students. The result showed that subjects had some difficulty in dihybrid inheritance question in different place. Most difficulty was on determining the number of different characteristic, parental genotype, gamete, and ratio of genotype and phenotype F2. Based on discussed during scaffolding showed that the subjects have some misunderstanding terms and difficulty to determine parental, gamete, genotype, and phenotype. Final result in this research showed that the subjects develop thinking process higher after scaffolding. Therefore the subjects can solve question properly.

Floral pipe: length in Petunia x hybrida heredability, number of genes and the interaction of the date with the character

OpenAIRE

Fatta, N.; Vazquez, M.; García, N.; Mascarini, A.; Grigioni, G.

2007-01-01

Petunia x hybrida, a floral summer of a economical importance in Buenos Aires, is nowadays produced with imported seed. The research presented is focused on the study of the feasibility to obtain locally competitive seed. The length of the floral pipe is a relevant character so the assay was designed in order to estimate the heredability, the number of genes intervener and the interactions with the date. The assay began with a F1 purchased from United States. In 2003, the F1 and F2 were sowed...

Heredity of flake- and stripe-variegated traits and their introduction into Japanese day-neutral winter-flowering sweet pea (Lathyrus odoratus L.) cultivars.

Science.gov (United States)

Yagishita, Yoshimi; Hara, Yasuhide; Nakayama, Masayoshi

2018-01-01

Sweet pea ( Lathyrus odoratus L.) is a major cut flower in Japan, generally grown in greenhouses in winter to spring. The wild-type sweet pea is a long-day summer-flowering plant. The day-neutral winter-flowering ability, which allows cut-flower production in Japan, is a recessive phenotype that emerged by spontaneous mutation. Although Japanese winter-flowering cultivars and additionally spring-flowering cultivars, which have semi-long-day flowering ability generated by crossing the winter- and summer-flowering cultivars, have superior phenotypes for cut flowers, they have limited variation in color and fragrance. In particular, variegated phenotypes do not appear in modern winter- and spring-flowering cultivars, only in summer-flowering cultivars. We try to expand the phenotypic diversity of Japanese cut flower cultivars. In the processes, we introduced the variegated phenotypes by crossing with summer-flowering cultivars, and succeeded in breeding some excellent cultivars. During breeding, we analyzed the segregation ratios and revealed the heredity of the phenotypes. Here we review the heredity of these variegated phenotypes and winter-flowering phenotypes and their related genes. We also describe how we introduced the trait into winter-flowering cultivars, tracing their pedigrees to show both phenotypes and genotypes of the progeny at each generation. This knowledge is useful for the efficient breeding of new variegated cultivars.

An improved sheep flock heredity algorithm for job shop scheduling and flow shop scheduling problems

Directory of Open Access Journals (Sweden)

Chandramouli Anandaraman

2011-10-01

Full Text Available Job Shop Scheduling Problem (JSSP and Flow Shop Scheduling Problem (FSSP are strong NP-complete combinatorial optimization problems among class of typical production scheduling problems. An improved Sheep Flock Heredity Algorithm (ISFHA is proposed in this paper to find a schedule of operations that can minimize makespan. In ISFHA, the pairwise mutation operation is replaced by a single point mutation process with a probabilistic property which guarantees the feasibility of the solutions in the local search domain. A Robust-Replace (R-R heuristic is introduced in place of chromosomal crossover to enhance the global search and to improve the convergence. The R-R heuristic is found to enhance the exploring potential of the algorithm and enrich the diversity of neighborhoods. Experimental results reveal the effectiveness of the proposed algorithm, whose optimization performance is markedly superior to that of genetic algorithms and is comparable to the best results reported in the literature.

Early colonization with a group of Lactobacilli decreases the risk for allergy at five years of age despite allergic heredity.

Directory of Open Access Journals (Sweden)

Maria A Johansson

Full Text Available BACKGROUND: Microbial deprivation early in life can potentially influence immune mediated disease development such as allergy. The aims of this study were to investigate the influence of parental allergy on the infant gut colonization and associations between infant gut microbiota and allergic disease at five years of age. METHODS AND FINDINGS: Fecal samples were collected from 58 infants, with allergic or non-allergic parents respectively, at one and two weeks as well as at one, two and twelve months of life. DNA was extracted from the fecal samples and Real time PCR, using species-specific primers, was used for detection of Bifidobacterium (B. adolescentis, B. breve, B. bifidum, Clostridium (C. difficile, a group of Lactobacilli (Lactobacillus (L. casei, L. paracasei and L. rhamnosus as well as Staphylococcus (S. aureus. Infants with non-allergic parents were more frequently colonized by Lactobacilli compared to infants with allergic parents (p = 0.014. However, non-allergic five-year olds acquired Lactobacilli more frequently during their first weeks of life, than their allergic counterparts, irrespectively of parental allergy (p = 0.009, p = 0.028. Further the non-allergic children were colonized with Lactobacilli on more occasions during the first two months of life (p = 0.038. Also, significantly more non-allergic children were colonized with B. bifidum at one week of age than the children allergic at five years (p = 0.048. CONCLUSION: In this study we show that heredity for allergy has an impact on the gut microbiota in infants but also that early Lactobacilli (L. casei, L. paracasei, L. rhamnosus colonization seems to decrease the risk for allergy at five years of age despite allergic heredity.

At issue: siblings of patients with schizophrenia: sibling bond, coping patterns, and fear of possible schizophrenia heredity.

Science.gov (United States)

Stålberg, Gabriella; Ekerwald, Hedvig; Hultman, Christina M

2004-01-01

Siblings of schizophrenia patients are from the patient's perspective important support providers, but most studies on family burden have focused on the parental role. This study aims to develop a detailed analysis of the psychological aspects of having a sibling with schizophrenia. We did a qualitative study with audiotaped semistructured interviews of 16 siblings. The reliability of the inductive categorization of data was high. A unifying theme appeared to be an emotional sibling bond characterized by feelings of love, sorrow, anger, envy, guilt, and shame. The major categories linked to coping with the situation were avoidance, isolation, normalization, caregiving, and grieving. A third major theme consisted of a fear of possible schizophrenia heredity. The siblings described concerns about the impact of a family history of psychiatric illness, a fear of becoming mentally ill, and reflections about "bad genes." Our findings support earlier findings of coping patterns but complement them by providing a model that includes awareness of genetic vulnerability as an important part of siblings' subjective burden.

[Summary of results of a study of heredity of intelligence in a sample of the Czech population. III. Longitudinal and genealogic study of twins and their families].

Science.gov (United States)

Drábková, H

1993-06-01

The author presents further results of the longitudinal study of inheritance of intelligence, its components and structure in twins. Summarized results are presented for the age period from 0-15 years as well as detailed results of individual components and the global IQ in the age group of 8-15 years. The paper follows after two previous ones published in 1988 where the applied methods and statistical evaluation were described. Evidence was provided that heredity of intelligence is involved in children from a very early age, i.e. 0-3 years. After the age of 4 heredity predominates markedly over environmental influences up to the age of 15 years investigated so far by the author. (A slight decline occurs during the prepubertal period-age 13 and 14 years.) The author found that in particular the following components of intellect are inborn: abstract thinking, logic, talent for mathematics, concentration, inquisitiveness. Very detailed tables are presented for possible comparison with data in the literature and data from adults. The author found that the development of intelligence from childhood to adult age is very irregular. This uneven character is also mostly inborn. Statistical evaluation revealed several basic types of developmental curves and extreme variants. This will, however, be discussed in another paper. The theoretical results can be used also in practice in school education, counselling psychologic and psychiatric out-patient departments.

The Contributions - and Collapse - of Lamarckian Heredity in Pasteurian Molecular Biology: 1. Lysogeny, 1900-1960.

Science.gov (United States)

Loison, Laurent; Gayon, Jean; Burian, Richard M

2017-02-01

This article shows how Lamarckism was essential in the birth of the French school of molecular biology. We argue that the concept of inheritance of acquired characters positively shaped debates surrounding bacteriophagy and lysogeny in the Pasteurian tradition during the interwar period. During this period the typical Lamarckian account of heredity treated it as the continuation of protoplasmic physiology in daughter cells. Félix d'Hérelle applied this conception to argue that there was only one species of bacteriophage and Jules Bordet applied it to develop an account of bacteriophagy as a transmissible form of autolysis and to analyze the new phenomenon of lysogeny. In a long-standing controversy with Bordet, Eugène Wollman deployed a more morphological understanding of the inheritance of acquired characters, yielding a particulate, but still Lamarckian, account of lysogeny. We then turn to André Lwoff who, with several colleagues, completed Wollman's research program from 1949 to 1953. We examine how he gradually set aside the Lamarckian background, finally removing inheritance of acquired characters from the resulting account of bacteriophagy and lysogeny. In the conclusion, we emphasize the complex dual role of Lamarckism as it moved from an assumed explanatory framework to a challenge that the nascent molecular biology had to overcome.

H3ABioNet, a sustainable pan-African bioinformatics network for human heredity and health in Africa

Science.gov (United States)

Mulder, Nicola J.; Adebiyi, Ezekiel; Alami, Raouf; Benkahla, Alia; Brandful, James; Doumbia, Seydou; Everett, Dean; Fadlelmola, Faisal M.; Gaboun, Fatima; Gaseitsiwe, Simani; Ghazal, Hassan; Hazelhurst, Scott; Hide, Winston; Ibrahimi, Azeddine; Jaufeerally Fakim, Yasmina; Jongeneel, C. Victor; Joubert, Fourie; Kassim, Samar; Kayondo, Jonathan; Kumuthini, Judit; Lyantagaye, Sylvester; Makani, Julie; Mansour Alzohairy, Ahmed; Masiga, Daniel; Moussa, Ahmed; Nash, Oyekanmi; Ouwe Missi Oukem-Boyer, Odile; Owusu-Dabo, Ellis; Panji, Sumir; Patterton, Hugh; Radouani, Fouzia; Sadki, Khalid; Seghrouchni, Fouad; Tastan Bishop, Özlem; Tiffin, Nicki; Ulenga, Nzovu

2016-01-01

The application of genomics technologies to medicine and biomedical research is increasing in popularity, made possible by new high-throughput genotyping and sequencing technologies and improved data analysis capabilities. Some of the greatest genetic diversity among humans, animals, plants, and microbiota occurs in Africa, yet genomic research outputs from the continent are limited. The Human Heredity and Health in Africa (H3Africa) initiative was established to drive the development of genomic research for human health in Africa, and through recognition of the critical role of bioinformatics in this process, spurred the establishment of H3ABioNet, a pan-African bioinformatics network for H3Africa. The limitations in bioinformatics capacity on the continent have been a major contributory factor to the lack of notable outputs in high-throughput biology research. Although pockets of high-quality bioinformatics teams have existed previously, the majority of research institutions lack experienced faculty who can train and supervise bioinformatics students. H3ABioNet aims to address this dire need, specifically in the area of human genetics and genomics, but knock-on effects are ensuring this extends to other areas of bioinformatics. Here, we describe the emergence of genomics research and the development of bioinformatics in Africa through H3ABioNet. PMID:26627985

Human Heredity and Health (H3) in Africa Kidney Disease Research Network: A Focus on Methods in Sub-Saharan Africa.

Science.gov (United States)

Osafo, Charlotte; Raji, Yemi Raheem; Burke, David; Tayo, Bamidele O; Tiffin, Nicki; Moxey-Mims, Marva M; Rasooly, Rebekah S; Kimmel, Paul L; Ojo, Akinlolu; Adu, Dwomoa; Parekh, Rulan S

2015-12-07

CKD affects an estimated 14% of adults in sub-Saharan Africa, but very little research has been done on the cause, progression, and prevention of CKD there. As part of the Human Heredity and Health in Africa (H3Africa) Consortium, the H3Africa Kidney Disease Research Network was established to study prevalent forms of kidney disease in sub-Saharan Africa and increase the capacity for genetics and genomics research. The study is performing comprehensive phenotypic characterization and analyzing environmental and genetic factors from nine clinical centers in four African countries (Ghana, Nigeria, Ethiopia, and Kenya) over a 5-year period. Approximately 4000 participants with specified kidney disease diagnoses and 4000 control participants will be enrolled in the four African countries. In addition, approximately 50 families with hereditary glomerular disease will be enrolled. The study includes both pediatric and adult participants age research infrastructure can be successfully established in Africa. This study will provide clinical, biochemical, and genotypic data that will greatly increase the understanding of CKD in sub-Saharan Africa. Copyright © 2015 by the American Society of Nephrology.

Prevalence and management of familial hypercholesterolemia in patients with coronary artery disease: The heredity survey.

Science.gov (United States)

Faggiano, Pompilio; Pirillo, Angela; Griffo, Raffaele; Ambrosetti, Marco; Pedretti, Roberto; Scorcu, Giampaolo; Werren, Marika; Febo, Oreste; Malfatto, Gabriella; Favretto, Giuseppe; Sarullo, Filippo; Antonini-Canterin, Francesco; Zobbi, Gianni; Temporelli, Pierluigi; Catapano, Alberico L

2018-02-01

Familial hypercholesterolemia (FH) is a genetic disorder characterized by high levels of low density lipoprotein cholesterol (LDL-C) predisposing to premature cardiovascular disease. Its prevalence varies and has been estimated around 1 in 200-500. The Heredity survey evaluated the prevalence of potential FH and the therapeutic approaches among patients with established coronary artery disease (CAD) or peripheral artery disease (PAD) in which it is less well documented. Data were collected in patients admitted to programs of rehabilitation and secondary prevention in Italy. Potential FH was estimated using Dutch Lipid Clinic Network (DLCN) criteria. Potential FH was defined as having a total score≥6. Among the 1438 consecutive patients evaluated, the prevalence of potential FH was 3.7%. The prevalence was inversely related to age, with a putative prevalence of 1:10 in those with Definite FH (DLCN score>8) had the highest percentages of patients after an ACS (75% vs 52.5% in the whole study population). At discharge, most patients were on high intensity statin therapy, but despite this, potential FH group still had a higher percentage of patients with LDL-C levels not at target and having a distance from the target higher than 50%. Among patients with established coronary heart disease, the prevalence of potential FH is higher than in the general population; the results suggest that a correct identification of potential FH, especially in younger patients, may help to better manage their high cardiovascular risk. Copyright © 2017 Elsevier Ireland Ltd. All rights reserved.

Genetik og hypertension

DEFF Research Database (Denmark)

Ellervik, Christina; Tarnow, Lisa; Pedersen, Erling Bjerregaard

2009-01-01

Monogenic forms of hypertension are very rare, but have a well-characterized heredity. Primary hypertension is very common with a complex and polygenic heredity. Primary hypertension arises due to an interaction between multiple genetic and environmental factors. Its heredity is unknown, although...

El concurso de la Académie Royale de Médecine de Paris, 1843: Análisis contextual de la emergencia de los primeros trabajos acerca de la herencia de la locura (A. Gaussail y E. Gintrac The Académie Royale de Médecine de París' contest, 1843: Contextual analysis of the emergence of the first publications concerning the heredity of madness (A. Gaussail and E. Gintrac

Directory of Open Access Journals (Sweden)

Mauro Vallejo

2010-12-01

Full Text Available El objetivo del presente trabajo es analizar la emergencia de las primeras publicaciones francesas enteramente dedicadas a la temática de la herencia de las enfermedades mentales. Tal y como ha sido demostrado por otros investigadores, Francia fue el territorio donde con más insistencia y ahínco se abordó el problema de la herencia desde un punto de vista médico. A partir de 1850, gran parte del alienismo de ese país consideró que el fenómeno hereditario era un componente esencial de las patologías nerviosas. Luego de describir qué lugar asignaban a ese factor los psiquiatras de comienzos de siglo, este escrito propone considerar el saber médico sobre la herencia antes de 1850 a los fines de comprender cómo y porqué aparecen, a instancias de un concurso auspiciado por la Académie Royale de Médecine, los primeros tratados acerca del asunto, escritos por A. Gaussail y E. Gintrac.The purpose of this work is to analyze the appearance of the first French publications dealing with the heredity of mental illnesses. As it has been shown by others scholars, France was the country where the hereditarian subject was specially observed from a medical point of view. From 1850 a great part of the alienist profession considered that the heredity was a essential component of the mental pathologies. After describing the relevance that until 1850 the psychiatrists gave to that factor, this paper shows that the medical knowledge about heredity must be taken into account in order to understand how and why, ant thanks to a contest announced by the académie royale de médecine, the first treatises dealing with the subject (written by A. Gaussail and E. Gintrac finally appeared.

Plants and Photosynthesis: Level III, Unit 3, Lesson 1; The Human Digestive System: Lesson 2; Functions of the Blood: Lesson 3; Human Circulation and Respiration: Lesson 4; Reproduction of a Single Cell: Lesson 5; Reproduction by Male and Female Cells: Lesson 6; The Human Reproductive System: Lesson 7; Genetics and Heredity: Lesson 8; The Nervous System: Lesson 9; The Glandular System: Lesson 10. Advanced General Education Program. A High School Self-Study Program.

Science.gov (United States)

Manpower Administration (DOL), Washington, DC. Job Corps.

This self-study program for the high-school level contains lessons in the following subjects: Plants and Photosynthesis; The Human Digestive System; Functions of the Blood; Human Circulation and Respiration; Reproduction of a Single Cell; Reproduction by Male and Female Cells; The Human Reproductive System; Genetics and Heredity; The Nervous…

[Constant or break? On the relations between human genetics and eugenics in the Twentieth Century].

Science.gov (United States)

Germann, Pascal

2015-07-01

The history of human genetics has been a neglected topic in history of science and medicine for a long time. Only recently, have medical historians begun to pay more attention to the history of human heredity. An important research question deals with the interconnections between human genetics and eugenics. This paper addresses this question: By focusing on a Swiss case study, the investigation of the heredity of goiter, I will argue that there existed close but also ambiguous relations between heredity research and eugenics in the twentieth century. Studies on human heredity often produced evidence that challenged eugenic aims and ideas. Concurrently, however, these studies fostered visions of genetic improvement of human populations.

Forecast of hourly global horizontal irradiance based on structured Kernel Support Vector Machine: A case study of Tibet area in China

International Nuclear Information System (INIS)

Jiang, He; Dong, Yao

2017-01-01

Highlights: • The structured variable selection in Kernel SVM is implemented using two ways. • The two-way interaction model is considered to enforce Heredity Principle. • SVMIC is used to select the kernel parameter in proposed approaches. • Simple and fast computations algorithms are derived. - Abstract: Various applications of forecasting effective global horizontal irradiance play increasingly vital role in grid-connected photovoltaic installations, but suffer from forecasting inaccuracy and prohibitively expensive computational cost. Although Support Vector Machine (SVM) is one of the most powerful forecasting approaches, it does not provide an interpretable model. This motivates penalized variable selection methods to be introduced to SVM to select important variables. However, in some forecasting problems, there are some underlying logic or hierarchical structure such as heredity principle among the variables. Penalized Kernel SVM approaches do not take heredity principles into consideration when enforcing sparsity. This paper investigates structural variable selection in Kernel SVM based approach which pursues heredity principle and sparsity simultaneously. To achieve heredity principle, both optimization and procedure based structural variable selection approaches are studied in the Kernel SVM. Computationally, we derive fast and simple-to-implement algorithms to perform structural variable selection and solar irradiance forecasting. Furthermore, Support Vector Machines Information Criterion is utilized to select the kernel parameters to guarantee the model consistency. Real data experiments directly reveal that our proposed KSVM-SVS based approach following heredity principle delivers superior performances in terms of forecasting accuracy comparing with other competitors.

Heredity of chronic bronchitis

DEFF Research Database (Denmark)

Meteran, Howraman; Backer, Vibeke; Kyvik, Kirsten Ohm

2014-01-01

BACKGROUND: Smoking is a major risk factor for lung diseases and lower respiratory symptoms, but since not all smokers develop chronic bronchitis and since chronic bronchitis is also diagnosed in never-smokers, it has been suggested that some individuals are more susceptible to develop chronic br...

Heredity for triangular operators

Directory of Open Access Journals (Sweden)

Henry Crawford Rhaly Jr.

2013-12-01

Full Text Available A proof is given that if the lower triangular infinite matrix $T$ acts boundedly on $\\ell^2$ and U is the unilateral shift, the sequence $(U^*^nTU^n$ inherits from $T$ the following properties: posinormality, dominance, $M$-hyponormality, hyponormality, normality, compactness, and noncompactness.  Also, it is demonstrated that the upper triangular matrix $T^*$ is dominant if and only if $T$ is a diagonal matrix.

The Influence of Causal Explanations and Diagnostic Labeling on Psychology Students' Beliefs About Treatments, Prognosis, Dangerousness and Unpredictability in Schizophrenia.

Science.gov (United States)

Magliano, Lorenza; Read, John; Rinaldi, Angela; Costanzo, Regina; De Leo, Renata; Schioppa, Giustina; Petrillo, Miriam

2016-04-01

This study explored views of 566 Italian psychology students about schizophrenia. The most frequently cited causes were psychological traumas (68 %) and heredity (54 %). Thirty-three percent of students firmly believed that people with the condition could recover. Reporting heredity among the causes, and identifying schizophrenia were both associated with prognostic pessimism, greater confidence in pharmacological treatments and lower confidence in psychological treatments. Schizophrenia labeling was also associated with higher perception of unpredictability and dangerousness. Compared to first year students, fourth/fifth year students more frequently reported heredity among the causes, and were more pessimistic about schizophrenia recovery. Stigma topics should be included in future psychologists' education.

História natural e as idéias de geração e herança no século XVIII: Buffon e Bonnet Natural history and eighteenth-century ideas regarding generation and heredity: Buffon and Bonnet

Directory of Open Access Journals (Sweden)

Luzia Aurelia Castañeda

1995-10-01

the ideas of generation and heredity ascribed a reproductive history to living things, a history where the act of one fellow creature being formed by another plays an important role in coming to understand the workings of life. The paper analyzes these conceptual approaches from the perspectives of Buffon's and Bonnet's ideas on reproduction and heredity, which represented opposite schools of thought: epigenesis and preformation.

Mendel and the Path to Genetics: Portraying Science as a Social Process

Science.gov (United States)

Kampourakis, Kostas

2013-01-01

Textbook descriptions of the foundations of Genetics give the impression that besides Mendel's no other research on heredity took place during the nineteenth century. However, the publication of the "Origin of Species" in 1859, and the criticism that it received, placed the study of heredity at the centre of biological thought. Consequently,…

On S.N. Bernstein's derivation of Mendel's Law and 'rediscovery' of the Hardy-Weinberg distribution

Directory of Open Access Journals (Sweden)

Alan Stark

2012-01-01

Full Text Available Around 1923 the soon-to-be famous Soviet mathematician and probabilist Sergei N. Bernstein started to construct an axiomatic foundation of a theory of heredity. He began from the premise of stationarity (constancy of type proportions from the first generation of offspring. This led him to derive the Mendelian coefficients of heredity. It appears that he had no direct influence on the subsequent development of population genetics. A basic assumption of Bernstein was that parents coupled randomly to produce offspring. This paper shows that a simple model of non-random mating, which nevertheless embodies a feature of the Hardy-Weinberg Law, can produce Mendelian coefficients of heredity while maintaining the population distribution. How W. Johannsen's monograph influenced Bernstein is discussed.

Power and Energy: Geopolitical Aspects of the Transnational Natural Gas Pipelines from the Caspian Sea Basin to Europe

Science.gov (United States)

2010-06-01

part of all three of which is the heredity of the Soviet regime. In order to understand the development of the post-Soviet republics in Central...mirrors, foodstuff, plants and other items, promoted economic and cultural trade between the Mediterranean and Persia, India, and China. By the end...wars, and religious tensions in the Caucasian and Central Asian countries—which are partly the heredity of the Soviet regime—remain unresolved. 50

Distinct Gene Expression Signatures in Lynch Syndrome and Familial Colorectal Cancer Type X

DEFF Research Database (Denmark)

Valentin, Mev; Therkildsen, Christina; Veerla, Srinivas

2013-01-01

Heredity is estimated to cause at least 20% of colorectal cancer. The hereditary nonpolyposis colorectal cancer subset is divided into Lynch syndrome and familial colorectal cancer type X (FCCTX) based on presence of mismatch repair (MMR) gene defects.......Heredity is estimated to cause at least 20% of colorectal cancer. The hereditary nonpolyposis colorectal cancer subset is divided into Lynch syndrome and familial colorectal cancer type X (FCCTX) based on presence of mismatch repair (MMR) gene defects....

Dědičnost kardiovaskulárních onemocnění

OpenAIRE

Košatová, Andrea

2013-01-01

The main purpose of this text is to conclude the known facts about the influence of heredity over cardiovascular diseases. It is targeted at the general public, but also at those who take a deeper interest in medicine, civilization diseases and their causes. The diseases of heart and vessels are the most common cause of sickness and death in the countries of so-called Western civilization. Heredity is one of the major risk factors that affect the probability of such diseases' outbreak. The so...

The inheritance of groin hernia

DEFF Research Database (Denmark)

Burcharth, J; Pommergaard, H C; Rosenberg, Jacob

2013-01-01

Groin hernia has been proposed to be hereditary; however, a clear hereditary pattern has not been established yet. The purpose of this review was to analyze studies evaluating family history and inheritance patterns and to investigate the possible heredity of groin hernias.......Groin hernia has been proposed to be hereditary; however, a clear hereditary pattern has not been established yet. The purpose of this review was to analyze studies evaluating family history and inheritance patterns and to investigate the possible heredity of groin hernias....

Simulated experiments

International Nuclear Information System (INIS)

Bjerknes, R.

1977-01-01

A cybernetic model has been developed to elucidate some of the main principles of the growth regulation system in the epidermis of the hairless mouse. A number of actual and theoretical biological experiments have been simulated on the model. These included simulating the cell kinetics as measured by pulse labelling with tritiated thymidine and by continuous labelling with tritiated thymidine. Other simulated experiments included steady state, wear and tear, painting with a carcinogen, heredity and heredity and tumour. Numerous diagrams illustrate the results of these simulated experiments. (JIW)

Electromagnetic Basis of Metabolism and Heredity

Science.gov (United States)

Freund, Friedemann; Stolc, Viktor

2016-01-01

Living organisms control their cellular biological clocks to maintain functional oscillation of the redox cycle, also called the "metabolic cycle" or "respiratory cycle". Organization of cellular processes requires parallel processing on a synchronized time-base. These clocks coordinate the timing of all biochemical processes in the cell, including energy production, DNA replication, and RNA transcription. When this universal time keeping function is perturbed by exogenous induction of reactive oxygen species (ROS), the rate of metabolism changes. This causes oxidative stress, aging and mutations. Therefore, good temporal coordination of the redox cycle not only actively prevents chemical conflict between the reductive and oxidative partial reactions; it also maintains genome integrity and lifespan. Moreover, this universal biochemical rhythm can be disrupted by ROS induction in vivo. This in turn can be achieved by blocking the electron transport chain either endogenously or exogenously by various metabolites, e.g. hydrogen sulfide (H2S), highly diffusible drugs, and carbon monoxide (CO). Alternatively, the electron transport in vivo can be attenuated via a coherent or interfering transfer of energy from exogenous ultralow frequency (ULF) and extremely low frequency (ELF) electromagnetic (EM) fields, suggesting that-on Earth-such ambient fields are an omnipresent (and probably crucially important) factor for the time-setting basis of universal biochemical reactions in living cells. Our work demonstrated previously un-described evidence for quantum effects in biology by electromagnetic coupling below thermal noise at the universal electron transport chain (ETC) in vivo.

Pathophysiology of AAA: heredity vs environment.

Science.gov (United States)

Björck, Martin; Wanhainen, Anders

2013-01-01

Abdominal aortic aneurysm (AAA) has a complex pathophysiology, in which both environmental and genetic factors play important roles, the most important being smoking. The recently reported falling prevalence rates of AAA in northern Europe and Australia/New Zeeland are largely explained by healthier smoking habits. Dietary factors and obesity, in particular abdominal obesity, are also of importance. A family history of AAA among first-degree relatives is present in approximately 13% of incident cases. The probability that a monozygotic twin of a person with an AAA has the disease is 24%, 71 times higher than that for a monozygotic twin of a person without AAA. Approximately 1000 SNPs in 100 candidate genes have been studied, and three genome-wide association studies were published, identifying different diverse weak associations. An example of interaction between environmental and genetic factors is the effect of cholesterol, where genetic and dietary factors affect levels of both HDL and LDL. True epigenetic studies have not yet been published. Copyright © 2013 Elsevier Inc. All rights reserved.

[Heredity in renal and prostatic neoplasia].

Science.gov (United States)

Prayer Galetti, T; D'Arrigo, L; De Zorzi, L; Patarnello, T

1997-09-01

There is an ever growing report of data supporting the evidence that accumulated genetic changes underlie the development of neoplasia. The paradigma of this multistep process is colon cancer were cancer onset is associated, over decades, with at least seven genetic events. The number of genetic alterations increases moving from adenomatous lesions to colon cancer and, although the genetic alterations occur according to a preferred sequence, the total accumulation of changes rather than their sequential order is responsible of tumor biological behavior. It is noteworthy that, at least for this neoplasia, carcinogenesis appears to arise as a result of the mutational activation of oncogenes coupled with the mutational inactivation of tumor suppressor genes. In some cases mutant suppressor genes appear to exert a phenotypic effect even when present in the heterozygous state thus been non "recessive" at the cellular level. The general features of this model may apply also to renal cell cancer (RCC) and prostate cancer (CaP). Extensive literature exists on the cytogenetic and molecular findings in RCC. Only 2% of RCC are familiar, but molecular genetic studies of these cancers have provided important informations on RCC pathogenesis. As with other cancers, familiar RCC is characterized by an early age of onset and frequent multicentricity. A pathological classification useful in studying these patients subdivide renal cancers in papillary (pRCC) and non papillary (RCC) neoplasms. The most common cause of inherited RCC is the Von Hippel Lindau disease (VHL) a dominantly inherited multisystem disorder characterized by retinal and cerebellar hemangioblastomas, pheochromocytomas, pancreatic cysts and RCC. Over 70% of these patients will develop an RCC by their sixth decade. In 1993 the isolation of the tumor suppressor gene in VHL disease at the level of chromosome 3p25-p26 have lead to a better understanding of RCC. Most missense mutations are associated with high risk of RCC, but some are associated with high risk of pheochromocytoma and low risk of RCC. The VHL gene is evolutionary conserved and encodes for a specific protein (pVHL). VHL protein downregulates transcriptional elongation and so suppresses the expression of proto-oncogenes and growth factors. Recently reintroduction of wild-type, non mutant, VHL gene into VHL deficient RCC cell line 786-O had no demonstrable effect on their in vitro growth but inhibited their ability to form tumors in nude mice. So far, VHL mutations or hypermethylations have been found in 76% of sporadic RCC. On the contrary, up to now, no 3p allele loss or VHL mutations have been detected in pRCC. Preliminary studies in familiar pRCC are pointing on genetic changes on chromosomes 1, 7, 16 and 17. As far as prostate cancer is regarded, men with a family history of prostate cancer have an age dependent, significantly increased PCa risk. For familiar clustering, of PCa the two main factors are early age at onset of the disease and the number of multiple affected family members. Hereditary prostate cancer is a subset of familiar prostate cancer with a pattern of distribution consistent with Mendelian inheritance. Hereditary prostate cancer is clinically defined as a clustering of 3 or more relatives within any nuclear family; or the occurrence of prostate cancer in each of 3 generations in either the probands paternal or maternal lineage; or a cluster of 2 relatives affected within 55 years of age or less. Therefore, hereditary prostate cancer may be seen as a multistep carcinogenesis, and clustering may be explained by Mendelian inheritance of a rare (frequency in population 0.36%) dominant, highly penetrant, allele. The estimated cumulative risk of developing PCa, is 88% for carriers as compared with 5% for non carriers. There are conflicting reports of an associated increased incidence of breast cancer in female relatives of men with familiar prostate cancer. In conclusion, there is a clear associatio

Johannsen's criticism of the chromosome theory.

Science.gov (United States)

Roll-Hansen, Nils

2014-01-01

The genotype theory of Wilhelm Johannsen (1857-1927) was an important contribution to the founding of classical genetics. This theory built on Johannsen's experimental demonstration that hereditary change is discontinuous, not continuous as had been widely assumed. Johannsen is also known for his criticism of traditional Darwinian evolution by natural selection, as well as his criticism of the classical Mendelian chromosome theory of heredity. He has often been seen as one of the anti-Darwinians that caused the "eclipse of Darwinism" in the early 20th century, before it was saved by the Modern Synthesis. This article focuses on Johannsen's criticism of the chromosome theory. He was indeed skeptical of the notion of the chromosomes as the sole carriers of heredity, but he praised the mapping of Mendelian genes on the chromosomes as a major step forward. Johannsen objected that these genes could not account for the whole of heredity, and that the stability of the genotype depended on much more than the stability of Mendelian genes. For Johannsen, the genotype, as a property of the whole organism, was the fundamental and empirically well-established entity.

Women as Mendelians and Geneticists

Science.gov (United States)

Richmond, Marsha L.

2015-01-01

After the rediscovery of Mendel's laws of heredity in 1900, the biologists who began studying heredity, variation, and evolution using the new Mendelian methodology—performing controlled hybrid crosses and statistically analyzing progeny to note the factorial basis of characters—made great progress. By 1910, the validity of Mendelism was widely recognized and the field William Bateson christened `genetics' was complemented by the chromosome theory of heredity of T. H. Morgan and his group in the United States. Historians, however, have largely overlooked an important factor in the early establishment of Mendelism and genetics: the large number of women who contributed to the various research groups. This article examines the social, economic, and disciplinary context behind this new wave of women's participation in science and describes the work of women Mendelians and geneticists employed at three leading experimental research institutes, 1900-1940. It argues that the key to more women working in science was the access to higher education and the receptivity of emerging interdisciplinary fields such as genetics to utilize the expertise of women workers, which not only advanced the discipline but also provided new opportunities for women's employment in science.

Heredity of supraglottic exercise-induced laryngeal obstruction

DEFF Research Database (Denmark)

Walsted, Emil Schwarz; Hvedstrup, Jeppe; Eiberg, Hans

2017-01-01

Respiratory symptoms on exertion, such as shortness of breath and wheezing, are commonly associated with asthma, but might also arise from the larynx [1–3]. In recent years, the emergence of exercise laryngoscopy [4] has led to a better understanding of laryngeal movement during exercise, and ins...

Prognosis of Lung Cancer: Heredity or Environment

Science.gov (United States)

2015-06-01

and white patients in an equal access health system. Cancer Epidemiol Biomarkers Prev 2012;21:1841–1847. 19. Hardy D, Xia R, Liu CC, Cormier JN...Nurgalieva Z, Du XL. Racial dis- parities and survival for nonsmall-cell lung cancer in a large cohort of black and white elderly patients. Cancer 2009;115...P. In lung cancer patients, age, race-ethnicity, gender and smoking predict adverse comor- bidity, which in turn predicts treatment and survival. J

Siblings and Mental Illness: Heredity vs. Environment.

Science.gov (United States)

Rowe, David C.; Elam, Patricia

1987-01-01

Siblings are far more likely to be different than alike in personality and psychopathology. Different genes and different environmental experiences can account for why one sibling becomes mentally ill and another is not affected. Environmental experiences play a much greater role in sibling differentiation than has been previously recognized.…

The Transmission mechanisms of the position and Functions of Prophets in Abrahamic Religions

Directory of Open Access Journals (Sweden)

Mohammad Reza Vasfi

2013-09-01

Full Text Available Prophethood, possesses a profound significance in the Abrahamic religions. Prophets act as mediums, through whom the message of God is received and delivered to people, and thus fulfill two kinds of epistemological and Responsible functions: one related to the prophetic “gnosis” of the divine message and the other to the missionary “responsibility” of enacting it. But do the position and functions of the prophets come to an end with his death? For the Abrahamic religions, the answer is ‘No’. In these religions, we are faced with a phenomenon that can be called the “Transmission of the position and functions of prophets”. This article attempts to explain this phenomenon in the context of the holy texts of these three religions and in the terms of the three mechanisms of Blessedness, Heredity and Successorship. Although, the separation between this mechanisms in analysis, necessarily, they are not separate in instances. The first mechanism of such Transmission, by which the prophet transmits on his position and functions to his Children's, is Blessedness. Blessedness is a special covenant between God and Abraham, and is reported twice in the Old covenant. By this mechanism, God blesses to Abraham and promises to bless his Children's, to make them as many as the dust of the earth, and to make them victorious in the face of their enemies. Thus, the mechanism of blessedness becomes institutionalized in Abraham’s family and household, and passes on from one generation to the next. In the New covenant, Jesus and Virgin Mary are called “the Blessed Ones”, Jesus is described as the Source of Blessedness for everyone, and all the true Christian believers are considered as the heirs to Abraham’s Blessedness. In the noble Quran, not only the covenant of God’s Blessedness with Abraham and Isaac is mentioned, but also Jesus is referred to as “the Blessed One” (“Mubarak”. However, it can be said that mechanism of Blessedness

The Transmission mechanisms of the position and Functions of Prophets in Abrahamic Religions

Directory of Open Access Journals (Sweden)

S. Roohollah Shafiee

2013-08-01

Full Text Available Prophethood, possesses a profound significance in the Abrahamic religions. Prophets act as mediums, through whom the message of God is received and delivered to people, and thus fulfill two kinds of epistemological and Responsible functions: one related to the prophetic “gnosis” of the divine message and the other to the missionary “responsibility” of enacting it. But do the position and functions of the prophets come to an end with his death? For the Abrahamic religions, the answer is ‘No’. In these religions, we are faced with a phenomenon that can be called the “Transmission of the position and functions of prophets”. This article attempts to explain this phenomenon in the context of the holy texts of these three religions and in the terms of the three mechanisms of Blessedness, Heredity and Successorship. Although, the separation between this mechanisms in analysis, necessarily, they are not separate in instances. The first mechanism of such Transmission, by which the prophet transmits on his position and functions to his Children's, is Blessedness. Blessedness is a special covenant between God and Abraham, and is reported twice in the Old covenant. By this mechanism, God blesses to Abraham and promises to bless his Children's, to make them as many as the dust of the earth, and to make them victorious in the face of their enemies. Thus, the mechanism of blessedness becomes institutionalized in Abraham’s family and household, and passes on from one generation to the next. In the New covenant, Jesus and Virgin Mary are called “the Blessed Ones”, Jesus is described as the Source of Blessedness for everyone, and all the true Christian believers are considered as the heirs to Abraham’s Blessedness. In the noble Quran, not only the covenant of God’s Blessedness with Abraham and Isaac is mentioned, but also Jesus is referred to as “the Blessed One” (“Mubarak”. However, it can be said that mechanism of Blessedness

The Transmission mechanisms of the position and Functions of Prophets in Abrahamic Religions

Directory of Open Access Journals (Sweden)

Mohammad Reza Vasfi

Full Text Available Prophethood, possesses a profound significance in the Abrahamic religions. Prophets act as mediums, through whom the message of God is received and delivered to people, and thus fulfill two kinds of epistemological and Responsible functions: one related to the prophetic “gnosis” of the divine message and the other to the missionary “responsibility” of enacting it. But do the position and functions of the prophets come to an end with his death? For the Abrahamic religions, the answer is ‘No’. In these religions, we are faced with a phenomenon that can be called the “Transmission of the position and functions of prophets”. This article attempts to explain this phenomenon in the context of the holy texts of these three religions and in the terms of the three mechanisms of Blessedness, Heredity and Successorship. Although, the separation between this mechanisms in analysis, necessarily, they are not separate in instances. The first mechanism of such Transmission, by which the prophet transmits on his position and functions to his Children's, is Blessedness. Blessedness is a special covenant between God and Abraham, and is reported twice in the Old covenant. By this mechanism, God blesses to Abraham and promises to bless his Children's, to make them as many as the dust of the earth, and to make them victorious in the face of their enemies. Thus, the mechanism of blessedness becomes institutionalized in Abraham’s family and household, and passes on from one generation to the next. In the New covenant, Jesus and Virgin Mary are called “the Blessed Ones”, Jesus is described as the Source of Blessedness for everyone, and all the true Christian believers are considered as the heirs to Abraham’s Blessedness. In the noble Quran, not only the covenant of God’s Blessedness with Abraham and Isaac is mentioned, but also Jesus is referred to as “the Blessed One” (“Mubarak”. However, it can be said that mechanism of Blessedness

Phylogenetics in plant biotechnology: principles, obstacles and ...

African Journals Online (AJOL)

GREGO

2007-03-19

examples are Molecular Ecology and Heredity) no longer accept .... Appropriate genetic distance measures: Homoplasy is expected under the ..... Character quality is assessed by a ..... 75:2868-2872. Kluge AG, Farris JS (1969).

Mesenchymal Stem Cells in the Bone Marrow Provide a Supportive Niche for Early Disseminated Breast Tumor-Initiating Cells

Science.gov (United States)

2011-04-01

Laboratory Summer internship Responsibilities: - Making agar plates - Maintaining cotton plant population - Glassware 2 Curriculum...undergraduate non-science majors in Heredity and Society Lab Research Interests: - Cancer Biology/Genetics - Cancer metastasis - Stem cell

[AN ENTRY FOR A "DICTIONARY OF GENETICS" GENERATION AND ASPECTS OF HEREDITY FROM THE PRESOCRATICS TO GALEN: THE MAIN NOTIONS AND THE TECHNICAL TERMINOLOGY].

Science.gov (United States)

Giorgianni, Franco; Provenza, Antonietta

2015-01-01

This article aims at dealing with the historical development and the terminology of the notion of generation in ancient Greece, taking as well into consideration several aspects of the notion of heredity, for, at present, research in this field lacks a consistent encyclopedic entry on such subjects. The Presocratic - mainly Empedoclean - notions of 'mixing' and 'separation' lurk behind the Hippocratic treatise De genitura/De natura pueri, in which the process of generation is explained through the 'mixing' mechanism of a female semen and a male one. Semen comes from each part of both parents, so it is sound from the sound parts, and unhealthy from the unhealthy parts. It is considered as the "foam of blood" (Diogenes, A 24 DK), gathering itself into a web of blood vessels that bring it to the genital organs. The mixed semen keeps on fixing itself in the womb thanks to pneuma ('breath'), until the embryo takes human shape. Generation is influenced by both the environment (Airs, Waters, Places) and dietetics (On Regimen, I). Male and female are on different levels in CH, since the former is characterized as hot and strong, and the latter is considered as cold and weak; as a consequence of this, the articulation takes longer in the case of a female embryo. On the other hand, the pangenesis and the preformism theory claim for a strong mutual relationship. Sex determination depends from the 'prevalence' of the male or female semen. The generation of twins of different sex depends from such 'prevalence', as well as from the conformation of the womb and its places (right/male, left/female). Both nature (physis) and use (nomos) have a role in the mechanism of inheritance, as the case of the Macrocephalians in Airs Waters Places shows. On the other hand, Plato's Timaeus exemplifies the theory according to which semen derives from the spinal marrow. The structures of the body - bones, flesh, nerves - aim at protecting marrow itself for the sake of maintaining the continuity

Human genes and genomes: science, health, society

National Research Council Canada - National Science Library

Rosenberg, Leon E; Rosenberg, Diane Drobnis

2012-01-01

"In the nearly 60 years since Watson and Crick proposed the double helical structure of DNA, the molecule of heredity, waves of discoveries have made genetics the most thrilling field in the sciences...

Neoosmanism: Turkey between yesterday and tomorrow

Directory of Open Access Journals (Sweden)

Galijašević Dževad

2011-01-01

Full Text Available Geostrategic integrity of the Balkans and the Danube region and the strategic ambitions of powerful countries that were inherited from previous centuries define the start points of European streams in XX century. German 'drang nach osten', Russian spread to south and an ambition of primate in struggle for the Turkish heredity, Turkish strivings to bring its Empire out of death with reforms, and remain right-sided to Sava-Danube river basin, preserving it as its natural border, and the strivings of Balkan peoples for liberation, shaped geopolitical, strategic and state-legal traits of the phenomenon called 'Eastern question'. The conquests form south east towards north and northwest and vice versa pointed that geostrategic traits of Balkans were not separation and geographic in-connectivity, but connection and permeation, which open strategic ways to domination over the Eurasian knot and warm seas of Mediterranean and Middle East. The fact that Balkans aren't the only connection between Europe and Asia does not lessen their geostrategic and geopolitical importance. On the contrary. This question, that was an eastern one for powerful countries, and one of a life importance for the people of southeast Europe, goes back into deep past. It was formed and a geostrategic position of a whole area that it related to by conflicted interest of people, religions and whole civilizations that faced each others there. However, if looking for a more narrow historical sense of the term Eastern question, we will find it in a collision of Europe and Islamic world, which was brought by Turkish penetration into Europe. During the rise of the Ottoman Empire, it was a matter of survival of European countries that were struck by Ottoman conquest, and after the decline of the Ottoman power it turned into a struggle for Turkish heredity. Today, the Struggle form Ottoman heredity strongly includes Turkey as well. Turkish engagement in a struggle for its own historical

Genetics 101 --The Hereditary Material of Life

Science.gov (United States)

... of this page please turn Javascript on. Feature: Genetics 101 Genetics 101 — The Hereditary Material of Life Past Issues / Summer 2013 Table of Contents Genetics is the study of heredity, the process in ...

Fine structures in Fe3Al alloy layer of a new hot dip aluminized steel

Indian Academy of Sciences (India)

Unknown

*National Key Laboratory of Advanced Welding Production Technology, Harbin ... †Key Lab of Liquid Structure and Heredity of Materials, Ministry of Education, Shandong University, ... improve the adhesion of the liquid aluminum to the base.

Retinitis Pigmentosa.

Science.gov (United States)

Carr, Ronald E.

1979-01-01

The author describes the etiology of retinitis pigmentosa, a visual dysfunction which results from progressive loss of the retinal photoreceptors. Sections address signs and symptoms, ancillary findings, heredity, clinical diagnosis, therapy, and research. (SBH)

Epigenetics: ambiguities and implications.

Science.gov (United States)

Stotz, Karola; Griffiths, Paul

2016-12-01

Everyone has heard of 'epigenetics', but the term means different things to different researchers. Four important contemporary meanings are outlined in this paper. Epigenetics in its various senses has implications for development, heredity, and evolution, and also for medicine. Concerning development, it cements the vision of a reactive genome strongly coupled to its environment. Concerning heredity, both narrowly epigenetic and broader 'exogenetic' systems of inheritance play important roles in the construction of phenotypes. A thoroughly epigenetic model of development and evolution was Waddington's aim when he introduced the term 'epigenetics' in the 1940s, but it has taken the modern development of molecular epigenetics to realize this aim. In the final sections of the paper we briefly outline some further implications of epigenetics for medicine and for the nature/nurture debate.

Heredity In Sarcoidosis - A Registry-Based Twin Study

DEFF Research Database (Denmark)

Sverrild, Asger; Backer, Vibeke; Kyvik, Kirsten Ohm

2008-01-01

BACKGROUND: Sarcoidosis is a multiorgan, granulomatous, inflammatory disease with unknown aetiology. Familial clustering of cases and ethnic variation in the epidemiology suggests a genetic influence on the disease susceptibility. AIM: This paper reports twin concordance and heritability estimates...... of sarcoidosis in order to assess the overall contribution of genetic factors to the disease susceptibility. METHODS: Monozygotic and dizygotic twins enrolled in either the Danish or the Finnish population-based, national Twin Cohorts (61,662 pairs in total) were linked to diagnostic information on sarcoidosis.......012. Compared to the general population we found an 80-fold increased risk of developing sarcoidosis in co-twins of affected monozygotic brothers or sisters. The increased risk in dizygotic twins was on the other hand only 7-fold. Aetiological model fitting gave a heritability of sarcoidosis of 0.66 (95% CI 0...

Walter Sutton and the Chromosome Theory of Heredity

Indian Academy of Sciences (India)

Admin

and played basketball, a young sport hardly ten-years-old started by D r. Jam es N ... course ofthese studies that Sutton m ade the im portant connection betw een ... his tw o sem inalpapers in 1902 and 1903 in the journal B iological B ulletin.

R-ES-ONA--NCE

Indian Academy of Sciences (India)

Mendel's Laws oflnheritance, heredity was still a mystery to biologists, and ... of paternal and maternal influences, the segregation of parental types in ... Genes on X and Y chromosomes, or those on mitochondrial or chloroplast DNA, are.

Coronary Artery Disease - Coronary Heart Disease

Science.gov (United States)

... not as great as men's. Heredity (Including Race) Children of parents with heart disease are more likely to develop it themselves. African Americans have more severe high blood pressure than Caucasians and a higher risk of heart ...

Understand Your Risk of Heart Attack

Science.gov (United States)

... not as great as men's. Heredity (Including Race) Children of parents with heart disease are more likely to develop it themselves. African Americans have more severe high blood pressure than Caucasians and a higher risk of heart ...

Differences in views of schizophrenia during medical education: a comparative study of 1st versus 5th-6th year Italian medical students.

Science.gov (United States)

Magliano, Lorenza; Read, John; Sagliocchi, Alessandra; Patalano, Melania; D'Ambrosio, Antonio; Oliviero, Nicoletta

2013-10-01

This study explored medical students' causal explanations and views of schizophrenia, and whether they changed during medical education. The survey was carried out on medical students of the Second University of Naples, Italy, who attended their first-year and their fifth- or sixth-year of lessons. The 381 who accepted were asked to read a case-vignette describing a person who met the ICD-10 criteria for schizophrenia and then fill in the Opinions on mental illness Questionnaire. The most frequently cited causes were psychological traumas (60%) and stress (56%), followed by misuse of street drugs (47%), and heredity (42%). 28% of students stated that persons with the disorder could be well again, and 28% that they were unpredictable. Labeling the case as "schizophrenia" and naming heredity among the causes were associated with pessimism about recovery and higher perception of social distance. First-year students more frequently reported psychological traumas among the causes (76 vs. 45%), and less frequently heredity (35 vs. 81%) and stress (42 vs. 69%), and they perceived less social distance from the "schizophrenics" than fifth/sixth-year students. In particular, 18% percent of first-year versus 38% of fifth/sixth-year students believed that these persons were kept at a distance by the other, and 45 versus 57% felt frightened by persons with the condition. These results indicate a need to include education on stigma and recovery in schizophrenia in the training of medical students.

Fine structure in the inter-critical heat-affected zone of HQ130 super ...

Indian Academy of Sciences (India)

Unknown

†Key Laboratory of Liquid Structure and Heredity of Materials, Ministry of Education, ... The microstructure in the inter-critical heat-affected zone (ICHAZ) of HQ130 steel, has been .... Ac3. The microhardness was measured by using the.

Micro-Albuminuria In Adolescent/Young Adult Offsprings Of ...

African Journals Online (AJOL)

young adult offsprings of Nigeria hypertensive adults. Background: On the premise that micro-albuminuria is a predictor of early stage hypertensive disease and the fact that heredity plays an important role in the aetiology of essential hypertension, ...

Effect of weld heat input on toughness and structure of HAZ of a new ...

Indian Academy of Sciences (India)

Unknown

Key Laboratory of Liquid Structure and Heredity of Materials, Ministry of Education, School of Materials Science .... should be controlled (t8/5 = 10 ~ 20 s) to improve tough- ness in the .... nology, Harbin Institute of Technology, People's Repub-.

The evolutionary implications of epigenetic inheritance.

Science.gov (United States)

Jablonka, Eva

2017-10-06

The Modern Evolutionary Synthesis (MS) forged in the mid-twentieth century was built on a notion of heredity that excluded soft inheritance, the inheritance of the effects of developmental modifications. However, the discovery of molecular mechanisms that generate random and developmentally induced epigenetic variations is leading to a broadening of the notion of biological heredity that has consequences for ideas about evolution. After presenting some old challenges to the MS that were raised, among others, by Karl Popper, I discuss recent research on epigenetic inheritance, which provides experimental and theoretical support for these challenges. There is now good evidence that epigenetic inheritance is ubiquitous and is involved in adaptive evolution and macroevolution. I argue that the many evolutionary consequences of epigenetic inheritance open up new research areas and require the extension of the evolutionary synthesis beyond the current neo-Darwinian model.

Patient-reported causes of heart failure in a large European sample

DEFF Research Database (Denmark)

Timmermans, Ivy; Denollet, Johan; Pedersen, Susanne S.

2018-01-01

), psychosocial (35%, mainly (work-related) stress), and natural causes (32%, mainly heredity). There were socio-demographic, clinical and psychological group differences between the various categories, and large discrepancies between prevalence of physical risk factors according to medical records and patient...... distress (OR = 1.54, 95% CI = 0.94–2.51, p = 0.09), and behavioral causes and a less threatening view of heart failure (OR = 0.64, 95% CI = 0.40–1.01, p = 0.06). Conclusion: European patients most frequently reported comorbidities, smoking, stress, and heredity as heart failure causes, but their causal......Background: Patients diagnosed with chronic diseases develop perceptions about their disease and its causes, which may influence health behavior and emotional well-being. This is the first study to examine patient-reported causes and their correlates in patients with heart failure. Methods...

Gálapagos Islands and Darwin's Theory of Evolution

Indian Academy of Sciences (India)

work. In spite of his lack of knowledge about the mechanisms of heredity or the material .... were different varieties adapted to the prevailing environment of ..... in the Station (by which time, they are safe from the introduced predators such as ...

Dry Macular Degeneration

Science.gov (United States)

... a combination of heredity and environmental factors, including smoking and diet. The condition develops as the eye ages. Dry ... nonsmokers. Ask your doctor for help to stop smoking. Maintain a ... controlling your diet. Choose a diet rich in fruits and vegetables. ...

ORIGINAL ARTICLES Haemophilia patients aged 0 - 18 years in the ...

African Journals Online (AJOL)

2003-06-06

Jun 6, 2003 ... education (and upbringing) of the child after they had learnt of .... parent). Only 14 guardians (29%) had some form of medical insurance. Although ... history and the role of heredity, which in turn may explain why children with ...

Bulletin of Materials Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

Author Affiliations. Wang Juan1 Li Yajiang1 Wu Huiqiang1 Ren Jiangwei1. Key Lab of Liquid Structure and Heredity of Materials, Ministry of Education, School of Materials Science and Engineering, Shandong University, Jinan 250061, P.R. China ...

Increased expression of Th17 cytokines in patients with psoriasis

African Journals Online (AJOL)

AJL

2012-02-16

Feb 16, 2012 ... immune, heredity, psychology and environment factors ... ground with mortar and pestle, cooled by liquid nitrogen of the ground tissue .... Figure 1. Correction between expression of IL-17A mRNA and IL-23P19 mRNA. skin.

Hormones & growth regulators can be useful to foresters

Science.gov (United States)

Albert G., Jr. Snow

1959-01-01

Trees, like other plants, contain many natural chemicals of the sort that we call hormones. Research is gradually revealing that, in the behavior of a tree, these chemicals may be almost as important as the basic influences of heredity and environment.

Effect of Cr and Ni on diffusion bonding of Fe3Al with steel

Indian Academy of Sciences (India)

Unknown

*Key Lab of Liquid Structure and Heredity of Materials, Ministry of Education, Shandong University, ... †National Key Lab of Advanced Bonding Production Technology, Harbin Institute of .... to Fe3Al can affect the dynamic balance at the Fe3Al/.

Breastfeeding and allergic disease

DEFF Research Database (Denmark)

van Odijk, J; Kull, I; Borres, M P

2003-01-01

concluded that breastfeeding seems to protect from the development of atopic disease. The effect appears even stronger in children with atopic heredity. If breast milk is unavailable or insufficient, extensively hydrolysed formulas are preferable to unhydrolysed or partially hydrolysed formulas in terms...

Inexorable spread: inexorable death? The fate of neo-XY ...

Indian Academy of Sciences (India)

2011-12-07

Dec 7, 2011 ... us since the earliest times of Mendelism and the chromo- some theory of heredity ... gotes and these may have reduced fertility due to meiotic seg- regation .... species of Drosophila, the rate of gene gain in the investi- gated Y ...

The mutagenic effect of streptomyces and aspergillus niger with fast neutron irradiation

International Nuclear Information System (INIS)

Zhang Shengjun; Zhou Shuxin; Fang Xiaoming

1992-01-01

The authors describe the effect of irradiation on some Streptomyces and Aspergillus niger with fast neutron. The death rate(%), production rate(%, W/V), and heredities were determined and analysed. Particularly, five variant types of Strepto. griseous No.1 will be researched in depth

Bulletin of Materials Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

National Key Laboratory of Advanced Welding Production Technology, Harbin Institute of Technology, Harbin 150001, PR China; Key Lab of Liquid Structure and Heredity of Materials, Ministry of Education, Shandong University, Jinan 250061, PR China; Computer Engineering Department, University of Northern Virginia, ...

March to Disaster: Major General Edward Braddock and the Monongahela Campaign

Science.gov (United States)

2008-12-12

cabins and clearing timber to plant crops; the Indians recognized that the British did not intend to leave. Frustrated and pressured from two sides...Essentially, heredity , wealth, intelligence, and leadership all emerged from social standing. Only the privileged espoused the characteristics and

Biological Effects of Short, High-Level Exposure to Gases: Nitrogen Oxides.

Science.gov (United States)

1980-07-01

of explosives in confined spaces; welding, brazing, and oxyacetylene cutting; industrial plant operations involving nitra- tion, acid dipping, etc...von Nieding), heredity , and age. The paper finds a conflict between (a) the work of Ehrlich and of Coffin on increased susceptibility to bacterial

Weldon's Search for a Direct Proof of Natural Selection and the ...

Indian Academy of Sciences (India)

Plants under Domestication in 1868, there was considerable dis- agreement about whether natural selection could indeed work the. Keywords. Evolution, struggle for existence, natural selection, type, variations, heredity, biometrics, Mendelism. way Darwin had suggested and be the driving engine of adap- tive evolution.

A glacial relict in the Carpathian caves – population variability or a species complex?

Czech Academy of Sciences Publication Activity Database

Parimuchová, A.; Kováč, Ľ.; Žurovcová, Martina; Miklisová, D.; Paučulová, L.

2017-01-01

Roč. 75, č. 3 (2017), s. 351-362 ISSN 1863-7221 Institutional support: RVO:60077344 Keywords : Collembola * geographic isolation * haplotypes Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.357, year: 2016

Polymorphisms in NAT2, CYP2D6, CYP2C19 and GSTP1 and their association with prostate cancer

DEFF Research Database (Denmark)

Wadelius, Mia; Autrup, Judith; Stubbins, Michael J.

1999-01-01

The development of prostate cancer is dependent on heredity, androgenic influences, and exposure to environmental agents. A high intake of dietary fat is associated with an increased risk of prostate cancer, either through influence on steroid hormone profiles or through production of carcinogeni...

Crime and Child-Rearing.

Science.gov (United States)

Roth, Byron M.

1996-01-01

Examines the notion that heredity plays a powerful role in criminal behavior, including genetic evidence that can allow for antisocial behavior. Reviews suggestions for reversing rising crime rates in light of the hereditary connection, policy development, family cohesion, and child raising. (GR)

Practical animal breeding as the key to an integrated view of genetics, eugenics and evolutionary theory: Arend L. Hagedoorn (1885-1953).

Science.gov (United States)

Theunissen, Bert

2014-06-01

In the history of genetics Arend Hagedoorn (1885-1953) is mainly known for the 'Hagedoorn effect', which states that part of the changes in variability that populations undergo over time are due to chance effects. Leaving this contribution aside, Hagedoorn's work has received scarcely any attention from historians. This is mainly due to the fact that Hagedoorn was an expert in animal breeding, a field that historians have only recently begun to explore. His work provides an example of how a prominent geneticist envisaged animal breeding to be reformed by the new science of heredity. Hagedoorn, a pupil of Hugo de Vries, tried to integrate his insights as a Mendelian geneticist and an animal breeding expert in a unified view of heredity, eugenics and evolution. In this paper I aim to elucidate how these fields were connected in Hagedoorn's work. Copyright © 2014 Elsevier Ltd. All rights reserved.

Review of genetic concepts

International Nuclear Information System (INIS)

Robinson, A.

1984-01-01

In recent years, practitioners of medicine have become increasingly aware of the importance of genetics in the understanding of physical and mental health and in the management of disease. The last decades have witnessed unprecedented developments in genetics that have increased our understanding of the basic processes of heredity enormously. New techniques and understanding have provided insights directly applicable to medicine. The fundamental fact of heredity may be considered the ability of living organisms to produce offspring that resemble their parents more than others. One of the basic characteristics of the human condition is the uniqueness and diversity of all individuals. This results from their genetic individuality (with the exception of identical twins) and the interaction of the genetic constitution (the genome) with the environment, which is generally unique to the individual as well. In short, the interaction of genes with the environment is what confers biologic uniqueness to all humans

High Satisfaction and Low Distress in Breast Cancer Patients One Year after BRCA-Mutation Testing without Prior Face-to-Face Genetic Counseling.

Science.gov (United States)

Sie, Aisha S; Spruijt, Liesbeth; van Zelst-Stams, Wendy A G; Mensenkamp, Arjen R; Ligtenberg, Marjolijn J L; Brunner, Han G; Prins, Judith B; Hoogerbrugge, Nicoline

2016-06-01

According to standard practice following referral to clinical genetics, most high risk breast cancer (BC) patients in many countries receive face-to-face genetic counseling prior to BRCA-mutation testing (DNA-intake). We evaluated a novel format by prospective study: replacing the intake consultation with telephone, written and digital information sent home. Face-to-face counseling then followed BRCA-mutation testing (DNA-direct). One year after BRCA-result disclosure, 108 participants returned long-term follow-up questionnaires, of whom 59 (55 %) had previously chosen DNA-direct (intervention) versus DNA-intake (standard practice i.e., control: 45 %). Questionnaires assessed satisfaction and psychological distress. All participants were satisfied and 85 % of DNA-direct participants would choose this procedure again; 10 % would prefer DNA-intake and 5 % were undecided. In repeated measurements ANOVA, general distress (GHQ-12, p = 0.01) and BC-specific distress (IES-bc, p = 0.03) were lower in DNA-direct than DNA-intake at all time measurements. Heredity-specific distress (IES-her) did not differ significantly between groups. Multivariate regression analyses showed that choice of procedure did not significantly contribute to either general or heredity-specific distress. BC-specific distress (after BC diagnosis) did contribute to both general and heredity-specific distress. This suggests that higher distress scores reflected BC experience, rather than the type of genetic diagnostic procedure. In conclusion, the large majority of BC patients that used DNA-direct reported high satisfaction without increased distress both in the short term, and 1 year after conclusion of genetic testing.

Limits of imagination: the 150th Anniversary of Mendel's Laws, and why Mendel failed to see the importance of his discovery for Darwin's theory of evolution.

Science.gov (United States)

Singh, Rama S

2015-09-01

Mendel is credited for discovering Laws of Heredity, but his work has come under criticism on three grounds: for possible falsification of data to fit his expectations, for getting undue credit for the laws of heredity without having ideas of segregation and independent assortment, and for being interested in the development of hybrids rather than in the laws of heredity. I present a brief review of these criticisms and conclude that Mendel deserved to be called the father of genetics even if he may not, and most likely did not, have clear ideas of segregation and particulate determiners as we know them now. I argue that neither Mendel understood the evolutionary significance of his findings for the problem of genetic variation, nor would Darwin have understood their significance had he read Mendel's paper. I argue that the limits to imagination, in both cases, came from their mental framework being shaped by existing paradigms-blending inheritance in the case of Darwin, hybrid development in the case of Mendel. Like Einstein, Darwin's natural selection was deterministic; like Niels Bohr, Mendel's Laws were probabilistic-based on random segregation of trait-determining "factors". Unlike Einstein who understood quantum mechanics, Darwin would have been at a loss with Mendel's paper with no guide to turn to. Geniuses in their imaginations are like heat-seeking missiles locked-in with their targets of deep interests and they generally see things in one dimension only. Imagination has limits; unaided imagination is like a bird without wings--it goes nowhere.

Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies

NARCIS (Netherlands)

A. González-Neira (Anna); J.M. Rosa-Rosa; A. Osorio (Ana); E. Gonzalez (Emilio); M.C. Southey (Melissa); O. Sinilnikova (Olga); H. Lynch (Henry); R.A. Oldenburg (Rogier); C.J. van Asperen (Christi); N. Hoogerbrugge (Nicoline); G. Pita (Guillermo); P. Devilee (Peter); D. Goldgar (David); J. Benítez (Javier)

2007-01-01

textabstractBackground: The recent development of new high-throughput technologies for SNP genotyping has opened the possibility of taking a genome-wide linkage approach to the search for new candidate genes involved in heredity diseases. The two major breast cancer susceptibility genes BRCA1 and

Controlling complexity: the clinical relevance of mouse complex genetics

Czech Academy of Sciences Publication Activity Database

Forejt, Jiří

2013-01-01

Roč. 21, č. 11 (2013), s. 1191-1196 ISSN 1018-4813 Institutional support: RVO:68378050 Keywords : Mouse model * Forward genetics * Rewiev Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 4.225, year: 2013

Factors associated with the time to the first wheezing episode in infants : a cross-sectional study from the International Study of Wheezing in Infants (EISL)

NARCIS (Netherlands)

Pacheco-Gonzalez, Rosa M.; Mallol, Javier; Sole, Dirceu; Brand, Paul L. P.; Perez-Fernandez, Virginia; Sanchez-Solis, Manuel; Garcia-Marcos, Luis

2016-01-01

Male gender, asthmatic heredity, perinatal tobacco smoke exposure and respiratory infections have been associated with wheeze in the first years of life, among other risk factors. However, information about what factors modify the time to the first episode of wheeze in infants is lacking. The

Association analysis of SNPs in the porcine CYP2E1 gene with skatole, indole, and androstenone levels in backfat of a crossbred pig population

Czech Academy of Sciences Publication Activity Database

Zadinová, K.; Stupka, R.; Stratil, Antonín; Čítek, J.; Vehovský, K.; Lebedová, N.; Šprysl, M.; Okrouhlá, M.

2017-01-01

Roč. 131, č. 1 (2017), s. 68-73 ISSN 0309-1740 Institutional support: RVO:67985904 Keywords : boar taint * PCR-RFLP * HPLC Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.126, year: 2016

African Journal of Biotechnology - Vol 9, No 53 (2010)

African Journals Online (AJOL)

Analysis of combining ability and heredity parameters of glucosinolates in Chinese kale · EMAIL FREE FULL TEXT EMAIL FREE FULL TEXT DOWNLOAD FULL TEXT DOWNLOAD FULL TEXT. G-J Chen, Y Si, B-H Cao, E-Y Feng, J-J Lei, 9026-9031 ...

Radiation and heredity: genetic aspects of protection against radiation

International Nuclear Information System (INIS)

Mosseh, I.B.

1990-01-01

Primary radiogenetic effects and delayed genetic radiation effects are considered. Experimental and published data on possibility to protect organisms and populations against single and long-term (during life of several generations) effect of ionizing radiation are given. Problem concerning population adaptation to low dose irradiation is discussed. 490 refs., 28 figs., 43 tabs

Making Heredity Matter: Samuel Butler's Idea of Unconscious Memory.

Science.gov (United States)

Turbil, Cristiano

2018-03-01

Butler's idea of evolution was developed over the publication of four books, several articles and essays between 1863 and 1890. These publications, although never achieving the success expected by Butler, proposed a psychological elaboration of evolution (robustly enforced by Lamarck's philosophy), called 'unconscious memory'. This was strongly in contrast with the materialistic approach suggested by Darwin's natural selection. Starting with a historical introduction, this paper aspires to ascertain the logic, meaning and significance of Butler's idea of 'unconscious memory' in the post-Darwinian physiological and psychological Pan-European discussion. Particular attention is devoted to demonstrating that Butler was not only a populariser of science but also an active protagonist in the late Victorian psychological debate.

Eugenics and Curriculum: 1860-1929.

Science.gov (United States)

Selden, Steven

1978-01-01

Examines ideas about heredity, racism, and the development of the eugenics movement, which influenced curriculum thinkers in the period of the "naturalistic mind" and progressivism; the eugenics movement's influence upon education for the gifted; and continuing similar attitudes as to the limited effect of environment on individuals…

Evolution of Karyotypes in Chameleons

Czech Academy of Sciences Publication Activity Database

Rovatsos, M.; Altmanová, M.; Johnson Pokorná, Martina; Velenský, P.; Baca, A. S.; Kratochvíl, L.

2017-01-01

Roč. 8, č. 12 (2017), č. článku 382. ISSN 2073-4425 Institutional support: RVO:67985904 Keywords : karyotype evolution * ITS * rDNA Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.600, year: 2016

Effect of oxalic acid on the mite Varroa destructor and its host the honey bee Apis mellifera

Czech Academy of Sciences Publication Activity Database

Papežíková, I.; Palíková, M.; Kremserová, Silvie; Zachová, A.; Peterová, H.; Babák, V.; Navrátil, S.

2017-01-01

Roč. 56, č. 4 (2017), s. 400-408 ISSN 0021-8839 Institutional support: RVO:68081707 Keywords : programmed cell-death * temperate climate * colony losses Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 1.364, year: 2016

Het immuunsysteem en de ziekte van Alzheimer

NARCIS (Netherlands)

van Exel, E.; Eikelenboom, P.; Comijs, H. C.; Kurniawan, C.; Frölich, M.; Smit, J. H.; Stek, M. L.; Scheltens, P.; Eefsting, J. E.; Westendorp, R. G. J.

2011-01-01

It has still not been established unequivocally whether vascular risk factors and inflammatory reactions, determined by heredity, are a cause or a result of Alzheimer's disease If the offspring of parents with AD have more risk factors and more frequent and severe inflammatory reactions than the

Molecular characterization of circulating tumor cells from patients with metastatic breast cancer reflects evolutionary changes in gene expression under the pressure of systemic therapy

Czech Academy of Sciences Publication Activity Database

Aaltonen, K. E.; Novosadová, Vendula; Bendahl, P.-O.; Graffman, C.; Larsson, A.-M.; Ryden, L.

2017-01-01

Roč. 8, č. 28 (2017), s. 45544-45565 ISSN 1949-2553 Institutional support: RVO:86652036 Keywords : metastatic breast cancer * circulating tumor cells * gene expression Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 5.168, year: 2016

Bulletin of Materials Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

Author Affiliations. Li Yajiang1 2 Wang Juan2 Yin Yansheng2 Ma Haijun2. Key Lab of Liquid Structure and Heredity of Materials, Ministry of Education, Shandong University, Jinan 250061, China; National Key Lab of Advanced Welding Technology, Harbin Institute of Technology, Harbin 150001, China ...

The complete mitochondrial transcript of the red tail loach Yasuhikotakia modesta as assembled from RNAseq (Teleostei: Botiidae)

Czech Academy of Sciences Publication Activity Database

Grau, J. H.; Hilgers, L.; Altmüller, J.; Šlechtová, Vendula; Bohlen, Jörg

2017-01-01

Roč. 2, č. 1 (2017), s. 46-47 ISSN 2380-2359 R&D Projects: GA ČR GA13-37277S Institutional support: RVO:67985904 Keywords : Yasuhikotakia modesta * loach * Botiidae Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3)

Revised Guidelines for Comprehensive Health Education, Grades 10-12.

Science.gov (United States)

Nebraska State Dept. of Education, Lincoln. Div. of Instructional Services.

These health curriculum guidelines were designed for teachers of secondary students. Four major topic areas are covered: 1) anatomy, physiology, tissues, systems, heredity, physical activity, and nutriition; 2) family structures, functions, and responsibilities; 3) values, stress, and drug abuse; and 4) the environment, disease control, cancer,…

Genetic analysis and QTL mapping of maize yield and associate ...

African Journals Online (AJOL)

STORAGESEVER

2008-06-17

Jun 17, 2008 ... strongly influenced by both genotype and environment, and the interaction of ... associated with yield components as well as secondary ... QTLs that control grain yield under drought ... statistical analysis (ANOVA etc) of phenotypic traits was carried out .... which means that the loci had stable heredity.

The holist tradition in twentieth century genetics. Wilhelm Johannsen's genotype concept.

Science.gov (United States)

Roll-Hansen, Nils

2014-06-01

The terms 'genotype', 'phenotype' and 'gene' originally had a different meaning from that in the Modern Synthesis. These terms were coined in the first decade of the twentieth century by the Danish plant physiologist Wilhelm Johannsen. His bean selection experiment and his theoretical analysis of the difference between genotype and phenotype were important inputs to the formation of genetics as a well-defined special discipline. This paper shows how Johannsen's holistic genotype theory provided a platform for criticism of narrowly genocentric versions of the chromosome theory of heredity that came to dominate genetics in the middle decades of the twentieth century. Johannsen came to recognize the epoch-making importance of the work done by the Drosophila group, but he continued to insist on the incompleteness of the chromosome theory. Genes of the kind that they mapped on the chromosomes could only give a partial explanation of biological heredity and evolution. © 2014 The Author. The Journal of Physiology © 2014 The Physiological Society.

Parameter determination of hereditary models of deformation of composite materials based on identification method

Science.gov (United States)

Kayumov, R. A.; Muhamedova, I. Z.; Tazyukov, B. F.; Shakirzjanov, F. R.

2018-03-01

In this paper, based on the analysis of some experimental data, a study and selection of hereditary models of deformation of reinforced polymeric composite materials, such as organic plastic, carbon plastic and a matrix of film-fabric composite, was pursued. On the basis of an analysis of a series of experiments it has been established that organo-plastic samples behave like viscoelastic bodies. It is shown that for sufficiently large load levels, the behavior of the material in question should be described by the relations of the nonlinear theory of heredity. An attempt to describe the process of deformation by means of linear relations of the theory of heredity leads to large discrepancies between the experimental and calculated deformation values. The use of the theory of accumulation of micro-damages leads to much better description of the experimental results. With the help of the hierarchical approach, a good approximation of the experimental values was successful only in the first three sections of loading.

Eugenics and public health in American history.

Science.gov (United States)

Pernick, M S

1997-11-01

Supporters of eugenics, the powerful early 20th-century movement for improving human heredity, often attacked that era's dramatic improvements in public health and medicine for preserving the lives of people they considered hereditarily unfit. Eugenics and public health also battled over whether heredity played a significant role in infectious diseases. However, American public health and eugenics had much in common as well. Eugenic methods often were modeled on the infection control techniques of public health. The goals, values, and concepts of disease of these two movements also often overlapped. This paper sketches some of the key similarities and differences between eugenics and public health in the United States, and it examines how their relationship was shaped by the interaction of science and culture. The results demonstrate that eugenics was not an isolated movement whose significance is confined to the histories of genetics and pseudoscience, but was instead an important and cautionary part of past public health and a general medical history as well.

Ovarian cancer at young age: the contribution of mismatch-repair defects in a population-based series of epithelial ovarian

DEFF Research Database (Denmark)

Domanska, K; Malander, S; Måsbäck, A

2007-01-01

age is a hallmark of heredity, and ovarian cancers associated with HNPCC have been demonstrated to develop at a particularly early age. We used the Swedish Cancer Registry to identify a population-based series of 98 invasive epithelial ovarian cancers that developed before 40 years. Mucinous......At least one of ten patients with ovarian cancer is estimated to develop their tumor because of heredity with the breast and ovarian cancer syndrome due to mutations in the BRCA1 and BRCA2 genes and hereditary nonpolyposis colorectal cancer (HNPCC) being the major genetic causes. Cancer at young...... and endometrioid cancers were overrepresented and were diagnosed in 27% and 16% of the tumors, respectively. Immunostaining using antibodies against MLH1, PMS2, MSH2, and MSH6 was used to assess the mismatch-repair status and revealed loss of expression of MLH1/PMS2 in two cases, loss of MSH2/MSH6 in one case...

Gregor Mendel, OSA (1822-1884), founder of scientific genetics.

Science.gov (United States)

Dunn, P M

2003-11-01

Gregor Mendel, an Augustinian monk and part-time school teacher, undertook a series of brilliant hybridisation experiments with garden peas between 1857 and 1864 in the monastery gardens and, using statistical methods for the first time in biology, established the laws of heredity, thereby establishing the discipline of genetics.

From Phenotype to Genotype: Exploring Middle School Students' Understanding of Genetic Inheritance in a Web-Based Environment

Science.gov (United States)

Williams, Michelle; Montgomery, Beronda L.; Manokore, Viola

2012-01-01

Research shows that students face challenges as they learn about genetic inheritance. The challenges could emanate from the fact that genetic inheritance involves unseen processes at different organizational levels. We explored students' understanding of heredity and related concepts such as cells and reproduction using a Web-based Science Inquiry…

Association assessment of Interleukine-10 gene polymorphism and ...

African Journals Online (AJOL)

Seyedeh Zahra Mousavi

eral factors increase the risk of CAD such as age, gender, heredity, smoking, high blood cholesterol, high blood pressure, physical inactivity, and obesity. These factors make people prone to the coronary heart disease [3]. The cytokines are potent inflammatory factors that regulate each stage of atherosclerosis and leading ...

Variabilité génétique et compréhension de la transmission de l ...

African Journals Online (AJOL)

Moreover, other minor genes could be implicated. The findings will extend the genetic diversity used to optimize commercial seed production with low acidity. These findings open the way to research other genes probably implicated in the variation of palm oil acidity. Keywords: acidity, genetic variability, heredity, oil palm ...

PITYRIASIS VERSICOLOR – POSSIBLE GENETIC BASIS ...

African Journals Online (AJOL)

Non-occurrence of Pityriasis versicolor (PV) in spouses of individuals with this superficial fungal infection despite several years of cohabitation suggests that heredity might play an important role in those affected. Forty subjects who were married were studied in two phases. The first phase involved using a detailed ...

Genetic Determinism vs. Phenotypic Plasticity in Protist Morphology

Czech Academy of Sciences Publication Activity Database

Mulot, M.; Marcisz, K.; Grandgirard, L.; Lara, E.; Kosakyan, Anush; Robroek, B. J. M.; Lamentowicz, M.; Payne, R. J.; Mitchell, E.A.D.

2017-01-01

Roč. 64, č. 6 (2017), s. 729-739 ISSN 1066-5234 Institutional support: RVO:60077344 Keywords : Body size * protozoa * soil moisture * testate amoebae * water table depth Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.692, year: 2016

Genetics and developmental biology of cooperation

Czech Academy of Sciences Publication Activity Database

Kasper, C.; Vierbuchen, M.; Ernst, Ulrich R.; Fischer, S.; Radersma, R.; Raulo, A.; Cunha-Saraiva, F.; Wu, M.; Mobley, K. B.; Taborsky, B.

2017-01-01

Roč. 26, č. 17 (2017), s. 4364-4377 ISSN 0962-1083 Institutional support: RVO:61388963 Keywords : altruism * behaviour * indirect genetic effects * social behaviour * social effects Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 6.086, year: 2016

Bulletin of Materials Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

Author Affiliations. Li Yajiang1 2 Wang Juan2 Liu Peng2. National Key Laboratory of Advanced Welding Production Technology, Harbin Institute of Technology, Harbin 150001, P.R. China; Key Laboratory of Liquid Structure and Heredity of Materials, Ministry of Education, Shandong University, Jinan 250061, P.R. China ...

Genetic diversity and phylogeny of the Christmas Island flying fox (Pteropus melanotus natalis)

Czech Academy of Sciences Publication Activity Database

Phalen, D. N.; Hall, J.; Ganesh, G.; Hartigan, Ashlie; Smith, C.; De Jong, C.; Field, H.; Rose, K.

2017-01-01

Roč. 98, č. 2 (2017), s. 428-437 ISSN 0022-2372 Institutional support: RVO:60077344 Keywords : diversity * flying fox * mitochondrial DNA * phylogeny * Pteropus melanotus natalis Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 1.630, year: 2016

Weldon's Search for a Direct Proof of Natural Selection and the ...

Indian Academy of Sciences (India)

fused, reception to Darwin's principle of natural selection in the .... This was the context in which he developed a particulate theory of heredity – 'pangenesis'. He ... Thereafter, following the independent rediscovery of Mendelian laws by de Vries, .... differences in traits among individuals that could be transmitted to offspring.

[Sex-linked juvenile retinoschisis].

Science.gov (United States)

François, P; Turut, P; Soltysik, C; Hache, J C

1976-02-01

About 13 observations of sexe linked juvenile retinoschisis, the authors describe the ophthalmoscopic, fluorographic and functional aspects of the disease whose caracteristics are:--its sexe linked recessive heredity; --its clinical characterestics associating: a microcystic macular degeneration, peripheral retinal lesions, vitreous body alterations, --an electroretinogram of the negative type.

Neural Differentiation Is Inhibited through HIF1 alpha/ beta-Catenin Signaling in Embryoid Bodies

Czech Academy of Sciences Publication Activity Database

Veceřa, J.; Kudová, Jana; Kučera, J.; Kubala, Lukáš; Pachernik, J.

2017-01-01

Roč. 2017, č. 2017 (2017), č. článku 8715798. ISSN 1687-966X Institutional support: RVO:68081707 Keywords : stem- cell fate * hypoxia * oxygen Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.540, year: 2016

Similar group mean scores, but large individual variations, in patient-relevant outcomes over 2 years in meniscectomized subjects with and without radiographic knee osteoarthritis

DEFF Research Database (Denmark)

Paradowski, Przemyslaw T; Englund, Martin; Roos, Ewa M.

2004-01-01

Epidemiological studies have, so far, identified factors associated with increased risk for incident or progressive OA, such as age, sex, heredity, obesity, and joint injury. There is, however, a paucity of long-term data that provide information on the nature of disease progression on either gro...... knee osteoarthritis (OA)....

The Learning Needs of Children.

Science.gov (United States)

Taylor, Mary; Sister Valerie

1990-01-01

The child's psychosocial and physiological development are discussed in terms of a limiting environment and program expectations. Some factors to consider are (1) heredity and heritage; (2) experience; (3) maturation; (4) social transmission; and (5) equilibration. Sensitive educators must prepare the environment for the child, not for the…

From Mendel's discovery on pea to today's plant genetics and breeding : Commemorating the 150th anniversary of the reading of Mendel's discovery.

Science.gov (United States)

Smýkal, Petr; K Varshney, Rajeev; K Singh, Vikas; Coyne, Clarice J; Domoney, Claire; Kejnovský, Eduard; Warkentin, Thomas

2016-12-01

This work discusses several selected topics of plant genetics and breeding in relation to the 150th anniversary of the seminal work of Gregor Johann Mendel. In 2015, we celebrated the 150th anniversary of the presentation of the seminal work of Gregor Johann Mendel. While Darwin's theory of evolution was based on differential survival and differential reproductive success, Mendel's theory of heredity relies on equality and stability throughout all stages of the life cycle. Darwin's concepts were continuous variation and "soft" heredity; Mendel espoused discontinuous variation and "hard" heredity. Thus, the combination of Mendelian genetics with Darwin's theory of natural selection was the process that resulted in the modern synthesis of evolutionary biology. Although biology, genetics, and genomics have been revolutionized in recent years, modern genetics will forever rely on simple principles founded on pea breeding using seven single gene characters. Purposeful use of mutants to study gene function is one of the essential tools of modern genetics. Today, over 100 plant species genomes have been sequenced. Mapping populations and their use in segregation of molecular markers and marker-trait association to map and isolate genes, were developed on the basis of Mendel's work. Genome-wide or genomic selection is a recent approach for the development of improved breeding lines. The analysis of complex traits has been enhanced by high-throughput phenotyping and developments in statistical and modeling methods for the analysis of phenotypic data. Introgression of novel alleles from landraces and wild relatives widens genetic diversity and improves traits; transgenic methodologies allow for the introduction of novel genes from diverse sources, and gene editing approaches offer possibilities to manipulate gene in a precise manner.

William Keith Brooks and the naturalist's defense of Darwinism in the late-nineteenth century.

Science.gov (United States)

Nash, Richard

2015-06-01

William Keith Brooks was an American zoologist at Johns Hopkins University from 1876 until his death in 1908. Over the course of his career, Brooks staunchly defended Darwinism, arguing for the centrality of natural selection in evolutionary theory at a time when alternative theories, such as neo-Lamarckism, grew prominent in American biology. In his book The Law of Heredity (1883), Brooks addressed problems raised by Darwin's theory of pangenesis. In modifying and developing Darwin's pangenesis, Brooks proposed a new theory of heredity that sought to avoid the pitfalls of Darwin's hypothesis. In so doing he strengthened Darwin's theory of natural selection by undermining arguments for the inheritance of acquired characteristics. In later attacks on neo-Lamarckism, Brooks consistently defended Darwin's theory of natural selection on logical grounds, continued to challenge the idea of the inheritance of acquired characteristics, and argued that natural selection best explained a wide range of adaptations. Finally, he critiqued Galton's statistical view of heredity and argued that Galton had resurrected an outmoded typological concept of species, one which Darwin and other naturalists had shown to be incorrect. Brooks's ideas resemble the "biological species concept" of the twentieth century, as developed by evolutionary biologist Ernst Mayr and others. The late-nineteenth century was not a period of total "eclipse" of Darwinism, as biologists and historians have hitherto seen it. Although the "Modern Synthesis" refers to the reconciliation of post-Mendelian genetics with evolution by natural selection, we might adjust our understanding of how the synthesis developed by seeing it as the culmination of a longer discussion that extends back to the late-nineteenth century.

Deshayes, 1834

African Journals Online (AJOL)

SARAH

30 nov. 2013 ... “No correlation between inbreeding depression and delayed selfing in the freshwater snail. Physa acuta”. Évolution 61:2655–2670. Henry P. Y., Bousset L., Sourrouille P., & Jarne P.,. 2005. “Partial selfing, ecological disturbance and reproductive assurance in an invasive freshwater snail”. Heredity, 95, pp ...

Awareness of Societal Issues among High School Biology Teachers Teaching Genetics

Science.gov (United States)

Lazarowitz, Reuven; Bloch, Ilit

2005-01-01

The purpose of this study was to investigate how aware high school biology teachers are of societal issues (values, moral, ethic, and legal issues) while teaching genetics, genetics engineering, molecular genetics, human heredity, and evolution. The study includes a short historical review of World War II atrocities during the Holocaust when…

Seeds as emerging hotspot for maintenance of genome stability

Czech Academy of Sciences Publication Activity Database

Diaz, Mariana; Pečinka, Aleš

2017-01-01

Roč. 82, č. 5 (2017), s. 467-470 ISSN 0011-4545 Institutional support: RVO:61389030 Keywords : Chromatin * Chromosome * DNA damage repair * Genome stability * Seed * Structural maintenance of chromosome Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 0.913, year: 2016

Ostéo-onycho-dystrophie héréditaire chez l'enfant à propos d'un cas ...

African Journals Online (AJOL)

... osteo-onychodysplasia replies on a group of argument with mutation in LMX1B gene being at the forefront. We can then understand the diagnostic difficulties of such cases in under medicalised countries where genotypic workups are not yet routinely done. Keywords: Ostéo-onychodystroplasia, heredity, child, Yaounde, ...

Metabolism in time and space – exploring the frontier of developmental biology

Czech Academy of Sciences Publication Activity Database

Krejčí, Alena; Tennessen, J. M.

2017-01-01

Roč. 144, č. 18 (2017), s. 3193-3198 ISSN 0950-1991 Institutional support: RVO:60077344 Keywords : metabolism * mitochondria * aerobic glycolysis Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 5.843, year: 2016 http://dev.biologists.org/content/144/18/3193

Expanding the Qawm: Culturally Savvy Counterinsurgency and Nation-Building in Afghanistan

Science.gov (United States)

2010-03-31

and guidance. They will not tend to look to Kabul or the institutions of the central government. In addition to locale and heredity , qawms may...should provide space for a garden area Afghans take great pride in growing gardens. Provide a space for them to grow plants , flowers, fruits, and

Crumbling Diversity: Comparison of Historical Archived and Contemporary Natural Populations Indicate Reduced Genetic Diversity and Increasing Genetic Differentiation in the Golden-Cheeked Warbler

Science.gov (United States)

2011-06-01

clavata. Heredity 101:120–126 Crow JF, Denniston C (1988) Inbreeding and variance effective population numbers. Evolution 42:482–495 Dixo M, Metzger JP...University Press, Cambridge, pp 361–366 Young A, Boyle T, Brown T (1996) The population genetic consequences of habitat fragmentation for plants . Trends

A New Hope? Overcoming the Limitations of Effects-Based Operations

Science.gov (United States)

2007-05-10

sway. Nor does the equation of a “Warlord” to a Junta government apply because often the “Warlord” is the head of a tribe through heredity or has...operations. More communities without power give rise to a greater disenfranchised population. In considering power plants as a target to 12

Child Development and Curriculum in Waldorf Education.

Science.gov (United States)

Schmitt-Stegmann, Astrid

Every educational theory has behind it a particular image of human beings and their development that supports a particular view of the learning process. This paper examines the image of children underlying Waldorf education. The paper identifies the individual and unique Self as the "third factor," that together with heredity and…

The "Lethal Chamber": Further Evidence of the Euthanasia Option.

Science.gov (United States)

Elks, Martin A.

1993-01-01

Historical discussions of the euthanasia or "lethal chamber" option in relation to people with mental retardation are presented. The paper concludes that eugenic beliefs in the primacy of heredity over environment and the positive role of natural selection may have condoned the poor conditions characteristic of large, segregated institutions and…

The N-Terminal Part of the Dishevelled DEP Domain Is Required for Wnt/beta-Catenin Signaling in Mammalian Cells

Czech Academy of Sciences Publication Activity Database

Pacliková, P.; Bernatík, O.; Radaszkiewicz, T.W.; Bryja, Vítězslav

2017-01-01

Roč. 37, č. 18 (2017), č. článku e00145-17. ISSN 0270-7306 Institutional support: RVO:68081707 Keywords : beta-catenin * tumor-suppressor * planar polarity Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 4.398, year: 2016

Genetic parameters and correlations among linear type traits in the ...

African Journals Online (AJOL)

user

2011-02-28

Feb 28, 2011 ... of Holstein heredity (BLD), respectively. The fixed effect of technician was denoted by TEC, the random effect of animal additive genetic effect and residual effects were shown by A and E, respectively. Each of the fixed effects was investigated via SAS software (proc Generalized Linear Model). In this study,.

Anthropological significance of dermatoglyphic trait variation: an ...

African Journals Online (AJOL)

Heredity, 23: 53-58. Hajn V., Gasiorowski A., 1999. Quantitative values on fingers and palms in Czech and. Polish populations. Biologica, 37: 107- 115. Henneberg M.J., Lambert K.M., Leigh C.M., 1997. Fingerprint homoplasy: Koalas and humans. Natural Science. Holt S.B., 1968. The genetics of dermal ridges. Thomas ...

Journal of Biosciences | Indian Academy of Sciences

Indian Academy of Sciences (India)

2005-01-07

Jan 7, 2005 ... Role of heredity and lifestyle in sporadic cancers is well documented. Here we focus on the influence of low penetrance genes and habits, with emphasis on tobacco habit in causing head and neck cancers. Role of such gene-environment interaction can be well studied in individuals with multiple primary ...

Differential distribution of Y-chromosome haplotypes in Swiss and Southern European goat breeds

Czech Academy of Sciences Publication Activity Database

Vidal, O.; Drögemüller, C.; Obexer-Ruff, G.; Reber, I.; Jordana, J.; Martínez, A.; Bâlteanu, V. A.; Delgado, J. V.; Eghbalsaied, S.; Landi, V.; Goyache, F.; Traore, A.; Pazzola, M.; Vacca, G.M.; Badaoui, B.; Pilla, F.; D'Andrea, M.; Álvarez, I.; Capote, J.; Sharaf, Abdoallah; Pons, A.; Amills, M.

2017-01-01

Roč. 7, NOV 23 (2017), č. článku 16161. ISSN 2045-2322 Institutional support: RVO:60077344 Keywords : mitochondrial-dna * nucleotide diversity * genetic diversity * domestication * origins * phylogenies * east Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 4.259, year: 2016

Mutations in spliceosomal proteins and retina degeneration

Czech Academy of Sciences Publication Activity Database

Růžičková, Šárka; Staněk, David

2017-01-01

Roč. 14, č. 5 (2017), s. 544-552 ISSN 1547-6286 R&D Projects: GA MŠk LO1419 Institutional support: RVO:68378050 Keywords : Retinitis pigmentosa * snRNP * splicing Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.900, year: 2016

Sequence divergence between spelt and common wheat

Czech Academy of Sciences Publication Activity Database

Liu, M.; Zhao, Q.; Qi, F.; Stiller, J.; Tang, Q.; Miao, J.; Vrána, Jan; Holušová, Kateřina; Liu, D.; Doležel, Jaroslav; Manners, J. M.; Han, B. P.; Liu, C.

2018-01-01

Roč. 131, č. 5 (2018), s. 1125-1132 ISSN 0040-5752 R&D Projects: GA MŠk(CZ) LO1204 Institutional support: RVO:61389030 Keywords : BREAD WHEAT * DNA * DIVERSITY Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 4.132, year: 2016

The Design of Studies to Evaluate Hereditary and Environmental Contributions to the Etiology of Behavioral Disorders.

Science.gov (United States)

Rosenthal, David

The introductory discussion focuses on the change in the current scientific climate regarding the role of heredity in the etiology of behavioral disorders. The author and his colleagues embarked on a series of studies, using naturally occurring adoptions as their subject source, to tease apart hereditary and environmental factors thought to be…

A Doctor Talks to 9-to-12-Year Olds.

Science.gov (United States)

Larrigo, Marion O.; Cassidy, Michael A.

As a part of a series of books written by physicians for their patients, this publication explains heredity, birth, and growth patterns to pre-teen children. The chapters are written in language appropriate for children moving from childhood into their teens and deal with topics like: cells, conception, prenatal development, puberty, and changing…

A Mutation of the Prdm9 Mouse Hybrid Sterility Gene Carried by a Transgene

Czech Academy of Sciences Publication Activity Database

Mihola, Ondřej; Trachtulec, Zdeněk

2017-01-01

Roč. 63, č. 1 (2017), s. 27-30 ISSN 0015-5500 R&D Projects: GA MŠk(CZ) LQ1604 Institutional support: RVO:68378050 Keywords : Prdm9 * transgene * meiosis Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 0.939, year: 2016

A Socratic Method for Surveying Students' Readiness to Study Evolution

Science.gov (United States)

Stansfield, William D.

2013-01-01

Before beginning a series of presentations on evolution, it would be prudent to survey the general level of students' understanding of prerequisite basic concepts of reproduction, heredity, ontology, and phenotypic diversity so that teachers can avoid devoting time to well-known subjects of general knowledge and can spend more time on subjects…

Hypoxia Downregulates MAPK/ERK but Not STAT3 Signaling in ROS-Dependent and HIF-1-Independent Manners in Mouse Embryonic Stem Cells

Czech Academy of Sciences Publication Activity Database

Kučera, J.; Netušilová, J.; Sládeček, S.; Lanová, M.; Vašíček, Ondřej; Štefková, K.; Navrtilová, J.; Kubala, Lukáš; Pacherník, J.

2017-01-01

Roč. 2017, č. 2017 (2017), č. článku 386947. ISSN 1942-0900 Institutional support: RVO:68081707 Keywords : PROTEIN PHOSPHATASE 2A * CHLORIDE-INDUCED APOPTOSIS * INDUCIBLE FACTOR 1-ALPHA Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 4.593, year: 2016

Legionella becoming a mutualist: adaptive processes shaping the genome of symbiont in the louse Polyplax serrata

Czech Academy of Sciences Publication Activity Database

Říhová, J.; Nováková, Eva; Husník, F.; Hypša, Václav

2017-01-01

Roč. 9, č. 11 (2017), s. 2946-2957 ISSN 1759-6653 Grant - others:GA MŠk(CZ) LM2015042 Institutional support: RVO:60077344 Keywords : symbiosis * horizontal gene transfer * genome evolution Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.979, year: 2016

Family perspectives in lynch syndrome becoming a family at risk, patterns of communication and influence on relations

Directory of Open Access Journals (Sweden)

Bartuma Katarina

2012-05-01

Full Text Available Abstract Background A growing number of individuals are diagnosed with hereditary cancer. Though increased levels of anxiety and depression have been demonstrated around the time of genetic counselling, most individuals handle life at increased risk well. Data have, however, been collected on individual basis, which led us to focus on family perspectives of hereditary cancer. Methods Lynch syndrome represents a major type of hereditary colorectal and gynaecological cancer. We preformed open-ended interviews with 27 informants from 9 Lynch syndrome families. Inductive content analysis revealed three major themes: transition to a risk family, patterns of communication and influence on family relations and individual roles. Results Family members described how learning about Lynch syndrome shifted focus from daily issues to concerns about cancer. Changes in communication related to difficulties in talking to children about heredity and informing new family members and distant relatives about an increased risk of cancer. Influence on relations was exemplified by family members taking on different roles, e.g. females often being responsible for coordinating information about heredity and providing support. Families in which members had experienced cancer at young age typically informed children soon after learning about heredity and at young age, whereas families with experience of cancer at higher age postponed information and thereby also genetic counselling. Conclusions Three major family perspectives are described in Lynch syndrome families; becoming a risk family, patterns of communication and influence on family relations. Since these issues are central, our findings suggests that such family perspectives should be considered during genetic counselling in order to contribute to information spread, help family members cope with the increased risk, and motivate family members at risk to undergo surveillance.

Examining the evidence for major histocompatibility complex-dependent mate selection in humans and nonhuman primates

Czech Academy of Sciences Publication Activity Database

Winternitz, Jamie Caroline; Abbate, J. L.

2015-01-01

Roč. 6, 13 May (2015), s. 73-88 ISSN 1179-7274 R&D Projects: GA MŠk(CZ) EE2.3.30.0048 Institutional support: RVO:67985939 Keywords : secual selection * olfaction * facial attraction * inbreeding avoidance * parasite resistance Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3)

Microstructural characterization in diffusion bonded TiC–Al 2 O 3 ...

Indian Academy of Sciences (India)

The diffusion bonded TiC–Al2O3/Cr18–Ni8 joint was investigated by a variety of characterization techniques such as scanning electron microscope (SEM) with energy dispersion ... Key Lab of Liquid Structure and Heredity of Materials, Ministry of Education, Shandong University (South Campus), Jinan 250061, P.R. China ...

Mitochondrial DNA provides evidence of a double origin for the stone crayfish Austropotamobius torrentium in the Elbe basin

Czech Academy of Sciences Publication Activity Database

Petrusek, A.; Pešek, P.; Leština, Dan; Martin, P.; Fischer, D.; Kozák, P.; Vlach, P.

2017-01-01

Roč. 62, JAN 01 (2017), s. 77-83 ISSN 0075-9511 Institutional support: RVO:60077344 Keywords : stone crayfish * Austropotamobius torrentium * Elbe basin Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 1.427, year: 2016 https://www.sciencedirect.com/science/article/pii/S0075951116300901

Genetic effect of neutrons

International Nuclear Information System (INIS)

Luchnik, N.V.; Sevan'kaev, A.V.; Fesenko, Eh.V.

1984-01-01

Gene mutations resulting from neutron effect are considered, but attention is focused on chromosome mutations. Dose curves for different energy of neutrons obtained at different objects are obtained which makes it possible to consider RBE of neutrons depending on their energy and radiation dose and to get some information on the neutron effect on heredity

Site-Specific Differentiation of Fibroblasts in Normal and Scleroderma Skin

Science.gov (United States)

2009-06-01

the accordance in the structure and growth of animals and plants . London: The Syden- ham Society, 1–268 Sessa L, Breiling A, Lavorgna G, Silvestri L...targets. Heredity 97:88–96 Wolpert L (1969) Positional information and the spatial pattern of cellular differentiation. J Theor Biol 25:1–47 Yamaguchi Y

R-ES-ONANCE--I -Novem-be-r

Indian Academy of Sciences (India)

itself with heredity, the single most characteristic feature of the living world. Also ... They tried to see whether, by combining Mendel's laws with the. Darwinian ... The question of senescence or growing old is quite different from the ... females, which have two. .... Price was that the best thing for an individual to do when it.

Catalase in Leishmaniinae: With me or against me?

Czech Academy of Sciences Publication Activity Database

Kraeva, N.; Horáková, Eva; Kostygov, A.Y.; Kořený, Luděk; Butenko, A.; Yurchenko, V.; Lukeš, Julius

2017-01-01

Roč. 50, JUN (2017), s. 121-127 ISSN 1567-1348 R&D Projects: GA ČR(CZ) GA16-18699S Institutional support: RVO:60077344 Keywords : Catalase * Leishmania * Trypanosomatids * Gene loss Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.885, year: 2016

Centromeric and non-centromeric satellite DNA organisation differs in holocentric Rhynchospora species

Czech Academy of Sciences Publication Activity Database

Ribeiro, T.; Marques, A.; Novák, Petr; Schubert, V.; Vanzela, A.L.L.; Macas, Jiří; Houben, A.; Pedrosa-Harand, A.

2017-01-01

Roč. 126, September 19 (2017), s. 325-335 ISSN 0009-5915 R&D Projects: GA ČR GBP501/12/G090 Institutional support: RVO:60077344 Keywords : Chromocentre * Cyperaceae * Heterochromatin * Holocentric chromosome Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 4.414, year: 2016

Clinical Features of Primary Glaucoma in South East Nigeria ...

African Journals Online (AJOL)

Background: The clinical course of glaucoma depends on the type, onset, severity and response to treatment. The intraocular pressure and heredity also play a role in its presentation as members of the same family tend to have the same type of glaucoma. This paper seeks to address the problem of primary open angle ...

Establishment and evolution of the radiation risk concept for the man and human population in the 20th century

International Nuclear Information System (INIS)

Vassilev, G.; Hadjieva

2003-01-01

The concept of radiation risk (RR) is the main basis for human protection from the harmful effect of ionizing radiation. It concerns the expected unfavorable health effects upon the irradiated person and probably upon his/her progeny. The early period of the history of RR evaluation was grounded on the assessment of acute skin reactions (erythema, epilation, dermatitis, ulceration) and on the measures (erythema dose) taken to diminish them. The second period covers the appraisal, based on estimation of different somatic effects and expected heredity ( genetic effects). They could be avoided if irradiation does not exceed the maximum permissible dose - the concept of zero RR. The current (third) period estimates both irradiation effects: deterministic effects that have a dose-related threshold and stochastic non-threshold effects. The ultimate goal of radiation protection is to exclude all deterministic effects and to diminish probability of stochastic effects (carcinogenesis and heredity effects) down to an acceptable level. Seven postulates describe the modern concept of RR for the man and human population: globalization irreversibility, accumulation, non-threshold harm, stochastic, non-specificity and acceptance of the risk

Persönlichkeitsentwicklung als ziel der Bildung: Aus der Sicht eines Psychologen

Science.gov (United States)

Heinze, Burger

1990-06-01

Personality, which is a term almost always used in a positive sense, does not exist from the moment of birth, but it develops under the influence of heredity and environment. Adolescence, which is seen as a transition from childhood to adulthood, raises difficulties in many modern industrialized countries as a result of the often arduous search for individual identity. In this context identity is seen as an interaction between heredity and environment. While developing his own personality, the young person has to maintain an integral existence vis-à-vis himself, society and life. Psychology defines the personality as the sum of numerous psychological characteristics, through which differences between people are revealed. The development of these characteristics is to be seen in the environment, maturation and actions of the individual. It can be subdivided into causes, conditions and processes. Finally the article discusses various aspects of the general question of education. The author concludes that the development of the personality should be an aim of education, but that this aim is presently unattainable because of a lack of clarity in the concept of education.

From Mendel to epigenetics: History of genetics.

Science.gov (United States)

Gayon, Jean

2016-01-01

The origins of genetics are to be found in Gregor Mendel's memoir on plant hybridization (1865). However, the word 'genetics' was only coined in 1906, to designate the new science of heredity. Founded upon the Mendelian method for analyzing the products of crosses, this science is distinguished by its explicit purpose of being a general 'science of heredity', and by the introduction of totally new biological concepts (in particular those of gene, genotype, and phenotype). In the 1910s, Mendelian genetics fused with the chromosomal theory of inheritance, giving rise to what is still called 'classical genetics'. Within this framework, the gene is simultaneously a unit of function and transmission, a unit of recombination, and of mutation. Until the early 1950s, these concepts of the gene coincided. But when DNA was found to be the material basis of inheritance, this congruence dissolved. Then began the venture of molecular biology, which has never stopped revealing the complexity of the way in which hereditary material functions. Copyright © 2016 Académie des sciences. Published by Elsevier SAS. All rights reserved.

Radiation heredity: unusual structural-phase states and metallic crystals properties

International Nuclear Information System (INIS)

Melikhov, V.D.; Skakov, M.K.

1998-01-01

Some experimental results allowing to judge about possibilities of unusual structural phase states formation during use irradiation and high temperature treatment of metallic crystals are considered. During study of pure (99.99 %) and especially pure (99.999 %) aluminium it was established, that after heating of preliminary irradiated samples in reactor, and non-irradiated ones up to temperatures above melting point (660 deg C), but not higher than 820 deg C, and cooling an microstructure and substructure of both irradiated and non-irradiated metals have been essentially distinguished with each other. If first of them had typically polycrystal construction, that second one was monocrystal with good developed initial substructure. Radiation effects have been preserved even in liquid metal if it was not overheated higher critical point, which is determined by phase transition from quasi-liquid state to true liquid one. During study of irradiation and postradiation treatment of structure and properties of intermetallides Fe 3 Al it was revealed, that in initially irradiated regulated alloys the radiation effect is preserving at heating of above 0.85 T melt (that essentially exceed order-disorder transition temperature) (550 deg C) in non-irradiated alloys of prolonged exposure and hardening. At that, irradiated-hardened alloy distinguishing from not hardened one by lattice parameter (on 0.1 %), by configuration of nearest surrounding of iron atoms in elementary cell, by regulating extent of different kind of atoms in lattice knocks. It was revealed, that at fluence (5·10 24 n·m 2 ) an appearance of new phases, distinguishing from matrix by component content. It was shown, that irradiation and post-radiation treatment are methods for creation unusual structural-phase states and attach to metals and alloys new properties

Heredity, physiology and malt quality analysis of albino-lemma barley

International Nuclear Information System (INIS)

Jin Ting; Wu Kuanran; Yang Jianming; Jia Qiaojun; Wang Junmei; Hua Wei; Chen He; Qiao Hailong

2013-01-01

The barley 0601 is a spontaneous albino-lemma mutant from beer barley cultivar Supi3. Genetic control of albino-lemma trait in the mutant 0601 and, the agronomic traits (thousand kernel weight, kernel plumpness), physiological traits (chlorophyll content, proanthocyanidin content) and major malt qualities (diastatic power, malt extract, Kolbach index) were investigated. The results showed that the albino-lemma trait is controlled by one recessive gene, and there were significant differences between the mutant and its wild-type in thousand kernel weight, kernel plumpness, chlorophyll content, diastatic power, and the malt extract, whereas no significant difference in proanthocyanidin content was found. These results provide the basis on mapping and cloning the albino-lemma gene and also provide good material for genetic research. (authors)

Evidence for a major role of heredity in Graves' disease

DEFF Research Database (Denmark)

Brix, T H; Kyvik, K O; Christensen, Kaare

2001-01-01

The etiology of Graves' disease (GD), affecting up to 2% of a population in iodine-sufficient areas, is incompletely understood. According to current thinking, the development of GD depends on complex interactions among genetic, environmental, and endogenous factors. However, the relative...... contributions of the genetic and environmental factors remain to be clarified. In this study we report probandwise concordance rates for GD in a new cohort of same sex twin pairs born between 1953 and 1976 (young cohort), ascertained from the nationwide population-based Danish Twin Register. To elucidate...... the magnitude of the genetic and environmental influence in the etiology of GD, these new twin data were pooled with our previously published twin data on GD (old cohort). The old cohort consisted of 2338 same sex twin pairs born between 1870 and 1920 who had participated in questionnaire surveys during...

The complete mitochondrial genome of the phytopathogenic fungus Phomopsis longicolla

Czech Academy of Sciences Publication Activity Database

Koloniuk, Igor; Hrabáková, Lenka; Petrzik, Karel

2016-01-01

Roč. 27, č. 6 (2016), s. 3979-3980 ISSN 1940 -1736 R&D Projects: GA MŠk LH13136; GA MŠk(CZ) EE2.3.30.0032 Institutional support: RVO:60077344 Keywords : Diaporthales * Mitogenome * Phomopsis Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.350, year: 2016

Breeding of newly licensed wheat variety Huapei 8 and improved ...

African Journals Online (AJOL)

H2 was the best selection generation for traits with high heredity ability, and H3 was the best selection for grain traits and yield test. Consequently, we bred and licensed six new wheat varieties derived from anther culture and significantly reduced breeding time to three to five years. Huapei 8 was the newest released wheat ...

Assessing pre- and post-zygotic barriers between North Atlantic eels (Anguilla anguilla and A. rostrata)

DEFF Research Database (Denmark)

Jacobsen, M. W.; Smedegaard, L.; Sørensen, Sune Riis

2017-01-01

Elucidating barriers to gene flow is important for understanding the dynamics of speciation. Here we investigate pre- and post-zygotic mechanisms acting between the two hybridizing species of Atlantic eels: Anguilla anguilla and A. rostrata. Temporally varying hybridization was examined by analyz...... in natural hybrids.Heredity advance online publication, 9 November 2016; doi:10.1038/hdy.2016.96....

Fluctuations of pol I and fibrillarin contents of the nucleoli

Czech Academy of Sciences Publication Activity Database

Hornaceka, M.; Kováčik, L.; Mazel, T.; Cmarko, D.; Bártová, Eva; Raška, I.; Smirnov, E.

2017-01-01

Roč. 8, č. 4 (2017), s. 421-432 ISSN 1949-1034 R&D Projects: GA ČR GBP302/12/G157 Institutional support: RVO:68081707 Keywords : ribosomal-rna genes * transcription sites * human-lymphocytes Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.387, year: 2016

Third release of the plant rDNA database with updated content and information on telomere composition and sequenced plant genomes

Czech Academy of Sciences Publication Activity Database

Vitales, D.; D'Ambrosio, U.; Galvez, F.; Kovařík, Aleš; Garcia, S.

2017-01-01

Roč. 303, č. 8 (2017), s. 1115-1121 ISSN 0378-2697 R&D Projects: GA ČR(CZ) GC16-02149J Institutional support: RVO:68081707 Keywords : in-situ hybridization * ribosomal-rna genes * 5s rdna Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 1.239, year: 2016

RSM22, mtYsxC and PNKD-like proteins are required for mitochondrial translation in Trypanosoma brucei

Czech Academy of Sciences Publication Activity Database

Týč, Jiří; Novotná, L.; Peña-Diaz, Priscila; Maslov, D. A.; Lukeš, Julius

2017-01-01

Roč. 34, MAY (2017), s. 67-74 ISSN 1567-7249 R&D Projects: GA ČR GA15-21974S Institutional support: RVO:60077344 Keywords : PNKD * YsxC * YihA * mitochondrial ribosome * LSU * SSU Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.704, year: 2016

The Gene: Time, Space and Spirit--Keys to Scientific Literacy Series.

Science.gov (United States)

Stonebarger, Bill

It has only been since the late nineteenth century that people have understood the mechanics of heredity and the discoveries of genes and DNA are even more recent. This booklet considers three aspects of genetics; time, space, and spirit. Time refers to a sense of history; space refers to geography; and spirit refers to life and thought. Several…

Tracking the evolutionary pathway of sex chromosomes among fishes: characterizing the unique XX/XY1Y2 system in Hoplias malabaricus (Teleostei, Characiformes)

Czech Academy of Sciences Publication Activity Database

de Oliveira, E. A.; Sember, Alexandr; Bertollo, L.A.C.; Yano, C. F.; Ezaz, T.; Moreira-Filho, O.; Hatanaka, T.; Trifonov, V.; Liehr, T.; Al-Rikabi, A. B. H.; Ráb, Petr; Pains, H.; de Bello Cioffi, M.

2018-01-01

Roč. 127, č. 1 (2018), s. 115-128 ISSN 0009-5915 R&D Projects: GA MŠk EF15_003/0000460 Institutional support: RVO:67985904 Keywords : fish cytogenetics * male-specific region * whole chromosome painting Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 4.414, year: 2016

The Work of The Fields Medallists: 19981

Indian Academy of Sciences (India)

To make the resulting theory independent of this auxiliary choice, one integrates over the parameter space of such choices, viz. M . g. It turns out that one has to consider a surface together with a choice of n labelled points on it. .... At present, my son and I are extremely interested in genetics and heredity. From: Gene Antics.

Overexpression of TET dioxygenases in seminomas associates with low levels of DNA methylation and hydroxymethylation

Czech Academy of Sciences Publication Activity Database

Benešová, Martina; Trejbalová, Kateřina; Kučerová, Dana; Vernerová, Z.; Hron, Tomáš; Szabo, A.; Amouroux, R.; Klezl, P.; Hajkova, P.; Hejnar, Jiří

2017-01-01

Roč. 56, č. 8 (2017), s. 1837-1850 ISSN 0899-1987 R&D Projects: GA MZd NT14601 Institutional support: RVO:68378050 Keywords : 5-hydroxymethylcytosine * 5-methylcytosine * germ cell tumor * seminoma * TET 1 Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 4.185, year: 2016

Morphologically indistinguishable hybrid Carassius female with 156 chromosomes: A threat for the threatened crucian carp, C. carassius, L

Czech Academy of Sciences Publication Activity Database

Knytl, M.; Kalous, L.; Rylková, K.; Choleva, Lukáš; Merilä, J.; Ráb, Petr

2018-01-01

Roč. 13, č. 1 (2018), č. článku e0190924. E-ISSN 1932-6203 R&D Projects: GA MŠk EF15_003/0000460 Institutional support: RVO:67985904 Keywords : Carrasius carrasius * chromosome Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.806, year: 2016

Gene conversion events and variable degree of homogenization of rDNA loci in cultivars of Brassica napus

Czech Academy of Sciences Publication Activity Database

Sochorova, Jana; Coriton, O.; Kuderová, Alena; Lunerová Bedřichová, Jana; Chevre, A.-M.; Kovařík, Aleš

2017-01-01

Roč. 119, č. 1 (2017), s. 13-26 ISSN 0305-7364 R&D Projects: GA ČR(CZ) GA13-10057S Institutional support: RVO:68081707 Keywords : ribosomal-rna genes * concerted evolution * intergenic spacer Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 4.041, year: 2016

Epidemiology Of Alcoholic Liver Disease

Directory of Open Access Journals (Sweden)

А.Г. Мартынова

2009-12-01

Full Text Available One of the main factors of chronic liver disease is alcohol. The level of alcoholic liver disease incidence and cirrhosis mortality has increased considerably in the recent years in many countries. The risk of development and disease progression are determined by the effect of endogenous and exogenous factors: "drinking mode", female gender, heredity and genetic predisposition, obesity, concomitant viral hepatitis

Regulation of MLH1 mRNA and protein expression by promoter methylation in primary colorectal cancer

DEFF Research Database (Denmark)

Jensen, Lars Henrik; Rasmussen, Anders Aamann; Byriel, Lene

2013-01-01

In colorectal cancer MLH1 deficiency causes microsatellite instability, which is relevant for the patient's prognosis and treatment, and its putative heredity. Dysfunction of MLH1 is caused by sporadic gene promoter hypermethylation or by hereditary mutations as seen in Lynch Syndrome. The aim...... of this study was to determine in detail how DNA methylation regulates MLH1 expression and impacts clinical management....

Karyotypes and Distribution of Tandem Repeat Sequences in Brassica nigra Determined by Fluorescence in situ Hybridization

Czech Academy of Sciences Publication Activity Database

Wang, G.; He, Q.; Macas, Jiří; Novák, Petr; Neumann, Pavel; Meng, D.; Zhao, H.; Guo, N.; Han, S.; Zong, M.; Jin, W.; Liu, F.

2017-01-01

Roč. 152, č. 3 (2017), s. 158-165 ISSN 1424-8581 R&D Projects: GA ČR GBP501/12/G090 Institutional support: RVO:60077344 Keywords : asymmetric somatic hybridization * Fluorescence in situ hybridization * Karyotype * (Peri) centromere Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 1.354, year: 2016

100 million years of multigene family evolution: origin and evolution of the avian MHC class IIB

Czech Academy of Sciences Publication Activity Database

Goebel, J.; Promerová, Marta; Bonadonna, F.; McCoy, K. D.; Serbielle, C.; Strandh, M.; Yannic, G.; Burri, R.; Fumagalli, L.

2017-01-01

Roč. 18, č. 460 (2017), s. 1-9 ISSN 1471-2164 R&D Projects: GA ČR GAP505/10/1871 Institutional support: RVO:68081766 Keywords : Birds * Birth -death evolution * Concerted evolution * Gene duplication * Gene conversion * Major histocompatibility complex * Recombination Subject RIV: EG - Zoology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.729, year: 2016

Epigenetic control of reproductive development

Czech Academy of Sciences Publication Activity Database

Lorenzo, J.L.R.; Hobza, Roman; Vyskot, Boris

2017-01-01

Roč. 303, č. 8 (2017), s. 991-1000 ISSN 0378-2697 R&D Projects: GA ČR GBP501/12/G090 Institutional support: RVO:68081707 Keywords : ribosomal-rna genes * demeter dna glycosylase * flowering time * arabidopsis-thaliana Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 1.239, year: 2016

Tandem affinity purification of AtTERT reveals putative interaction partners of plant telomerase in vivo

Czech Academy of Sciences Publication Activity Database

Majerská, J.; Schrumpfová, P.; Dokládal, Ladislav; Schorová, Š.; Stejskal, K.; Obořil, M.; Honys, D.; Kozáková, L.; Polanská, P.; Sýkorová, Eva

2017-01-01

Roč. 254, č. 4 (2017), s. 1547-1562 ISSN 0033-183X R&D Projects: GA ČR GA13-06943S Institutional support: RVO:68081707 Keywords : single-stranded-dna * genome-wide screen * arabidopsis-thaliana * reverse-transcriptase Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.870, year: 2016

Concerted evolution rapidly eliminates sequence variation in rDNA coding regions but not in intergenic spacers in Nicotiana tabacum allotetraploid

Czech Academy of Sciences Publication Activity Database

Lunerová Bedřichová, Jana; Renny-Byfield, S.; Matyášek, Roman; Leitch, A.; Kovařík, Aleš

2017-01-01

Roč. 303, č. 8 (2017), s. 1043-1060 ISSN 0378-2697 R&D Projects: GA ČR(CZ) GA17-11642S; GA ČR(CZ) GC16-02149J Institutional support: RVO:68081707 Keywords : Concerted evolution * Immunomodulation * Neutrophils Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 1.239, year: 2016

Asexual queen succession mediates an accelerated colony life cycle in the termite Silvestritermes minutus

Czech Academy of Sciences Publication Activity Database

Fougeyrollas, R.; Křivánek, Jan; Roy, V.; Dolejšová, Klára; Frechault, S.; Roisin, Y.; Hanus, Robert; Sillam-Dusses, D.

2017-01-01

Roč. 26, č. 12 (2017), s. 3295-3308 ISSN 0962-1083 R&D Projects: GA ČR(CZ) GA14-12774S Institutional support: RVO:61388963 Keywords : asexual queen succession * breeding system * life history * parthenogenesis * Silvestritermes minutus * termites Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 6.086, year: 2016

Oscar Riddle's Science, a Special Bird, & the Founding of the NABT

Science.gov (United States)

Vandervoort, Frances S.

2013-01-01

Oscar Riddle, born in Indiana in 1877, was an ardent evolutionist and a key player in the founding of the National Association of Biology Teachers in 1938. He studied heredity and behavior in domestic pigeons and doves with Charles O. Whitman of the University of Chicago, received his Ph.D. in zoology in 1907, and in 1912 began a long career at…

100 million years of multigene family evolution: origin and evolution of the avian MHC class IIB

Czech Academy of Sciences Publication Activity Database

Goebel, J.; Promerová, Marta; Bonadonna, F.; McCoy, K. D.; Serbielle, C.; Strandh, M.; Yannic, G.; Burri, R.; Fumagalli, L.

2017-01-01

Roč. 18, č. 460 (2017), s. 1-9 ISSN 1471-2164 R&D Projects: GA ČR GAP505/10/1871 Institutional support: RVO:68081766 Keywords : Birds * Birth-death evolution * Concerted evolution * Gene duplication * Gene conversion * Major histocompatibility complex * Recombination Subject RIV: EG - Zoology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.729, year: 2016

Integrating plant and animal biology for the search of novel DNA damage biomarkers

Czech Academy of Sciences Publication Activity Database

Nikitaki, Z.; Holá, Marcela; Donà, M.; Pavlopoulou, A.; Michalopoulos, I.; Angelis, Karel; Georgakilas, A. G.; Macovei, I.; Balestrazzi, A.

2018-01-01

Roč. 775, JAN-MAR (2018), s. 21-38 ISSN 1383-5742 R&D Projects: GA ČR GA16-01137S Institutional support: RVO:61389030 Keywords : DNA damage response * Ionizing radiation * Radiation exposure monitoring * Radiotolerance * Ultraviolet radiation Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 5.500, year: 2016

Sex Chromosome Evolution and Genomic Divergence in the Fish Hoplias malabaricus (Characiformes, Erythrinidae)

Czech Academy of Sciences Publication Activity Database

Sember, Alexandr; Bertollo, L.A.C.; Ráb, Petr; Yano, C. F.; Hatanaka, T.; de Oliveira, E. A.; de Bello Cioffi, M.

2018-01-01

Roč. 9, č. 1 (2018), č. článku 71. ISSN 1664-8021 R&D Projects: GA MŠk EF15_003/0000460 Institutional support: RVO:67985904 Keywords : fish cytogenetics * multiple sex chromosomes * sex-determining region Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.789, year: 2016

Elainella gen. nov.: a new tropical cyanobacterium characterized using a complex genomic approach

Czech Academy of Sciences Publication Activity Database

Jahodářová, E.; Dvořák, P.; Hašler, P.; Holušová, Kateřina; Poulíčková, A.

2018-01-01

Roč. 53, č. 1 (2018), s. 39-51 ISSN 0967-0262 R&D Projects: GA MŠk(CZ) LO1204 Institutional support: RVO:61389030 Keywords : 16S rRNA * genome sequencing * new genus * phylogenomics * Pseudophormidium * tropical cyanobacteria Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.412, year: 2016

Dynamics of tandemly repeated DNA sequences during evolution of diploid and tetraploid botiid loaches (Teleostei: Cobitoidea: Botiidae)

Czech Academy of Sciences Publication Activity Database

Sember, Alexandr; Bohlen, Jörg; Šlechtová, Vendula; Altmanová, Marie; Pelikánová, Šárka; Ráb, Petr

2018-01-01

Roč. 13, č. 3 (2018), č. článku e0195054. E-ISSN 1932-6203 R&D Projects: GA ČR GA13-37277S; GA MŠk EF15_003/0000460 Institutional support: RVO:67985904 Keywords : polyploidization * loach Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.806, year: 2016

Transcriptional stimulation of rate-limiting components of the autophagic pathway improves plant fitness

Czech Academy of Sciences Publication Activity Database

Minina, E. A.; Moschou, P. N.; Vetukuri, R. R.; Sanchez-Vera, V.; Cardoso, C.; Liu, Q.; Elander, P. H.; Dalman, K.; Beganovic, M.; Lindberg Yilmaz, J.; Marmon, S.; Shabala, S.; Suarez, M.; Ljung, K.; Novák, Ondřej; Shabala, S.; Stymne, S.; Hofius, D.; Bozhkov, P. V.

2018-01-01

Roč. 69, č. 6 (2018), s. 1415-1432 ISSN 0022-0957 Institutional support: RVO:61389030 Keywords : Aging * ATG genes * Autophagy * Autophagy-related ubiquitin-like conjugation systems * Biomass * Oil content * Ratelimiting components of autophagic flux * Seed yield * Stress resistance * Transcriptional regulation Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 5.830, year: 2016

A Genetic Study of Wild Populations and Evolution A Genetic Study of Wild Populations and Evolution

Directory of Open Access Journals (Sweden)

Hovanitz William

1944-06-01

Full Text Available The determination of the scientific basis of heredity within the last two decades and the verification of the principal conclusions in many different plants and animals has made possible the application of analytical methods in the study of variations in wild populations. As with the physical and chemical sciences, genetics has been enabled to make use of mathematics to compound (often theoretically out of simple units, the genes, the complexity known as an organism, much in the same way as a chemist compounds molecules with atoms and the physicist compounds atoms with protons and electrons. The determination of the scientific basis of heredity within the last two decades and the verification of the principal conclusions in many different plants and animals has made possible the application of analytical methods in the study of variations in wild populations. As with the physical and chemical sciences, genetics has been enabled to make use of mathematics to compound (often theoretically out of simple units, the genes, the complexity known as an organism, much in the same way as a chemist compounds molecules with atoms and the physicist compounds atoms with protons and electrons.

Cultural differences in rated typicality and perceived causes of memory changes in adulthood.

Science.gov (United States)

Bottiroli, Sara; Cavallini, Elena; Fastame, Maria Chiara; Hertzog, Christopher

2013-01-01

This study examined cultural differences in stereotypes and attributions regarding aging and memory. Two subcultures belonging to the same country, Italy, were compared on general beliefs about memory. Sardinians live longer than other areas of Italy, which is a publically shared fact that informs stereotypes about that subculture. An innovative instrument evaluating simultaneously aging stereotypes and attributions about memory and memory change in adulthood was administered to 52 Sardinian participants and 52 Milanese individuals divided into three age groups: young (20-30), young-old (60-70), and old-old (71-85) adults. Both Milanese and Sardinians reported that memory decline across the life span is more typical than a pattern of stability or improvement. However, Sardinians viewed stability and improvement in memory as more typical than did the Milanese. Interestingly, cultural differences emerged in attributions about memory improvement. Although all Sardinian age groups rated nutrition and heredity as relevant causes in determining the memory decline, Sardinians' rated typicality of life-span memory improvement correlated strongly with causal attributions to a wide number of factors, including nutrition and heredity. Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

Eugenics and American social history, 1880-1950.

Science.gov (United States)

Allen, G E

1989-01-01

Eugenics, the attempt to improve the human species socially through better breeding was a widespread and popular movement in the United States and Europe between 1910 and 1940. Eugenics was an attempt to use science (the newly discovered Mendelian laws of heredity) to solve social problems (crime, alcoholism, prostitution, rebelliousness), using trained experts. Eugenics gained much support from progressive reform thinkers, who sought to plan social development using expert knowledge in both the social and natural sciences. In eugenics, progressive reformers saw the opportunity to attack social problems efficiently by treating the cause (bad heredity) rather than the effect. Much of the impetus for social and economic reform came from class conflict in the period 1880-1930, resulting from industrialization, unemployment, working conditions, periodic depressions, and unionization. In response, the industrialist class adopted firmer measures of economic control (abandonment of laissez-faire principles), the principles of government regulation (interstate commerce, labor), and the cult of industrial efficiency. Eugenics was only one aspect of progressive reform, but as a scientific claim to explain the cause of social problems, it was a particularly powerful weapon in the arsenal of class conflict at the time.

Lost in translation: Defects in transfer RNA modifications and neurological disorders

Czech Academy of Sciences Publication Activity Database

Bednářová, Andrea; Hanna, M.; Durham, I.; Van Cleave, T.; England, A.; Chaudhuri, A.; Krishnan, N.

2017-01-01

Roč. 10, MAY 09 (2017), č. článku 135. ISSN 1662-5099 Grant - others:GA ČR(CZ) L200961701 Institutional support: RVO:60077344 Keywords : transfer RNA modifications * modified nucleosides * neurological disease Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 5.076, year: 2016 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5422465/

Chromosomal Evolution in Lower Vertebrates: Sex Chromosomes in Neotropical Fishes

Czech Academy of Sciences Publication Activity Database

Cioffi, M. de B.; Yano, C. F.; Sember, Alexandr; Bertollo, L.A.C.

2017-01-01

Roč. 8, č. 10 (2017), č. článku 258. ISSN 2073-4425 R&D Projects: GA MŠk EF15_003/0000460 Institutional support: RVO:67985904 Keywords : alternative evolutionary models * simple and multiple sex chromosomes * independent and common origins Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.600, year: 2016

Nonfamilial cherubism

Directory of Open Access Journals (Sweden)

A Trivedi

2013-01-01

Full Text Available Cherubism is a non neoplastic progressive heredity disease affecting the jaw bones. It is a benign disease with a characteristic symmetrical involvement of the maxilla and mandible. It usually affects children before 5 years of age, with painless progressive swelling of the cheeks, frequently associated with dental malformations. Here, we are presenting a case report of a 12-year-old boy suffering from cherubism.

Parents experiences and opinions about childrenˈs emotions

OpenAIRE

Prašnikar, Barbara

2013-01-01

Different authors may give different interpretations of emotions, however everyone agrees, that emotions affect all areas of life: health, learning, interpersonal relationships and behaviour. The development of emotion alongside the broader environment and heredity, is also largely influenced by teachers in kindergarten who may have beneficial effects on the emotional development of preschool children. With conversation, storytelling, explanations ... they develop children’s communication s...

Higher-order organisation of extremely amplified, potentially functional and massively methylated 5S rDNA in European pikes (Esox sp.)

Czech Academy of Sciences Publication Activity Database

Symonová, R.; Ocalewicz, K.; Kirtiklis, L.; Delmastro, G. B.; Pelikánová, Šárka; Garcia, S.; Kovařík, Aleš

2017-01-01

Roč. 18, č. 391 (2017), č. článku 391. ISSN 1471-2164 R&D Projects: GA ČR GA14-02940S; GA ČR GBP501/12/G090 Institutional support: RVO:67985904 ; RVO:68081707 Keywords : rDNA * evolution * chromosome Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.729, year: 2016

Targeting of BCL2 Family Proteins with ABT-199 and Homoharringtonine Reveals BCL2- and MCL1-Dependent Subgroups of Diffuse Large B-Cell Lymphoma

Czech Academy of Sciences Publication Activity Database

Klanova, M.; Anděra, Ladislav; Bražina, Jan; Švadlenka, Jan; Benešová, Simona; Soukup, J.; Průková, D.; Vejmelkova, D.; Jaksa, R.; Helman, K.; Vockova, P.; Lateckova, L.; Molinsky, J.; Maswabi, B.C.; Alam, M.; Kodet, R.; Pytlik, R.; Trneny, M.; Klener, P.

2016-01-01

Roč. 22, č. 5 (2016), s. 1138-1149 ISSN 1078-0432 R&D Projects: GA ČR GA14-19590S Institutional support: RVO:68378050 Keywords : NON-HODGKINS-LYMPHOMA * PROGNOSTIC-SIGNIFICANCE * OMACETAXINE MEPESUCCINATE * GENE-EXPRESSION * APOPTOSIS * REARRANGEMENT * SURVIVAL * LEUKEMIA * CANCER * AGENTS Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 9.619, year: 2016

Loss of lamin B receptor is necessary to induce cellular senescence

Czech Academy of Sciences Publication Activity Database

Lukášová, Emilie; Kovařík, Aleš; Bačíková, Alena; Falk, Martin; Kozubek, Stanislav

2017-01-01

Roč. 474 (2017), s. 281-300 ISSN 0264-6021 R&D Projects: GA ČR GBP302/12/G157; GA ČR GBP501/12/G090 Institutional support: RVO:68081707 Keywords : oncogene-induced senescence * inner nuclear-membrane * dna-damage response Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.797, year: 2016

Clique Relaxations in Biological and Social Network Analysis Foundations and Algorithms

Science.gov (United States)

2015-10-26

NUMBER 9. SPONSORING/MONITORING AGENCY NAME(S) AND ADDRESS(ES) Optimization and Discrete Mathematics Mathematics , Information and Life Sciences Air...Business Media, 2013, pp.149-174. J. Pattillo, Y. Wang, and S. Butenko. Approximating 2-cliques in unit disk graphs. Discrete Applied Mathematics 166 (2014...for developing effective combinatorial branch-and-bound strategies for detection of maximum clique relaxation structures. The concepts of weak heredity

Variability of rooting in a small second-generation population of the hybrid Pinus attenuradiata

Science.gov (United States)

J. W. Duffield; A. R. Liddicoet

1949-01-01

Propagation of conifers by rooting of cuttings is an old art that has recently benefited by the findings of the plant physiologist. The forest tree breeder may now use rooting as a tool in his efforts to evaluate the heredity of his trees. In a study undertaken to use vegetative propagation of members of a variable hybrid population as a guide for selecting superior...

De novo transcriptome assembly facilitates characterisation of fast-evolving gene families, MHC class I in the bank vole (Myodes glareolus)

Czech Academy of Sciences Publication Activity Database

Migalska, M.; Sebastian, A.; Konczal, M.; Kotlík, Petr; Radwan, J.

2017-01-01

Roč. 118, č. 4 (2017), s. 348-357 ISSN 0018-067X R&D Projects: GA ČR GAP506/11/1872; GA ČR(CZ) GA16-03248S Institutional support: RVO:67985904 Keywords : bank vole * major histocompatibility complex * RNA-seq data Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.961, year: 2016

Impact of cytomixis on meiosis, pollen viability and pollen size in ...

Indian Academy of Sciences (India)

Srinivas

mother cells of Medicago sativa L.; J. Heredity 94 512–516. Bhat T A, Parveen S and Khan A H 2006 MMS-induced cytomixis in pollen mother cells of broad bean (Vicia faba L.); Turk. J. Bot. 30 273–279. Bione N C P, Pagliarini M S and de Toledo J F F 2000 Meiotic behavior of several Brazilian soybean varieties; Genet.

The H3Africa policy framework: negotiating fairness in genomics.

Science.gov (United States)

de Vries, Jantina; Tindana, Paulina; Littler, Katherine; Ramsay, Michèle; Rotimi, Charles; Abayomi, Akin; Mulder, Nicola; Mayosi, Bongani M

2015-03-01

Human Heredity and Health in Africa (H3Africa) research seeks to promote fair collaboration between scientists in Africa and those from elsewhere. Here, we outline how concerns over inequality and exploitation led to a policy framework that places a firm focus on African leadership and capacity building as guiding principles for African genomics research. Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.

Spermatogenesis in the parasitoid Diachasmimorpha longicaudata (Hymenoptera: Braconidae)

Czech Academy of Sciences Publication Activity Database

Carabajal Paladino, Leonela Z.; Lo Nostro, F.; Papeschi, A.; Cladera, J.; Bressa, M. J.

2017-01-01

Roč. 98, č. 1 (2017), s. 38-43 ISSN 0001-7272 R&D Projects: GA MŠk(CZ) EE2.3.30.0032 Institutional support: RVO:60077344 Keywords : Hymenoptera * modified meiosis * abortive division Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 1.211, year: 2016 http://onlinelibrary.wiley.com/doi/10.1111/azo.12148/pdf

Barriers to Breast Cancer Screening among Latinas in the U.S.-Mexico Border Region

Science.gov (United States)

2011-05-01

Services, Directorate for Information Operations and Reports (0704-0188), 1215 Jefferson Davis Highway, Suite 1204, Arlington, VA 22202- 4302...have the disease.3,5 Latina perceptions of heredity and vulnerability have operated within a framework of uneven and delayed screening encompassing...levels of awareness of these tests across racial and ethnic groups. According to the 2000 National Health Interview Survey ( NHIS ), 49.9% of non-Hispanic

The impact of high-throughput sequencing technology on speciation research: maintaining perspective

Czech Academy of Sciences Publication Activity Database

Baird, Stuart J. E.

2017-01-01

Roč. 30, č. 8 (2017), s. 1482-1487 ISSN 1010-061X R&D Projects: GA ČR GA15-13265S; GA ČR(CZ) GA17-25320S Institutional support: RVO:68081766 Keywords : hybrid incompatibilities * selection * introgression * populations * evolution * diversity Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.792, year: 2016

Glycosidases in porcine follicular fluid and their effect on zona pellucida-AWN 1 spermadhesin interaction

Czech Academy of Sciences Publication Activity Database

Dráb, T.; Ren, Štěpán; Maňásková-Postlerová, Pavla; Tichá, M.; Jonáková, Věra; Liberda, J.

2017-01-01

Roč. 100, SEP 15 2017 (2017), s. 80-87 ISSN 0093-691X R&D Projects: GA ČR GA14-05547S; GA MŠk(CZ) ED1.1.00/02.0109 Institutional support: RVO:86652036 Keywords : Glycosidases * Oocyte development * Zona pellucida * Follicle Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 1.986, year: 2016

Early exposure to secondhand tobacco smoke and the development of allergic diseases in 4 year old children in Malmö, Sweden.

Science.gov (United States)

Hansen, Kristina; Mangrio, Elisabeth; Lindström, Martin; Rosvall, Maria

2010-08-23

Earlier studies have shown an association between secondhand tobacco smoke and allergy development in children. Furthermore, there is an increased risk of developing an allergy if the parents have an allergy. However, there are only few studies investigating the potential synergistic effect of secondhand tobacco smoke and allergic heredity on the development of an allergy. The study was population-based cross-sectional with retrospective information on presence of secondhand tobacco smoke during early life. The study population consisted of children who visited the Child Health Care (CHC) centres in Malmö for their 4-year health checkup during 2006-2008 and whose parents answered a self-administered questionnaire (n = 4,278 children). The questionnaire was distributed to parents of children registered with the CHC and invited for the 4-year checkup during the study period. There was a two to four times increased odds of the child having an allergy or having sought medical care due to allergic symptoms if at least one parent had an allergy, while there were rather small increased odds related to presence of secondhand smoke during the child's first month in life or at the age of 8 months. However, children with heredity for allergies and with presence of secondhand tobacco smoke during their first year in life had highly increased odds of developing an allergy and having sought medical care due to allergic symptoms at 4 years of age. Thus, there was a synergistic effect enhancing the independent effects of heredity and exposure to secondhand tobacco smoke on allergy development. Children with a family history of allergies and early exposure to secondhand tobacco smoke is a risk group that prevention and intervention should pay extra attention to. The tobacco smoke effect on children is an essential and urgent question considering it not being self chosen, possibly giving life lasting negative health effects and being possible to reduce.

Early exposure to secondhand tobacco smoke and the development of allergic diseases in 4 year old children in Malmö, Sweden

Directory of Open Access Journals (Sweden)

Hansen Kristina

2010-08-01

Full Text Available Abstract Background Earlier studies have shown an association between secondhand tobacco smoke and allergy development in children. Furthermore, there is an increased risk of developing an allergy if the parents have an allergy. However, there are only few studies investigating the potential synergistic effect of secondhand tobacco smoke and allergic heredity on the development of an allergy. Methods The study was population-based cross-sectional with retrospective information on presence of secondhand tobacco smoke during early life. The study population consisted of children who visited the Child Health Care (CHC centres in Malmö for their 4-year health checkup during 2006-2008 and whose parents answered a self-administered questionnaire (n = 4,278 children. The questionnaire was distributed to parents of children registered with the CHC and invited for the 4-year checkup during the study period. Results There was a two to four times increased odds of the child having an allergy or having sought medical care due to allergic symptoms if at least one parent had an allergy, while there were rather small increased odds related to presence of secondhand smoke during the child's first month in life or at the age of 8 months. However, children with heredity for allergies and with presence of secondhand tobacco smoke during their first year in life had highly increased odds of developing an allergy and having sought medical care due to allergic symptoms at 4 years of age. Thus, there was a synergistic effect enhancing the independent effects of heredity and exposure to secondhand tobacco smoke on allergy development. Conclusions Children with a family history of allergies and early exposure to secondhand tobacco smoke is a risk group that prevention and intervention should pay extra attention to. The tobacco smoke effect on children is an essential and urgent question considering it not being self chosen, possibly giving life lasting negative health

Obtaining subjects' consent to publish identifying personal information: current practices and identifying potential issues.

Science.gov (United States)

Yoshida, Akiko; Dowa, Yuri; Murakami, Hiromi; Kosugi, Shinji

2013-11-25

In studies publishing identifying personal information, obtaining consent is regarded as necessary, as it is impossible to ensure complete anonymity. However, current journal practices around specific points to consider when obtaining consent, the contents of consent forms and how consent forms are managed have not yet been fully examined. This study was conducted to identify potential issues surrounding consent to publish identifying personal information. Content analysis was carried out on instructions for authors and consent forms developed by academic journals in four fields (as classified by Journal Citation Reports): medicine general and internal, genetics and heredity, pediatrics, and psychiatry. An online questionnaire survey of editors working for journals that require the submission of consent forms was also conducted. Instructions for authors were reviewed for 491 academic journals (132 for medicine general and internal, 147 for genetics and heredity, 100 for pediatrics, and 112 for psychiatry). Approximately 40% (203: 74 for medicine general and internal, 31 for genetics and heredity, 58 for pediatrics, and 40 for psychiatry) stated that subject consent was necessary. The submission of consent forms was required by 30% (154) of the journals studied, and 10% (50) provided their own consent forms for authors to use. Two journals mentioned that the possible effects of publication on subjects should be considered. Many journal consent forms mentioned the difficulties in ensuring complete anonymity of subjects, but few addressed the study objective, the subjects' right to refuse consent and the withdrawal of consent. The main reason for requiring the submission of consent forms was to confirm that consent had been obtained. Approximately 40% of journals required subject consent to be obtained. However, differences were observed depending on the fields. Specific considerations were not always documented. There is a need to address issues around the study

Obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues

Science.gov (United States)

2013-01-01

Background In studies publishing identifying personal information, obtaining consent is regarded as necessary, as it is impossible to ensure complete anonymity. However, current journal practices around specific points to consider when obtaining consent, the contents of consent forms and how consent forms are managed have not yet been fully examined. This study was conducted to identify potential issues surrounding consent to publish identifying personal information. Methods Content analysis was carried out on instructions for authors and consent forms developed by academic journals in four fields (as classified by Journal Citation Reports): medicine general and internal, genetics and heredity, pediatrics, and psychiatry. An online questionnaire survey of editors working for journals that require the submission of consent forms was also conducted. Results Instructions for authors were reviewed for 491 academic journals (132 for medicine general and internal, 147 for genetics and heredity, 100 for pediatrics, and 112 for psychiatry). Approximately 40% (203: 74 for medicine general and internal, 31 for genetics and heredity, 58 for pediatrics, and 40 for psychiatry) stated that subject consent was necessary. The submission of consent forms was required by 30% (154) of the journals studied, and 10% (50) provided their own consent forms for authors to use. Two journals mentioned that the possible effects of publication on subjects should be considered. Many journal consent forms mentioned the difficulties in ensuring complete anonymity of subjects, but few addressed the study objective, the subjects’ right to refuse consent and the withdrawal of consent. The main reason for requiring the submission of consent forms was to confirm that consent had been obtained. Conclusion Approximately 40% of journals required subject consent to be obtained. However, differences were observed depending on the fields. Specific considerations were not always documented. There is a need

Selfing for the design of genomic selection experiments in biparental plant populations.

Science.gov (United States)

McClosky, Benjamin; LaCombe, Jason; Tanksley, Steven D

2013-11-01

Self-fertilization (selfing) is commonly used for population development in plant breeding, and it is well established that selfing increases genetic variance between lines, thus increasing response to phenotypic selection. Furthermore, numerous studies have explored how selfing can be deployed to maximal benefit in the context of traditional plant breeding programs (Cornish in Heredity 65:201-211,1990a, Heredity 65:213-220,1990b; Liu et al. in Theor Appl Genet 109:370-376, 2004; Pooni and Jinks in Heredity 54:255-260, 1985). However, the impact of selfing on response to genomic selection has not been explored. In the current study we examined how selfing impacts the two key aspects of genomic selection-GEBV prediction (training) and selection response. We reach the following conclusions: (1) On average, selfing increases genomic selection gains by more than 70 %. (2) The gains in genomic selection response attributable to selfing hold over a wide range population sizes (100-500), heritabilities (0.2-0.8), and selection intensities (0.01-0.1). However, the benefits of selfing are dramatically reduced as the number of QTLs drops below 20. (3) The major cause of the improved response to genomic selection with selfing is through an increase in the occurrence of superior genotypes and not through improved GEBV predictions. While performance of the training population improves with selfing (especially with low heritability and small population sizes), the magnitude of these improvements is relatively small compared with improvements observed in the selection population. To illustrate the value of these insights, we propose a practical genomic selection scheme that substantially shortens the number of generations required to fully capture the benefits of selfing. Specifically, we provide simulation evidence that indicates the proposed scheme matches or exceeds the selection gains observed in advanced populations (i.e. F 8 and doubled haploid) across a broad range of

Science of breeding and heredity from ancient Persia to modern Iran.

Science.gov (United States)

Kariminejad, Mohammad H; Khorshidian, Ardeshir

2012-01-01

About 1700 years BC, the prophet Zoroaster declared equal right for women and men to choose their "own ways." There is much evidence that ancient Persians believed in the equal contribution of women and men toward producing a child, and all its hereditary characteristics.Even more surprising are the phrases in Vandidad book, which were gathered by Mobedans in the Mad dynasty about egg extraction (gametes) from animal reproductive organs (gonads) and their storage for future conception.Centuries later, Western philosopher beliefs in regard to reproduction were contrary to Persian knowledge. The Greek philosophers believed that man's water (semen) contains all human characteristics, and the female uterus is only responsible for nurturing and development of fetus. After detection of the ovum (de Graaf 2(nd) half 17 century) Malpigy proposed the preformation theory (ovist) which means there is a miniature human inside ovum, that grows after Semen has entered the uterus and grow into a well-developed fetus. This hypothesis was later delegated to spermatozoa. These contradictory and inappropriate beliefs were subject to discussions and dispute, until C.E. Wolf demonstrated that the embryo is a product of the fertilization of ovum by spermatozoa.800 years prior this the sage Ferdowsi "The Great Iranian Poet" explains nicely the equal participation of man and woman in the production of the fetus and transmission of characters.After the renaissance and especially in recent years, tremendous achievements have been made in unraveling biological secrets of reproduction. There was no work o n genetics in Iran until 1936, when a genetic course was added to the biology curriculum in related colleges and universities; Iranian Genetics Society was founded in 1966, initiating a steady movement in this field.Although there was an inevitable gap during the revolution and war in our country, now there is great effort by researchers to eliminate the gap and bring us into the mainstream of world science, and development in biomedical sciences in the third millennium.

Heredity nonpolyposis colorectal cancer : studies on tumor development and preventive strategies

NARCIS (Netherlands)

Rijcken, Fleur Elise Marie

2006-01-01

HNPCC is een relatief vaak voorkomend erfelijk kankersyndroom. Fleur Rijcken onderzocht de ontstaanswijze van de twee meest voorkomende HNPCC-tumoren, dikkedarm- en baarmoederkanker. Zij toonde aan dat de voorlopers van darmkanker, de dysplastische poliepen, vooral in het rechter deel van de darm

Rht18 Semidwarfism in Wheat Is Due to Increased GA 2-oxidaseA9 Expression and Reduced GA Content

Czech Academy of Sciences Publication Activity Database

Ford, B. A.; Foo, E.; Sharwood, R.; Karafiátová, Miroslava; Vrána, Jan; MacMillan, C.; Nichols, D. S.; Steuernagel, B.; Uauy, C.; Doležel, Jaroslav; Chandler, M.; Spielmeyer, W.

2018-01-01

Roč. 177, č. 1 (2018), s. 168-180 ISSN 0032-0889 R&D Projects: GA MŠk(CZ) LO1204; GA ČR GBP501/12/G090 Institutional support: RVO:61389030 Keywords : green-revolution * gibberellin biosynthesis * ectopic expression * common wheat * gene * rice * barley * mutant * chromosomes Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 6.456, year: 2016

The Lω-Compactness in Lω-Spaces

Directory of Open Access Journals (Sweden)

Shui-Li Chen

2013-01-01

Full Text Available The concepts of αω-remote neighborhood family, γω-cover, and Lω-compactness are defined in Lω-spaces. The characterizations of Lω-compactness are systematically discussed. Some important properties of Lω-compactness such as ω-closed heredity, arbitrarily multiplicative property, and preserving invariance under ω-continuous mappings are obtained. Finally, the Alexander ω-subbase lemma and the Tychonoff product theorem with respect to Lω-compactness are given.

Comparative Phylogeography of Neotropical Birds

Science.gov (United States)

2009-05-01

birds, butterflies, plants , soil type, and precipitation (Whitmore and Prance 1987); (C) study populations based largely on neo-tropical lowland...Caballero, A. 1994. Developments in the prediction of effective population size. Heredity 73:657- 679. Camargo, A., R. O. De Sa, and W. R. Heyer. 2006...157-183. Hamrick, J. L., and M. J. W. Godt. 1996. Effects of life history traits on genetic diversity in plant species. Philosophical Transactions Of

All-male hybrids of a tetrapod Pelophylax esculentus share its origin and genetics of maintenance

Czech Academy of Sciences Publication Activity Database

Doležálková-Kaštánková, Marie; Pruvost, N. B. M.; Plötner, J.; Reyer, H. U.; Janko, Karel; Choleva, Lukáš

2018-01-01

Roč. 9, č. 1 (2018), č. článku 13. ISSN 2042-6410 R&D Projects: GA MŠk EF15_003/0000460; GA ČR GJ15-19947Y; GA ČR GA13-12580S Institutional support: RVO:67985904 Keywords : Pelophylax * water frog * hemiclone Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.635, year: 2016

Inheritance of malignant melanoma in the MeLiM strain of miniature pigs

Czech Academy of Sciences Publication Activity Database

Hruban, V.; Horák, Vratislav; Fortýn, Karel; Hradecký, Jan; Klaudy, Jiří; Smith, D. M.; Reisnerová, H.; Majzlík, I.

2004-01-01

Roč. 49, č. 12 (2004), s. 453-459 ISSN 0375-8427 R&D Projects: GA ČR GA523/98/0229; GA ČR GA524/01/0162; GA AV ČR IBS5045113; GA AV ČR KSK5011112 Institutional research plan: CEZ:AV0Z5045916 Keywords : heredity of porcine melanoblastoma * animal model * cutaneous tumour Subject RIV: ED - Physiology Impact factor: 0.790, year: 2004

Comparative Dermatoglyphic Study between Autistic Patients and Normal People in Iran

OpenAIRE

Mansoureh Kazemi; Mohammad Reza Fayyazi-Bordbar; Nasser Mahdavi-Shahri

2017-01-01

Autism is a neurodevelopmental disorder originating from early childhood; nevertheless, its diagnosis is in older ages. In addition to heredity, environmental factors are also of great significance in the etiology of the disease. Dermatoglyphic patterns, albeit varied, remain stable for a lifetime and yield a large number of patterns upon examination. Studies have shown a significant association between dermatoglyphics and some diseases, especially genetic ones. We compared fingerprints betwe...

What?s in a Surname? Physique, Aptitude, and Sports Type Comparisons between Tailors and Smiths

OpenAIRE

Voracek, Martin; Rieder, Stephan; Stieger, Stefan; Swami, Viren

2015-01-01

Combined heredity of surnames and physique, coupled with past marriage patterns and trade-specific physical aptitude and selection factors, may have led to differential assortment of bodily characteristics among present-day men with specific trade-reflecting surnames (Tailor vs. Smith). Two studies reported here were partially consistent with this genetic-social hypothesis, first proposed by Bäumler (1980). Study 1 (N = 224) indicated significantly higher self-rated physical aptitude for prot...

Testing the phenotype-linked fertility hypothesis in the presence and absence of inbreeding

Czech Academy of Sciences Publication Activity Database

Forstmeier, W.; Ihle, M.; Opatová, Pavlína; Martin, K.; Knief, U.; Albrechtová, Jana; Albrecht, Tomáš; Kempenaers, B.

2017-01-01

Roč. 30, č. 5 (2017), s. 968-976 ISSN 1010-061X R&D Projects: GA ČR(CZ) GAP506/12/2472 Institutional support: RVO:68081766 Keywords : display behaviour * mate choice * phenotype-linked fertility hypothesis * precopulatory traits * sexual selection * sperm abnormalities * sperm quality * sperm velocity Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.792, year: 2016

86Rubidium uptake in mononuclear leucocytes from young subjects at increased risk of developing essential hypertension

DEFF Research Database (Denmark)

Nielsen, J R; Johansen, Torben; Pedersen, K E

1988-01-01

This study was designed to assess any changes in mononuclear leucocytes from young men at increased risk of developing essential hypertension and to determine whether any changes found were associated with borderline hypertension and/or heredity. To this end we used mononuclear leucocytes......, and especially in those borderline hypertensives with at least one hypertensive parent. The latter group was also the group at greatest risk of developing essential hypertension....

Tebufenozide resistance is associated with sex-linked inheritance in Plutella xylostella.

Science.gov (United States)

Cao, Guang-Chun; Han, Zhao-Jun

2015-04-01

The diamondback moth (DBM), Plutella xylostella (L.), is a major pest of cruciferous crops. Tebufenozide, a novel nonsteroidal ecdysone agonist, exhibits good efficacy and has played an increasingly important role in the control of Lepidopteran pests in China. For its resistance management, the genetic basis of tebufenozide resistance was studied using a laboratory selected resistant strain of DBM (resistant ratio, RR = 268). A series of crosses with laboratory susceptible and resistant strains revealed that tebufenozide resistance in this pest was partially biased toward female heredity, with a large difference in RR for F1 (RR = 29) and rF1 progeny (RR = 147). The dominance calculated for these 2 cross progeny was -0.788 and 0.09, respectively. Further analysis showed that the susceptible male and female larvae were similar in their sensitivity to tebufenozide, but the resistant female larvae showed significantly higher resistance than the resistant male larvae. The heredity of tebufenozide resistance in DBM might be linked with the W sex chromosome, which suggested that DBM has the ability to develop high levels of resistance to tebufenozide. This is the first report of sex-linked inheritance of tebufenozide resistance in P. xylostella (L.). © 2013 Institute of Zoology, Chinese Academy of Sciences.

Molecular genetics of a Chinese family with spinocerebellar ataxia

Directory of Open Access Journals (Sweden)

Dan-dan WU

2015-10-01

Full Text Available Objective　To study the genotype of the members of a Chinese family with spinocerebellar ataxia (SCA. Methods　The peripheral blood samples of 6 patients and 40 asymptomatic people belonged to the family were collected. Referring to the clinical manifestations of the proband and second-generation sequencing results, the CAG trinucleotide repeats of the pathogenic gene ATXN2 were amplified by polymerase chain reaction (PCR. The repeated times of the trinucleotide in normally and abnormally amplified alleles were defined by agarose gel electrophoresis and PCR products sequencing. Results　Autosomal dominant heredity was the cause of the SCA in this family. Six out of 46 in the fourth-generation were SCA2 patients, 7 were the carriers of pathogenic allele. The repeated times of CAG trinucleotide were within the normal range in one of the two alleles of ATXN2, but they were in abnormal range in the another one. The repeated times of CAG trinucleotide were 40-46 in abnormal alleles of patients. Conclusion　Autosomal dominant heredity SCA2 has been diagnosed in this family caused by the dynamic nutation of CAG trinucleotide repeats, and 7 pathogenic allele carriers in this family were confirmed by genetic diagnosis. DOI: 10.11855/j.issn.0577-7402.2015.08.07

Clinical study of the oral manifestations and related factors in type 2 diabetics patients.

Science.gov (United States)

Sousa, Maria Goretti de Menezes; Costa, Antonio de Lisboa Lopes; Roncalli, Angelo Giuseppe

2011-01-01

Diabetes Mellitus (DM) is reported with and associated to oral alterations, with conflicting results. The aim of this study was to identify the prevalence of oral soft tissue alterations in type 2 diabetes mellitus patients. Socioeconomic variables, gender, heredity, capillary glucose control and local factors (prosthesis, dry mouth sensation) were analyzed in 196 diabetic and non-diabetic patients enrolled in HIPERDIA, at 41 Health units of Natal, Brazil. A case study. The last blood glucose mean was 177.0 mg/dl for diabetics and 89.46 mg/dl for non-diabetics. Mean capillary blood glucose was elevated in diabetics (215.95 mg/dl); it was 102.31 mg/dl in non-diabetics. The family history confirmed the heredity nature of the disease in 68.8% of diabetic patients (n = 66) (p salivary flow was 49% (n = 47) in diabetics, and 34% (n = 34) in non-diabetics. Candidiasis was present in 30.5% of diabetic patients (n=29) and 36% of non-diabetics (n=36). Both groups had lesions in the palate - 81.4% (n = 35) in diabetics, and 71.1% in non-diabetics (n = 27) (p = 0.68). The alterations are not related to diabetes and are present independently of having or not type 2 Diabetes Mellitus.

The double pedigree: a method for studying culturally and genetically inherited behavior in tandem.

Directory of Open Access Journals (Sweden)

Etienne Danchin

Full Text Available Transgenerational sources of biological variation have been at the center of evolutionary studies ever since Darwin and Wallace identified natural selection. This is because evolution can only operate on traits whose variation is transmitted, i.e. traits that are heritable. The discovery of genetic inheritance has led to a semantic shift, resulting in the tendency to consider that only genes are inherited across generations. Today, however, concepts of heredity are being broadened again to integrate the accruing evidence of non-genetic inheritance, and many evolutionary biologists are calling for the inclusion of non-genetic inheritance into an inclusive evolutionary synthesis. Here, we focus on social heredity and its role in the inheritance of behavioral traits. We discuss quantitative genetics methods that might allow us to disentangle genetic and non-genetic transmission in natural populations with known pedigrees. We then propose an experimental design based on cross-fostering among animal cultures, environments and families that has the potential to partition inherited phenotypic variation into socially (i.e. culturally and genetically inherited components. This approach builds towards a new conceptual framework based on the use of an extended version of the animal model of quantitative genetics to integrate genetic and cultural components of behavioral inheritance.

Features of the organization of bread wheat chromosome 5BS based on physical mapping

Czech Academy of Sciences Publication Activity Database

Salina, E.A.; Nesterov, V.; Frenkel, Z.; Kiseleva, V. I.; Timonova, E. M.; Magni, F.; Vrána, Jan; Šafář, Jan; Šimková, Hana; Doležel, Jaroslav; Korol, A.; Sergeeva, E.M.

2018-01-01

Roč. 19, FEB 9 (2018), č. článku 80. ISSN 1471-2164 R&D Projects: GA ČR GBP501/12/G090; GA MŠk(CZ) LO1204 Institutional support: RVO:61389030 Keywords : Chromosome 5BS * Genetic markers * Hexaploid wheat * Physical mapping * Sequencing * Synteny * Triticum aestivum Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 3.729, year: 2016

New forms of -compactness with respect to hereditary classes

Directory of Open Access Journals (Sweden)

Abdo Mohammed Qahis

2019-01-01

Full Text Available A hereditary class on a set X is a nonempty collection of subsets closed under heredity. The aim of this paper is to introduce and study strong forms of u-compactness in generalized topological spaces with respect to a hereditary class, called  SuH-compactness and S- SuH-compactness. Also several of their properties are presented. Finally some eects of various kinds of functions on them are studied.

The Heritability of Cluster B Personality Disorders Assessed both by Personal Interview and Questionnaire

OpenAIRE

Torgersen, Svenn; Myers, John; Reichborn-Kjennerud, Ted; Røysamb, Espen; Kubarych, Thomas S.; Kendler, Kenneth S.

2012-01-01

Whereas the heritability of common personality traits has been firmly established, the results of the few published studies on personality disorders (PDs) are highly divergent, with some studies finding high heredity and others very low. A problem with assessing personality disorders by means of interview is errors connected with interviewer bias. A way to overcome the problem is to use self-report questionnaires in addition to interviews. This study used both interview and questionnaire for ...

Elusive Parnassius mnemosyne (Linnaeus, 1758) larvae: habitat selection, sex determination and sex ratio (Lepidoptera: Papilionidae)

Czech Academy of Sciences Publication Activity Database

Vlašánek, Petr; Bartoňová, Alena; Marec, František; Konvička, Martin

2017-01-01

Roč. 45, č. 180 (2017), s. 561-569 ISSN 0300-5267 R&D Projects: GA ČR GAP505/10/2167; GA AV ČR IAA600960925; GA ČR(CZ) GA17-13713S EU Projects: European Commission(XE) 669609 - Diversity6continents Institutional support: RVO:60077344 Keywords : Lepidoptera * Papilionidae * habitat Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 0.264, year: 2016

Familial colorectal cancer type X

DEFF Research Database (Denmark)

Dominguez-Valentin, Mev; Therkildsen, Christina; Da Silva, Sabrina

2015-01-01

Heredity is a major cause of colorectal cancer, but although several rare high-risk syndromes have been linked to disease-predisposing mutations, the genetic mechanisms are undetermined in the majority of families suspected of hereditary cancer. We review the clinical presentation, histopathologic...... features, and the genetic and epigenetic profiles of the familial colorectal cancer type X (FCCTX) syndrome with the aim to delineate tumor characteristics that may contribute to refined diagnostics and optimized tumor prevention....

Thrombus Size is Associated with Etiology of Deep Venous Thrombosis – A Cross-Sectional Study

OpenAIRE

Vučić, Nikša; Magdić, Tihana; Krnić, Anton; Včev, Aleksandar; Božić, Dubravko

2005-01-01

The aim of this study was to evaluate the impact of risk factors for deep vein thrombosis (DVT) on thrombus sizes in lower extremities. The size and extent of thrombus was scored according to International Consensus Committee for venous disease classification. After the diagnosis of DVT was established and its size scored, predominant risk factors for DVT in each patient were identified (malignant disease, thrombophilia, postoperative state, hormonal therapy, heredity, limb trauma, immobiliza...

High-Resolution Maps of Mouse Reference Populations

Czech Academy of Sciences Publication Activity Database

Šimeček, Petr; Forejt, Jiří; Williams, R. W.; Shiroishi, T.; Takada, T.; Lu, L.; Johnson, T. E.; Bennett, B.; Deschepper, C. F.; Scott-Boyer, M.P.; de Villena, F.P.M.; Churchill, G. A.

2017-01-01

Roč. 7, č. 10 (2017), s. 3427-3434 ISSN 2160-1836 R&D Projects: GA ČR GA16-01969S; GA MŠk(CZ) LM2015040; GA MŠk(CZ) LQ1604 Institutional support: RVO:68378050 Keywords : chromosome substitution strains * recombinant inbred strains * mouse diversity genotyping array * gene conversions Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.861, year: 2016

Molecular cytogenetic differentiation of paralogs of Hox paralogs in duplicated and re-diploidized genome of the North American paddlefish (Polyodon spathula)

Czech Academy of Sciences Publication Activity Database

Symonová, Radka; Havelka, M.; Amemiya, C. T.; Howell, M. W.; Kořínková, Tereza; Flajšhans, M.; Gela, D.; Ráb, Petr

2017-01-01

Roč. 18, č. 1 (2017), č. článku 19. ISSN 1471-2156 R&D Projects: GA ČR GA14-02940S; GA MŠk EF15_003/0000460 Institutional support: RVO:67985904 Keywords : hoxA/D paralogs mapping * sturgeon whole genome duplication * ancient fish genome * rediploidization Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.266, year: 2016

Distinctiveness of Initial Preform Properties in Renovation

Directory of Open Access Journals (Sweden)

V. M. Yaroslavtsev

2015-01-01

Full Text Available Technologies of renovation form a special group of resource-and energy saving technological processes as they are, by definition, already aimed either at increasing resource of the objects satisfying needs of the society life support and practical activities in different spheres, or at extension of their life cycle including a reuse of material from which they are made. Renovation is used where there is a material object, which does not meet requirements of standard or technical documentation.A characteristic feature of the renovation technologies is lack of procedure for a choice of the preform as in all cases an initial preform is the renovation object itself. Thus each object, acting as an initial preform, has the exclusively individual properties, including technological ones.Distinctiveness of renovation object properties is correlated, first of all, with the personified conditions of formation and (or change of condition of their properties in time at all stages of life cycle (production – transportation – warehousing – operation starting with a preform material when manufacturing under all types of loadings (technological and operational. As a result each object forms its "history" of loading and damages and, therefore, its information base which has to consider the phenomenon of “heredity of life cycle”. The term "heredity of life cycle" characterizes information support of object at any moment under review, including both information of technological inheritance, and data of operational heredity.As a result at every moment of time we have a product with a set of new, uncertain properties caused by the phenomena of heredity of life cycle. These properties are individual for each object to be renovated, which changed its status for the status of initial preform for different types of renovation technologies. This is one of the most important distinctions of renovation technology from the technology used to manufacture a new

Self-reported chemicals exposure, beliefs about disease causation, and risk of breast cancer in the Cape Cod Breast Cancer and Environment Study: a case-control study

Science.gov (United States)

2010-01-01

Background Household cleaning and pesticide products may contribute to breast cancer because many contain endocrine disrupting chemicals or mammary gland carcinogens. This population-based case-control study investigated whether use of household cleaners and pesticides increases breast cancer risk. Methods Participants were 787 Cape Cod, Massachusetts, women diagnosed with breast cancer between 1988 and 1995 and 721 controls. Telephone interviews asked about product use, beliefs about breast cancer etiology, and established and suspected breast cancer risk factors. To evaluate potential recall bias, we stratified product-use odds ratios by beliefs about whether chemicals and pollutants contribute to breast cancer; we compared these results with odds ratios for family history (which are less subject to recall bias) stratified by beliefs about heredity. Results Breast cancer risk increased two-fold in the highest compared with lowest quartile of self-reported combined cleaning product use (Adjusted OR = 2.1, 95% CI: 1.4, 3.3) and combined air freshener use (Adjusted OR = 1.9, 95% CI: 1.2, 3.0). Little association was observed with pesticide use. In stratified analyses, cleaning products odds ratios were more elevated among participants who believed pollutants contribute "a lot" to breast cancer and moved towards the null among the other participants. In comparison, the odds ratio for breast cancer and family history was markedly higher among women who believed that heredity contributes "a lot" (OR = 2.6, 95% CI: 1.9, 3.6) and not elevated among others (OR = 0.7, 95% CI: 0.5, 1.1). Conclusions Results of this study suggest that cleaning product use contributes to increased breast cancer risk. However, results also highlight the difficulty of distinguishing in retrospective self-report studies between valid associations and the influence of recall bias. Recall bias may influence higher odds ratios for product use among participants who believed that chemicals and

Self-reported chemicals exposure, beliefs about disease causation, and risk of breast cancer in the Cape Cod Breast Cancer and Environment Study: a case-control study.

Science.gov (United States)

Zota, Ami R; Aschengrau, Ann; Rudel, Ruthann A; Brody, Julia Green

2010-07-20

Household cleaning and pesticide products may contribute to breast cancer because many contain endocrine disrupting chemicals or mammary gland carcinogens. This population-based case-control study investigated whether use of household cleaners and pesticides increases breast cancer risk. Participants were 787 Cape Cod, Massachusetts, women diagnosed with breast cancer between 1988 and 1995 and 721 controls. Telephone interviews asked about product use, beliefs about breast cancer etiology, and established and suspected breast cancer risk factors. To evaluate potential recall bias, we stratified product-use odds ratios by beliefs about whether chemicals and pollutants contribute to breast cancer; we compared these results with odds ratios for family history (which are less subject to recall bias) stratified by beliefs about heredity. Breast cancer risk increased two-fold in the highest compared with lowest quartile of self-reported combined cleaning product use (Adjusted OR = 2.1, 95% CI: 1.4, 3.3) and combined air freshener use (Adjusted OR = 1.9, 95% CI: 1.2, 3.0). Little association was observed with pesticide use. In stratified analyses, cleaning products odds ratios were more elevated among participants who believed pollutants contribute "a lot" to breast cancer and moved towards the null among the other participants. In comparison, the odds ratio for breast cancer and family history was markedly higher among women who believed that heredity contributes "a lot" (OR = 2.6, 95% CI: 1.9, 3.6) and not elevated among others (OR = 0.7, 95% CI: 0.5, 1.1). Results of this study suggest that cleaning product use contributes to increased breast cancer risk. However, results also highlight the difficulty of distinguishing in retrospective self-report studies between valid associations and the influence of recall bias. Recall bias may influence higher odds ratios for product use among participants who believed that chemicals and pollutants contribute to breast cancer

Self-reported chemicals exposure, beliefs about disease causation, and risk of breast cancer in the Cape Cod Breast Cancer and Environment Study: a case-control study

Directory of Open Access Journals (Sweden)

Rudel Ruthann A

2010-07-01

Full Text Available Abstract Background Household cleaning and pesticide products may contribute to breast cancer because many contain endocrine disrupting chemicals or mammary gland carcinogens. This population-based case-control study investigated whether use of household cleaners and pesticides increases breast cancer risk. Methods Participants were 787 Cape Cod, Massachusetts, women diagnosed with breast cancer between 1988 and 1995 and 721 controls. Telephone interviews asked about product use, beliefs about breast cancer etiology, and established and suspected breast cancer risk factors. To evaluate potential recall bias, we stratified product-use odds ratios by beliefs about whether chemicals and pollutants contribute to breast cancer; we compared these results with odds ratios for family history (which are less subject to recall bias stratified by beliefs about heredity. Results Breast cancer risk increased two-fold in the highest compared with lowest quartile of self-reported combined cleaning product use (Adjusted OR = 2.1, 95% CI: 1.4, 3.3 and combined air freshener use (Adjusted OR = 1.9, 95% CI: 1.2, 3.0. Little association was observed with pesticide use. In stratified analyses, cleaning products odds ratios were more elevated among participants who believed pollutants contribute "a lot" to breast cancer and moved towards the null among the other participants. In comparison, the odds ratio for breast cancer and family history was markedly higher among women who believed that heredity contributes "a lot" (OR = 2.6, 95% CI: 1.9, 3.6 and not elevated among others (OR = 0.7, 95% CI: 0.5, 1.1. Conclusions Results of this study suggest that cleaning product use contributes to increased breast cancer risk. However, results also highlight the difficulty of distinguishing in retrospective self-report studies between valid associations and the influence of recall bias. Recall bias may influence higher odds ratios for product use among participants who believed

Amino acid composition of lamb meat from the North East Bulgarian fine fleece breed and its crossbreds with Australian merino and Ile de France from internal breeding

Directory of Open Access Journals (Sweden)

R. Slavov

2016-09-01

Full Text Available Abstract. A comparative analysis of amino acid composition of lamb meat from the North East Bulgarian fine fleece breed (I gr. and its crossbreds from internal breeding with 25% heredity from the Australian merino (II gr. and Ile de France (III gr. breeds was conducted. Upon starting the experiment lambs were equal and during the experiment they were placed under similar conditions of feeding and rearing. To establish the amino acid composition of meat slaughter analyses were performed at 100 and 130 days of age. From the carcass of each slaughtered animal individual mean samples were taken. Studies were carried out in the Research Laboratory of the Faculty of Agriculture at Trakia University. As a result of the studies the following conclusions were made: ¼ Ile de France crossbreds in a sophisticated crossing have the highest total amino acid content, including essential amino acids in the meat of 100- and 130-day-old lambs, 6.87% and 7.36%, respectively. The lysine/arginine ratio, relating to protein atherogenicity, varies within narrow ranges among groups and marks slight increase with age – from 1.31-1.37 at 100 days to 1.41-1.46 at 130 days. With the increase of age in crossbreds from internal breeding total protein amino acid content grows, that being most prominent in lambs from the III group – from 41.92 to 43.49%. The values of total protein indices increase compared to the reference protein (from 117.97% to 118.22% for II group and from 116.44% to 120.80% for III group and the whole egg protein (from 89.39% to 91.92% for II group and from 90.53% to 93.93 for III group. It has been found that internal breeding of crossbreds with 25% heredity from the Ile de France breed has positive effect concerning the total amino acid content of lamb meat at 100 and 130 days of age, essential amino acid content in it and the levels of total amino acid indices. Internal breeding of crossbreds with 25% heredity from the Australian merino breed

Chromosomal distribution of interstitial telomeric sequences as signs of evolution through chromosome fusion in six species of the giant water bugs (Hemiptera, Belostoma)

Czech Academy of Sciences Publication Activity Database

Chirino, M. G.; Dalíková, Martina; Marec, František; Bressa, M. J.

2017-01-01

Roč. 7, č. 14 (2017), s. 5227-5235 ISSN 2045-7758 R&D Projects: GA ČR(CZ) GA17-13713S Grant - others:GA ČR(CZ) GA17-17211S Institutional support: RVO:60077344 Keywords : chromosomal fusion * interstitial telomeric repeats * karyotype evolution Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.440, year: 2016 http://onlinelibrary.wiley.com/doi/10.1002/ece3.3098/full

Butyrate alters expression of cytochrome P450 1A1 and metabolism of benzo[a] pyrene via its histone deacetylase activity in colon epithelial cell models

Czech Academy of Sciences Publication Activity Database

Zapletal, Ondřej; Tylichová, Zuzana; Neča, J.; Kohoutek, J.; Machala, M.; Milcová, Alena; Pokorná, M.; Topinka, Jan; Moyer, M.P.; Hofmanová, Jiřina; Kozubík, Alois; Vondráček, Jan

2017-01-01

Roč. 91, č. 5 (2017), s. 2135-2150 ISSN 0340-5761 R&D Projects: GA ČR(CZ) GA13-09766S; GA MŠk(CZ) LM2015073 Institutional support: RVO:68081707 ; RVO:68378041 Keywords : aryl- hydrocarbon receptor * polycyclic aromatic- hydrocarbon s * beta-catenin Subject RIV: EB - Genetics ; Molecular Biology; EB - Genetics ; Molecular Biology (UEM-P) OBOR OECD: Biochemistry and molecular biology; Genetics and heredity (medical genetics to be 3) (UEM-P) Impact factor: 5.901, year: 2016

A Digital Humanities Approach to the History of Science Eugenics Revisited in Hidden Debates by Means of Semantic Text Mining

OpenAIRE

Huijnen, Pim; Laan, Fons; de Rijke, Maarten; Pieters, Toine

2014-01-01

Comparative historical research on the the intensity, diversity and fluidity of public discourses has been severely hampered by the extraordinary task of manually gathering and processing large sets of opinionated data in news media in different countries. At most 50,000 documents have been systematically studied in a single comparative historical project in the subject area of heredity and eugenics. Digital techniques, like the text mining tools WAHSP and BILAND we have developed in two succ...

Monitoring changes in genetic diversity

CSIR Research Space (South Africa)

Bruford, MW

2018-01-01

Full Text Available has thrived in many different environments over the billions of years, encoding its solutions into DNA—the heredity material. Thanks to this genetic patrimony, many species are equipped with sufficient evolutionary resi- lience to overcome rapid... for food, shelter, medicines, fuel and ecotourism income but may also include those that are ecologically important providing other key ecosystem services such as 120 M.W. Bruford et al. pollination, nutrient cycling and pest regulation (Bailey 2011...

[Correcting influence of vitamin E short chain derivatives on lipid peroxidation, liver cell membrane, and chromatin structure when rats are exposed to embichin].

Science.gov (United States)

Kovalenko, V M; Byshovets', T F; Hubs'kyĭ, Iu I; Levyts'kyĭ, Ie L; Shaiakhmetova, H M; Marchenko, O M; Voloshyna, O S; Saĭfetdinova, H A; Okhrimenko, V O; Donchenko, H V

2000-01-01

Embikhin causes activation of LPO processes in endoplasmic reticulum and in nuclear chromatine fractions of rat liver cells. The latter is accompanied by the impairment of repressive and active nuclear chromatine fractions structure. Derivate of vitamin E in these conditions renders correcting action on parameters of lipid peroxidation in the investigated subcellular structures, testifying its positive influence on the cell heredity apparatus state. The normalizing action of tocopherol derivative on cytochromes P450 and b5 levels is shown.

PROSPECTS OF CONCEPTUALIZATION OF THE NOTION “HEREDITY”

Directory of Open Access Journals (Sweden)

A. A. Kochergin

2015-01-01

Full Text Available The article examines the prospects for further development of the conceptualization of the notion “heredity” in a wide range of biological and socio-humanitarian aspects. Further development of genetics closely relates to the disclosure of interaction of genetic, interdisciplinary, general scientific, ethical, legal and philosophical categories, its complex dialectics. The doctrine of heredity in the post-nonclassical stage of its development is increasingly taking on the traits of humanities, of a science of human.

THE INVESTIGATION OF THE RELATIONSHIP BETWEEN FINGERPRINT PATTERNS AND CRIME TYPES

OpenAIRE

DELİCE, Murat; DUMAN, Ali; ÖZEL, Şaban Ali

2014-01-01

The exclusivity of prints at the tip of each individuals fingers is known for thousands of years and these prints are used for security purposes for a long time. Recent developments have pointed out that fingerprint patterns are related to gender, heredity, diseases, blood types and even character. However, the relationship between fingerprint patterns and crime types has not been explored. In order to meet this need, this research study examines the fingerprint patterns of suspects who are i...

Paradigma Revolusi Mental Dalam Pembentukan Karakter Bangsa Berbasis Sinergitas Islam Dan Filsafat Pendidikan

OpenAIRE

Siregar, Maragustam

2015-01-01

Mental revolution associated with a massive revamp of the human mind which manifests in three mindset patterns, confident, and patterns of taste-spirituality that bear behavior. That three patterns were based on the values that is planted in a person, they are: religion, culture-tradition, and philosophy of the nation. The existence of a person's mental character is influenced by many factors, namelyeducation, environment, heredity and global culture. The global culture is useful to make ever...

Ruth Rendell and Barbara Vine – family matters

OpenAIRE

Peters, F

2017-01-01

This article traces themes and preoccupations that work across Ruth Rendell’s work, writing both as Rendell and also as Barbara Vine. It investigates the ways in which the\\ud use of a pseudonym allows her to delve deeper into areas that she also explores as Rendell – the dysfunctional family and heredity, both in relation to physical disease and the fruitless search for origins, the latter discussed by her through the lens of Freudian psychoanalysis.

Obesity Differentially Affects Phenotypes of Polycystic Ovary Syndrome

OpenAIRE

Moran, Carlos; Arriaga, Monica; Rodriguez, Gustavo; Moran, Segundo

2012-01-01

Obesity or overweight affect most of patients with polycystic ovary syndrome (PCOS). Phenotypes are the clinical characteristics produced by the interaction of heredity and environment in a disease or syndrome. Phenotypes of PCOS have been described on the presence of clinical hyperandrogenism, oligoovulation and polycystic ovaries. The insulin resistance is present in the majority of patients with obesity and/or PCOS and it is more frequent and of greater magnitude in obese than in non obese...

Nutrition meets heredity: a case of RNA-mediated transmission of acquired characters.

Science.gov (United States)

Rassoulzadegan, Minoo; Cuzin, François

2018-04-01

RNA-based inheritance provides a reasonable hypothesis to explain multigenerational maintenance of the disease in the progeny of either a male or female parent suffering from the metabolic syndrome (obesity and type 2 diabetes) induced by abnormal diet. Although, it is still difficult to formulate a complete rational mechanism, study of inheritance is a most direct way to learn about the epigenetic control of gene expression and we wished to summarised our current approach along this line.

Heredity, pet ownership, and confounding control in a population-based birth cohort.

Science.gov (United States)

Almqvist, Catarina; Egmar, Ann-Charlotte; van Hage-Hamsten, Marianne; Berglind, Niklas; Pershagen, Göran; Nordvall, S Lennart; Svartengren, Magnus; Hedlin, Gunilla; Wickman, Magnus

2003-04-01

The association between pet ownership in childhood and subsequent allergic disease is controversial. Bias related to selection of pet exposure has been suggested as a reason for contradictory study results. The purpose of this investigation was to elucidate how pet exposure depends on family history of allergic disease, smoking, and socioeconomic factors in a prospective birth cohort. Parents of 4089 two-month-old children answered a questionnaire that included detailed questions about family history of asthma (maternal, paternal, and sibling), rhinoconjunctivitis, atopic eczema/dermatitis syndrome, pollen and pet allergy, smoking habits, parental occupation, and family pet ownership (cat and dog). Dust samples collected from the mothers' beds were analyzed for Fel d 1 and Can f 1 in a subgroup of the cohort. Cats were less frequently kept in families with parental asthma, rhinoconjunctivitis, or pet or pollen allergy (3.5% to 5.8%) than in families without parental allergic disease (10.8% to 11.8%). Dogs were less common in families with (3.3%) than in families without (5.9%) parental atopic eczema/dermatitis syndrome. Families with smoking mothers and those with low socioeconomic index kept cats and dogs more frequently. Cat allergen levels were lower in homes with than in homes without maternal pet allergy, and this tended to hold true even for homes without a cat. Cat ownership decreased from birth to 2 years of age, especially in families with parental history of allergic diseases. There seems to be a selection of pet exposure based on parental history of allergy, maternal smoking, and socioeconomic factors. This has to be taken into consideration in evaluations of risk associations between pet exposure and allergic disease in childhood.

Heredity of stress-related response in androgenetic common carp (Cyprinus carpio L.)

NARCIS (Netherlands)

Tanck, M.W.T.; Vermeulen, K.J.; Bovenhuis, H.; Komen, J.

2001-01-01

The aim of this paper was to estimate the heritability for the intensity of the stress-related cortisol response in common carp (Cyprinus carpio L.) using androgenetic progeny groups. For this, 660 androgenetic individuals (age: 110 days) were subjected to a 9°C cold shock and blood sampled 20 min

The Allusion of the Gene: Misunderstandings of the Concepts Heredity and Gene

Science.gov (United States)

Falk, Raphael

2014-01-01

Life sciences became Biology, a formal scientific discipline, at the turn of the nineteenth century, when it adopted the methods of reductive physics and chemistry. Mendel's hypothesis of inheritance of discrete factors further introduced a quantitative reductionist dimension into biology. In 1910 Johannsen differentiated between the…

Consciousness, Social Heredity, and Development: The Evolutionary Thought of James Mark Baldwin

Science.gov (United States)

Wozniak, Robert H.

2009-01-01

James Mark Baldwin is one of the most important and least known early American scientific psychologists. Drawing inspiration from Charles Darwin and other evolutionists of the period, Baldwin developed a biosocial theory of psychological development that influenced both Jean Piaget and Lev S. Vygotsky; and he proposed a mechanism relating learned…

Clinical study of the oral manifestations and related factors in type 2 diabetics patients Estudo clínico das manifestações orais e fatores relacionados em pacientes diabéticos tipo 2

Directory of Open Access Journals (Sweden)

Maria Goretti de Menezes Sousa

2011-04-01

Full Text Available Diabetes Mellitus (DM is reported with and associated to oral alterations, with conflicting results. The aim of this study was to identify the prevalence of oral soft tissue alterations in type 2 diabetes mellitus patients. MATERIAL AND METHODS: Socioeconomic variables, gender, heredity, capillary glucose control and local factors (prosthesis, dry mouth sensation were analyzed in 196 diabetic and non-diabetic patients enrolled in HIPERDIA, at 41 Health units of Natal, Brazil. STUDY DESIGN: A case study. RESULTS: The last blood glucose mean was 177.0 mg/dl for diabetics and 89.46 mg/dl for non-diabetics. Mean capillary blood glucose was elevated in diabetics (215.95 mg/dl; it was 102.31 mg/dl in non-diabetics. The family history confirmed the heredity nature of the disease in 68.8% of diabetic patients (n = 66 (p < 0.001; salivary flow was 49% (n = 47 in diabetics, and 34% (n = 34 in non-diabetics. Candidiasis was present in 30.5% of diabetic patients (n=29 and 36% of non-diabetics (n=36. Both groups had lesions in the palate - 81.4% (n = 35 in diabetics, and 71.1% in non-diabetics (n = 27 (p = 0.68. CONCLUSION: The alterations are not related to diabetes and are present independently of having or not type 2 Diabetes Mellitus.

Indoor environmental risk factors in young asthmatics: a case-control study.

Science.gov (United States)

Lindfors, A; Wickman, M; Hedlin, G; Pershagen, G; Rietz, H; Nordvall, S L

1995-11-01

One hundred and ninety three children with asthma and 318 controls aged 1-4 years were evaluated for atopic heredity and exposure to possible indoor risk factors for asthma-for example exposure to furred pets, tobacco smoke, and home dampness. A subgroup of cases were classified as cat and/or dog allergic on the basis of skin prick tests. Heredity for asthma was a significant risk factor (odds ratio (OR) 3.0, confidence interval (CI) 2.1 to 4.6). Environmental tobacco smoke was associated with an excess risk for asthma (OR 1.7, CI 1.1 to 2.3) and signs of home dampness tended to increase this risk (OR 1.3, CI 0.9 to 2.0). High dose exposure to cat and/or dog resulted in an increased risk only in asthma cases sensitised to cat and/or dog (OR 2.7, CI 1.0 to 7.3). A combination of high dose exposure to cat and/or dog, environmental tobacco smoke and damp housing was associated with an OR of 8.0 (CI 1.9 to 34.1). Raised indoor humidity has been shown to reflect low air exchange, which may also lead to increased doses of inhaled aeroallergens and tobacco smoke, and contribute to the interaction between the three risk factors.

Horticulture: the font for the baptism of genetics.

Science.gov (United States)

Olby, R C

2000-10-01

This year marks the centenary of the rediscovery of the laws of heredity, and their introduction to the English-speaking world. Here I introduce the main events and the characters who figure in this story before turning to the task of this essay--to ask why it was that support in England for the emerging science of genetics, or Mendelism as it was then called, came chiefly from horticulture, and was only belatedly accepted into the mainstream of British academic biology.

Novel resistance to Cydia pomonella granulovirus (CpGV) in codling moth shows autosomal and dominant inheritance and confers cross-resistance to different CpGV genome groups

Czech Academy of Sciences Publication Activity Database

Sauer, A. J.; Fritsch, E.; Undorf-Spahn, K.; Nguyen, Petr; Marec, František; Heckel, D. G.; Jehle, J. A.

2017-01-01

Roč. 12, č. 6 (2017), č. článku e0179157. E-ISSN 1932-6203 R&D Projects: GA ČR(CZ) GA14-22765S; GA ČR(CZ) GP14-35819P Institutional support: RVO:60077344 Keywords : Cydia pomonella granulovirus * inheritance * resistance Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.806, year: 2016 http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0179157

Pitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia

OpenAIRE

Kolahdouz, Mahsa; Mohammadi, Zahra; Kolahdouz, Parisa; Tajamolian, Masoud; Khanahmad, Hossein

2015-01-01

Congenital adrenal hyperplasia (CAH) is a putative error of metabolism with autosomal recessive heredity pattern. The main manifestations of classic form of CAH are salt-wasting, dehydration and simple virilization in both sexes and ambiguous genitalia in female gender. 21-hyroxylase (CYP21A2) impairment with prevalence value of 1 in 10,000?15,000 live births is the most common etiology of CAH. Because of consanguineous marriages, the frequency of the CAH in Iran is very high. A wide range of...

The corkscrew sperm defect in Danish bulls - a possible indicator of nuclear fallout

International Nuclear Information System (INIS)

Blom, Erik

1978-01-01

In spite of the fact that the sterilizing corkscrew sperm defect was described about 20 years ago, very little is as yet known about a possible causal factor and about the genesis of the defect. Up to now 60 Danish cases have been recorded showing no proof whatsoever of heredity. The cases have predominantly been found in older bulls of the Red Danish breed and during a period with a rather high degree of atmospheric pollution from nuclear fallout. (author)

Air Officer’s Education

Science.gov (United States)

2012-08-01

variety and relationships of living organisms and the influences of heredity and environment in the evolution of life. A review of the field of science...by bold thinking done in the Air Force or not at all. The so-called Air Defense will not protect the United States and its productive plant from the...atomic bomb. It may be that this plant has to take on a different shape and for this reason economics in our sense of the term is a compulsory

Changes in plasma membrane aquaporin gene expression under osmotic stress and blue light in tomato

Czech Academy of Sciences Publication Activity Database

Balarynová, Jana; Danihlík, J.; Fellner, Martin

2018-01-01

Roč. 40, č. 2 (2018), č. článku 27. ISSN 0137-5881 R&D Projects: GA MŠk(CZ) LO1204 Institutional support: RVO:61389030 Keywords : male-sterile mutant * arabidopsis-thaliana * seed-germination * abscisic-acid * solanum-lycopersicon * nitric-oxide * 7b-1 * protein * hypocotyl * responses * Tomato * Seed * Aquaporins * Blue light * 7B-1 mutant * Mannitol * PIPs Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 1.364, year: 2016

Faktor-faktor Gaya Hidup yang Berhubungan dengan Obesitas Anak Sekolah Dasar Swasta Bernardus dan Hj Isriati Kelas 4-6 di Semarang

OpenAIRE

Wuryanto, Arie; Susanto, Henry Setiawan; Nilasari, Griska Erfiana

2015-01-01

Obesity in children is a complex problem. Currently, excessive nutrients and obesity is an epidemic in Australia, New Zealand and Singapore and rapidly spread in the population of Pacific islands and in a certain Asian country. Obesity can result in varied chronic diseases. The purpose of this case control study is to find out the relation of pattern of heredity, consumption, and physical activity, to the incident of obesity in the students of elementary school Bernardus and Hj Isriati in Sem...

Neo-sex chromosomes in the monarch butterfly, Danaus plexippus

Czech Academy of Sciences Publication Activity Database

Mongue, A. J.; Nguyen, Petr; Voleníková, Anna; Walters, J. R.

2017-01-01

Roč. 7, č. 10 (2017), s. 3281-3294 ISSN 2160-1836 R&D Projects: GA ČR(CZ) GA14-22765S; GA ČR(CZ) GP14-35819P Grant - others:GA JU(CZ) 159/2016/P Institutional support: RVO:60077344 Keywords : sex chromosomes * evolution * Lepidoptera Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.861, year: 2016 http://www.g3journal.org/content/7/10/3281.long

Differential diagnosis and management of human-directed aggression in cats.

Science.gov (United States)

Frank, Diane; Dehasse, Joel

2003-03-01

Human-directed aggression in cats should be evaluated as a multifactorial problem. It results from the combined actions of heredity, environment, learning, human social requirements (or needs), client interactions, lack of understanding of normal feline behavior, unrealistic client expectations, and lack of meeting the cat's basic ethologic needs. Managing human-directed aggression in cats encompasses the use of environmental modification, therapies, and, when and if needed, regulatory drugs so as to increase learning capabilities and adaptation and decrease danger to the human victims.

The role of diclofenack on inducing of aplasia cutis congenita: a case report

OpenAIRE

Pajaziti, Laura; Rexhepi, Syzana; Shatri-Mu?a, Ylfete; Ferizi, Mybera

2009-01-01

Background Aplasia cutis congenita is a disorder where e newborn child is missing skin from certain areas. It is a rare condition with no particular race or sex more at risk. May occur by itself or be associated with other physical syndromes or disorders. A classification system exists for aplasia cutis congenital consisting of 9 groups, based on the number and location of the skin defects and the presence or absence of other malformations. Causes of aplasia congenital could be heredity, tera...

Sources of Wilhelm Johannsen's genotype theory.

Science.gov (United States)

Roll-Hansen, Nils

2009-01-01

This paper describes the historical background and early formation of Wilhelm Johannsen's distinction between genotype and phenotype. It is argued that contrary to a widely accepted interpretation (For instance, W. Provine, 1971. The Origins of Theoretical Population Genetics. Chicago: The University of Chicago Press; Mayr, 1973; F. B. Churchill, 1974. Journal of the History of Biology 7: 5-30; E. Mayr, 1982. The Growth of Biological Thought, Cambridge: Harvard University Press; J. Sapp, 2003. Genesis. The Evolution of Biology. New York: Oxford University Press) his concepts referred primarily to properties of individual organisms and not to statistical averages. Johannsen's concept of genotype was derived from the idea of species in the tradition of biological systematics from Linnaeus to de Vries: An individual belonged to a group - species, subspecies, elementary species - by representing a certain underlying type (S. Müller-Wille and V. Orel, 2007. Annals of Science 64: 171-215). Johannsen sharpened this idea theoretically in the light of recent biological discoveries, not least those of cytology. He tested and confirmed it experimentally combining the methods of biometry, as developed by Francis Galton, with the individual selection method and pedigree analysis, as developed for instance by Louis Vilmorin. The term "genotype" was introduced in W. Johannsen's 1909 (Elemente der Exakten Erblichkeitslehre. Jena: Gustav Fischer) treatise, but the idea of a stable underlying biological "type" distinct from observable properties was the core idea of his classical bean selection experiment published 6 years earlier (W. Johannsen, 1903. Ueber Erblichkeit in Populationen und reinen Linien. Eine Beitrag zur Beleuchtung schwebender Selektionsfragen, Jena: Gustav Fischer, pp. 58-59). The individual ontological foundation of population analysis was a self-evident presupposition in Johannsen's studies of heredity in populations from their start in the early 1890s till his

Mutant-inducing effect of γ-ray irradiation for hybrid rice F1 derived from cross of black glutinous rice x wild rice

International Nuclear Information System (INIS)

Mao Dezhi; Tang Yilan

1998-01-01

The hybrid rice F 1 plant derived from the back crossing of glutinous rice x wild rice was irradiated with γ-ray. The result of investigation to the induced mutant showed that through the selection and backcross, a black glutinous rice strain with the short stem, cold tolerance and high yield was developed. The analysis of the ability of heredity variance showed that the selection was effective for the husk colour, black glutinous and black Indica rice, but ineffective for the white Indica rice and seed setting

A leucine aminopeptidase is involved in kinetoplast DNA segregation in Trypanosoma brucei

Czech Academy of Sciences Publication Activity Database

Peña-Diaz, Priscila; Vancová, Marie; Resl, C.; Field, M.C.; Lukeš, Julius

2017-01-01

Roč. 13, č. 4 (2017), č. článku e1006310. E-ISSN 1553-7374 R&D Projects: GA MŠk(CZ) EE2.3.30.0032; GA ČR(CZ) GA16-18699S Institutional support: RVO:60077344 Keywords : site-specific recombination * basal body movements * mitochondrial-dna * leucyl aminopeptidase * crithidia-fasciculata * escherichia-coli * cell-cycle * minicircle replication * phylogenetic analysis * genome segregation Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 7.003, year: 2015

Clinical features of diabetes mellitus in Japan as observed in a hospital outpatient clinic

Energy Technology Data Exchange (ETDEWEB)

Wada, Sunao; Toda, Shintaro; Omori, Yoshiaki; Yamakido, Michio; Blackard, W G

1963-04-18

A university diabetes clinic in Japan was characterized by age at examination, age at onset, sex ratio, microangiopathies, atherosclerotic complications, weight, heredity, and diet. The findings in this clinic, along with those from other diabetes clinics in Japan, were compared with studies on Western diabetics. The similarities between the 2 diabetic populations far outnumbered the dissimilarities. However, diabetes mellitus in Japan is distinguished by infrequent occurrence of juvenile diabetes and ketosis, relative lack of atherosclerotic complications, and reversal of the sex ratio. 39 references, 7 tables.

W-enriched satellite sequence in the Indian meal moth, Plodia interpunctella (Lepidoptera, Pyralidae)

Czech Academy of Sciences Publication Activity Database

Dalíková, Martina; Zrzavá, Magda; Kubíčková, S.; Marec, František

2017-01-01

Roč. 25, 3-4 (2017), s. 241-252 ISSN 0967-3849 R&D Projects: GA ČR(CZ) GA14-22765S; GA ČR(CZ) GA17-13713S Grant - others:GA ČR(CZ) GA17-17211S Institutional support: RVO:60077344 Keywords : satellite DNA * sex chromosomes * transcription Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.385, year: 2016 https://link.springer.com/article/10.1007%2Fs10577-017-9558-8

Breastfeeding and allergic disease: a multidisciplinary review of the literature (1966-2001) on the mode of early feeding in infancy and its impact on later atopic manifestations

DEFF Research Database (Denmark)

Odijk, J.; Kull, I.; Borres, M.

2003-01-01

Background: Strategies to prevent children from developing allergy have been elaborated on the basis of state-of-the-art reviews of the scientific literature regarding pets and allergies, building dampness and health, and building ventilation and health. A similar multidisciplinary review of infant...... concluded that breastfeeding seems to protect from the development of atopic disease. The effect appears even stronger in children with atopic heredity. If breast milk is unavailable or insufficient, extensively hydrolysed formulas are preferable to unhydrolysed or partially hydrolysed formulas in terms...

Biological consequences of nuclear war

International Nuclear Information System (INIS)

Dubinin, N.P.

1986-01-01

Irradiation probability due to radionuclide fallout is shown to exceed 1 Gy even for the territories which have not been affected by nuclear weapons direct explosions. If some people survive in the nuclear war, their heredity would be affected. Genetic consequences of nuclear war complete the process of Homo sapiens disappearance from the Earth. Space weapons development will deteriorate the prospects of civilization ruin as a result of biological aftereffects of nuclear war and possible application of new arms, as well as chemical and biologic weapons

Chemistry and biology by new multiple choice

International Nuclear Information System (INIS)

Seo, Hyeong Seok; Kim, Seong Hwan

2003-02-01

This book is divided into two parts, the first part is about chemistry, which deals with science of material, atom structure and periodic law, chemical combination and power between molecule, state of material and solution, chemical reaction and an organic compound. The second part give description of biology with molecule and cell, energy in cells and chemical synthesis, molecular biology and heredity, function on animal, function on plant and evolution and ecology. This book has explanation of chemistry and biology with new multiple choice.

Trichorhinophalangeal syndrome

Energy Technology Data Exchange (ETDEWEB)

Tuzovic, S.; Fiebach, B.J.O.; Magnus, L.; Sauerbrei, H.U.

1982-11-01

This article reports on 14 cases of a trichorhinophalangeal syndrome in five successive generations. Besides the well-known characteristics of the TRPS the following symptoms observed in this family are new: Teething was considerably delayed, intelligence was reduced, and there were skin manifestations resembling eczema. Besides, struma colli and colitis ulcerosa were also observed. Subsequent observations have to clarify whether these symptoms are a facultative part of the TRPS pattern. The constant appearance of carriers of these characteristics during five generation points to dominant heredity.

The trichorhinophalangeal syndrome

International Nuclear Information System (INIS)

Tuzovic, S.; Fiebach, B.J.O.; Magnus, L.; Sauerbrei, H.U.

1982-01-01

This article reports on 14 cases of a trichorhinophalangeal syndrome in five successive generations. Besides the well-known characteristics of the TRPS the following symptoms observed in this family are new: Teething was considerably delayed, intelligence was reduced, and there were skin manifestations resembling eczema. Besides, struma colli and colitis ulcerosa were also observed. Subsequent observations have to clarify whether these symptoms are a facultative part of the TRPS pattern. The constant appearance of carriers of these characteristics during five generation points to dominant heredity. (orig.) [de

A revision of the genus Geitlerinema and a description of the genus Anagnostidinema gen. nov (Oscillatoriophycidae, Cyanobacteria)

Czech Academy of Sciences Publication Activity Database

Strunecký, O.; Bohunická, Markéta; Johansen, J. R.; Čapková, Kateřina; Raabová, L.; Dvořák, P.; Komárek, Jiří

2017-01-01

Roč. 17, č. 1 (2017), s. 114-126 ISSN 1802-5439 R&D Projects: GA ČR GA15-00113S; GA ČR(CZ) GA15-11912S; GA ČR GA13-13368S Grant - others:CENAKVA(CZ) CZ.1.05/2.1.00/01.0024; GA MŠk(CZ) LO1205 Institutional support: RVO:67985939 Keywords : morphology * ecology * Anagnostifdinema Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 1.350, year: 2016

Two-tailed RT-qPCR: a novel method for highly accurate miRNA quantification

Czech Academy of Sciences Publication Activity Database

Androvič, Peter; Valihrach, Lukáš; Elling, J.; Sjöback, R.; Kubista, Mikael

2017-01-01

Roč. 45, č. 15 (2017), č. článku e144. ISSN 0305-1048 R&D Projects: GA ČR(CZ) GA16-10214S; GA ČR(CZ) GA16-10214S; GA MŠk(CZ) ED1.1.00/02.0109 Institutional support: RVO:86652036 Keywords : rolling circle amplification * microrna biogenesis pathways * real-time pcr * neurodegenerative diseases Subject RIV: EB - Gene tics ; Molecular Biology OBOR OECD: Gene tics and heredity (medical gene tics to be 3) Impact factor: 10.162, year: 2016

Consanguinidad, sífilis, herencia y matrimonio: el lento advenimiento de la intervención médica en las leyes mexicanas del matrimonio

Directory of Open Access Journals (Sweden)

Carlos López Beltrán

2009-12-01

Full Text Available The noun “heredity”, in its biological sense, first circulated in France during the 1830s. During that century, heredity was linked to the pessimistic notion of degeneration, the control of which became a tool for the academic and political projects of French physicians to be included in those of the Nation. Something similar occurred in Mexico. After two generations of late 19th and early 20th centuries physicians, which incorporated the manipulation of heredity into their projects and questioned, just as their French colleagues, consanguineous marriages, medical supervision of every union –consanguineous or not– became compulsory within the civil marriage regulations, coinciding with the institutionalization of the Mexican eugenic movement. Even if they had moved from Europe to Mexico, notions of heredity, degeneration, consanguinity and eugenics were adjusted and justified according to the local situation and prevailing values of the Mexican society.//El sustantivo “herencia” en su sentido biológico comenzó a circular en Francia en la década de los años treinta del siglo XIX. En ese mismo siglo la herencia fue vinculada a la pesimista noción de degeneración y el control sobre la misma se convirtió en una herramienta de los médicos franceses para incluir sus proyectos académicos y políticos en los de la nación francesa. En México sucedió una cosa similar. Después de dos generaciones distinguibles de médicos de finales del siglo XIX y principios del XX que incorporaron a sus proyectos la manipulación de la herencia en el mismo tenor que había tenido en Francia y en las que se cuestionaron los matrimonios consanguíneos, se instaló como parte de las leyes que rigen al matrimonio civil la necesidad de la vigilancia médica de todas las uniones, y no sólo las de este tipo. Esto ocurrió justo en el momento en el que movimiento eugenésico mexicano se institucionalizó. A pesar de haberse trasladado desde Europa a la

Fissuras lábio-palatais: estudo caso-controle Oral clefts: a case-control study

Directory of Open Access Journals (Sweden)

Leonor de Castro Monteiro Loffredo

1994-06-01

Full Text Available Realizou-se um estudo caso-controle com o propósito de se detectar possíveis fatores de risco para o aparecimento de fissuras orais. Foram objeto de análise: local de moradia da mãe nos quatro primeiros meses de gestação, poluição, aplicação de pesticida/herbicida na lavoura, doenças dos pais, doenças da mãe nos quatro primeiros meses de gestação, ingestão medicamentosa nesse período, hereditariedade, tabagismo, consumo de bebida alcoólica e exposição a raio-X. Foram aplicados formulários às mães referentes aos 450 casos, sendo 354 portadores de fissuras labiais ou lábio-palatais e 96 de fissuras palatinas, e às mães referentes aos 450 controles. Empregou-se análise multivariada e as variáveis hereditariedade (RR=4,96, epilepsia na mãe (RR=2,39 e ingestão de anti-inflamatório (RR=2,59 foram consideradas fatores de risco para fissuras labiais ou lábio-palatais. As variáveis hereditariedade (RR=2,82 e poluição (RR=2,58 foram consideradas fatores de risco para fissuras palatinas.This study relates to a case-control analysis for the purpose of verifying the association between oral clefts and possible risk factors. The analysed variables were: place of mother's residence (urban/ rural, pollution, parental diseases, mother's diseases during the first four months of pregnancy, intake of drugs related to this period, heredity, smoking habits, alcohol consumption and X-ray examinations during pregnancy or X-ray examinations prior to preganacy. There were 450 cases of clefts of whom 354 had a cleft lip with or without cleft palate and 96 had a cleft palate. The relative risk (RR for each variable by was estimated points and at a 95% of confidence interval and multivariate analysis was applied. As regards cleft lip with or without cleft palate, the risk factors are heredity (RR = 4.96, epilepsy in the mother (RR = 2.39 and the intake of drugs such as anti-inflammatory substance in the first four months of pregnancy (RR

Heredity and Environment in Etiology of Eating Disorders. I. Review of Twin Studies

Directory of Open Access Journals (Sweden)

Meshkova T.A.

2015-06-01

Full Text Available Twin studies of eating disorders (anorexia nervosa, bulimia nervosa, and binge eating are reviewed. Historically, eating disorders (ED was viewed as a disorders primarily influenced by sociocultural factors, however, over the past decade, this perception has been challenged. Twin studies demonstrate that genetic factors significantly influence the risk for ED and substantially contribute to the observed association between ED and other disorders and personal traits (major depression, anxiety disorders, substance use disorders, perfectionism. Among environmental factors nonshared (unique environment plays the main role, except of early puberty.

[Breast cancer and heredity: results of a population case-control study in Girona].

Science.gov (United States)

de Sanjosé, S; Viladiu, P; Cordón, F; Vilardell, L; Marcos, R; Izquìerdo, A

1998-03-21

To characterise the relationship between breast cancer and different aspects of the reproductive life, use of drugs and alcohol by family history of breast cancer. From the cancer registry of Girona, Spain, 330 women were identified with histologically confirmed breast cancer during 1986-1989. For each case, a control woman was selected from a random sample of the population living in the matched area to the case by age (+/- 5 yr.). The information was collected by a personal interview and included: family history of breast cancer, reproductive history, presence of acne during the teenage years, use of oral contraceptives and drugs for sleep and anxiety disorders, and alcohol consumption. 18.5% of breast cancer cases and 8.9% of all controls had a family history of breast cancer. Family history on a first degree relative (mother or sister) was present in 10.6% of the cases and 2.8% of controls, which represented an odds ratio for breast cancer of 3.7 (95% CI, 1.8-7.8) higher than the general population. Women with a first degree family history of breast cancer were at higher risk for breast cancer if they had a history of acne during the teenage period (OR = 2.4; 95% CI, 1.1-5.2) and if they referred long menstrual periods in the early years of menarche (OR = 3.1; 95% CI, 1.3-7.0). Women with no family history had a higher breast cancer risk if they had a late menarche, long menstrual periods, late first full term pregnancy, and history of acne during puberty. Alcohol consumption and use of drugs for anxiety and sleep disorders were associated with a decreased risk of breast cancer. First degree family history of breast cancer seems to be the best risk indicator for developing breast cancer. Long menstrual periods and presence of acne during puberty may indicate hormonal imbalance that act independently of the family history in breast cancer development.

'Semen contains vitality and heredity, not germs': seminal discourse in the AIDS era.

Science.gov (United States)

Khan, Sharful Islam; Hudson-Rodd, Nancy; Saggers, Sherry; Bhuiyan, Mahbubul Islam; Bhuiya, Abbas; Karim, Syed Afzalul; Rauyajin, Oratai

2006-12-01

Perspectives of public health generally ignore culture-bound sexual health concerns, such as semen loss, and primarily attempt to eradicate sexually transmitted infections (STIs), including human immunodeficiency virus (HIV). Like in many other countries, sexual health concerns of men in Bangladesh have also received less attention compared to STIs in the era of AIDS. This paper describes the meanings of non-STI sexual health concerns, particularly semen loss, in the masculinity framework. In a qualitative study on male sexuality, 50 men, aged 18-55 years, from diverse sociodemographic backgrounds and 10 healthcare practitioners were interviewed. Men considered semen the most powerful and vital body fluid representing their sexual performance and reproductive ability. Rather than recognizing the vulnerability to transmission of STIs, concerns about semen were grounded in the desire of men to preserve and nourish seminal vitality. Traditional practitioners supported semen loss as a major sexual health concern where male heritage configures male sexuality in a patriarchal society. Currently, operating HIV interventions in the framework of disease and death may not ensure participation of men in reproductive and sexual health programmes and is, therefore, less likely to improve the quality of sexual life of men and women.

Low awareness of risk factors among bladder cancer survivors: New evidence and a literature overview.

Science.gov (United States)

Westhoff, Ellen; Maria de Oliveira-Neumayer, Julia; Aben, Katja K; Vrieling, Alina; Kiemeney, Lambertus A

2016-06-01

Data on urinary bladder cancer (UBC) patients' perceptions about causes of bladder cancer is limited, while this may be important knowledge for health prevention and education. We evaluated self-reported perceptions and beliefs about the causes of bladder cancer among UBC survivors in the Netherlands. UBC survivors identified through the Netherlands Cancer Registry from 2007 to 2012 were invited to participate. Patients who consented were asked to fill out a questionnaire, including questions on lifestyle characteristics, occupational and medical history, and family history of cancer. The final question was 'You have been diagnosed with bladder cancer. Do you have any idea what may have been the cause of your cancer?'. Of the 1793 UBC survivors included, 366 (20%) reported a possible cause for their bladder cancer. The most frequently reported suspected causes were smoking (10%), occupational exposure (5%), and heredity (2%). Smoking, occupational exposure and heredity were mentioned only slightly more frequently by participants with these risk factors (11%, 8%, and 5%, respectively) compared to the total population. Most UBC survivors did not suspect any cause that might have contributed to the development of their cancer. Even among participants with established risk factors for bladder cancer, these risk factors were not commonly perceived. This finding probably reflects the superficial knowledge of risk factors for bladder cancer in the population and highlights the importance of effective education on cancer prevention. Copyright © 2016 The Authors. Published by Elsevier Ltd.. All rights reserved.

In the Beginning was a Mutualism - On the Origin of Translation

Science.gov (United States)

Vitas, Marko; Dobovišek, Andrej

2018-04-01

The origin of translation is critical for understanding the evolution of life, including the origins of life. The canonical genetic code is one of the most dominant aspects of life on this planet, while the origin of heredity is one of the key evolutionary transitions in living world. Why the translation apparatus evolved is one of the enduring mysteries of molecular biology. Assuming the hypothesis, that during the emergence of life evolution had to first involve autocatalytic systems which only subsequently acquired the capacity of genetic heredity, we propose and discuss possible mechanisms, basic aspects of the emergence and subsequent molecular evolution of translation and ribosomes, as well as enzymes as we know them today. It is possible, in this sense, to view the ribosome as a digital-to-analogue information converter. The proposed mechanism is based on the abilities and tendencies of short RNA and polypeptides to fold and to catalyse biochemical reactions. The proposed mechanism is in concordance with the hypothesis of a possible chemical co-evolution of RNA and proteins in the origin of the genetic code or even more generally at the early evolution of life on Earth. The possible abundance and availability of monomers at prebiotic conditions are considered in the mechanism. The hypothesis that early polypeptides were folding on the RNA scaffold is also considered and mutualism in molecular evolutionary development of RNA and peptides is favoured.

Influence of substrate preparation on the shaping of the topography of the surface of nanoceramic oxide layers

Science.gov (United States)

Bara, Marek; Kubica, Marek

2014-02-01

The paper discusses the shaping mechanism and changes occurring in the structure and topography of the surface of nanoceramic oxide layers during their formation. The paper presents the influence of substrate preparation on the surface topography of oxide layers. The layers were produced via hard anodizing on the EN AW-5251 aluminum alloy. The layers obtained were subjected to microscope examinations, image and chemical composition analyses, and stereometric examinations. Heredity of substrate properties in the topography of the surface of nanoceramic oxide layers formed as a result of electrochemical oxidation has been shown.

The differentiated approach in forming swimming abilities and skills of students

Directory of Open Access Journals (Sweden)

Nikolskiy A.U.

2010-09-01

Full Text Available It is considered the directions of organization and methods of conducting of lessons with students. In experiment took part students of the 17-20 years old. The criteria of forming of typological educational groups are presented on the initial stage of teaching swimming of students. The degree of connection of the hereditarily conditioned swimming coordinating inclination is certain with the indexes of formed swimming abilities and skills of students. It is well-proven that a process of capture motive habits is under unreserved influence of conservative heredity of individual.

Conceptual and methodological biases in network models.

Science.gov (United States)

Lamm, Ehud

2009-10-01

Many natural and biological phenomena can be depicted as networks. Theoretical and empirical analyses of networks have become prevalent. I discuss theoretical biases involved in the delineation of biological networks. The network perspective is shown to dissolve the distinction between regulatory architecture and regulatory state, consistent with the theoretical impossibility of distinguishing a priori between "program" and "data." The evolutionary significance of the dynamics of trans-generational and interorganism regulatory networks is explored and implications are presented for understanding the evolution of the biological categories development-heredity, plasticity-evolvability, and epigenetic-genetic.

22nd International Conference on Soft Computing

CERN Document Server

2017-01-01

This proceeding book contains a collection of selected accepted papers of the Mendel conference held in Brno, Czech Republic in June 2016. The proceedings book contains three chapters which present recent advances in soft computing including intelligent image processing. The Mendel conference was established in 1995 and is named after the scientist and Augustinian priest Gregor J. Mendel who discovered the famous Laws of Heredity. The main aim of the conference is to create a regular possibility for students, academics and researchers to exchange ideas and novel research methods on a yearly basis.

Mutation breeding of banana tube-buds in vitro. Pt. 5: Genomic variation of Zhangjiao No.8 strain detected by RAPD

International Nuclear Information System (INIS)

Guo Jianhui; Cai Enxing; Chen Liping; Huang Xidong; Shen Mingshan; Hong Fuxiang

2003-01-01

Zhangjiao No.8, a new variety induced from irradiation by 60 Co γ-rays, was analyzed by RAPD using 20 random primers against Mus AAA Grand Cavendish. The result showed that 68 bands could be amplified by 12 primers, 53 were homologous, accounted for 77.9%, of total bands; only 22.1% were differential bands, the polymorphism difference up to 24.6% between Zhangjiao No.8 and CK, indicating its stable heredity. Three differential bands from S 10 and S 19 could be used as markers for identification and anti-degeneration of Zhangjiao No.8

Chronic low-dose pro-oxidant treatment stimulates transcriptional activity of telomeric retroelements and incerases telomere lenght in Drosophila

Czech Academy of Sciences Publication Activity Database

Korandová, Michala; Krůček, Tomáš; Szakosová, Klára; Kodrík, Dalibor; Kühnlein, R. P.; Tomášková, Jindřiška; Čapková Frydrychová, Radmila

2018-01-01

Roč. 104, JAN 10 (2018), s. 1-8 ISSN 0022-1910 R&D Projects: GA ČR(CZ) GA17-03253S EU Projects: European Commission(XE) 316304 - MODBIOLIN Grant - others:GA JU(CZ) 052/2013/P; GA JU(CZ) 038/2014/P Institutional support: RVO:60077344 Keywords : Drosophila * oxidative stress * telomeres Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.227, year: 2016 https://www. science direct.com/ science /article/pii/S0022191017303098?via%3Dihub

Risk assessment of bronchial asthma development in children with atopic dermatitis

Science.gov (United States)

Vуsotska, Olena V.; Klymenko, Viktoriia A.; Trubitcin, Alexei A.; Pecherska, Anna I.; Savchuk, Tamara O.; Kolimoldayev, Maksat; Wójcik, Waldemar; Szatkowska, Małgorzata; Burlibay, Aron

2017-08-01

This article offers a risk assessment of bronchial asthma development in children with atopic dermatitis by applying fuzzy-set theory to accumulated statistical data. It is shown that with a view to executing the said task one should exercise a complex approach involving factors such as "IgE level", "existence of obstructions" and "burdened bronchial asthma heredity of immediate relatives". The obtained results will assist in making adequate and well-informed medical decisions as well as facilitate the decrease of the risk of developing bronchial asthma in children with atopic dermatitis.

Dietary prevention of allergic diseases in infants and small children. Part III

DEFF Research Database (Denmark)

Muraro, Antonella; Dreborg, Sten; Halken, Susanne

2004-01-01

-reviewed observational and interventional studies was performed following the statements of evidence as defined by WHO. The results of the analysis indicate that breastfeeding is highly recommended for all infants irrespective of atopic heredity. A dietary regimen is unequivocally effective in the prevention of allergic...... diseases in high-risk children. In these patients breastfeeding combined with avoidance of solid food and cow's milk for at least 4-6 months is the most effective preventive regimen. In the absence of breast milk, formulas with documented reduced allergenicity for at least 4-6 months should be used....

Different biogenetic causal explanations and attitudes towards persons with major depression, schizophrenia and alcohol dependence: is the concept of a chemical imbalance beneficial?

Science.gov (United States)

Speerforck, Sven; Schomerus, Georg; Pruess, Susanne; Angermeyer, Matthias C

2014-10-01

It is unclear whether different biogenetic causal beliefs affect stigmatization of mentally-ill patients differently. It has been argued that in particular believing in a 'chemical imbalance' as a cause of mental disorder might be associated with more tolerant attitudes. In a representative population survey in Germany (n=3642), using unlabelled case vignettes of persons with depression, schizophrenia, or alcohol dependence, we elicited agreement with three different biogenetic explanations of the illness: 'Chemical imbalance of the brain', 'brain disease' and 'heredity'. We further investigated emotional reactions as well as the desire for social distance. For each vignette condition we calculated linear regressions with each biogenetic explanation as independent and emotional reactions as well as social distance as dependent variable controlling for socio-demographic variables. Our cross-sectional study does not allow statements regarding causality and the explanatory power of our statistical models was low. 'Chemical imbalance of the brain' and 'brain disease' were both associated with a stronger desire for social distance in schizophrenia and depression, and with more social acceptance in alcohol dependence, whereas 'heredity' was not significantly associated with social distance in any of the investigated illnesses. All three biogenetic causal beliefs were associated with more fear in all three illnesses. Our study corroborates findings that biogenetic explanations have different effects in different disorders, and seem to be harmful in depression and schizophrenia. A particular de-stigmatizing potential of the causal belief 'chemical imbalance' could not be found. Implications for useful anti-stigma messages are discussed. Copyright © 2014 Elsevier B.V. All rights reserved.

The role of genealogy and clinical family histories in documenting possible inheritance patterns for diabetes mellitus in the pre-insulin era: part 1. The clinical case of Josephine Imperato.

Science.gov (United States)

Imperato, Pascal James; Imperato, Gavin H

2009-10-01

Establishing the role of heredity in type 2 diabetes mellitus (type 2 DM) is challenging. While type 2 DM frequently displays a pattern of familial aggregation, many other risk factors are responsible for the clinical expression of the disease. This paper reviews a number of the early twentieth-century studies of inheritance patterns for type 2 DM and presents in detail the history of Josephine Foniciello Imperato (Maria Giuseppa Foniciello) who died from the disease in New York City at the age of 52 years on 14 November 1921, ten months before commercial insulin became available.

The Role of Degeneration Theory in the Understanding of Mental Illness, Colombia First Half of the Twentieth Century

Directory of Open Access Journals (Sweden)

María Fernanda Vásquez Valencia

2018-01-01

Full Text Available Based on medical journals and theses from the first half of the twentieth century, this article analyzes the role played by the theory of degeneration in the understanding of mental illness in Colombia. It is particularly interesting to show how Colombian physicians have appropriated concepts such as degeneration, diathesis, morbid heredity and stigmas of degeneration since the early 20th century to describe, classify and define mental illnesses present in Colombian territory. During this period the theory of degeneration served as the conceptual and theoretical framework for understanding the etiology, genesis and evolution of mental illness.

Hybrid asexuality as a primary postzygotic barrier between nascent species: On the interconnection between asexuality, hybridization and speciation

Czech Academy of Sciences Publication Activity Database

Janko, K.; Pačes, Jan; Wilkinson-Herbots, H.; Costa, R. J.; Roslein, J.; Drozd, P.; Iakovenko, N.; Rídl, Jakub; Hroudová, Miluše; Kočí, J.; Reifová, R.; Šlechtová, V.; Choleva, L.

2018-01-01

Roč. 27, č. 1 (2018), s. 248-263 ISSN 0962-1083 R&D Projects: GA AV ČR KJB600450902; GA MŠk(CZ) LM2015047; GA ČR GA13-12580S; GA ČR GA206/09/1298; GA ČR GAP506/10/1155; GA ČR GJ15-19947Y; GA MŠk EF15_003/0000460 Institutional support: RVO:68378050 ; RVO:67985904 Keywords : balance hypothesis * coalescence * evolution of asexuality * hybridization * phylogeography * speciation Subject RIV: CE - Biochemistry OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 6.086, year: 2016

New insights into the evolution of the W Chromosome in Lepidoptera

Czech Academy of Sciences Publication Activity Database

Dalíková, Martina; Zrzavá, Magda; Hladová, Irena; Nguyen, Petr; Šonský, Ivan; Flegrová, Martina; Kubíčková, S.; Voleníková, Anna; Kawahara, A. Y.; Peters, R. S.; Marec, František

2017-01-01

Roč. 108, č. 7 (2017), s. 709-719 ISSN 0022-1503. [Evolutionary Genomics of Sex 2016. Tempe, 17.11.2016-19.11.2016] R&D Projects: GA ČR(CZ) GA14-22765S; GA ČR(CZ) GA17-13713S; GA ČR(CZ) GP14-35819P Grant - others:GA JU(CZ) 159/2016/P Institutional support: RVO:60077344 Keywords : comparative genomic hybridization * laser microdissection * quantitative PCR Subject RIV: EB - Genetics ; Molecular Biology OBOR OECD: Genetics and heredity (medical genetics to be 3) Impact factor: 2.432, year: 2016 https://academic.oup.com/jhered/article/108/7/709/3978917

Conference report "Stoffwechsel. Histories of metabolism", workshop organized by Mathias Grote at Technische Universität Berlin, November 28-29th, 2014.

Science.gov (United States)

Grote, Mathias; Keuck, Lara

2015-06-01

Historical analyses of what metabolism has been conceived of, how concepts of metabolism were related to disciplines such as nineteenth-century nutritional physiology or twentieth-century biochemistry, and how their genealogies relate to the current developments may be helpful to understand the various, at times polemic, ways in which the boundaries between metabolism and heredity have been re-drawn. Against this background, a small number of scholars gathered in Berlin for a workshop that equally aimed at bringing new stories to the fore, and at considering seemingly known ones in a new light. Some aspects of the discussions are summarized in this paper.

Aldred Scott Warthin's Family 'G' : The American Plot Against Cancer and Heredity (1895-1940)

NARCIS (Netherlands)

Pieters, A.H.L.M.

2017-01-01

According to many, the genetic technology used in cancer is a promising test case of twenty-first century ‘genomic medicine’. However, it is important to realize that accounting for the genetic or hereditary factors in cancer medicine is not new. Since at least the eighteenth century, medical

A linear time algorithm for minimum fill-in and treewidth for distance heredity graphs

NARCIS (Netherlands)

Broersma, Haitze J.; Dahlhaus, E.; Kloks, A.J.J.; Kloks, T.

2000-01-01

A graph is distance hereditary if it preserves distances in all its connected induced subgraphs. The MINIMUM FILL-IN problem is the problem of finding a chordal supergraph with the smallest possible number of edges. The TREEWIDTH problem is the problem of finding a chordal embedding of the graph

Cellular heredity in haploid cultures of somatic cells. Progress report, August 1977--August 1978

International Nuclear Information System (INIS)

Freed, J.J.

1978-09-01

Studies in progress on cultured frog and fish cells, exploring the relation between the frequency of mutation after ultraviolet irradiation and the pathway through which DNA repair takes place are reported. The rationale is that the mutation frequency induced by a uv exposure is determined not only by the dose delivered but by the fidelity of the DNA repair process. Since frog cells express photoreversal enzyme, whether repair takes place by error-free photoreversal or by other, error-prone, mechanisms can be determined experimentally. An important question is whether an inducible, error-prone mutagenic form of repair is demonstrable. During the past year, methods necessary to determine uv survival and mutation frequency over a range of uv exposures were worked out. Using these methods, we have tested for alteration of the uv survival curve by previous conditioning exposures in frog cells was studied and uv survival and photoreversal capacity in fish cells were determined. The relation between uv survival and induction of ouabain resistance by an alkylating agent (MNNG) was examined as a background for further studies with uv. A procedure intended to accomplish DNA-mediated transfer of frog DNA photolyase enzyme to Chinese hamster cells is described

Cellular heredity in haploid cultures of somatic cells. Comprehensive report, April 1975--June 1977

International Nuclear Information System (INIS)

Freed, J.J.

1977-07-01

This report reviews genetic studies carried out since 1975 on a haploid cultured cell line from frog embryos (ICR 2A). Although a single chromosome set would be expected to facilitate recovery of recessive mutants, experiments suggested that cell culture variants might arise through processes more complex than the selection of simple mutational changes. Therefore, the objectives of the work reported here have been to throw light on just how cell culture variants arise in this system. First, we have continued to characterize the ICR 2A line, with emphasis on stability of karyotype and DNA content. Second, we have studied in detail the origin of two classes of drug-resistant variants. Bromodeoxyuridine resistance of the thymidine deficiency type has been shown to arise through sequential loss of two forms of thymidine-phosphorylating enzyme; loss of the second form of enzyme is complex, suggesting that changes more complex than simple recessive mutations may be involved. Another form of resistance, in which tolerance of high levels of bromodeoxyuridine is found in cells that continue to express thymidine kinase, remains under study. Variants resistant to microtubule inhibitors were isolated. It was found that these haploid strains have properties distinguishing them from analogous resistant strains isolated from diploid mammalian cell cultures in other laboratories. In order to understand better how mutagens are involved in the origin of cell culture variants, we have examined the effect of different forms of DNA repair on the frequency of drug-resistant colonies induced by ultraviolet radiation. Preliminary experiments suggest that the frequency of such colonies is greater when repair takes place through (presumably error-prone) dark repair than when (error-free) photoreversal is allowed to occur. Such experiments can determine whether new phenotypes arise from alterations in DNA, and thus whether, in a broad sense, they are likely to be mutational in nature

Cellular heredity in haploid cultures of somatic cells, March 1968-April 1981. Final report

International Nuclear Information System (INIS)

Freed, J.J.

1982-03-01

An account is given of the development and application to cell-culture genetics of unique haploid cell lines from frog embryo developed in this laboratory. Since 1968, the main aim of this project has been to develop the haploid cell system for studies of mutagenesis in culture, particularly by ultraviolet radiation. In the course of this work we isolated chromosomally stable cell lines, derived and characterized a number of variants, and adapted cell hybridization and other methods to this material. Particular emphasis was placed on ultraviolet photobiology, including studies of cell survival, mutagenesis, and pathways of repair of uv-damaged DNA. Although at present less widely used for genetic experiments than mammalian cell lines, the frog cells offer the advantages of authentic haploidy and a favorable repertory of DNA repair pathways for study of uv mutagenesis

Sorderas neurosensoriales no sindrómicas: Análisis de la herencia en 10 familias

Directory of Open Access Journals (Sweden)

Ibis Menéndez

1998-06-01

Full Text Available Se reportan los árboles genealógicos de 10 probandos afectados con sorderas neurosensoriales no sindrómicas de aparición familiar. El análisis genético practicado permitió reconocer la clara segregación de un único gen de sordera en 7 familias (3 autosómicas recesivas, 2 autosómicas dominantes, 1 ligada al cromosoma X, 1 con herencia mitocondrial. En las 3 familias restantes resultó difícil el análisis y se propuso la herencia recesiva como la más probable, sobre la base, fundamentalmente, de las características de la pérdida auditiva (congénita, bilateral, severa o profunda. En general las sorderas autosómicas recesivas fueron las más frecuentes. Se corrobora que estos estudios suelen ser complicados por la gran heterogeneidad que pueden presentar a todos los niveles las sorderas neurosensoriales no sindrómicas.The pedigress of 10 examiness affected with non syndrome neurosensorial deafness of familial appearance were erported. The genetical analysis made allowed to recognize the clear segregation of a sale gene of deafness in 7 families (3 recessive autosomal, 2 dominant autosomal, 1 linked to cromosome X, and 1 with mitochondrial heredity. In the other 3 hamilies the analysis was difficult and the recessive heredity was suggested as the most probable, based mainly on the characteristics of auditive loss (congenital, bilateral, severe or deep. In general, the recessive autosomal deafness was the most common. It was corroborated that these studies are usually complicated due to the great heterogeneity that the non syndromic neurosensorial deafness may present at all levels.

Storytelling, statistics and hereditary thought: the narrative support of early statistics.

Science.gov (United States)

López-Beltrán, Carlos

2006-03-01

This paper's main contention is that some basically methodological developments in science which are apparently distant and unrelated can be seen as part of a sequential story. Focusing on general inferential and epistemological matters, the paper links occurrences separated by both in time and space, by formal and representational issues rather than social or disciplinary links. It focuses on a few limited aspects of several cognitive practices in medical and biological contexts separated by geography, disciplines and decades, but connected by long term transdisciplinary representational and inferential structures and constraints. The paper intends to show a given set of knowledge claims based on organizing statistically empirical data can be seen to have been underpinned by a previous, more familiar, and probably more natural, narrative handling of similar evidence. To achieve that this paper moves from medicine in France in the late eighteenth and early nineteenth century to the second half of the nineteenth century in England among gentleman naturalists, following its subject: the shift from narrative depiction of hereditary transmission of physical peculiarities to posterior statistical articulations of the same phenomena. Some early defenders of heredity as an important (if not the most important) causal presence in the understanding of life adopted singular narratives, in the form of case stories from medical and natural history traditions, to flesh out a special kind of causality peculiar to heredity. This work tries to reconstruct historically the rationale that drove the use of such narratives. It then shows that when this rationale was methodologically challenged, its basic narrative and probabilistic underpinings were transferred to the statistical quantificational tools that took their place.

Long-term course of severe depression: late remission and recurrence may be found in a follow-up after 38-53 years

Directory of Open Access Journals (Sweden)

Lisa Crona

2012-07-01

Full Text Available This study is a follow-up of inpatients diagnosed with severe depression/melancholia between 1956 and 1969. During this period, all inpatients at the Department of Psychiatry, University Hospital, Lund, were rated on a multidimensional diagnostic schedule on discharge. There were 471 patients born from 1920 onward. In the present follow-up, 2006 to 2010, 169 survivors could be traced. They were asked to participate in the study involving a telephone interview, in which a structured life chart was used. Of the patients contacted, 16 were ill or confused and 3 did not remember ever being depressed, leaving 150 who could participate. Seventy-five of these agreed to participate in the study. Long-term course of depression was evaluated by cluster analysis and compared to background variables, such as heredity for depression, perceived parental rearing behaviour, and treatment of index depressive episode. Using a cluster analysis the patients could be separated into six clusters describing the course: i single or few episodes followed by long-lasting remission; ii single or few episodes followed by long-lasting remission, although shorter; iii single or few episodes followed by late recurrence; iv single or few episodes, but more frequently ill, followed by late recurrence; v several episodes followed by lasting remission; vi chronic course of episodes. Remission or recurrence could there- fore occur even after more than a decade. In summary, there was a short-term course with or without recurrence or a chronic course with or without late remission. Heredity for depression was significantly related to a chronic course with or without late remission.

Raza, alteridad y exclusión en Alemania durante la década de 1920

Directory of Open Access Journals (Sweden)

Alejandro Castillejo Cuéllar

2007-04-01

Full Text Available In 1927, under the umbrella of the Kaiser Wilhelm Gesellschaft, the institution responsible for directing Germany's research policies, the Kaiser Wilhelm Institut für Anthropologie, Menschliche, Erblehre und Eugenic (Kaiser Wilhelm Institute for Anthropology, Human Heredity and Eugenics was founded. The institution represented the apex of the German eugenics movement that had developed in the previous decades, and the birth of oneof the intellectual centers where the Reich's ideology of social engineering was founded. This article discusses some of the historic elements that linked racial ideology, the bedrock of Nazi policy of extermination, and the social sciences during the Weimar period

Theories of genetics and evolution and the development of medical entomology in France (1900-1939).

Science.gov (United States)

Gachelin, G; Opinel, A

2008-12-01

The development of entomology and medical entomology in France is discussed in the context of the prevalence of Lamarckian ideas concerning heredity and evolution. Lamarckian ideas have greatly influenced research carried out at the Institut Pasteur by Emile Roubaud and more generally in Felix Mesnil's laboratory, as well as research in general entomology at the Museum national d'histoire naturelle. By contrast, it did not influence research and teaching at the Faculté de médecine of Paris or that of physicians more generally including those in overseas Instituts Pasteur, which clearly kept away from theoretical discussion concerning the origin of variations and adaptation in insects of medical interest.

Bad habits and bad genes: early 20th-century eugenic attempts to eliminate syphilis and associated "defects" from the United States.

Science.gov (United States)

Wilson, Philip K

2003-01-01

American eugenists in the early 20th century distinguished "degenerates," including syphilitics, prostitutes, alcoholics and criminals, from the "normal" population by their particular bad habits. From eugenists' viewpoint, these bad habits were derived from bad character, a flaw that stemmed from an individual's bad genes. This essay explores how eugenists during this period characterized syphilitics and those with associated character "defects" in terms of heredity. Additionally, it examines the methods eugenists most frequently advocated to rectify these bad habits. These methods included marriage restriction, immigration control and reproductive sterilization. Overall, eugenists directed their efforts not so much at the "degenerate" as at his or her germ line.

STUDIES ON WILD HOUSE MICE .4. ON THE HEREDITY OF TESTOSTERONE AND READINESS TO ATTACK

NARCIS (Netherlands)

VANOORTMERSSEN, GA; BENUS, RF; SLUYTER, F

1992-01-01

An attempt was made to determine the role of the Y chromosome in the development of aggression in wild house mice. The aggression-eliciting property of testosterone depends not only on circulating adult testosterone, but also on perinatal sensitization of the central nervous system to this steroid.

Errores innatos del metabolismo: Enfermedades lisosomales

Directory of Open Access Journals (Sweden)

Caridad Menéndez Saínz

2002-03-01

Full Text Available Dentro de los errores innatos del metabolismo se encuentran las enfermedades de almacenamiento lisosomal o enzimopatías lisosomales, las cuáles se caracterizan por un déficit enzimático específico, la excreción de metabolitos por la orina y la acumulación de los compuestos no degradados en diferentes órganos y tejidos que ocasionan la disfución de éstos. Tienen un patrón de herencia autosómico recesivo, excepto para la enfermedad de Fabry y la enfermedad de Hunter en las que el patrón de herencia está ligado al cromosoma X. Estas enfermedades tienen una baja incidencia en general, aunque hay poblaciones donde algunas de ellas tienen una alta incidencia. Su importancia radica en la magnitud que representan como problema de salud, por la pobre calidad de vida de esos pacientes, así como su fallecimiento prematuro, motivo por el cual hay que evitar los nacimientos de nuevos niños afectados.Among the metabolism inborn errors, there are the lysosomal storage diseases or lysosomal enzymopathies that are characterized by an specific enzymatic deficiency, excretion of metabollites in urine and accumulation of non-degraded compounds in various organs and tissues causing their dysfunction. These diseases have a recessive autosomal heredity, except for Fabry´s disease and Hunter’s disease in which the pattern of heredity is chromosome X-linked. These diseases have a low incidence in general although there are populations where they show a high incidence. Their importance lies in what they represent as a health problem because of the poor quality of life of these patients and their early death, therefore, it is necessary to prevent the birth of new infants affected with these diseases.

Infant wheeze, comorbidities and school age asthma.

Science.gov (United States)

Neuman, Asa; Bergström, Anna; Gustafsson, Per; Thunqvist, Per; Andersson, Niklas; Nordvall, Lennart; Kull, Inger; Wickman, Magnus

2014-06-01

Factors associated with early onset of wheeze have been described, but there is limited knowledge on which of these infant wheezers who will have developed asthma in school age. The aim was to identify clinical risk factors for asthma in the 8-yr-old children that wheezed during infancy in a population-based setting. Three thousand two hundred and fifty-one children from a population-based birth cohort followed prospectively from infancy until age 8 yr were included in the study. Data were analyzed using multivariate logistic regression analysis. Parents reported any wheeze episode before age 2 yr in 823 subjects (25%). Infant wheezers had an almost fourfold risk of asthma at age 8 [adjusted odds ratio (aOR) 3.68, 95% CI 2.74-4.96], equivalent to an asthma prevalence of 14% compared with 4% among non-wheezers (p < 0.001). After adjustments for sex, exposure to tobacco smoke and indoor dampness/mould, allergic heredity (aOR 1.53, 95% CI 1.02-2.30), increased frequency of wheeze (aOR 3.41, 95% CI 2.09-5.56 for children with ≥3 episodes compared with ≤2 episodes during the first 2 yr of life), infant eczema (aOR 2.31, 95% CI 1.52-3.49), and recurrent abdominal pain (aOR 2.33, 95% CI 1.30-4.16) remained risk factors for school age asthma in the infant wheezing group. Among infant wheezers, allergic heredity, increased severity of wheeze, infant eczema, and recurrent abdominal pain were independent risk factors for asthma at age 8 yr. Among children with three or four of these risk factors, 38% had asthma at school age. © 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

A population-based study of gastroesophageal reflux disease and sleep problems in elderly twins.

Directory of Open Access Journals (Sweden)

Anna Lindam

Full Text Available BACKGROUND & AIMS: Previous studies indicate an association between sleep problems and gastroesophageal reflux disease (GERD. Although both these conditions separately have moderate heritabilities, confounding by genetic factors has not previously been taken into account. This study aimed to reveal the association between sleep problems and GERD, while adjusting for heredity and other potential confounding factors. METHODS: This cross-sectional population-based study included all 8,014 same-sexed twins of at least 65 years of age and born in Sweden between 1886 and 1958, who participated in telephone interviews in 1998-2002. Three logistic regression models were used 1 external control analysis, 2 within-pair co-twin analysis with dizygotic (DZ twin pairs discordant for GERD, and 3 within-pair co-twin analysis with monozygotic (MZ twin pairs discordant for GERD. Odds ratios (ORs with 95% confidence intervals (CIs were calculated and adjusted for established risk factors for GERD, i.e. sex, age, body mass index (BMI, tobacco smoking, and educational level. RESULTS: A dose-response association was identified between increasing levels of sleep problems and GERD in the external control analysis. Individuals who often experienced sleep problems had a two-fold increased occurrence of GERD compared to those who seldom had sleep problems (OR 2.0, 95% CI 1.8-2.4. The corresponding association was of similar strength in the co-twin analysis including 356 DZ pairs (OR 2.2, 95% CI 1.6-3.4, and in the co-twin analysis including 210 MZ pairs (OR 1.5, 95% CI 0.9-2.7. CONCLUSION: A dose-dependent association between sleep problems and GERD remains after taking heredity and other known risk factors for GERD into account.

Epigenética, más allá de la Genética Epigenética, más allá de la Genética

Directory of Open Access Journals (Sweden)

Ángeles Rangel-Serrano

2012-02-01

Full Text Available Epigenetics is the study of reversible inheritable changes in gene function that occur without a change in the sequence of nuclear DNA and is transmitted from one generation of cells or organisms to the next. The chemical modifications to DNA and its associated proteins help to determine the selective use of genes and influence cell fate. Epigenetic modifications of the genome are involved in regulating many cellular processes. These include embryonic development, X chromosome inactivation and genomic imprinting. Abnormal epigenetic modifications and control can cause disease, including cancer and autoimmune diseases. Identification of inheritable epigenetic patterns such as DNA methylation and histone acetylation has been proposed as a useful marker for the early detection and prognosis of diseases caused by epigenetic errors.La epigenética es el estudio de los cambios heredables reversibles en la función de los genes que ocurren sin cambios en la secuencia de ADN. Las modificaciones químicas del ADN y sus proteínas asociadas determinan la expresión selectiva de genes y su influencia en el comportamiento de las células. Las modificaciones epigenéticas del genoma regulan muchos procesos celulares, tales como el desarrollo embrionario, la inactivación del cromosoma X, la impronta genómica y, la estabilidad de los cromosomas. La alteración de las modificaciones epigenéticas o la pérdida de su control, pueden causar enfermedades como el cáncer y contribuir al desarrollo de enfermedades autoinmunes. Por lo anterior, se ha propuesto que la identificación de los patrones epigenéticos heredables tales como la metilación del ADN y la acetilación de histonas sería una herramienta útil en el diagnóstico y pronóstico de las enfermedades causadas por errores epigenéticos.

Opinion evolution in different social acquaintance networks

Science.gov (United States)

Chen, Xi; Zhang, Xiao; Wu, Zhan; Wang, Hongwei; Wang, Guohua; Li, Wei

2017-11-01

Social acquaintance networks influenced by social culture and social policy have a great impact on public opinion evolution in daily life. Based on the differences between socio-culture and social policy, three different social acquaintance networks (kinship-priority acquaintance network, independence-priority acquaintance network, and hybrid acquaintance network) incorporating heredity proportion ph and variation proportion pv are proposed in this paper. Numerical experiments are conducted to investigate network topology and different phenomena during opinion evolution, using the Deffuant model. We found that in kinship-priority acquaintance networks, similar to the Chinese traditional acquaintance networks, opinions always achieve fragmentation, resulting in the formation of multiple large clusters and many small clusters due to the fact that individuals believe more in their relatives and live in a relatively closed environment. In independence-priority acquaintance networks, similar to Western acquaintance networks, the results are similar to those in the kinship-priority acquaintance network. In hybrid acquaintance networks, similar to the Chinese modern acquaintance networks, only a few clusters are formed indicating that in modern China, opinions are more likely to reach consensus on a large scale. These results are similar to the opinion evolution phenomena in modern society, proving the rationality and applicability of network models combined with social culture and policy. We also found a threshold curve pv+2 ph=2.05 in the results for the final opinion clusters and evolution time. Above the threshold curve, opinions could easily reach consensus. Based on the above experimental results, a culture-policy-driven mechanism for the opinion dynamic is worth promoting in this paper, that is, opinion dynamics can be driven by different social cultures and policies through the influence of heredity and variation in interpersonal relationship networks. This

Origin and distribution of epipolythiodioxopiperazine (ETP gene clusters in filamentous ascomycetes

Directory of Open Access Journals (Sweden)

Gardiner Donald M

2007-09-01

Full Text Available Abstract Background Genes responsible for biosynthesis of fungal secondary metabolites are usually tightly clustered in the genome and co-regulated with metabolite production. Epipolythiodioxopiperazines (ETPs are a class of secondary metabolite toxins produced by disparate ascomycete fungi and implicated in several animal and plant diseases. Gene clusters responsible for their production have previously been defined in only two fungi. Fungal genome sequence data have been surveyed for the presence of putative ETP clusters and cluster data have been generated from several fungal taxa where genome sequences are not available. Phylogenetic analysis of cluster genes has been used to investigate the assembly and heredity of these gene clusters. Results Putative ETP gene clusters are present in 14 ascomycete taxa, but absent in numerous other ascomycetes examined. These clusters are discontinuously distributed in ascomycete lineages. Gene content is not absolutely fixed, however, common genes are identified and phylogenies of six of these are separately inferred. In each phylogeny almost all cluster genes form monophyletic clades with non-cluster fungal paralogues being the nearest outgroups. This relatedness of cluster genes suggests that a progenitor ETP gene cluster assembled within an ancestral taxon. Within each of the cluster clades, the cluster genes group together in consistent subclades, however, these relationships do not always reflect the phylogeny of ascomycetes. Micro-synteny of several of the genes within the clusters provides further support for these subclades. Conclusion ETP gene clusters appear to have a single origin and have been inherited relatively intact rather than assembling independently in the different ascomycete lineages. This progenitor cluster has given rise to a small number of distinct phylogenetic classes of clusters that are represented in a discontinuous pattern throughout ascomycetes. The disjunct heredity of

Properties of low content uranium-molybdenum alloys which may be used as nuclear fuels

International Nuclear Information System (INIS)

Lehmann, J.; Decours, J.

1964-01-01

Metallurgical properties are given in this report of uranium-molybdenum alloys containing 0,5 to 3 per cent of molybdenum. Since some of these alloys are used in EDF power reactors are given: briefly the operating conditions imposed on nuclear fuels: maximum temperature, temperature gradient and external pressure. In the first part are considered the structural properties of the alloys correlation with the phase transformation kinetics; a description is given of the effects of certain physico-metallurgical factors on the morphology and the crystalline structure of the materials: - solidification conditions and the heredity of the γ structure, - cooling rate at the transformation points, - whether or not the intermediate γ → β transformation is suppressed In the second part we show how a knowledge of the phase transformation processes has made it possible to define the optimum preparation conditions for these materials in the form of fuel tubes intended for the EDF reactors: casting conditions, controlled cooling treatments, weldability. In the third part we study the thermal, stability during the long duration high temperature treatments and the cycles in the two zones of the diagram α + γ; β + γ the effects of the morphology (in particular the two types of α pseudo-grains observed) and of the cooling rate during the transformation point transitions are described. In the fourth part are discussed the mechanical properties: resistance to a tractive force, resistance to creep, resilience. These properties can also be affected by the γ structure heredity and by the cooling rate to which the alloy has been subjected. In conclusion we discuss the reasons which led to the choice of some of these alloys for the first EDF reactors in particular the advantages of their high creep resistance between 450 and 600 deg C for use in the form of tubes subjected to an external pressure. (authors) [fr

Generalization of exponential based hyperelastic to hyper-viscoelastic model for investigation of mechanical behavior of rate dependent materials.

Science.gov (United States)

Narooei, K; Arman, M

2018-03-01

In this research, the exponential stretched based hyperelastic strain energy was generalized to the hyper-viscoelastic model using the heredity integral of deformation history to take into account the strain rate effects on the mechanical behavior of materials. The heredity integral was approximated by the approach of Goh et al. to determine the model parameters and the same estimation was used for constitutive modeling. To present the ability of the proposed hyper-viscoelastic model, the stress-strain response of the thermoplastic elastomer gel tissue at different strain rates from 0.001 to 100/s was studied. In addition to better agreement between the current model and experimental data in comparison to the extended Mooney-Rivlin hyper-viscoelastic model, a stable material behavior was predicted for pure shear and balance biaxial deformation modes. To present the engineering application of current model, the Kolsky bars impact test of gel tissue was simulated and the effects of specimen size and inertia on the uniform deformation were investigated. As the mechanical response of polyurea was provided over wide strain rates of 0.0016-6500/s, the current model was applied to fit the experimental data. The results were shown more accuracy could be expected from the current research than the extended Ogden hyper-viscoelastic model. In the final verification example, the pig skin experimental data was used to determine parameters of the hyper-viscoelastic model. Subsequently, a specimen of pig skin at different strain rates was loaded to a fixed strain and the change of stress with time (stress relaxation) was obtained. The stress relaxation results were revealed the peak stress increases by applied strain rate until the saturated loading rate and the equilibrium stress with magnitude of 0.281MPa could be reached. Copyright © 2017 Elsevier Ltd. All rights reserved.

Why are children in the same family so different from one another?

Science.gov (United States)

Plomin, Robert; Daniels, Denise

2011-06-01

One of the most important findings that has emerged from human behavioral genetics involves the environment rather than heredity, providing the best available evidence for the importance of environmental influences on personality, psychopathology, and cognition. The research also converges on the remarkable conclusion that these environmental influences make two children in the same family as different from one another as are pairs of children selected randomly from the population. The theme of the target article is that environmental differences between children in the same family (called "nonshared environment") represent the major source of environmental variance for personality, psychopathology, and cognitive abilities. One example of the evidence that supports this conclusion involves correlations for pairs of adopted children reared in the same family from early in life. Because these children share family environment but not heredity, their correlation directly estimates the importance of shared family environment. For most psychological characteristics, correlations for adoptive "siblings" hover near zero, which implies that the relevant environmental influences are not shared by children in the same family. Although it has been thought that cognitive abilities represent an exception to this rule, recent data suggest that environmental variance that affects IQ is also of the nonshared variety after adolescence. The article has three goals: (1) To describe quantitative genetic methods and research that lead to the conclusion that nonshared environment is responsible for most environmental variation relevant to psychological development, (2) to discuss specific nonshared environmental influences that have been studied to date, and (3) to consider relationships between nonshared environmental influences and behavioral differences between children in the same family. The reason for presenting this article in BBS is to draw attention to the far

Review and prospect of nuclear technology agriculture application in Zhejiang province

International Nuclear Information System (INIS)

Lu Yanting; Xiong Lidong; Wu Qing; Jin Qingsheng

2012-01-01

The discipline development, main progress and achievements of nuclear agricultural sciences in past 50 years in Zhejiang Province were reviewed in the paper. The great progress were obtained in radiation mutation breeding and related heredity mechanism, radiation sterile insect technique and related molecular biology mechanism, the agricultural products storage and preservation of irradiation processing. There were remarkable achievements in isotope tracer technique for animal and plant physiology and biochemistry research and agricultural chemicals safety usage standard. There was also distinct progress in space mutation breeding. From now on, there will be a close combination for the nuclear agricultural sciences with the modern bio-technology and the information technology, which will unceasingly promote the nuclear agricultural sciences development. (authors)

Research advances in susceptibility genes and their role in the pathogenesis of nonalcoholic fatty liver disease

Directory of Open Access Journals (Sweden)

XUAN Shiying

2016-03-01

Full Text Available Currently the incidence of nonalcoholic fatty liver disease (NAFLD is increasing, and the age of onset is getting younger worldwide, resulting in a heavy economic burden for both individuals and the society. Since NAFLD is closely related to heredity, metabolism, and the environment, genetic factors play an important role in the development and progression of NAFLD. With the development and wide application of the techniques from the genome-wide association studies, new research advances have been achieved in the susceptibility genes of NAFLD. This review summarizes the related research findings at home and abroad, and investigates the pathogenic factors for NAFLD and related mechanisms with a focus on the polymorphisms of susceptibility genes.

The adjuvant effect of phthalate exposure on IgE sensitisation in early childhood

DEFF Research Database (Denmark)

Callesen, M.; Weschler, Charles J.; Jensen, T.

2012-01-01

on internationally accepted criteria. Result: In the group of randomly selected children IgE sensitization was associated with the total phthalate exposure (P ...E sensitization in children. Method: A cross-sectional case-cohort study (n = 500) based on 2835 children, aged 3–5 years, responding to a questionnaire in the Danish Indoor Environment and Children’s Health study consisted of 300 subjects randomly selected and 200 cases with at least two parentally reported...... doctor diagnosed allergic diseases (asthma, allergic rhinoconjunctivitis or atopic dermatitis). The same physician conducted a clinical examination of all the 500 children including a structured interview on allergic heredity, clinical and medical history Specific serum-IgE against inhalant and food...

Genetic profiles distinguish different types of hereditary ovarian cancer

DEFF Research Database (Denmark)

Domanska, Katarina; Malander, Susanne; Staaf, Johan

2010-01-01

(HBOC) syndrome and the hereditary non-polyposis colorectal cancer (HNPCC) syndrome. Genome-wide array comparative genomic hybridization was applied to 12 HBOC associated tumors with BRCA1 mutations and 8 HNPCC associated tumors with mismatch repair gene mutations with 24 sporadic ovarian cancers......Heredity represents the strongest risk factor for ovarian cancer with disease predisposing mutations identified in 15% of the tumors. With the aim to identify genetic classifiers for hereditary ovarian cancer, we profiled hereditary ovarian cancers linked to the hereditary breast and ovarian cancer...... that HBOC and HNPCC associated ovarian cancer develop along distinct genetic pathways and genetic profiles can thus be applied to distinguish between different types of hereditary ovarian cancer....

Connecting Cancer to Its Causes Requires Incorporation of Effects on Tissue Microenvironments.

Science.gov (United States)

DeGregori, James

2017-11-15

In a recent article in Science , Tomasetti and colleagues present an expanded model for cancer risk, which they claim demonstrates the relative contribution of mutations caused by replication errors, environment, and heredity. The foundation of this model is the theory that the overwhelming driver of cancer risk is mutations. This perspective will present experimental evidence and evolutionary theory to challenge the basis of this underlying theory. An argument will be presented that the mutation-centric model of cancer suggests unrealistic solutions to cancer and distracts the research community from more promising approaches that consider tissue context. Cancer Res; 77(22); 6065-8. ©2017 AACR . ©2017 American Association for Cancer Research.

Environmental carcinogenesis and genetic variability

International Nuclear Information System (INIS)

Knudsen, A.G. Jr

1977-01-01

It was found that carcinogenesis in man may involve the interaction of genetic and environmental forces, and that mutation, whether germinal or somatic, seems to be involved in the origin of many, perhaps all cancers. The cancers of man may be visualized as occurring in four groups of individuals according to whether (1) neither genetic nor environmental factors are dominant, i.e. 'background' or 'spontaneous' cancer, (2) heredity alone is dominant, (3) environment alone is important, or (4) both are operating (Knudsen, 1977). The last two groups together are widely thought to contribute 70-80% of cancer cases in the United States; the relative contribution of each group is a major question to be answered

In between mental evolution and unconscious memory: Lamarckism, Darwinism, and professionalism in late Victorian Britain.

Science.gov (United States)

Turbil, Cristiano

2017-09-01

In 1884 Samuel Butler published a collection of essays entitled Remarks on George Romanes' Mental Evolution, where he attempted to show how Romanes' idea of mental evolution presented similarities with his theory of unconscious memory. By looking at Romanes' work through Butler's writing, this article will reevaluate some aspects of their works regarding the complex debate about memory, heredity, and instinct. This paper will explore the main differences and similarities between Romanes' science and Butler's writing on science both in terms of their ideas and contents. It will then look into their different professional relationships with Darwin and how this determined the professional and public reception of their theories. © 2017 Wiley Periodicals, Inc.

Differentiation of Students in the Early Danish Welfare State

DEFF Research Database (Denmark)

Ydesen, Christian; Andreasen, Karen Egedal; Hamre, Bjørn Frithiof

2018-01-01

Historically, differentiation of students has been influenced by to numerous contextual factors. Scholars and practitioners consider it a context-sensitive practice subject to negotiations and entanglements among various agents, groups, interests, ideas, and values. This article pursues the pract......Historically, differentiation of students has been influenced by to numerous contextual factors. Scholars and practitioners consider it a context-sensitive practice subject to negotiations and entanglements among various agents, groups, interests, ideas, and values. This article pursues...... of the education system. This entailed an increased division of labour among professional groups; debates reflecting different ideas about eugenics, heredity, and social equality; the schooling of psychologists and psychiatrists in Denmark; and the development of psychology and psychiatry as academic disciplines....

Heredity of medium-range order structure from melts to the microstructure of Ni-Cr-W superalloy

Energy Technology Data Exchange (ETDEWEB)

Gao, Zhongtang; Hu, Rui; Wang, Jun; Li, Jinshan [Northwestern Polytechnical University, State Key Laboratory of Solidification Processing, Xi' an (China)

2015-07-15

The structure factor S(Q), intensities and pair distribution function g(r) of liquid Ni-Cr-W superalloy at different temperatures have been measured by a high-temperature X-ray diffractometer. Coordination N{sub min}, correlation radius r{sub c}, the nearest atomic distance r{sub 1}, solidification microstructure and compression performance have been studied. The results show that a pre-peak exists on the structure factor curve at the liquidus temperature, and a fine structure of equiaxed, globular and non-dendritic primary grains can be achieved by casting the alloy at liquidus temperature. Liquid structure feature of Ni-Cr-W superalloy is found to depend on temperature. During the solidification, some structural information carried by the medium-range order (MRO) structure is inherited from the melt to the microstructure, which is beneficial for grain refinement. The maximum yield strength measured from typical microstructure of the equiaxed and non-dendritic grains at 1400 C is 543 MPa. The results show that refinement and non-dendritic grain is beneficial to the improvement of the yield strength. (orig.)

Family environment, not heredity, accounts for family resemblances in food preferences and attitudes: a twin study.

Science.gov (United States)

Rozin, P; Millman, L

1987-04-01

Monozygotic and same-sex dizygotic twin pairs reported on their food preferences, the variety of foods of the same general category (e.g. types of soup) in their diet, and their concern about contact of their food with disgusting or other unacceptable substances (contamination sensitivity). Although there was substantial resemblance between siblings for many of these items, there was no clear evidence for a heritable component on any item. The only case for which there was an interpretable and significantly greater resemblance among monozygotic than among dizygotic twins (out of 23 questions) was preferred degree of hotness resulting from chili pepper in foods. These results confirm the prediction that in omnivorous animals, such as humans, genetic predispositions will be minimal with respect to food. The modest sibling resemblances on a number of measures are primarily attributable to a shared environment.

Cellular heredity in haploid cultures of somatic cells. Comprehensive report, April 1975--June 1977. [UV radiation

Energy Technology Data Exchange (ETDEWEB)

Freed, J.J.

1977-07-01

This report reviews genetic studies carried out since 1975 on a haploid cultured cell line from frog embryos (ICR 2A). Although a single chromosome set would be expected to facilitate recovery of recessive mutants, experiments suggested that cell culture variants might arise through processes more complex than the selection of simple mutational changes. Therefore, the objectives of the work reported here have been to throw light on just how cell culture variants arise in this system. First, we have continued to characterize the ICR 2A line, with emphasis on stability of karyotype and DNA content. Second, we have studied in detail the origin of two classes of drug-resistant variants. Bromodeoxyuridine resistance of the thymidine deficiency type has been shown to arise through sequential loss of two forms of thymidine-phosphorylating enzyme; loss of the second form of enzyme is complex, suggesting that changes more complex than simple recessive mutations may be involved. Another form of resistance, in which tolerance of high levels of bromodeoxyuridine is found in cells that continue to express thymidine kinase, remains under study. Variants resistant to microtubule inhibitors were isolated. It was found that these haploid strains have properties distinguishing them from analogous resistant strains isolated from diploid mammalian cell cultures in other laboratories. In order to understand better how mutagens are involved in the origin of cell culture variants, we have examined the effect of different forms of DNA repair on the frequency of drug-resistant colonies induced by ultraviolet radiation. Preliminary experiments suggest that the frequency of such colonies is greater when repair takes place through (presumably error-prone) dark repair than when (error-free) photoreversal is allowed to occur. Such experiments can determine whether new phenotypes arise from alterations in DNA, and thus whether, in a broad sense, they are likely to be mutational in nature.

¿Hacer tabla rasa de la historia?: la analogía entre herencia fisiológica y memoria en el anarquismo español (1870-1914

Directory of Open Access Journals (Sweden)

Girón, Álvaro

2000-12-01

Full Text Available

The expansion of Darwinism stimulated a great deal of interest about the phenomena associated with heredity during the 1870-1930 years. Spanish anarchists, even though they were not specifically interested in the causes of variation and heredity, manifested an explicit concern about its potential effects. In fact, the analogy between memory and heredity, normally linked with Neolamarckian theories, proved to be extremely useful to rationalise those aspects of social and historical reality more difficult to accept from a libertarian point of view.