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Sample records for cdv strains detected

  1. Heterogeneity within the hemagglutinin genes of canine distemper virus (CDV) strains detected in Italy

    DEFF Research Database (Denmark)

    Martella, V.; Cirone, F.; Elia, G.

    2006-01-01

    along with CDVs of the Arctic lineage, the highest identity being to strain GR88 (98.0 and 98.4% aa, respectively). The full-length sequence of a red fox CDV strain, 207/00 was also determined and analyzed. The H protein of the fox CDV strain was unrelated to strains within the major European lineage...

  2. A multiplex reverse transcription-nested polymerase chain reaction for detection and differentiation of wild-type and vaccine strains of canine distemper virus

    Directory of Open Access Journals (Sweden)

    Cui Shang-jin

    2010-05-01

    Full Text Available Abstract A multiplex reverse transcription-nested polymerase chain reaction (RT-nPCR method was developed for the detection and differentiation of wild-type and vaccine strains of canine distemper virus (CDV. A pair of primers (P1 and P4 specific for CDV corresponding to the highly conserved region of the CDV genome were used as a common primer pair in the first-round PCR of the nested PCR. Primers P2 specific for CDV wild-type strains, were used as the forward primer together with the common reverse primer P4 in the second round of nested PCR. Primers P3, P5 specific for CDV wild-type strain or vaccine strain, were used as the forward primer together with the common reverse primer P4+P6 in the second round of nested PCR. A fragment of 177 bp was amplified from vaccine strain genomic RNA, and a fragment of 247 bp from wild-type strain genomic RNA in the RT-nPCR, and two fragments of 247 bp and 177 bp were amplified from the mixed samples of vaccine and wild-type strains. No amplification was achieved for uninfected cells, or cells infected with Newcastle disease virus (NDV, canine parvovirus (CPV, canine coronavirus (CCV, rabies virus (RV, or canine adenovirus (CAV. The RT-nPCR method was used to detect 30 field samples suspected of canine distemper from Heilongjiang and Jilin Provinces, and 51 samples in Shandong province. As a result of 30 samples, were found to be wild-type-like, and 5 to be vaccine-strain-like. The RT-nPCR method can be used to effectively detect and differentiate wild-type CDV-infected dogs from dogs vaccinated with CDV vaccine, and thus can be used in clinical detection and epidemiological surveillance.

  3. Lights and shades on an historical vaccine canine distemper virus, the Rockborn strain

    DEFF Research Database (Denmark)

    Martella, V.; Blixenkrone-Møller, Merete; Elia, G.

    2011-01-01

    to differ from the commonly used vaccine strain, Onderstepoort (93.0% nt and 91.7% aa), and to resemble more closely (99.6% nt and 99.3% aa) a CDV strain detected in China from a Lesser Panda (Ailurus fulgens). An additional four CDV strains matching (>99% nt identity) the Rockborn virus were identified...

  4. Genotyping canine distemper virus (CDV) by a hemi-nested multiplex PCR provides a rapid approach for investigation of CDV outbreaks

    DEFF Research Database (Denmark)

    Blixenkrone-Møller, Merete; Martella, Vito

    2007-01-01

    CDV is a highly contagious viral pathogen causing a lethal systemic disease in dogs and other carnivores. Several lineages or genotypes of CDV exist that are variously distributed throughout several continents. Legal or uncontrolled trading of animals may modify the epidemiology of CDV, introducing...... novel strains in CDV-naïve areas or accounting for the resurgence of CDV in areas where vaccine prophylaxis was effective and successful to control the disease. A hemi-nested PCR system was developed to genotype strains of the major CDV lineages, America-1, Europe, Asia-1, Asia-2 and Arctic. The assay...

  5. Crenarchaeal CdvA forms double-helical filaments containing DNA and interacts with ESCRT-III-like CdvB.

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    Christine Moriscot

    Full Text Available BACKGROUND: The phylum Crenarchaeota lacks the FtsZ cell division hallmark of bacteria and employs instead Cdv proteins. While CdvB and CdvC are homologues of the eukaryotic ESCRT-III and Vps4 proteins, implicated in membrane fission processes during multivesicular body biogenesis, cytokinesis and budding of some enveloped viruses, little is known about the structure and function of CdvA. Here, we report the biochemical and biophysical characterization of the three Cdv proteins from the hyperthermophilic archaeon Metallospherae sedula. METHODOLOGY/PRINCIPAL FINDINGS: Using sucrose density gradient ultracentrifugation and negative staining electron microscopy, we evidenced for the first time that CdvA forms polymers in association with DNA, similar to known bacterial DNA partitioning proteins. We also observed that, in contrast to full-lengh CdvB that was purified as a monodisperse protein, the C-terminally deleted CdvB construct forms filamentous polymers, a phenomenon previously observed with eukaryotic ESCRT-III proteins. Based on size exclusion chromatography data combined with detection by multi-angle laser light scattering analysis, we demonstrated that CdvC assembles, in a nucleotide-independent way, as homopolymers resembling dodecamers and endowed with ATPase activity in vitro. The interactions between these putative cell division partners were further explored. Thus, besides confirming the previous observations that CdvB interacts with both CdvA and CdvC, our data demonstrate that CdvA/CdvB and CdvC/CdvB interactions are not mutually exclusive. CONCLUSIONS/SIGNIFICANCE: Our data reinforce the concept that Cdv proteins are closely related to the eukaryotic ESCRT-III counterparts and suggest that the organization of the ESCRT-III machinery at the Crenarchaeal cell division septum is organized by CdvA an ancient cytoskeleton protein that might help to coordinate genome segregation.

  6. Canine distemper virus (CDV) in another big cat: should CDV be renamed carnivore distemper virus?

    Science.gov (United States)

    Terio, Karen A; Craft, Meggan E

    2013-09-17

    One of the greatest threats to the conservation of wild cat populations may be dogs or, at least, one of their viruses. Canine distemper virus (CDV), a single-stranded RNA virus in the Paramyxoviridae family and genus Morbillivirus, infects and causes disease in a variety of species, not just canids. An outbreak of CDV in wild lions in the Serengeti, Tanzania, in 1994 was a wake-up call for conservationists, as it demonstrated that an infectious disease could swiftly impact a previously healthy felid population. To understand how this virus causes disease in noncanid hosts, researchers have focused on specific mutations in the binding site of the CDV hemagglutinin gene. Now, Seimon et al. provide information on CDV in its latest feline victim, the endangered wild Amur tiger (Panthera tigris altaica) [T. A. Seimon et al., mBio 4(4):e00410-13, 2013, doi:10.1128/mBio.00410-13]. Their findings of CDV strains infecting tigers, in combination with recent information from other felids, paints a different picture, one in which CDV strains from a variety of geographic lineages and with a variety of amino acid residues in the hemagglutinin gene binding site can infect cats and cause disease. Although CDV has been known as a multihost disease since its discovery in domestic dogs in 1905, perhaps it is time to reconsider whether these noncanid species are not just incidental or "spillover" hosts but, rather, a normal part of the complex ecology of this infectious disease.

  7. Strain-Detecting Composite Materials

    Science.gov (United States)

    Wallace, Terryl A. (Inventor); Smith, Stephen W. (Inventor); Piascik, Robert S. (Inventor); Horne, Michael R. (Inventor); Messick, Peter L. (Inventor); Alexa, Joel A. (Inventor); Glaessgen, Edward H. (Inventor); Hailer, Benjamin T. (Inventor)

    2016-01-01

    A composite material includes a structural material and a shape-memory alloy embedded in the structural material. The shape-memory alloy changes crystallographic phase from austenite to martensite in response to a predefined critical macroscopic average strain of the composite material. In a second embodiment, the composite material includes a plurality of particles of a ferromagnetic shape-memory alloy embedded in the structural material. The ferromagnetic shape-memory alloy changes crystallographic phase from austenite to martensite and changes magnetic phase in response to the predefined critical macroscopic average strain of the composite material. A method of forming a composite material for sensing the predefined critical macroscopic average strain includes providing the shape-memory alloy having an austenite crystallographic phase, changing a size and shape of the shape-memory alloy to thereby form a plurality of particles, and combining the structural material and the particles at a temperature of from about 100-700.degree. C. to form the composite material.

  8. Propagation of Asian isolates of canine distemper virus (CDV in hamster cell lines

    Directory of Open Access Journals (Sweden)

    Yamaguchi Ryoji

    2009-10-01

    Full Text Available Abstract Backgrounds The aim of this study was to confirm the propagation of various canine distemper viruses (CDV in hamster cell lines of HmLu and BHK, since only a little is known about the possibility of propagation of CDV in rodent cells irrespective of their epidemiological importance. Methods The growth of CDV in hamster cell lines was monitored by titration using Vero.dogSLAMtag (Vero-DST cells that had been proven to be susceptible to almost all field isolates of CDV, with the preparations of cell-free and cell-associated virus from the cultures infected with recent Asian isolates of CDV (13 strains and by observing the development of cytopathic effect (CPE in infected cultures of hamster cell lines. Results Eleven of 13 strains grew in HmLu cells, and 12 of 13 strains grew in BHK cells with apparent CPE of cell fusion in the late stage of infection. Two strains and a strain of Asia 1 group could not grow in HmLu cells and BHK cells, respectively. Conclusion The present study demonstrates at the first time that hamster cell lines can propagate the majority of Asian field isolates of CDV. The usage of two hamster cell lines suggested to be useful to characterize the field isolates biologically.

  9. Emergence of canine distemper virus strains with modified molecular signature and enhanced neuronal tropism leading to high mortality in wild carnivores.

    Science.gov (United States)

    Origgi, F C; Plattet, P; Sattler, U; Robert, N; Casaubon, J; Mavrot, F; Pewsner, M; Wu, N; Giovannini, S; Oevermann, A; Stoffel, M H; Gaschen, V; Segner, H; Ryser-Degiorgis, M-P

    2012-11-01

    An ongoing canine distemper epidemic was first detected in Switzerland in the spring of 2009. Compared to previous local canine distemper outbreaks, it was characterized by unusually high morbidity and mortality, rapid spread over the country, and susceptibility of several wild carnivore species. Here, the authors describe the associated pathologic changes and phylogenetic and biological features of a multiple highly virulent canine distemper virus (CDV) strain detected in and/or isolated from red foxes (Vulpes vulpes), Eurasian badgers (Meles meles), stone (Martes foina) and pine (Martes martes) martens, from a Eurasian lynx (Lynx lynx), and a domestic dog. The main lesions included interstitial to bronchointerstitial pneumonia and meningopolioencephalitis, whereas demyelination--the classic presentation of CDV infection--was observed in few cases only. In the brain lesions, viral inclusions were mainly in the nuclei of the neurons. Some significant differences in brain and lung lesions were observed between foxes and mustelids. Swiss CDV isolates shared together with a Hungarian CDV strain detected in 2004. In vitro analysis of the hemagglutinin protein from one of the Swiss CDV strains revealed functional and structural differences from that of the reference strain A75/17, with the Swiss strain showing increased surface expression and binding efficiency to the signaling lymphocyte activation molecule (SLAM). These features might be part of a novel molecular signature, which might have contributed to an increase in virus pathogenicity, partially explaining the high morbidity and mortality, the rapid spread, and the large host spectrum observed in this outbreak.

  10. Importance of canine distemper virus (CDV) infection in free-ranging Iberian lynxes (Lynx pardinus).

    Science.gov (United States)

    Meli, Marina L; Simmler, Pascale; Cattori, Valentino; Martínez, Fernando; Vargas, Astrid; Palomares, Francisco; López-Bao, José V; Simón, Miguel A; López, Guillermo; León-Vizcaino, Luis; Hofmann-Lehmann, Regina; Lutz, Hans

    2010-11-20

    Canine distemper virus (CDV) is a morbillivirus that is the etiological agent of one of the most important viral diseases affecting canids and an expanding range of other carnivores. Using real-time RT-PCR, CDV RNA was detected in organs of an Iberian lynx (Lynx pardinus) found dead in the Doñana National Park, Southwestern Andalusia, Spain. This finding may be of great importance for the conservation of the species; at present the Iberian lynx is the most critically endangered wild felid. The aim of the present study was to elucidate the significance of CDV for the Iberian lynx population. High viral loads were evident in the dead lynx, suggesting an etiological involvement of CDV in its death. When carnivores from the same region were analyzed by CDV RT-PCR, a stone marten (Martes foina) was positive. Phylogenetic analyses demonstrated high identity of the two detected CDVs and a close relationship to the European dog lineage of CDV. Antibodies to CDV were detected in 14.8% of 88 tested free-ranging Iberian lynxes. The sample seroprevalence was significantly higher in lynxes from the Doñana Natural Space (22.9%) than Sierra Morena (5%). The stone marten and a red fox (Vulpes vulpes) also tested seropositive. In conclusion, CDV is present in the Iberian lynx population, especially in the Doñana region, with sporadic cases of disease. To reduce the infectious pressure of CDV on this endangered population, a mass dog vaccination should be considered. Copyright © 2010 Elsevier B.V. All rights reserved.

  11. Lights and shades on an historical vaccine canine distemper virus, the Rockborn strain.

    Science.gov (United States)

    Martella, V; Blixenkrone-Møller, M; Elia, G; Lucente, M S; Cirone, F; Decaro, N; Nielsen, L; Bányai, K; Carmichael, L E; Buonavoglia, C

    2011-02-01

    Both egg- and cell-adapted canine distemper virus (CDV) vaccines are suspected to retain residual virulence, especially if administered to immuno-suppressed animals, very young pups or to highly susceptible animal species. In the early 1980s, post-vaccine encephalitis was reported in dogs from various parts of Britain after administration of a particular batch of combined CDV Rockborn strain/canine adenovirus type-1 vaccine, although incrimination of the Rockborn strain was subsequently retracted. Notwithstanding, this, and other reports, led to the view that the Rockborn strain is less attenuated and less safe than other CDV vaccines, and the Rockborn strain was officially withdrawn from the markets in the mid 1990s. By sequencing the H gene of the strain Rockborn from the 46th laboratory passage, and a commercial vaccine (Candur(®) SH+P, Hoechst Rousell Vet GmbH), the virus was found to differ from the commonly used vaccine strain, Onderstepoort (93.0% nt and 91.7% aa), and to resemble more closely (99.6% nt and 99.3% aa) a CDV strain detected in China from a Lesser Panda (Ailurus fulgens). An additional four CDV strains matching (>99% nt identity) the Rockborn virus were identified in the sequence databases. Also, Rockborn-like strains were identified in two vaccines currently in the market. These findings indicate that Rockborn-like viruses may be recovered from dogs or other carnivores with distemper, suggesting cases of residual virulence of vaccines, or circulation of vaccine-derived Rockborn-like viruses in the field. Copyright © 2010 Elsevier Ltd. All rights reserved.

  12. Antagonistic pleiotropy and fitness trade-offs reveal specialist and generalist traits in strains of canine distemper virus.

    Directory of Open Access Journals (Sweden)

    Veljko M Nikolin

    Full Text Available Theoretically, homogeneous environments favor the evolution of specialists whereas heterogeneous environments favor generalists. Canine distemper is a multi-host carnivore disease caused by canine distemper virus (CDV. The described cell receptor of CDV is SLAM (CD150. Attachment of CDV hemagglutinin protein (CDV-H to this receptor facilitates fusion and virus entry in cooperation with the fusion protein (CDV-F. We investigated whether CDV strains co-evolved in the large, homogeneous domestic dog population exhibited specialist traits, and strains adapted to the heterogeneous environment of smaller populations of different carnivores exhibited generalist traits. Comparison of amino acid sequences of the SLAM binding region revealed higher similarity between sequences from Canidae species than to sequences from other carnivore families. Using an in vitro assay, we quantified syncytia formation mediated by CDV-H proteins from dog and non-dog CDV strains in cells expressing dog, lion or cat SLAM. CDV-H proteins from dog strains produced significantly higher values with cells expressing dog SLAM than with cells expressing lion or cat SLAM. CDV-H proteins from strains of non-dog species produced similar values in all three cell types, but lower values in cells expressing dog SLAM than the values obtained for CDV-H proteins from dog strains. By experimentally changing one amino acid (Y549H in the CDV-H protein of one dog strain we decreased expression of specialist traits and increased expression of generalist traits, thereby confirming its functional importance. A virus titer assay demonstrated that dog strains produced higher titers in cells expressing dog SLAM than cells expressing SLAM of non-dog hosts, which suggested possible fitness benefits of specialization post-cell entry. We provide in vitro evidence for the expression of specialist and generalist traits by CDV strains, and fitness trade-offs across carnivore host environments caused by

  13. Specific detection of Xylella fastidiosa Pierce's disease strains.

    Science.gov (United States)

    Banks, D; Albibi, R; Chen, J; Lamikanra, O; Jarret, R L; Smith, B J

    1999-08-01

    Pierce's disease (PD, Xylella fastidiosa) of grapevine is the primary pathogen limiting vinifera grape production in Florida and other regions of the southeastern United States. Quick and accurate detection of PD strains is essential for PD studies and control. A unique random amplified polymorphic DNA (PD1-1-2) was isolated from a PD strain from Florida. Fragment PD1-1-2 was cloned, sequenced, and found to be 1005 bp in length. PCR primers were designed to utilize these sequence data for PD strain detection. One primer set (XF176f-XF954r) amplified a 779-bp DNA fragment from 34 PD strains including seven pathotypes of X. fastidiosa, but not from strains of Xanthomonas campestris pv. campestris, Xan. vesicatoria or Escherichia coli. A second primer set (XF176f and XF686r) amplified a 511-bp fragment specific to 98 PD strains, but not from strains of citrus variegated chlorosis, mulberry leaf scorch, oak leaf scorch, periwinkle wilt, phony peach, or plum leaf scald. Sequence analysis indicated that RAPD fragment PD1-1-2 contains a Ser-tRNA gene. The PD-specific region includes a TaqI restriction site (TCGA) and is 150 bp downstream of the Ser-tRNA gene.

  14. Prevalence of positive antibody test results for canine parvovirus (CPV) and canine distemper virus (CDV) and response to modified live vaccination against CPV and CDV in dogs entering animal shelters.

    Science.gov (United States)

    Litster, Annette; Nichols, Jamieson; Volpe, Allison

    2012-05-25

    Canine parvovirus (CPV) and canine distemper virus (CDV) infections are relatively common in animal shelters and are important population management issues since the immune status of incoming dogs is usually unknown. This study aimed to determine the prevalence of positive antibody test results for CPV and CDV in incoming dogs aged ≥ 4 months and to measure antibody response over 2 weeks following vaccination with a modified live vaccine (MLV). Dogs aged 4-24 months entering an adoption-guarantee shelter (Shelter 1, n=51) and aged ≥ 4 months entering a limited admission shelter (Shelter 2; n=51) were enrolled. Dogs from Shelter 1 had been vaccinated with MLV at a municipal shelter 5 days before enrollment, whereas dogs from Shelter 2 had no known history of vaccination at enrollment. Sera were obtained on day 1, immediately prior to CPV/CDV MLV, and tested using an in-clinic ELISA kit to detect CPV/CDV antibodies. Dogs negative for CPV and/or CDV were retested at day 6-8 and those dogs still negative at day 6-8 were retested at day 13-15. Prior to CPV/CDV MLV on day 1, more dogs tested positive for CPV (Shelter 1 - 68.6%; Shelter 2 - 84.3%) than for CDV (Shelter 1 - 37.3%; Shelter 2 - 41.2%). On day 1, prior to MLV, all spayed/neutered animals tested CPV antibody-positive (n=17/102) and CPV antibody-positive dogs were older than serologically negative dogs (Shelter 1, P=0.0029; Shelter 2, P=0.0042). By day 13-15, almost all dogs were CPV antibody-positive (Shelter 1 - 97.9%; Shelter 2 - 100.0%) and CDV antibody-positive (Shelter 1 - 93.8%; Shelter 2 - 97.8%). MLV induces protective antibody titers against CPV/CDV in almost all dogs after 13-15 days. Copyright © 2011 Elsevier B.V. All rights reserved.

  15. Early detection of left ventricular dysfunction in asymptomatic diabetic patient using strain and strain rate echocardiographic imaging

    Directory of Open Access Journals (Sweden)

    Rania Gaber

    2014-03-01

    Conclusion: Type 2 diabetes mellitus deteriorate both LV systolic and diastolic performance. Strain and strain rate by tissue Doppler Imaging is superior to conventional Doppler in early detection and evaluation of systolic and diastolic dysfunction in type 2 diabetic patients.

  16. Large strain cruciform biaxial testing for FLC detection

    Science.gov (United States)

    Güler, Baran; Efe, Mert

    2017-10-01

    Selection of proper test method, specimen design and analysis method are key issues for studying formability of sheet metals and detection of their forming limit curves (FLC). Materials with complex microstructures may need an additional micro-mechanical investigation and accurate modelling. Cruciform biaxial test stands as an alternative to standard tests as it achieves frictionless, in-plane, multi-axial stress states with a single sample geometry. In this study, we introduce a small-scale (less than 10 cm) cruciform sample allowing micro-mechanical investigation at stress states ranging from plane strain to equibiaxial. With successful specimen design and surface finish, large forming limit strains are obtained at the test region of the sample. The large forming limit strains obtained by experiments are compared to the values obtained from Marciniak-Kuczynski (M-K) local necking model and Cockroft-Latham damage model. This comparison shows that the experimental limiting strains are beyond the theoretical values, approaching to the fracture strain of the two test materials: Al-6061-T6 aluminum alloy and DC-04 high formability steel.

  17. An Intelligent Strain Gauge with Debond Detection and Temperature Compensation

    Science.gov (United States)

    Jensen, Scott L.

    2012-01-01

    The harsh rocket propulsion test environment will expose any inadequacies associated with preexisting instrumentation technologies, and the criticality for collecting reliable test data justifies investigating any encountered data anomalies. Novel concepts for improved systems are often conceived during the high scrutiny investigations by individuals with an in-depth knowledge from maintaining critical test operations. The Intelligent Strain Gauge concept was conceived while performing these kinds of activities. However, the novel concepts are often unexplored even if it has the potential for advancing the current state of the art. Maturing these kinds of concepts is often considered to be a tangential development or a research project which are both normally abandoned within the propulsion-oriented environment. It is also difficult to justify these kinds of projects as a facility enhancement because facility developments are only accepted for mature and proven technologies. Fortunately, the CIF program has provided an avenue for bringing the Intelligent Strain Gauge to fruition. Two types of fully functional smart strain gauges capable of performing reliable and sensitive debond detection have been successfully produced. Ordinary gauges are designed to provide test article data and they lack the ability to supply information concerning the gauge itself. A gauge is considered to be a smart gauge when it provides supplementary data relating other relevant attributes for performing diagnostic function or producing enhanced data. The developed strain gauges provide supplementary signals by measuring strain and temperature through embedded Karma and nickel chromium (NiCr) alloy elements. Intelligently interpreting the supplementary data into valuable information can be performed manually, however, integrating this functionality into an automatic system is considered to be an intelligent gauge. This was achieved while maintaining a very low mass. The low mass enables

  18. Detection of antibody to canine distemper virus in wild raccoons (Procyon lotor) in Japan.

    Science.gov (United States)

    Nakano, Hitoshi; Kameo, Yuki; Sato, Hiroshi; Mochizuki, Masami; Yokoyama, Mayumi; Uni, Shigehiko; Shibasaki, Takahiro; Maeda, Ken

    2009-12-01

    Canine distemper virus (CDV) causes a lethal disease among members of the Carnivora. To clarify the distribution of CDV in wild animals, we examined 106 raccoon sera collected from two prefectures in Japan, Hyogo and Osaka, from 2005 to 2007. Among them, 34 raccoons (32.1%) possessed a virus-neutralizing (VN) antibody to KDK-1 strain (genotype Asia-1). There was no significant difference in seroprevalence of CDV regardless of places, gender, and body weights. In Hyogo, a geometric mean of VN titers to KDK-1 was significantly higher than that to Onderstepoort (vaccine strain), indicating that KDK-1-like CDV different from vaccine strain might have spread among raccoon population in Hyogo. In conclusion, CDV is epidemic among feral raccoons in Japan, suggesting that CDV might have been spreading among Japanese wild animals.

  19. Specific detection and analysis of a probiotic Bifidobacterium strain in infant feces

    NARCIS (Netherlands)

    Kok, RG; DeWaal, A; Schut, F; Welling, GW; Weenk, G; Hellingwerf, KJ

    1996-01-01

    For specific detection of the probiotic Bifidobacterium sp. strain LW420 in infant feces and for rapid quality control of this strain in culture, three strain-specific 16S rRNA gene-targeted primers have been developed. These primers allow specific detection of the organism via PCR. Specificity of

  20. Large strain detection of SRM composite shell based on fiber Bragg grating sensor

    Science.gov (United States)

    Zhang, Lei; Chang, Xinlong; Zhang, Youhong; Yang, Fan

    2017-12-01

    There may be more than 2% strain of carbon fiber composite material on solid rocket motor (SRM) in some extreme cases. A surface-bonded silica fiber Bragg grating (FBG) strain sensor coated by polymer is designed to detect the large strain of composite material. The strain transfer relation of the FBG large strain sensor is deduced, and the strain transfer mechanism is verified by finite element simulation. To calibrate the sensors, the tensile test is done by using the carbon fiber composite plate specimen attached to the designed strain sensor. The results show that the designed sensor can detect the strain more than 3%, the strain sensitivity is 0.0762 pm/μɛ, the resolution is 13.13μɛ, and the fitting degree of the wavelength-strain curve fitting function is 0.9988. The accuracy and linearity of the sensor can meet the engineering requirements.

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  8. File list: Unc.CDV.20.AllAg.Carotid_Arteries [Chip-atlas[Archive

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  1. File list: Unc.CDV.05.AllAg.Atrioventicular_canals [Chip-atlas[Archive

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  6. Recombinant canine distemper virus strain snyder hill expressing green or red fluorescent proteins causes meningoencephalitis in the ferret

    NARCIS (Netherlands)

    M. Ludlow (Martin); D.T. Nguyen (Tien); D. Silin; O. Lyubomska; R.D. de Vries (Rory); V. von Messling; S. McQuaid (Stephen); R.L. de Swart (Rik); W.P. Duprex (Paul)

    2012-01-01

    textabstractThe propensity of canine distemper virus (CDV) to spread to the central nervous system is one of the primary features of distemper. Therefore, we developed a reverse genetics system based on the neurovirulent Snyder Hill (SH) strain of CDV (CDVSH) and show that this virus rapidly

  7. Covariance of dynamic strain responses for structural damage detection

    Science.gov (United States)

    Li, X. Y.; Wang, L. X.; Law, S. S.; Nie, Z. H.

    2017-10-01

    A new approach to address the practical problems with condition evaluation/damage detection of structures is proposed based on the distinct features of a new damage index. The covariance of strain response function (CoS) is a function of modal parameters of the structure. A local stiffness reduction in structure would cause monotonous increase in the CoS. Its sensitivity matrix with respect to local damages of structure is negative and narrow-banded. The damage extent can be estimated with an approximation to the sensitivity matrix to decouple the identification equations. The CoS sensitivity can be calibrated in practice from two previous states of measurements to estimate approximately the damage extent of a structure. A seven-storey plane frame structure is numerically studied to illustrate the features of the CoS index and the proposed method. A steel circular arch in the laboratory is tested. Natural frequencies changed due to damage in the arch and the damage occurrence can be judged. However, the proposed CoS method can identify not only damage happening but also location, even damage extent without need of an analytical model. It is promising for structural condition evaluation of selected components.

  8. A stretchable strain sensor based on a metal nanoparticle thin film for human motion detection

    Science.gov (United States)

    Lee, Jaehwan; Kim, Sanghyeok; Lee, Jinjae; Yang, Daejong; Park, Byong Chon; Ryu, Seunghwa; Park, Inkyu

    2014-09-01

    Wearable strain sensors for human motion detection are being highlighted in various fields such as medical, entertainment and sports industry. In this paper, we propose a new type of stretchable strain sensor that can detect both tensile and compressive strains and can be fabricated by a very simple process. A silver nanoparticle (Ag NP) thin film patterned on the polydimethylsiloxane (PDMS) stamp by a single-step direct transfer process is used as the strain sensing material. The working principle is the change in the electrical resistance caused by the opening/closure of micro-cracks under mechanical deformation. The fabricated stretchable strain sensor shows highly sensitive and durable sensing performances in various tensile/compressive strains, long-term cyclic loading and relaxation tests. We demonstrate the applications of our stretchable strain sensors such as flexible pressure sensors and wearable human motion detection devices with high sensitivity, response speed and mechanical robustness.Wearable strain sensors for human motion detection are being highlighted in various fields such as medical, entertainment and sports industry. In this paper, we propose a new type of stretchable strain sensor that can detect both tensile and compressive strains and can be fabricated by a very simple process. A silver nanoparticle (Ag NP) thin film patterned on the polydimethylsiloxane (PDMS) stamp by a single-step direct transfer process is used as the strain sensing material. The working principle is the change in the electrical resistance caused by the opening/closure of micro-cracks under mechanical deformation. The fabricated stretchable strain sensor shows highly sensitive and durable sensing performances in various tensile/compressive strains, long-term cyclic loading and relaxation tests. We demonstrate the applications of our stretchable strain sensors such as flexible pressure sensors and wearable human motion detection devices with high sensitivity, response

  9. Detection of phosphatase activity in aquatic and terrestrial cyanobacterial strains

    Directory of Open Access Journals (Sweden)

    Babić Olivera B.

    2013-01-01

    Full Text Available Cyanobacteria, as highly adaptable microorganisms, are characterized by an ability to survive in different environmental conditions, in which a significant role belongs to their enzymes. Phosphatases are enzymes produced by algae in relatively large quantities in response to a low orthophosphate concentration and their activity is significantly correlated with their primary production. The activity of these enzymes was investigated in 11 cyanobacterial strains in order to determine enzyme synthesis depending on taxonomic and ecological group of cyanobacteria. The study was conducted with 4 terrestrial cyanobacterial strains, which belong to Nostoc and Anabaena genera, and 7 filamentous water cyanobacteria of Nostoc, Oscillatoria, Phormidium and Microcystis genera. The obtained results showed that the activity of acid and alkaline phosphatases strongly depended on cyanobacterial strain and the environment from which the strain originated. Higher activity of alkaline phosphatases, ranging from 3.64 to 85.14 μmolpNP/s/dm3, was recorded in terrestrial strains compared to the studied water strains (1.11-5.96 μmolpNP/s/dm3. The activity of acid phosphatases was higher in most tested water strains (1.67-6.28 μmolpNP/s/dm3 compared to the activity of alkaline phosphatases (1.11-5.96 μmolpNP/s/dm3. Comparing enzyme activity of nitrogen fixing and non-nitrogen fixing cyanobacteria, it was found that most nitrogen fixing strains had a higher activity of alkaline phosphatases. The data obtained in this work indicate that activity of phosphatases is a strain specific property. The results further suggest that synthesis and activity of phosphatases depended on eco-physiological characteristics of the examined cyanobacterial strains. This can be of great importance for the further study of enzymes and mechanisms of their activity as a part of cyanobacterial survival strategy in environments with extreme conditions. [Projekat Ministarstva nauke Republike

  10. Detecting strain in birefringent materials using spectral polarimetry

    Science.gov (United States)

    Ragucci, Anthony J. (Inventor); Cisar, Alan J. (Inventor); Huebschman, Michael L. (Inventor); Garner, Harold R. (Inventor)

    2010-01-01

    A method, computer program product and system for analyzing multispectral images from a plurality of regions of birefringent material, such as a polymer film, using polarized light and a corresponding polar analyzer to identify differential strain in the birefringent material. For example, the birefringement material may be low-density polyethylene (LDPE), high-density polyethylene (HDPE), polypropylene, polyethylene terephthalate (PET), polyvinyl chloride (PVC), polyvinylidene chloride, polyester, nylon, or cellophane film. Optionally, the method includes generating a real-time quantitative strain map.

  11. Speckle Tracking Based Strain Analysis Is Sensitive for Early Detection of Pathological Cardiac Hypertrophy.

    Science.gov (United States)

    An, Xiangbo; Wang, Jingjing; Li, Hao; Lu, Zhizhen; Bai, Yan; Xiao, Han; Zhang, Youyi; Song, Yao

    2016-01-01

    Cardiac hypertrophy is a key pathological process of many cardiac diseases. However, early detection of cardiac hypertrophy is difficult by the currently used non-invasive method and new approaches are in urgent need for efficient diagnosis of cardiac malfunction. Here we report that speckle tracking-based strain analysis is more sensitive than conventional echocardiography for early detection of pathological cardiac hypertrophy in the isoproterenol (ISO) mouse model. Pathological hypertrophy was induced by a single subcutaneous injection of ISO. Physiological cardiac hypertrophy was established by daily treadmill exercise for six weeks. Strain analysis, including radial strain (RS), radial strain rate (RSR) and longitudinal strain (LS), showed marked decrease as early as 3 days after ISO injection. Moreover, unlike the regional changes in cardiac infarction, strain analysis revealed global cardiac dysfunction that affects the entire heart in ISO-induced hypertrophy. In contrast, conventional echocardiography, only detected altered E/E', an index reflecting cardiac diastolic function, at 7 days after ISO injection. No change was detected on fractional shortening (FS), E/A and E'/A' at 3 days or 7 days after ISO injection. Interestingly, strain analysis revealed cardiac dysfunction only in ISO-induced pathological hypertrophy but not the physiological hypertrophy induced by exercise. Taken together, our study indicates that strain analysis offers a more sensitive approach for early detection of cardiac dysfunction than conventional echocardiography. Moreover, multiple strain readouts distinguish pathological cardiac hypertrophy from physiological hypertrophy.

  12. Human group A rotavirus infections in children in Denmark: detection of reassortant G9 strains and zoonotic P[14] strains.

    Science.gov (United States)

    Midgley, S; Böttiger, B; Jensen, T G; Friis-Møller, A; Person, L K; Nielsen, L; Barzinci, S; Fischer, T K

    2014-10-01

    One of the leading causes of severe childhood gastroenteritis are group A rotaviruses, and they have been found to be associated with ∼40% of the annual gastroenteritis-associated hospitalizations in young Danish children rotavirus strains circulating among young children rotavirus positive stool samples were genotyped in the study period, and the majority of samples (74%) were from hospitalized children. G and P genotypes were successfully determined for 826 of samples, with G1P[8] being the most commonly detected genotype. Detection of G1 showed a decreasing trend over time, and an inverse trend was seen for the emerging G9P. The common human genotypes (G1/G3/G4/G9P[8] and G2P[4]) were detected in the majority of samples (n=733, 88.2%). Rare genotype combinations such as G6P[14] were detected in genotype strains and strains which failed to amplify in genotyping RT-PCR were subjected to genetic characterization by sequencing one or all of the following genes; VP7, VP4, VP6 and NSP4. Sequences of sufficient length and quality were available for all 4 genes for 28 strains. Phylogenetic analysis revealed that reassortant G9P[4] strains circulated with 3 different genotype combinations. As rotavirus vaccines are not widely used in Denmark or its neighboring countries, the diversity of rotavirus strains identified in this study most likely reflects naturally occurring selection pressures and viral evolution. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. Self-adapted and tunable graphene strain sensors for detecting both subtle and large human motions.

    Science.gov (United States)

    Tao, Lu-Qi; Wang, Dan-Yang; Tian, He; Ju, Zhen-Yi; Liu, Ying; Pang, Yu; Chen, Yuan-Quan; Yang, Yi; Ren, Tian-Ling

    2017-06-22

    Conventional strain sensors rarely have both a high gauge factor and a large strain range simultaneously, so they can only be used in specific situations where only a high sensitivity or a large strain range is required. However, for detecting human motions that include both subtle and large motions, these strain sensors can't meet the diverse demands simultaneously. Here, we come up with laser patterned graphene strain sensors with self-adapted and tunable performance for the first time. A series of strain sensors with either an ultrahigh gauge factor or a preferable strain range can be fabricated simultaneously via one-step laser patterning, and are suitable for detecting all human motions. The strain sensors have a GF of up to 457 with a strain range of 35%, or have a strain range of up to 100% with a GF of 268. Most importantly, the performance of the strain sensors can be easily tuned by adjusting the patterns of the graphene, so that the sensors can meet diverse demands in both subtle and large motion situations. The graphene strain sensors show significant potential in applications such as wearable electronics, health monitoring and intelligent robots. Furthermore, the facile, fast and low-cost fabrication method will make them possible and practical to be used for commercial applications in the future.

  14. A duplex PCR assay for the detection of Ralstonia solanacearum phylotype II strains in Musa spp.

    Science.gov (United States)

    Cellier, Gilles; Moreau, Aurélie; Chabirand, Aude; Hostachy, Bruno; Ailloud, Florent; Prior, Philippe

    2015-01-01

    Banana wilt outbreaks that are attributable to Moko disease-causing strains of the pathogen Ralstonia solanacearum (Rs) remain a social and economic burden for both multinational corporations and subsistence farmers. All known Moko strains belong to the phylotype II lineage, which has been previously recognized for its broad genetic basis. Moko strains are paraphyletic and are distributed among seven related but distinct phylogenetic clusters (sequevars) that are potentially major threats to Musaceae, Solanaceae, and ornamental crops in many countries. Although clustered within the Moko IIB-4 sequevar, strains of the epidemiologically variant IIB-4NPB do not cause wilt on Cavendish or plantain bananas; instead, they establish a latent infection in the vascular tissues of plantains and demonstrate an expanded host range and high aggressiveness toward Solanaceae and Cucurbitaceae. Although most molecular diagnostic methods focus on strains that wilt Solanaceae (particularly potato), no relevant protocol has been described that universally detects strains of the Musaceae-infecting Rs phylotype II. Thus, a duplex PCR assay targeting Moko and IIB-4NPB variant strains was developed, and its performance was assessed using an extensive collection of 111 strains representing the known diversity of Rs Moko-related strains and IIB-4NPB variant strains along with certain related strains and families. The proposed diagnostic protocol demonstrated both high accuracy (inclusivity and exclusivity) and high repeatability, detected targets on either pure culture or spiked plant extracts. Although they did not belong to the Moko clusters described at the time of the study, recently discovered banana-infecting strains from Brazil were also detected. According to our comprehensive evaluation, this duplex PCR assay appears suitable for both research and diagnostic laboratories and provides reliable detection of phylotype II Rs strains that infect Musaceae.

  15. A duplex PCR assay for the detection of Ralstonia solanacearum phylotype II strains in Musa spp.

    Directory of Open Access Journals (Sweden)

    Gilles Cellier

    Full Text Available Banana wilt outbreaks that are attributable to Moko disease-causing strains of the pathogen Ralstonia solanacearum (Rs remain a social and economic burden for both multinational corporations and subsistence farmers. All known Moko strains belong to the phylotype II lineage, which has been previously recognized for its broad genetic basis. Moko strains are paraphyletic and are distributed among seven related but distinct phylogenetic clusters (sequevars that are potentially major threats to Musaceae, Solanaceae, and ornamental crops in many countries. Although clustered within the Moko IIB-4 sequevar, strains of the epidemiologically variant IIB-4NPB do not cause wilt on Cavendish or plantain bananas; instead, they establish a latent infection in the vascular tissues of plantains and demonstrate an expanded host range and high aggressiveness toward Solanaceae and Cucurbitaceae. Although most molecular diagnostic methods focus on strains that wilt Solanaceae (particularly potato, no relevant protocol has been described that universally detects strains of the Musaceae-infecting Rs phylotype II. Thus, a duplex PCR assay targeting Moko and IIB-4NPB variant strains was developed, and its performance was assessed using an extensive collection of 111 strains representing the known diversity of Rs Moko-related strains and IIB-4NPB variant strains along with certain related strains and families. The proposed diagnostic protocol demonstrated both high accuracy (inclusivity and exclusivity and high repeatability, detected targets on either pure culture or spiked plant extracts. Although they did not belong to the Moko clusters described at the time of the study, recently discovered banana-infecting strains from Brazil were also detected. According to our comprehensive evaluation, this duplex PCR assay appears suitable for both research and diagnostic laboratories and provides reliable detection of phylotype II Rs strains that infect Musaceae.

  16. Microminiature high-resolution linear displacement sensor for peak strain detection in smart structures

    Science.gov (United States)

    Arms, Steven W.; Guzik, David C.; Townsend, Christopher P.

    1998-07-01

    Critical civil and military structures require 'smart' sensors in order to report their strain histories; this can help to insure safe operation after exposure to potentially damaging loads. A passive resetable peak strain detector was developed by modifying the mechanics of a differential variable reluctance transducer. The peak strain detector was attached to an aluminum test beam along with a bonded resistance strain gauge and a standard DVRT. Strain measurements were recorded during cyclic beam deflections. DVRT output was compared to the bonded resistance strain gauge output, yielding correlation coefficients ranging from 0.9989 to 0.9998 for al teste, including re-attachment of the DVRT to the specimen. Peak bending strains were obtained by the modified peak detect DVRT to the specimen. Peak bending strains were obtained by the modified peak detect DVRT and this was compared to the peak bending strains as measured by the bonded strain gauge. The peak detect DVRT demonstrated an accuracy of approximately +/- 5 percent over a peak range of 2000 to 2800 microstrain.

  17. Genomic characterization of nontypeable rotaviruses and detection of a rare G8 strain in Delhi, India.

    Science.gov (United States)

    Sharma, Sumit; Paul, Vinod K; Bhan, Maharaj K; Ray, Pratima

    2009-12-01

    In the present investigation we molecularly characterized nontypeable rotavirus strains previously identified during surveillance in New Delhi, India. The majority of strains were demonstrated to belong to genotype G1 (54.5%) or P[8] (77.8%) on the basis of nucleotide sequencing of fragments from their VP7 and VP4 genes. The other genotypes detected included G2, G8, G9, G12, and P[4]. A G8P[6] strain, strain DS108, was detected for the first time in northern India. The VP7 gene of DS108 was most homologous with the VP7 gene of a bovine G8 strain, strain A5 (98.9%), indicating its bovine parentage. In contrast, the VP4 gene had a high degree of nucleotide sequence homology (92.9% to 99.1%) with the VP4 genes of human P[6] strains. The VP6 gene and nonstructural genes (NSP1 to NSP3 and NSP5) were most homologous with the VP6 gene and nonstructural genes of human rotaviruses belonging to the DS1 genogroup. Interestingly, the NSP4 gene of DS108 clustered within genotype E6 that until now had only two representative strains, both with G12P[6] specificity (strains RV176-00 and N26-02). Together, these results indicate that G8 strain DS108 belongs to the DS1 genogroup and could be the result of the acquisition of the VP7, VP4, and NSP4 genes by a human G2P[4] strain from more than one donor, similar to the evolution of G12P[6] strain RV176-00. The present study highlights the importance of characterizing multiple genes of nontypeable rotavirus strains to detect novel strains and get a more complete picture of rotavirus evolution.

  18. Early detection of oxacillin-resistant staphylococcal strains with hypertonic broth diluent for microdilution panels.

    Science.gov (United States)

    Dillon, L K; Howe, S E

    1984-01-01

    A total of 292 coagulase-positive and 111 coagulase-negative staphylococcal strains were tested in microdilution MIC panels containing 16 to 0.13 microgram of oxacillin per ml diluted in cation-supplemented Mueller-Hinton broth with and without an additional 2% NaCl. All strains were tested using the stationary-phase inoculum procedure with an incubation temperature of 35 degrees C. Test results were recorded after 16 to 20 h of incubation; staphylococcal strains susceptible to oxacillin (less than or equal to 2 micrograms/ml) were reincubated for 20 to 24 h, and endpoints were determined again. Oxacillin resistance was found in 27 (9%) of the 292 coagulase-positive strains and 39 (35%) of the 111 coagulase-negative strains. Of these resistant strains, 5 (19%) of the 27 coagulase-positive strains and 13 (33%) of the 39 coagulase-negative strains were detected 24 h earlier in cation-supplemented Mueller-Hinton broth with 2% NaCl than in cation-supplemented Mueller-Hinton broth without the additional NaCl. However, 9 (33%) of the 27 resistant coagulase-positive strains and 10 (26%) of the 39 resistant coagulase-negative strains were detected only after an additional 24 h of incubation. Oxacillin MICs for the 265 coagulase-positive susceptible strains and 72 coagulase-negative susceptible strains were not affected by the additional 2% NaCl. These results support the utility of adding 2% NaCl to the broth diluent for the early detection of oxacillin-resistant staphylococcal strains and the necessity of extended incubation for those strains which initially appear to be susceptible to oxacillin after only 16 to 20 h of incubation. PMID:6562124

  19. Detection of Novel Rotavirus Strain by Vaccine Postlicensure Surveillance

    OpenAIRE

    Weinberg, Geoffrey A.; Teel, Elizabeth N.; Mijatovic-Rustempasic, Slavica; Payne, Daniel C.; Roy, Sunando; Foytich, Kimberly; Parashar, Umesh D.; Gentsch, Jon R.; Bowen, Michael D.

    2013-01-01

    Surveillance for rotavirus-associated diarrhea after implementation of rotavirus vaccination can assess vaccine effectiveness and identify disease-associated genotypes. During active vaccine postlicensure surveillance in the United States, we found a novel rotavirus genotype, G14P[24], in a stool sample from a child who had diarrhea. Unusual rotavirus strains may become more prevalent after vaccine implementation.

  20. Prevalence of rotavirus infections and strain types detected among ...

    African Journals Online (AJOL)

    control strategies. However, development and application of appropriate rotavirus vaccines requires an understanding of the magnitude of diarrhoea associated with rotavirus infection, the age group most affected, the severity of diarrhoea associated with rotavirus infections and the strain types circulating in an area.

  1. Detection and transmission of extracellular fac-tor producing Streptococcus suis serotype 2 strains in pigs

    NARCIS (Netherlands)

    Swildens, B.

    2009-01-01

    DETECTION AND TRANSMISSION OF EXTRACELLULAR FACTOR PRODUCING STREPTOCOCCUS SUIS SEROTYPE 2 STRAINS IN PIGS INTRODUCTION Streptococcus suis (S.suis) has been implicated in the etiology of many diseases among which meningitis in pigs. The virulent extracellular factor-positive strains of S.suis

  2. Canine Distemper Virus (CDV) immune-stimulating complexes (iscoms), but not measles virus iscoms, protect dogs against CDV infection.

    NARCIS (Netherlands)

    P. de Vries (Petra); F.G.C.M. Uytdehaag (Fons); A.D.M.E. Osterhaus (Albert)

    1988-01-01

    textabstractThe potential of immune-stimulating complexes (iscoms), a novel form of antigenic presentation, for the induction of protective immunity against morbillivirus infection was shown by immunizing dogs with canine distemper virus (CDV) iscoms, which contained the fusion (F) protein and a

  3. A nanocrystal strain gauge for luminescence detection of mechanical forces

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Charina; Koski, Kristie; Olson, Andrew; Alivisatos, Paul

    2010-07-26

    Local microscale stresses play a crucial role in inhomogeneous mechanical processes from cell motility to material failure. However, it remains difficult to spatially resolve stress at these small length scales. While contact-probe and non-contact based techniques have been used to quantify local mechanical behavior in specific systems with high stiffness or stress and spatial resolution, these methods cannot be used to study a majority of micromechanical systems due to spectroscopic and geometrical constraints. We present here the design and implementation of a luminescent nanocrystal strain gauge, the CdSe/CdS core/shell tetrapod. The tetrapod can be incorporated into many materials, yielding a local stress measurement through optical fluorescence spectroscopy of the electronically confined CdSe core states. The stress response of the tetrapod is calibrated and utilized to study mechanical behavior in single polymer fibers. We expect that tetrapods can be used to investigate local stresses in many other mechanical systems.

  4. The Nitrosopumilus maritimus CdvB, but Not FtsZ, Assembles into Polymers

    Directory of Open Access Journals (Sweden)

    Kian-Hong Ng

    2013-01-01

    Full Text Available Euryarchaeota and Crenarchaeota are two major phyla of archaea which use distinct molecular apparatuses for cell division. Euryarchaea make use of the tubulin-related protein FtsZ, while Crenarchaea, which appear to lack functional FtsZ, employ the Cdv (cell division components to divide. Ammonia oxidizing archaeon (AOA Nitrosopumilus maritimus belongs to another archaeal phylum, the Thaumarchaeota, which has both FtsZ and Cdv genes in the genome. Here, we used a heterologous expression system to characterize FtsZ and Cdv proteins from N. maritimus by investigating the ability of these proteins to form polymers. We show that one of the Cdv proteins in N. maritimus, the CdvB (Nmar_0816, is capable of forming stable polymers when expressed in fission yeast. The N. maritimus CdvB is also capable of assembling into filaments in mammalian cells. However, N. maritimus FtsZ does not assemble into polymers in our system. The ability of CdvB, but not FtsZ, to polymerize is consistent with a recent finding showing that several Cdv proteins, but not FtsZ, localize to the mid-cell site in the dividing N. maritimus. Thus, we propose that it is Cdv proteins, rather than FtsZ, that function as the cell division apparatus in N. maritimus.

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  12. A duplex endpoint PCR assay for rapid detection and differentiation of Leptospira strains.

    Science.gov (United States)

    Benacer, Douadi; Zain, Siti Nursheena Mohd; Lewis, John W; Khalid, Mohd Khairul Nizam Mohd; Thong, Kwai Lin

    2017-01-01

    This study aimed to develop a duplex endpoint PCR assay for rapid detection and differentiation of Leptospira strains. Primers were designed to target the rrs (LG1/LG2) and ligB (LP1/LP2) genes to confirm the presence of the Leptospira genus and the pathogenic species, respectively. The assay showed 100% specificity against 17 Leptospira strains with a limit of detection of 23.1pg/µl of leptospiral DNA and sensitivity of 103 leptospires/ml in both spiked urine and water. Our duplex endpoint PCR assay is suitable for rapid early detection of Leptospira with high sensitivity and specificity.

  13. DETECTION OF VIRULENCE GENES IN ENVIRONMENTAL STRAINS OF Vibrio cholerae FROM ESTUARIES IN NORTHEASTERN BRAZIL

    Directory of Open Access Journals (Sweden)

    Francisca Gleire Rodrigues de Menezes

    2014-09-01

    Full Text Available The objectives of this study were to detect the presence of Vibrio cholerae in tropical estuaries (Northeastern Brazil and to search for virulence factors in the environmental isolates. Water and sediment samples were inoculated onto a vibrio-selective medium (TCBS, and colonies with morphological resemblance to V. cholerae were isolated. The cultures were identified phenotypically using a dichotomous key based on biochemical characteristics. The total DNA extracted was amplified by PCR to detect ompW and by multiplex PCR to detect the virulence genes ctx, tcp, zot and rfbO1. The results of the phenotypic and genotypic identification were compared. Nine strains of V. cholerae were identified phenotypically, five of which were confirmed by detection of the species-specific gene ompW. The dichotomous key was efficient at differentiating environmental strains of V. cholerae. Strains of V. cholerae were found in all four estuaries, but none possessed virulence genes.

  14. Detection of virulence genes in environmental strains of Vibrio cholerae from estuaries in northeastern Brazil.

    Science.gov (United States)

    Menezes, Francisca Gleire Rodrigues de; Neves, Soraya da Silva; Sousa, Oscarina Viana de; Vila-Nova, Candida Machado Vieira Maia; Maggioni, Rodrigo; Theophilo, Grace Nazareth Diogo; Hofer, Ernesto; Vieira, Regine Helena Silva dos Fernandes

    2014-01-01

    The objectives of this study were to detect the presence of Vibrio cholerae in tropical estuaries (Northeastern Brazil) and to search for virulence factors in the environmental isolates. Water and sediment samples were inoculated onto a vibrio-selective medium (TCBS), and colonies with morphological resemblance to V. cholerae were isolated. The cultures were identified phenotypically using a dichotomous key based on biochemical characteristics. The total DNA extracted was amplified by PCR to detect ompW and by multiplex PCR to detect the virulence genes ctx, tcp, zot and rfbO1. The results of the phenotypic and genotypic identification were compared. Nine strains of V. cholerae were identified phenotypically, five of which were confirmed by detection of the species-specific gene ompW. The dichotomous key was efficient at differentiating environmental strains of V. cholerae. Strains of V. cholerae were found in all four estuaries, but none possessed virulence genes.

  15. DETECTION OF VIRULENCE GENES IN ENVIRONMENTAL STRAINS OF Vibrio cholerae FROM ESTUARIES IN NORTHEASTERN BRAZIL

    Science.gov (United States)

    de Menezes, Francisca Gleire Rodrigues; Neves, Soraya da Silva; de Sousa, Oscarina Viana; Vila-Nova, Candida Machado Vieira Maia; Maggioni, Rodrigo; Theophilo, Grace Nazareth Diogo; Hofer, Ernesto; Vieira, Regine Helena Silva dos Fernandes

    2014-01-01

    The objectives of this study were to detect the presence of Vibrio cholerae in tropical estuaries (Northeastern Brazil) and to search for virulence factors in the environmental isolates. Water and sediment samples were inoculated onto a vibrio-selective medium (TCBS), and colonies with morphological resemblance to V. cholerae were isolated. The cultures were identified phenotypically using a dichotomous key based on biochemical characteristics. The total DNA extracted was amplified by PCR to detect ompW and by multiplex PCR to detect the virulence genes ctx, tcp, zot and rfbO1. The results of the phenotypic and genotypic identification were compared. Nine strains of V. cholerae were identified phenotypically, five of which were confirmed by detection of the species-specific gene ompW. The dichotomous key was efficient at differentiating environmental strains of V. cholerae. Strains of V. cholerae were found in all four estuaries, but none possessed virulence genes. PMID:25229224

  16. Detection of Dekkera-Brettanomyces strains in sherry by a nested PCR method.

    Science.gov (United States)

    Ibeas, J I; Lozano, I; Perdigones, F; Jimenez, J

    1996-01-01

    Brettanomyces sp. and its ascosporogenous sexual state, Dekkera sp., have been well documented as spoilage microorganisms, usually associated with barrel-aged red wines. In this report, we describe the genetic characterization, on the basis of DNA content per cell, electrophoretic karyotyping, and mitochondrial DNA restriction patterns, of a Dekkera yeast strain isolated from sherries and of a number of other Brettanomyces and Dekkera strains. By using a genomic DNA fragment of the isolated Dekkera strain, we developed a two-step PCR method which directs the specific amplification of target DNA from this strain and from other Brettanomyces-Dekkera strains. The method efficiently amplified the target DNA from intact cells, obviating DNA isolation, and yielded a detection limit of fewer than 10 yeast cells in contaminated samples of sherry. PMID:8975627

  17. Molecular detection of virulence factors among food and clinical Enterococcus faecalis strains in South Brazil

    Directory of Open Access Journals (Sweden)

    A.W. Medeiros

    2014-01-01

    Full Text Available The present report aimed to perform a molecular epidemiological survey by investigating the presence of virulence factors in E. faecalis isolated from different human clinical (n = 57 and food samples (n = 55 in Porto Alegre, Brazil, collected from 2006 to 2009. In addition, the ability to form biofilm in vitro on polystyrene and the β-haemolytic and gelatinase activities were determined. Clinical strains presented a higher prevalence of aggregation substance (agg, enterococcal surface protein (esp and cytolysin (cylA genes when compared with food isolates. The esp gene was found only in clinical strains. On the other hand, the gelatinase (gelE and adherence factor (ace genes had similar prevalence among the strains, showing the widespread occurrence of these virulence factors among food and clinical E. faecalis strains in South Brazil. More than three virulence factor genes were detected in 77.2% and 18.2% of clinical and food strains, respectively. Gelatinase and β-haemolysin activities were not associated with the presence of gelE and cylA genes. The ability to produce biofilm was detected in 100% of clinical and 94.6% of food isolates, and clinical strains were more able to form biofilm than the food isolates (Student's t-test, p < 0.01. Results from the statistical analysis showed significant associations between strong biofilm formation and ace (p = 0.015 and gelE (p = 0.007 genes in clinical strains. In conclusion, our data indicate that E. faecalis strains isolated from clinical and food samples possess distinctive patterns of virulence factors, with a larger number of genes that encode virulence factors detected in clinical strains.

  18. Whole genomic constellation of the first human G8 rotavirus strain detected in Japan.

    Science.gov (United States)

    Agbemabiese, Chantal Ama; Nakagomi, Toyoko; Doan, Yen Hai; Nakagomi, Osamu

    2015-10-01

    Human G8 Rotavirus A (RVA) strains are commonly detected in Africa but are rarely detected in Japan and elsewhere in the world. In this study, the whole genome sequence of the first human G8 RVA strain designated AU109 isolated in a child with acute gastroenteritis in 1994 was determined in order to understand how the strain was generated including the host species origin of its genes. The genotype constellation of AU109 was G8-P[4]-I2-R2-C2-M2-A2-N2-T2-E2-H2. Phylogenetic analyses of the 11 genome segments revealed that its VP7 and VP1 genes were closely related to those of a Hungarian human G8P[14] RVA strain and these genes shared the most recent common ancestors in 1988 and 1982, respectively. AU109 possessed an NSP2 gene closely related to those of Chinese sheep and goat RVA strains. The remaining eight genome segments were closely related to Japanese human G2P[4] strains which circulated around 1985-1990. Bayesian evolutionary analyses revealed that the NSP2 gene of AU109 and those of the Chinese sheep and goat RVA strains diverged from a common ancestor around 1937. In conclusion, AU109 was generated through genetic reassortment event where Japanese DS-1-like G2P[4] strains circulating around 1985-1990 obtained the VP7, VP1 and NSP2 genes from unknown ruminant G8 RVA strains. These observations highlight the need for comprehensive examination of the whole genomes of RVA strains of less explored host species. Copyright © 2015 Elsevier B.V. All rights reserved.

  19. Specific gene probe for detection of biotyped and serotyped Listeria strains.

    OpenAIRE

    Notermans, S; Chakraborty, T; Leimeister-Wächter, M; Dufrenne, J; Heuvelman, K J; Maas, H; Jansen, W; Wernars, K; Guinee, P

    1989-01-01

    A total of 284 strains of Listeria, including all known serovars and biovars together with Listeria grayi and Listeria murrayi, were biotyped and serotyped. Biotyping and serotyping could be done in 2 days. A gene probe encoding a delayed hypersensitivity factor (DTH) was used in the detection of pathogenic biotypes and serotypes of the tested strains. The gene was found in all 117 tested Listeria monocytogenes strains of serogroups 1/2a, 1/2b, 1/2c, 3a, 3b, 3c, 4c, 4d, 4e, 4ab, and 7. It was...

  20. Designing, manufacturing, and testing of embedded EFPI strain sensor for damage detection of smart composite beams

    Science.gov (United States)

    Sim, Lay M.; Zhou, Gang

    2005-04-01

    Designing a fiber optic sensor in the development of a real-time damage detection and evaluation system is important for providing reliable results. This paper describes the manufacturing and implementation of an Extrinsic Fabry-Perot Interferometer (EFPI) strain sensor for the non-destructive quantitative evaluation of carbon fiber reinforced composites. The EPFI strain sensors were examined for their integrity and performance. The integrity of the sensors was assessed experimentally by determining the bending strength of the glass tube, which was used in the fabrication of the sensor. Further validations on the survival of the sensors when embedded were also carried out with the application of the modified classical lamination theory (CLT). The sensor performance was examined extensively by either bonded on the surface or embedded in the tensile region of simple quasi-isotropic (QI) composite beams. These smart beams were loaded quasi-statically in three-point bend and cantilever loading The EFPI strain sensors have shown to surface a maximum tensile strain of up to 0.8%, which was adequate and reliable for strain measurements in the current system. The understanding of the EFPI strain sensors behaviour have paved way for the success in achieving a fiber optic strain sensor based damage detection and evaluation system (FODDAS).

  1. PCR detection of cytK gene in Bacillus cereus group strains isolated from food samples.

    Science.gov (United States)

    Oltuszak-Walczak, Elzbieta; Walczak, Piotr

    2013-11-01

    A method for detection of the cytotoxin K cytK structural gene and its active promoter preceded by the PlcR-binding box, controlling the expression level of this enterotoxin, was developed. The method was applied for the purpose of the analysis of 47 bacterial strains belonging to the Bacillus cereus group isolated from different food products. It was found that the majority of the analyzed strains carried the fully functional cytK gene with its PlcR regulated promoter. The cytK gene was not detected in four emetic strains of Bacillus cereus carrying the cesB gene and potentially producing an emetic toxin - cereulide. The cytotoxin K gene was detected in 4 isolates classified as Bacillus mycoides and one reference strain B. mycoides PCM 2024. The promoter region and the N-terminal part of the cytK gene from two strains of B. mycoides (5D and 19E) showed similarities to the corresponding sequences of Bacillus cereus W23 and Bacillus thuringiensis HD-789, respectively. It was shown for the first time that the cytK gene promoter region from strains 5D and 19E of Bacillus mycoides had a similar arrangement to the corresponding sequence of Bacillus cereus ATCC 14579. The presence of the cytK gene in Bacillus mycoides shows that this species, widely recognized as nonpathogenic, may pose potential biohazard to human beings. © 2013.

  2. QTL for body composition on chromosome 7 detected using a chromosome substitution mouse strain.

    Science.gov (United States)

    Reed, Danielle R; McDaniel, Amanda H; Avigdor, Mauricio; Bachmanov, Alexander A

    2008-02-01

    Previous studies in mice have detected quantitative trait loci (QTLs) on chromosome 7 that affect body composition. As a step toward identifying the responsible genes, we compared a chromosome 7 substitution strain C57BL/6J-Chr7(129S1/SvImJ)/Na (CSS-7) to its host (C57BL/6J) strain. Fourteen-week-old mice were measured for body size (weight, length), organ weight (brain, heart, liver, kidneys, and spleen), body and bone composition (fat and lean weight; bone area, mineral content, and density), and individual adipose depot weights (gonadal, retroperitoneal, mesenteric, inguinal, and subscapular). Differences between the CSS-7 strain and the host strain were interpreted as evidence for the presence of one or more QTLs on chromosome 7. Using this criterion, we detected QTLs for body weight, bone area, bone mineral content, brain, and heart weight, most adipose depot weights and some indices of fatness. A few strain differences were more pronounced in males (e.g., most adiposity measures) and others were more pronounced in females (e.g., bone area). QTLs for body length, lean weight, bone mineral density, and kidney, spleen, and liver weight were not detected. This study found several associations that suggest one or more QTLs specific to the weight of select tissues and organs exist on mouse chromosome 7. Because these loci are detectable on a fixed and uniform genetic background, they are reasonable targets for high-resolution mapping and gene identification using a congenic approach.

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  14. File list: Oth.CDV.50.RELA.AllCell [Chip-atlas[Archive

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    Full Text Available Oth.CDV.50.RELA.AllCell hg19 TFs and others RELA Cardiovascular SRX425264,SRX294971...,SRX425263,SRX112016,SRX367013,SRX367015,SRX112015,SRX367014,SRX425262,SRX367012 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.50.RELA.AllCell.bed ...

  15. File list: NoD.CDV.50.NA.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.50.NA.AllCell hg19 No description NA Cardiovascular SRX270959,SRX134734,DRX...8,DRX014600,DRX014570,SRX213916,SRX318770,SRX347269,SRX213926,SRX134740 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.50.NA.AllCell.bed ...

  16. File list: InP.CDV.05.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.05.AllAg.Carotid_Arteries hg19 Input control Cardiovascular Carotid Arterie...s DRX021453,DRX021454,DRX021452 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.05.AllAg.Carotid_Arteries.bed ...

  17. File list: NoD.CDV.20.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.20.AllAg.Carotid_Arteries hg19 No description Cardiovascular Carotid Arteri...es http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.20.AllAg.Carotid_Arteries.bed ...

  18. File list: DNS.CDV.50.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.50.AllAg.Carotid_Arteries hg19 DNase-seq Cardiovascular Carotid Arteries ht...tp://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.50.AllAg.Carotid_Arteries.bed ...

  19. File list: ALL.CDV.10.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.Carotid_Arteries hg19 All antigens Cardiovascular Carotid Arteries... DRX021452,DRX021453,DRX021454 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.10.AllAg.Carotid_Arteries.bed ...

  20. File list: InP.CDV.50.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.50.AllAg.Carotid_Arteries hg19 Input control Cardiovascular Carotid Arterie...s DRX021452,DRX021453,DRX021454 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.50.AllAg.Carotid_Arteries.bed ...

  1. File list: DNS.CDV.10.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.10.AllAg.Carotid_Arteries hg19 DNase-seq Cardiovascular Carotid Arteries ht...tp://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.10.AllAg.Carotid_Arteries.bed ...

  2. File list: Oth.CDV.10.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.10.AllAg.Carotid_Arteries hg19 TFs and others Cardiovascular Carotid Arteri...es http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.10.AllAg.Carotid_Arteries.bed ...

  3. File list: InP.CDV.10.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.10.AllAg.Carotid_Arteries hg19 Input control Cardiovascular Carotid Arterie...s DRX021452,DRX021453,DRX021454 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.10.AllAg.Carotid_Arteries.bed ...

  4. File list: ALL.CDV.05.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.Carotid_Arteries hg19 All antigens Cardiovascular Carotid Arteries... DRX021453,DRX021454,DRX021452 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.05.AllAg.Carotid_Arteries.bed ...

  5. File list: Pol.CDV.05.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.05.AllAg.Carotid_Arteries hg19 RNA polymerase Cardiovascular Carotid Arteri...es http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.05.AllAg.Carotid_Arteries.bed ...

  6. File list: Pol.CDV.50.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.50.AllAg.Carotid_Arteries hg19 RNA polymerase Cardiovascular Carotid Arteri...es http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.50.AllAg.Carotid_Arteries.bed ...

  7. File list: Pol.CDV.10.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.10.AllAg.Carotid_Arteries hg19 RNA polymerase Cardiovascular Carotid Arteri...es http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.10.AllAg.Carotid_Arteries.bed ...

  8. File list: InP.CDV.20.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.20.AllAg.Carotid_Arteries hg19 Input control Cardiovascular Carotid Arterie...s DRX021452,DRX021453,DRX021454 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.20.AllAg.Carotid_Arteries.bed ...

  9. File list: ALL.CDV.50.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.50.AllAg.Carotid_Arteries hg19 All antigens Cardiovascular Carotid Arteries... DRX021452,DRX021453,DRX021454 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.50.AllAg.Carotid_Arteries.bed ...

  10. File list: Oth.CDV.20.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.20.AllAg.Carotid_Arteries hg19 TFs and others Cardiovascular Carotid Arteri...es http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.20.AllAg.Carotid_Arteries.bed ...

  11. File list: DNS.CDV.20.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.20.AllAg.Carotid_Arteries hg19 DNase-seq Cardiovascular Carotid Arteries ht...tp://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.20.AllAg.Carotid_Arteries.bed ...

  12. File list: NoD.CDV.05.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.05.AllAg.Carotid_Arteries hg19 No description Cardiovascular Carotid Arteri...es http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.05.AllAg.Carotid_Arteries.bed ...

  13. File list: NoD.CDV.50.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.50.AllAg.Carotid_Arteries hg19 No description Cardiovascular Carotid Arteri...es http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.50.AllAg.Carotid_Arteries.bed ...

  14. File list: Oth.CDV.50.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.50.AllAg.Carotid_Arteries hg19 TFs and others Cardiovascular Carotid Arteri...es http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.50.AllAg.Carotid_Arteries.bed ...

  15. File list: Oth.CDV.05.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.AllAg.Carotid_Arteries hg19 TFs and others Cardiovascular Carotid Arteri...es http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.05.AllAg.Carotid_Arteries.bed ...

  16. File list: DNS.CDV.05.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.05.AllAg.Carotid_Arteries hg19 DNase-seq Cardiovascular Carotid Arteries ht...tp://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.05.AllAg.Carotid_Arteries.bed ...

  17. File list: ALL.CDV.20.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.Carotid_Arteries hg19 All antigens Cardiovascular Carotid Arteries... DRX021452,DRX021453,DRX021454 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.20.AllAg.Carotid_Arteries.bed ...

  18. File list: NoD.CDV.10.AllAg.Carotid_Arteries [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.10.AllAg.Carotid_Arteries hg19 No description Cardiovascular Carotid Arteri...es http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.10.AllAg.Carotid_Arteries.bed ...

  19. File list: ALL.CDV.50.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.50.AllAg.Brachiocephalic_endothelial_cells hg19 All antigens Cardiovascular Brachioceph...alic endothelial cells DRX014747 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.50.AllAg.Brachiocephalic_endothelial_cells.bed ...

  20. File list: Pol.CDV.10.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.10.AllAg.Brachiocephalic_endothelial_cells hg19 RNA polymerase Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.10.AllAg.Brachiocephalic_endothelial_cells.bed ...

  1. File list: Unc.CDV.20.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.20.AllAg.Brachiocephalic_endothelial_cells hg19 Unclassified Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.20.AllAg.Brachiocephalic_endothelial_cells.bed ...

  2. File list: Pol.CDV.05.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.05.AllAg.Brachiocephalic_endothelial_cells hg19 RNA polymerase Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.05.AllAg.Brachiocephalic_endothelial_cells.bed ...

  3. File list: Oth.CDV.20.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.20.AllAg.Brachiocephalic_endothelial_cells hg19 TFs and others Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.20.AllAg.Brachiocephalic_endothelial_cells.bed ...

  4. File list: DNS.CDV.05.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.05.AllAg.Brachiocephalic_endothelial_cells hg19 DNase-seq Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.05.AllAg.Brachiocephalic_endothelial_cells.bed ...

  5. File list: Oth.CDV.10.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.10.AllAg.Brachiocephalic_endothelial_cells hg19 TFs and others Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.10.AllAg.Brachiocephalic_endothelial_cells.bed ...

  6. File list: Oth.CDV.05.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.AllAg.Brachiocephalic_endothelial_cells hg19 TFs and others Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.05.AllAg.Brachiocephalic_endothelial_cells.bed ...

  7. File list: ALL.CDV.05.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.Brachiocephalic_endothelial_cells hg19 All antigens Cardiovascular Brachioceph...alic endothelial cells DRX014747 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.05.AllAg.Brachiocephalic_endothelial_cells.bed ...

  8. File list: Unc.CDV.10.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.10.AllAg.Brachiocephalic_endothelial_cells hg19 Unclassified Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.10.AllAg.Brachiocephalic_endothelial_cells.bed ...

  9. File list: ALL.CDV.10.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.Brachiocephalic_endothelial_cells hg19 All antigens Cardiovascular Brachioceph...alic endothelial cells DRX014747 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.10.AllAg.Brachiocephalic_endothelial_cells.bed ...

  10. File list: His.CDV.05.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.05.AllAg.Brachiocephalic_endothelial_cells hg19 Histone Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.05.AllAg.Brachiocephalic_endothelial_cells.bed ...

  11. File list: ALL.CDV.20.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.Brachiocephalic_endothelial_cells hg19 All antigens Cardiovascular Brachioceph...alic endothelial cells DRX014747 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.20.AllAg.Brachiocephalic_endothelial_cells.bed ...

  12. File list: His.CDV.10.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.10.AllAg.Brachiocephalic_endothelial_cells hg19 Histone Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.10.AllAg.Brachiocephalic_endothelial_cells.bed ...

  13. File list: Oth.CDV.50.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.50.AllAg.Brachiocephalic_endothelial_cells hg19 TFs and others Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.50.AllAg.Brachiocephalic_endothelial_cells.bed ...

  14. File list: Unc.CDV.50.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.50.AllAg.Brachiocephalic_endothelial_cells hg19 Unclassified Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.50.AllAg.Brachiocephalic_endothelial_cells.bed ...

  15. File list: Pol.CDV.50.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.50.AllAg.Brachiocephalic_endothelial_cells hg19 RNA polymerase Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.50.AllAg.Brachiocephalic_endothelial_cells.bed ...

  16. File list: Unc.CDV.05.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.05.AllAg.Brachiocephalic_endothelial_cells hg19 Unclassified Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.05.AllAg.Brachiocephalic_endothelial_cells.bed ...

  17. File list: Pol.CDV.20.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.20.AllAg.Brachiocephalic_endothelial_cells hg19 RNA polymerase Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.20.AllAg.Brachiocephalic_endothelial_cells.bed ...

  18. File list: His.CDV.50.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.50.AllAg.Brachiocephalic_endothelial_cells hg19 Histone Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.50.AllAg.Brachiocephalic_endothelial_cells.bed ...

  19. File list: His.CDV.20.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.20.AllAg.Brachiocephalic_endothelial_cells hg19 Histone Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.20.AllAg.Brachiocephalic_endothelial_cells.bed ...

  20. File list: DNS.CDV.20.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.20.AllAg.Brachiocephalic_endothelial_cells hg19 DNase-seq Cardiovascular Brachioceph...alic endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.20.AllAg.Brachiocephalic_endothelial_cells.bed ...

  1. File list: InP.CDV.20.Input_control.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.20.Input_control.AllCell hg19 Input control Input control Cardiovascular SR...SRX220068,SRX220065,SRX220067,SRX080409,DRX021454,SRX189947 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.20.Input_control.AllCell.bed ...

  2. File list: ALL.CDV.20.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.Sinoatrial_Node mm9 All antigens Cardiovascular Sinoatrial Node SR...X1030300,SRX1030299 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/ALL.CDV.20.AllAg.Sinoatrial_Node.bed ...

  3. File list: ALL.CDV.50.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.50.AllAg.Sinoatrial_Node mm9 All antigens Cardiovascular Sinoatrial Node SR...X1030300,SRX1030299 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/ALL.CDV.50.AllAg.Sinoatrial_Node.bed ...

  4. File list: Oth.CDV.50.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.50.AllAg.Sinoatrial_Node mm9 TFs and others Cardiovascular Sinoatrial Node ...SRX1030299 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.50.AllAg.Sinoatrial_Node.bed ...

  5. File list: Oth.CDV.20.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.20.AllAg.Sinoatrial_Node mm9 TFs and others Cardiovascular Sinoatrial Node ...SRX1030299 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.20.AllAg.Sinoatrial_Node.bed ...

  6. File list: NoD.CDV.50.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.50.AllAg.Sinoatrial_Node mm9 No description Cardiovascular Sinoatrial Node ...http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/NoD.CDV.50.AllAg.Sinoatrial_Node.bed ...

  7. File list: Unc.CDV.10.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.10.AllAg.Sinoatrial_Node mm9 Unclassified Cardiovascular Sinoatrial Node SR...X1030300 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Unc.CDV.10.AllAg.Sinoatrial_Node.bed ...

  8. File list: NoD.CDV.05.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.05.AllAg.Sinoatrial_Node mm9 No description Cardiovascular Sinoatrial Node ...http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/NoD.CDV.05.AllAg.Sinoatrial_Node.bed ...

  9. File list: ALL.CDV.10.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.Sinoatrial_Node mm9 All antigens Cardiovascular Sinoatrial Node SR...X1030300,SRX1030299 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/ALL.CDV.10.AllAg.Sinoatrial_Node.bed ...

  10. File list: Oth.CDV.05.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.AllAg.Sinoatrial_Node mm9 TFs and others Cardiovascular Sinoatrial Node ...SRX1030299 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.05.AllAg.Sinoatrial_Node.bed ...

  11. File list: InP.CDV.50.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.50.AllAg.Sinoatrial_Node mm9 Input control Cardiovascular Sinoatrial Node h...ttp://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.50.AllAg.Sinoatrial_Node.bed ...

  12. File list: Oth.CDV.10.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.10.AllAg.Sinoatrial_Node mm9 TFs and others Cardiovascular Sinoatrial Node ...SRX1030299 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.10.AllAg.Sinoatrial_Node.bed ...

  13. File list: Unc.CDV.50.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.50.AllAg.Sinoatrial_Node mm9 Unclassified Cardiovascular Sinoatrial Node SR...X1030300 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Unc.CDV.50.AllAg.Sinoatrial_Node.bed ...

  14. File list: NoD.CDV.20.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.20.AllAg.Sinoatrial_Node mm9 No description Cardiovascular Sinoatrial Node ...http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/NoD.CDV.20.AllAg.Sinoatrial_Node.bed ...

  15. File list: InP.CDV.10.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.10.AllAg.Sinoatrial_Node mm9 Input control Cardiovascular Sinoatrial Node h...ttp://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.10.AllAg.Sinoatrial_Node.bed ...

  16. File list: InP.CDV.20.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.20.AllAg.Sinoatrial_Node mm9 Input control Cardiovascular Sinoatrial Node h...ttp://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.20.AllAg.Sinoatrial_Node.bed ...

  17. File list: Unc.CDV.20.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.20.AllAg.Sinoatrial_Node mm9 Unclassified Cardiovascular Sinoatrial Node SR...X1030300 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Unc.CDV.20.AllAg.Sinoatrial_Node.bed ...

  18. File list: InP.CDV.05.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.05.AllAg.Sinoatrial_Node mm9 Input control Cardiovascular Sinoatrial Node h...ttp://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.05.AllAg.Sinoatrial_Node.bed ...

  19. File list: Unc.CDV.05.AllAg.Sinoatrial_Node [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.05.AllAg.Sinoatrial_Node mm9 Unclassified Cardiovascular Sinoatrial Node SR...X1030300 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Unc.CDV.05.AllAg.Sinoatrial_Node.bed ...

  20. File list: NoD.CDV.20.AllAg.HPAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.20.AllAg.HPAEC hg19 No description Cardiovascular HPAEC DRX014578,DRX014647...46,DRX014651,DRX014649 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.20.AllAg.HPAEC.bed ...

  1. File list: NoD.CDV.10.AllAg.HPAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.10.AllAg.HPAEC hg19 No description Cardiovascular HPAEC DRX014578,DRX014647...82,DRX014577,DRX014580 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.10.AllAg.HPAEC.bed ...

  2. File list: NoD.CDV.20.NA.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.20.NA.AllCell hg19 No description NA Cardiovascular SRX270959,SRX134734,DRX...1,SRX213916,DRX014649,DRX014602,DRX014562,SRX213918,SRX134740,SRX318770 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.20.NA.AllCell.bed ...

  3. File list: NoD.CDV.50.AllAg.HPAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.50.AllAg.HPAEC hg19 No description Cardiovascular HPAEC DRX014578,DRX014647...49,DRX014582,DRX014693 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.50.AllAg.HPAEC.bed ...

  4. File list: NoD.CDV.20.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.20.AllAg.HUVEC hg19 No description Cardiovascular HUVEC DRX014618,DRX014608...17,DRX014610,DRX014607,DRX014609 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.20.AllAg.HUVEC.bed ...

  5. File list: NoD.CDV.20.AllAg.Aorta [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.20.AllAg.Aorta hg19 No description Cardiovascular Aorta SRX134730,SRX134748...,SRX190787,SRX136957,SRX347265,SRX213926,SRX136951,SRX342280,SRX347269,SRX347278,SRX213918 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.20.AllAg.Aorta.bed ...

  6. File list: NoD.CDV.05.AllAg.HPAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.05.AllAg.HPAEC hg19 No description Cardiovascular HPAEC DRX014578,DRX014648...82,DRX014577,DRX014580 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.05.AllAg.HPAEC.bed ...

  7. File list: NoD.CDV.50.AllAg.HMVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.50.AllAg.HMVEC hg19 No description Cardiovascular HMVEC DRX014657,DRX014658...,DRX014656,DRX014660,ERX974778,DRX014664,DRX014659,DRX014661 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.50.AllAg.HMVEC.bed ...

  8. File list: NoD.CDV.10.NA.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.10.NA.AllCell hg19 No description NA Cardiovascular SRX270959,SRX190782,DRX...7,DRX014580,DRX014626,DRX014600,DRX014639,SRX318770,SRX213923,SRX347273 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.10.NA.AllCell.bed ...

  9. File list: NoD.CDV.10.AllAg.HMVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.10.AllAg.HMVEC hg19 No description Cardiovascular HMVEC DRX014657,DRX014658...,DRX014664,ERX974778,DRX014660,DRX014656,DRX014661,DRX014659 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.10.AllAg.HMVEC.bed ...

  10. File list: NoD.CDV.10.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.10.AllAg.HUVEC hg19 No description Cardiovascular HUVEC DRX014618,DRX014608...20,DRX014622,DRX014607,DRX014612 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.10.AllAg.HUVEC.bed ...

  11. File list: NoD.CDV.05.AllAg.HMVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.05.AllAg.HMVEC hg19 No description Cardiovascular HMVEC DRX014657,DRX014658...,DRX014664,ERX974778,DRX014660,DRX014656,DRX014661,DRX014659 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.05.AllAg.HMVEC.bed ...

  12. File list: NoD.CDV.10.AllAg.Aorta [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.10.AllAg.Aorta hg19 No description Cardiovascular Aorta SRX134730,SRX347278...,SRX347265,SRX136957,SRX134748,SRX190787,SRX342280,SRX213926,SRX136951,SRX347269,SRX213918 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.10.AllAg.Aorta.bed ...

  13. File list: NoD.CDV.20.AllAg.HMVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.20.AllAg.HMVEC hg19 No description Cardiovascular HMVEC DRX014657,DRX014664...,DRX014658,DRX014656,DRX014660,DRX014659,DRX014661,ERX974778 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.20.AllAg.HMVEC.bed ...

  14. File list: Pol.CDV.20.RNA_Polymerase_III.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.20.RNA_Polymerase_III.AllCell mm9 RNA polymerase RNA Polymerase III Cardiov...ascular http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Pol.CDV.20.RNA_Polymerase_III.AllCell.bed ...

  15. File list: Pol.CDV.10.RNA_polymerase_II.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.10.RNA_polymerase_II.AllCell hg19 RNA polymerase RNA polymerase II Cardiova...,SRX080152,SRX080153,SRX367018,SRX367016 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.10.RNA_polymerase_II.AllCell.bed ...

  16. File list: Pol.CDV.20.RNA_Polymerase_II.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.20.RNA_Polymerase_II.AllCell mm9 RNA polymerase RNA Polymerase II Cardiovas...X320034,SRX346170,SRX346169,SRX373605,SRX680476 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Pol.CDV.20.RNA_Polymerase_II.AllCell.bed ...

  17. File list: Pol.CDV.20.RNA_polymerase_II.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.20.RNA_polymerase_II.AllCell hg19 RNA polymerase RNA polymerase II Cardiova...,SRX346933,SRX346936,SRX367018,SRX367016 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.20.RNA_polymerase_II.AllCell.bed ...

  18. File list: Oth.CDV.10.KSHV_LANA.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.10.KSHV_LANA.AllCell hg19 TFs and others KSHV LANA Cardiovascular SRX503335...,SRX503336 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.10.KSHV_LANA.AllCell.bed ...

  19. File list: Oth.CDV.05.KSHV_LANA.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.KSHV_LANA.AllCell hg19 TFs and others KSHV LANA Cardiovascular SRX503335...,SRX503336 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.05.KSHV_LANA.AllCell.bed ...

  20. File list: Oth.CDV.20.KSHV_LANA.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.20.KSHV_LANA.AllCell hg19 TFs and others KSHV LANA Cardiovascular SRX503335...,SRX503336 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.20.KSHV_LANA.AllCell.bed ...

  1. File list: Oth.CDV.50.KSHV_LANA.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.50.KSHV_LANA.AllCell hg19 TFs and others KSHV LANA Cardiovascular SRX503335...,SRX503336 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.50.KSHV_LANA.AllCell.bed ...

  2. File list: His.CDV.05.AllAg.Cardiomyocytes [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.05.AllAg.Cardiomyocytes mm9 Histone Cardiovascular Cardiomyocytes SRX305918...,SRX305920,SRX1121699,SRX305919 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/His.CDV.05.AllAg.Cardiomyocytes.bed ...

  3. File list: His.CDV.20.AllAg.Cardiomyocytes [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.20.AllAg.Cardiomyocytes mm9 Histone Cardiovascular Cardiomyocytes SRX112169...9,SRX305918,SRX305920,SRX305919 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/His.CDV.20.AllAg.Cardiomyocytes.bed ...

  4. File list: ALL.CDV.50.AllAg.Cardiomyocytes [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.50.AllAg.Cardiomyocytes mm9 All antigens Cardiovascular Cardiomyocytes SRX3...05918,SRX305920,SRX305919,SRX1121699,SRX1121694 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/ALL.CDV.50.AllAg.Cardiomyocytes.bed ...

  5. File list: ALL.CDV.20.AllAg.Cardiomyocytes [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.Cardiomyocytes mm9 All antigens Cardiovascular Cardiomyocytes SRX1...121699,SRX305918,SRX305920,SRX305919,SRX1121694 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/ALL.CDV.20.AllAg.Cardiomyocytes.bed ...

  6. File list: His.CDV.10.AllAg.Cardiomyocytes [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.10.AllAg.Cardiomyocytes mm9 Histone Cardiovascular Cardiomyocytes SRX112169...9,SRX305919,SRX305918,SRX305920 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/His.CDV.10.AllAg.Cardiomyocytes.bed ...

  7. File list: ALL.CDV.05.AllAg.Cardiomyocytes [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.Cardiomyocytes mm9 All antigens Cardiovascular Cardiomyocytes SRX3...05918,SRX305920,SRX1121699,SRX305919,SRX1121694 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/ALL.CDV.05.AllAg.Cardiomyocytes.bed ...

  8. File list: His.CDV.50.AllAg.Cardiomyocytes [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.50.AllAg.Cardiomyocytes mm9 Histone Cardiovascular Cardiomyocytes SRX305918...,SRX305920,SRX305919,SRX1121699 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/His.CDV.50.AllAg.Cardiomyocytes.bed ...

  9. File list: Pol.CDV.50.RNA_polymerase_II.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.50.RNA_polymerase_II.AllCell hg19 RNA polymerase RNA polymerase II Cardiova...,SRX367018,SRX367016,SRX112014,SRX112013 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.50.RNA_polymerase_II.AllCell.bed ...

  10. File list: Pol.CDV.10.RNA_polymerase_III.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.10.RNA_polymerase_III.AllCell hg19 RNA polymerase RNA polymerase III Cardio...vascular http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.10.RNA_polymerase_III.AllCell.bed ...

  11. File list: Pol.CDV.05.RNA_polymerase_III.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.05.RNA_polymerase_III.AllCell hg19 RNA polymerase RNA polymerase III Cardio...vascular http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.05.RNA_polymerase_III.AllCell.bed ...

  12. File list: ALL.CDV.05.AllAg.Wharton_Jelly [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.Wharton_Jelly hg19 All antigens Cardiovascular Wharton Jelly SRX15...1548216,SRX1548219,SRX1548226,SRX1548220,SRX1548208 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.05.AllAg.Wharton_Jelly.bed ...

  13. File list: ALL.CDV.50.AllAg.Wharton_Jelly [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.50.AllAg.Wharton_Jelly hg19 All antigens Cardiovascular Wharton Jelly SRX15...1548228,SRX1548226,SRX1548227,SRX1548230,SRX1548220 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.50.AllAg.Wharton_Jelly.bed ...

  14. File list: Oth.CDV.10.AllAg.Wharton_Jelly [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.10.AllAg.Wharton_Jelly hg19 TFs and others Cardiovascular Wharton Jelly SRX...1548205,SRX1548207,SRX1548204,SRX1548209,SRX1548206,SRX1548208 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.10.AllAg.Wharton_Jelly.bed ...

  15. File list: Oth.CDV.05.AllAg.Wharton_Jelly [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.AllAg.Wharton_Jelly hg19 TFs and others Cardiovascular Wharton Jelly SRX...1548205,SRX1548207,SRX1548204,SRX1548209,SRX1548206,SRX1548208 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.05.AllAg.Wharton_Jelly.bed ...

  16. File list: His.CDV.50.Pan_lysine_crotonylation.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.50.Pan_lysine_crotonylation.AllCell mm9 Histone Pan lysine crotonylation Ca...rdiovascular http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/His.CDV.50.Pan_lysine_crotonylation.AllCell.bed ...

  17. File list: Oth.CDV.05.Crotonyl_lysine.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.Crotonyl_lysine.AllCell mm9 TFs and others Crotonyl lysine Cardiovascula...r http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.05.Crotonyl_lysine.AllCell.bed ...

  18. File list: His.CDV.20.Pan_lysine_crotonylation.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.20.Pan_lysine_crotonylation.AllCell mm9 Histone Pan lysine crotonylation Ca...rdiovascular http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/His.CDV.20.Pan_lysine_crotonylation.AllCell.bed ...

  19. File list: DNS.CDV.05.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.05.AllAg.Primary_endothelial_cells hg19 DNase-seq Cardiovascular Primary en...dothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.05.AllAg.Primary_endothelial_cells.bed ...

  20. File list: DNS.CDV.50.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.50.AllAg.Primary_endothelial_cells hg19 DNase-seq Cardiovascular Primary en...dothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.50.AllAg.Primary_endothelial_cells.bed ...

  1. File list: Pol.CDV.05.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.05.AllAg.Primary_endothelial_cells hg19 RNA polymerase Cardiovascular Primary... endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.05.AllAg.Primary_endothelial_cells.bed ...

  2. File list: Oth.CDV.50.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.50.AllAg.Primary_endothelial_cells hg19 TFs and others Cardiovascular Primary... endothelial cells SRX393516,SRX244128,SRX393518 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.50.AllAg.Primary_endothelial_cells.bed ...

  3. File list: Oth.CDV.05.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.AllAg.Primary_endothelial_cells hg19 TFs and others Cardiovascular Primary... endothelial cells SRX393518,SRX393516,SRX244128 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.05.AllAg.Primary_endothelial_cells.bed ...

  4. File list: His.CDV.50.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.50.AllAg.Primary_endothelial_cells hg19 Histone Cardiovascular Primary endo...thelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.50.AllAg.Primary_endothelial_cells.bed ...

  5. File list: His.CDV.10.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.10.AllAg.Primary_endothelial_cells hg19 Histone Cardiovascular Primary endo...thelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.10.AllAg.Primary_endothelial_cells.bed ...

  6. File list: Pol.CDV.20.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.20.AllAg.Primary_endothelial_cells hg19 RNA polymerase Cardiovascular Primary... endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.20.AllAg.Primary_endothelial_cells.bed ...

  7. File list: Pol.CDV.10.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.10.AllAg.Primary_endothelial_cells hg19 RNA polymerase Cardiovascular Primary... endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.10.AllAg.Primary_endothelial_cells.bed ...

  8. File list: Pol.CDV.50.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.50.AllAg.Primary_endothelial_cells hg19 RNA polymerase Cardiovascular Primary... endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.50.AllAg.Primary_endothelial_cells.bed ...

  9. File list: Oth.CDV.20.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.20.AllAg.Primary_endothelial_cells hg19 TFs and others Cardiovascular Primary... endothelial cells SRX393516,SRX393518,SRX244128 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.20.AllAg.Primary_endothelial_cells.bed ...

  10. File list: DNS.CDV.10.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.10.AllAg.Primary_endothelial_cells hg19 DNase-seq Cardiovascular Primary en...dothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.10.AllAg.Primary_endothelial_cells.bed ...

  11. File list: Unc.CDV.05.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.05.AllAg.Primary_endothelial_cells hg19 Unclassified Cardiovascular Primary... endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.05.AllAg.Primary_endothelial_cells.bed ...

  12. File list: Unc.CDV.10.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.10.AllAg.Primary_endothelial_cells hg19 Unclassified Cardiovascular Primary... endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.10.AllAg.Primary_endothelial_cells.bed ...

  13. File list: Oth.CDV.10.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.10.AllAg.Primary_endothelial_cells hg19 TFs and others Cardiovascular Primary... endothelial cells SRX393516,SRX393518,SRX244128 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.10.AllAg.Primary_endothelial_cells.bed ...

  14. File list: Unc.CDV.20.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.20.AllAg.Primary_endothelial_cells hg19 Unclassified Cardiovascular Primary... endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.20.AllAg.Primary_endothelial_cells.bed ...

  15. File list: His.CDV.20.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.20.AllAg.Primary_endothelial_cells hg19 Histone Cardiovascular Primary endo...thelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.20.AllAg.Primary_endothelial_cells.bed ...

  16. File list: Unc.CDV.50.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.50.AllAg.Primary_endothelial_cells hg19 Unclassified Cardiovascular Primary... endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.50.AllAg.Primary_endothelial_cells.bed ...

  17. File list: DNS.CDV.20.AllAg.Primary_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.20.AllAg.Primary_endothelial_cells hg19 DNase-seq Cardiovascular Primary en...dothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.20.AllAg.Primary_endothelial_cells.bed ...

  18. File list: NoD.CDV.20.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.20.AllAg.Atrioventicular_canals mm9 No description Cardiovascular Atriovent...icular canals http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/NoD.CDV.20.AllAg.Atrioventicular_canals.bed ...

  19. File list: ALL.CDV.10.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.Atrioventicular_canals mm9 All antigens Cardiovascular Atrioventic...ular canals SRX1271841 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/ALL.CDV.10.AllAg.Atrioventicular_canals.bed ...

  20. File list: ALL.CDV.05.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.Atrioventicular_canals mm9 All antigens Cardiovascular Atrioventic...ular canals SRX1271841 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/ALL.CDV.05.AllAg.Atrioventicular_canals.bed ...

  1. File list: DNS.CDV.50.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.50.AllAg.Atrioventicular_canals mm9 DNase-seq Cardiovascular Atrioventicula...r canals http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/DNS.CDV.50.AllAg.Atrioventicular_canals.bed ...

  2. File list: InP.CDV.05.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.05.AllAg.Atrioventicular_canals mm9 Input control Cardiovascular Atrioventi...cular canals http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.05.AllAg.Atrioventicular_canals.bed ...

  3. File list: Oth.CDV.05.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.AllAg.Atrioventicular_canals mm9 TFs and others Cardiovascular Atriovent...icular canals SRX1271841 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.05.AllAg.Atrioventicular_canals.bed ...

  4. File list: NoD.CDV.50.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.50.AllAg.Atrioventicular_canals mm9 No description Cardiovascular Atriovent...icular canals http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/NoD.CDV.50.AllAg.Atrioventicular_canals.bed ...

  5. File list: NoD.CDV.10.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.10.AllAg.Atrioventicular_canals mm9 No description Cardiovascular Atriovent...icular canals http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/NoD.CDV.10.AllAg.Atrioventicular_canals.bed ...

  6. File list: Pol.CDV.05.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.05.AllAg.Atrioventicular_canals mm9 RNA polymerase Cardiovascular Atriovent...icular canals http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Pol.CDV.05.AllAg.Atrioventicular_canals.bed ...

  7. File list: DNS.CDV.20.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.20.AllAg.Atrioventicular_canals mm9 DNase-seq Cardiovascular Atrioventicula...r canals http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/DNS.CDV.20.AllAg.Atrioventicular_canals.bed ...

  8. File list: DNS.CDV.10.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.10.AllAg.Atrioventicular_canals mm9 DNase-seq Cardiovascular Atrioventicula...r canals http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/DNS.CDV.10.AllAg.Atrioventicular_canals.bed ...

  9. File list: DNS.CDV.05.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.05.AllAg.Atrioventicular_canals mm9 DNase-seq Cardiovascular Atrioventicula...r canals http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/DNS.CDV.05.AllAg.Atrioventicular_canals.bed ...

  10. File list: InP.CDV.50.AllAg.Atrioventicular_canals [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.50.AllAg.Atrioventicular_canals mm9 Input control Cardiovascular Atrioventi...cular canals http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.50.AllAg.Atrioventicular_canals.bed ...

  11. File list: Unc.CDV.05.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.05.AllAg.Heart mm9 Unclassified Cardiovascular Heart SRX544840,SRX551543,SR...X544839 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Unc.CDV.05.AllAg.Heart.bed ...

  12. File list: InP.CDV.05.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.05.AllAg.Heart mm9 Input control Cardiovascular Heart SRX373597,SRX373596,S...6548,SRX275462,SRX275463,SRX275461 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.05.AllAg.Heart.bed ...

  13. File list: InP.CDV.10.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.10.AllAg.Heart mm9 Input control Cardiovascular Heart SRX373597,SRX373596,S...7691,SRX275462,SRX275461,SRX066549 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.10.AllAg.Heart.bed ...

  14. File list: Oth.CDV.10.AllAg.Heart_Atria [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.10.AllAg.Heart_Atria mm9 TFs and others Cardiovascular Heart Atria SRX27283...0,SRX272831 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.10.AllAg.Heart_Atria.bed ...

  15. File list: Oth.CDV.50.AllAg.Heart_Atria [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.50.AllAg.Heart_Atria mm9 TFs and others Cardiovascular Heart Atria SRX27283...0,SRX272831 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.50.AllAg.Heart_Atria.bed ...

  16. File list: InP.CDV.20.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.20.AllAg.Heart mm9 Input control Cardiovascular Heart SRX373596,SRX373597,S...0036,SRX275461,SRX275462,SRX066549 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.20.AllAg.Heart.bed ...

  17. File list: Unc.CDV.50.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.50.AllAg.Heart mm9 Unclassified Cardiovascular Heart SRX551543,SRX544840,SR...X544839 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Unc.CDV.50.AllAg.Heart.bed ...

  18. File list: ALL.CDV.05.AllAg.Heart_Atria [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.Heart_Atria mm9 All antigens Cardiovascular Heart Atria SRX272830,...SRX272831 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/ALL.CDV.05.AllAg.Heart_Atria.bed ...

  19. File list: ALL.CDV.20.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.Heart hg19 All antigens Cardiovascular Heart SRX201809,SRX099630,S...RX099629,SRX188944,SRX099628,SRX189389 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.20.AllAg.Heart.bed ...

  20. File list: ALL.CDV.10.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.Heart hg19 All antigens Cardiovascular Heart SRX099630,SRX201809,S...RX188944,SRX099628,SRX099629,SRX189389 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.10.AllAg.Heart.bed ...

  1. File list: His.CDV.20.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.20.AllAg.Heart mm9 Histone Cardiovascular Heart SRX373584,SRX680471,SRX6804...73599,SRX680470 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/His.CDV.20.AllAg.Heart.bed ...

  2. File list: Unc.CDV.20.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.20.AllAg.Heart mm9 Unclassified Cardiovascular Heart SRX551543,SRX544840,SR...X544839 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Unc.CDV.20.AllAg.Heart.bed ...

  3. File list: Pol.CDV.05.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.05.AllAg.Heart mm9 RNA polymerase Cardiovascular Heart SRX062958,SRX143815,...5,SRX346169,SRX680476 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Pol.CDV.05.AllAg.Heart.bed ...

  4. File list: Oth.CDV.20.AllAg.Heart_Atria [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.20.AllAg.Heart_Atria mm9 TFs and others Cardiovascular Heart Atria SRX27283...0,SRX272831 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.20.AllAg.Heart_Atria.bed ...

  5. File list: Pol.CDV.10.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.10.AllAg.Heart mm9 RNA polymerase Cardiovascular Heart SRX275458,SRX062958,...9,SRX373605,SRX680476 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Pol.CDV.10.AllAg.Heart.bed ...

  6. File list: ALL.CDV.05.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.Heart hg19 All antigens Cardiovascular Heart SRX099630,SRX201809,S...RX188944,SRX099628,SRX099629,SRX189389 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.05.AllAg.Heart.bed ...

  7. File list: Pol.CDV.20.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.20.AllAg.Heart mm9 RNA polymerase Cardiovascular Heart SRX275458,SRX062958,...9,SRX373605,SRX680476 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Pol.CDV.20.AllAg.Heart.bed ...

  8. File list: Oth.CDV.05.AllAg.Heart_Atria [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.AllAg.Heart_Atria mm9 TFs and others Cardiovascular Heart Atria SRX27283...0,SRX272831 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.05.AllAg.Heart_Atria.bed ...

  9. File list: ALL.CDV.50.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.50.AllAg.Heart hg19 All antigens Cardiovascular Heart SRX201809,SRX099630,S...RX099629,SRX188944,SRX099628,SRX189389 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.50.AllAg.Heart.bed ...

  10. File list: Unc.CDV.10.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.10.AllAg.Heart mm9 Unclassified Cardiovascular Heart SRX544840,SRX551543,SR...X544839 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Unc.CDV.10.AllAg.Heart.bed ...

  11. File list: His.CDV.05.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.05.AllAg.Heart mm9 Histone Cardiovascular Heart SRX377688,SRX680468,SRX3735...73602,SRX373599 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/His.CDV.05.AllAg.Heart.bed ...

  12. File list: InP.CDV.50.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.50.AllAg.Heart mm9 Input control Cardiovascular Heart SRX373597,SRX373596,S...0037,SRX275462,SRX275461,SRX066549 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.50.AllAg.Heart.bed ...

  13. File list: His.CDV.50.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.50.AllAg.Heart mm9 Histone Cardiovascular Heart SRX373584,SRX680467,SRX3735...77692,SRX680470 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/His.CDV.50.AllAg.Heart.bed ...

  14. File list: His.CDV.10.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.10.AllAg.Heart mm9 Histone Cardiovascular Heart SRX680468,SRX373585,SRX3735...73599,SRX680470 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/His.CDV.10.AllAg.Heart.bed ...

  15. File list: Pol.CDV.50.AllAg.Heart [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.50.AllAg.Heart mm9 RNA polymerase Cardiovascular Heart SRX275458,SRX062958,...6,SRX346170,SRX346169 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Pol.CDV.50.AllAg.Heart.bed ...

  16. File list: ALL.CDV.05.AllAg.HPAF [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.HPAF hg19 All antigens Cardiovascular HPAF SRX190075,SRX069148,SRX...069207,SRX111771,SRX080414,SRX080344,SRX080372,SRX190068 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.05.AllAg.HPAF.bed ...

  17. File list: ALL.CDV.50.AllAg.HPAF [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.50.AllAg.HPAF hg19 All antigens Cardiovascular HPAF SRX111771,SRX080344,SRX...080414,SRX190075,SRX069148,SRX069207,SRX190068,SRX080372 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.50.AllAg.HPAF.bed ...

  18. File list: ALL.CDV.10.AllAg.HPAF [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.HPAF hg19 All antigens Cardiovascular HPAF SRX069148,SRX111771,SRX...190075,SRX069207,SRX080414,SRX080344,SRX080372,SRX190068 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.10.AllAg.HPAF.bed ...

  19. File list: ALL.CDV.20.AllAg.HPAF [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.HPAF hg19 All antigens Cardiovascular HPAF SRX111771,SRX069148,SRX...069207,SRX080344,SRX080414,SRX190075,SRX080372,SRX190068 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.20.AllAg.HPAF.bed ...

  20. File list: Unc.CDV.10.Unclassified.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.10.Unclassified.AllCell mm9 Unclassified Unclassified Cardiovascular SRX544...840,SRX551543,SRX1030300,SRX544839 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Unc.CDV.10.Unclassified.AllCell.bed ...

  1. File list: Unc.CDV.05.Unclassified.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.05.Unclassified.AllCell hg19 Unclassified Unclassified Cardiovascular SRX38...1738,SRX080121,SRX080122,SRX189746,SRX189744,SRX189745,SRX189747,SRX031226,SRX381737 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.05.Unclassified.AllCell.bed ...

  2. File list: Unc.CDV.50.Unclassified.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.50.Unclassified.AllCell mm9 Unclassified Unclassified Cardiovascular SRX551...543,SRX544840,SRX544839,SRX1030300 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Unc.CDV.50.Unclassified.AllCell.bed ...

  3. File list: His.CDV.50.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.50.AllAg.HUVEC hg19 Histone Cardiovascular HUVEC SRX335069,SRX335068,SRX338...,SRX038619,SRX067454 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.50.AllAg.HUVEC.bed ...

  4. File list: Pol.CDV.50.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.50.AllAg.HUVEC hg19 RNA polymerase Cardiovascular HUVEC SRX067500,SRX338788...05,SRX080152,SRX080153,SRX346933,SRX346936,SRX150473,SRX112014,SRX112013 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.50.AllAg.HUVEC.bed ...

  5. File list: Pol.CDV.10.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.10.AllAg.HUVEC hg19 RNA polymerase Cardiovascular HUVEC SRX067500,SRX338788...05,SRX112013,SRX346934,SRX346933,SRX346936,SRX425265,SRX080152,SRX080153 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.10.AllAg.HUVEC.bed ...

  6. File list: Oth.CDV.20.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.20.AllAg.HUVEC hg19 TFs and others Cardiovascular HUVEC SRX150427,SRX335070...70878,SRX425253,SRX220061,SRX220063,SRX338783 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.20.AllAg.HUVEC.bed ...

  7. File list: Unc.CDV.10.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.10.AllAg.HUVEC hg19 Unclassified Cardiovascular HUVEC SRX080121,SRX080122,S...RX031226 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.10.AllAg.HUVEC.bed ...

  8. File list: Unc.CDV.05.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.05.AllAg.HUVEC hg19 Unclassified Cardiovascular HUVEC SRX080121,SRX080122,S...RX031226 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.05.AllAg.HUVEC.bed ...

  9. File list: DNS.CDV.05.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.05.AllAg.HUVEC hg19 DNase-seq Cardiovascular HUVEC SRX069168,SRX193600,SRX0...69126,SRX100902 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.05.AllAg.HUVEC.bed ...

  10. File list: His.CDV.20.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.20.AllAg.HUVEC hg19 Histone Cardiovascular HUVEC SRX335069,SRX335068,SRX338...,SRX335072,SRX067454 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.20.AllAg.HUVEC.bed ...

  11. File list: ALL.CDV.10.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.HUVEC hg19 All antigens Cardiovascular HUVEC SRX100257,SRX100256,S...X038609,SRX038606,SRX038608 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.10.AllAg.HUVEC.bed ...

  12. File list: Pol.CDV.05.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.05.AllAg.HUVEC hg19 RNA polymerase Cardiovascular HUVEC SRX067500,SRX338788...33,SRX112014,SRX103005,SRX112013,SRX425265,SRX080153,SRX346936,SRX080152 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.05.AllAg.HUVEC.bed ...

  13. File list: Oth.CDV.50.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.50.AllAg.HUVEC hg19 TFs and others Cardiovascular HUVEC SRX150427,SRX335070...57607,SRX425262,SRX346932,SRX338783,SRX220063 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.50.AllAg.HUVEC.bed ...

  14. File list: Oth.CDV.10.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.10.AllAg.HUVEC hg19 TFs and others Cardiovascular HUVEC SRX100257,SRX100256...31246,SRX670629,SRX220061,SRX220062,SRX220063 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.10.AllAg.HUVEC.bed ...

  15. File list: His.CDV.10.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.10.AllAg.HUVEC hg19 Histone Cardiovascular HUVEC SRX335069,SRX335068,SRX067...,SRX038606,SRX038608 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.10.AllAg.HUVEC.bed ...

  16. File list: DNS.CDV.10.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.10.AllAg.HUVEC hg19 DNase-seq Cardiovascular HUVEC SRX069168,SRX193600,SRX0...69126,SRX100902 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.10.AllAg.HUVEC.bed ...

  17. File list: DNS.CDV.50.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.50.AllAg.HUVEC hg19 DNase-seq Cardiovascular HUVEC SRX069168,SRX193600,SRX0...69126 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.50.AllAg.HUVEC.bed ...

  18. File list: ALL.CDV.20.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.HUVEC hg19 All antigens Cardiovascular HUVEC SRX335069,SRX335068,S...X038607,SRX335072,SRX067454 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.20.AllAg.HUVEC.bed ...

  19. File list: DNS.CDV.20.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.20.AllAg.HUVEC hg19 DNase-seq Cardiovascular HUVEC SRX069168,SRX193600,SRX0...69126,SRX100902 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.20.AllAg.HUVEC.bed ...

  20. File list: ALL.CDV.05.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.HUVEC hg19 All antigens Cardiovascular HUVEC SRX100257,SRX100256,S...X014612,SRX038607,SRX038608 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.05.AllAg.HUVEC.bed ...

  1. File list: Oth.CDV.05.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.AllAg.HUVEC hg19 TFs and others Cardiovascular HUVEC SRX100257,SRX100256...80337,SRX038603,SRX031246,SRX102980,SRX220063 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.05.AllAg.HUVEC.bed ...

  2. File list: InP.CDV.10.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.10.AllAg.HUVEC hg19 Input control Cardiovascular HUVEC SRX096361,SRX150426,...068,SRX425270,SRX220066,SRX220067,SRX220065,SRX220064 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.10.AllAg.HUVEC.bed ...

  3. File list: His.CDV.05.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.05.AllAg.HUVEC hg19 Histone Cardiovascular HUVEC SRX335069,SRX335068,SRX038...,SRX038607,SRX038608 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.05.AllAg.HUVEC.bed ...

  4. File list: Pol.CDV.20.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.20.AllAg.HUVEC hg19 RNA polymerase Cardiovascular HUVEC SRX067500,SRX338788...66,SRX425267,SRX346934,SRX103005,SRX080152,SRX080153,SRX346933,SRX346936 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.20.AllAg.HUVEC.bed ...

  5. File list: InP.CDV.50.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.50.AllAg.HUVEC hg19 Input control Cardiovascular HUVEC SRX096361,SRX150426,...065,SRX038620,SRX220066,SRX220068,SRX220067,SRX102981 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.50.AllAg.HUVEC.bed ...

  6. File list: InP.CDV.20.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.20.AllAg.HUVEC hg19 Input control Cardiovascular HUVEC SRX096361,SRX150426,...620,SRX220064,SRX220066,SRX220068,SRX220065,SRX220067 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.20.AllAg.HUVEC.bed ...

  7. File list: InP.CDV.05.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.05.AllAg.HUVEC hg19 Input control Cardiovascular HUVEC SRX220065,SRX294968,...271,SRX425273,SRX220068,SRX425270,SRX190192,SRX220067 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.05.AllAg.HUVEC.bed ...

  8. File list: His.CDV.20.AllAg.HAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.20.AllAg.HAEC hg19 Histone Cardiovascular HAEC SRX469904,SRX143109,SRX14311...2422,SRX062423,SRX143118,SRX062425,SRX143121,SRX062420,SRX469907,SRX469908,SRX469909,SRX143124 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.20.AllAg.HAEC.bed ...

  9. File list: ALL.CDV.50.AllAg.HAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.50.AllAg.HAEC hg19 All antigens Cardiovascular HAEC SRX143123,SRX469912,SRX...8,SRX469909,SRX143118,SRX062422,SRX062425,SRX143124 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.50.AllAg.HAEC.bed ...

  10. File list: InP.CDV.10.AllAg.HAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.10.AllAg.HAEC hg19 Input control Cardiovascular HAEC SRX143129,SRX143128,SR...X469916,SRX469917,SRX143127,SRX469918 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.10.AllAg.HAEC.bed ...

  11. File list: InP.CDV.05.AllAg.HAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.05.AllAg.HAEC hg19 Input control Cardiovascular HAEC SRX143129,SRX143128,SR...X469916,SRX469917,SRX143127,SRX469918 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.05.AllAg.HAEC.bed ...

  12. File list: His.CDV.05.AllAg.HAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.05.AllAg.HAEC hg19 Histone Cardiovascular HAEC SRX469899,SRX469901,SRX46991...3119,SRX062422,SRX469909,SRX062420,SRX143124,SRX143121,SRX469908,SRX062423,SRX143118,SRX469907 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.05.AllAg.HAEC.bed ...

  13. File list: ALL.CDV.10.AllAg.HAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.HAEC hg19 All antigens Cardiovascular HAEC SRX143129,SRX143128,SRX...4,SRX143118,SRX062423,SRX062425,SRX469907,SRX062420 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.10.AllAg.HAEC.bed ...

  14. File list: InP.CDV.20.AllAg.HAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.20.AllAg.HAEC hg19 Input control Cardiovascular HAEC SRX143129,SRX469916,SR...X143128,SRX469917,SRX143127,SRX469918 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.20.AllAg.HAEC.bed ...

  15. File list: His.CDV.50.AllAg.HAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.50.AllAg.HAEC hg19 Histone Cardiovascular HAEC SRX143123,SRX469912,SRX46991...2423,SRX143121,SRX062420,SRX469907,SRX469908,SRX469909,SRX143118,SRX062422,SRX062425,SRX143124 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.50.AllAg.HAEC.bed ...

  16. File list: ALL.CDV.20.AllAg.HAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.HAEC hg19 All antigens Cardiovascular HAEC SRX143129,SRX469904,SRX...1,SRX062420,SRX469907,SRX469908,SRX469909,SRX143124 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.20.AllAg.HAEC.bed ...

  17. File list: ALL.CDV.05.AllAg.HAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.HAEC hg19 All antigens Cardiovascular HAEC SRX143129,SRX469899,SRX...4,SRX143121,SRX469908,SRX062423,SRX143118,SRX469907 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.05.AllAg.HAEC.bed ...

  18. File list: His.CDV.10.AllAg.HAEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.10.AllAg.HAEC hg19 Histone Cardiovascular HAEC SRX469913,SRX469910,SRX46991...3121,SRX469908,SRX062422,SRX469909,SRX143124,SRX143118,SRX062423,SRX062425,SRX469907,SRX062420 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.10.AllAg.HAEC.bed ...

  19. File list: InP.CDV.10.Input_control.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.10.Input_control.AllCell mm9 Input control Input control Cardiovascular SRX...4,SRX373590,SRX1304811,SRX1304812,SRX377394,SRX377691,SRX275462,SRX275461,SRX066549 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.10.Input_control.AllCell.bed ...

  20. File list: Oth.CDV.05.5-Methylcytosine.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.5-Methylcytosine.AllCell mm9 TFs and others 5-Methylcytosine Cardiovascu...lar http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.05.5-Methylcytosine.AllCell.bed ...

  1. File list: Oth.CDV.10.5-Methylcytosine.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.10.5-Methylcytosine.AllCell hg19 TFs and others 5-Methylcytosine Cardiovasc...ular http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.10.5-Methylcytosine.AllCell.bed ...

  2. File list: Oth.CDV.05.5-Methylcytosine.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.5-Methylcytosine.AllCell hg19 TFs and others 5-Methylcytosine Cardiovasc...ular http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.05.5-Methylcytosine.AllCell.bed ...

  3. File list: Oth.CDV.50.5-Methylcytosine.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.50.5-Methylcytosine.AllCell hg19 TFs and others 5-Methylcytosine Cardiovasc...ular http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.50.5-Methylcytosine.AllCell.bed ...

  4. File list: Oth.CDV.20.5-Methylcytosine.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.20.5-Methylcytosine.AllCell hg19 TFs and others 5-Methylcytosine Cardiovasc...ular http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.20.5-Methylcytosine.AllCell.bed ...

  5. File list: Oth.CDV.20.Crotonyl_lysine.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.20.Crotonyl_lysine.AllCell mm9 TFs and others Crotonyl lysine Cardiovascula...r http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.20.Crotonyl_lysine.AllCell.bed ...

  6. File list: Oth.CDV.50.Crotonyl_lysine.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.50.Crotonyl_lysine.AllCell mm9 TFs and others Crotonyl lysine Cardiovascula...r http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/Oth.CDV.50.Crotonyl_lysine.AllCell.bed ...

  7. File list: Pol.CDV.10.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.10.AllAg.Endocardial_cells hg19 RNA polymerase Cardiovascular Endocardial c...ells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.10.AllAg.Endocardial_cells.bed ...

  8. File list: NoD.CDV.20.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.20.AllAg.Endocardial_cells hg19 No description Cardiovascular Endocardial c...ells DRX014674 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.20.AllAg.Endocardial_cells.bed ...

  9. File list: InP.CDV.05.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.05.AllAg.Endocardial_cells hg19 Input control Cardiovascular Endocardial ce...lls http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.05.AllAg.Endocardial_cells.bed ...

  10. File list: ALL.CDV.20.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.Endocardial_cells hg19 All antigens Cardiovascular Endocardial cel...ls DRX014674 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.20.AllAg.Endocardial_cells.bed ...

  11. File list: Pol.CDV.05.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.05.AllAg.Endocardial_cells hg19 RNA polymerase Cardiovascular Endocardial c...ells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.05.AllAg.Endocardial_cells.bed ...

  12. File list: Pol.CDV.20.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.20.AllAg.Endocardial_cells hg19 RNA polymerase Cardiovascular Endocardial c...ells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.20.AllAg.Endocardial_cells.bed ...

  13. File list: Oth.CDV.05.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.AllAg.Endocardial_cells hg19 TFs and others Cardiovascular Endocardial c...ells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.05.AllAg.Endocardial_cells.bed ...

  14. File list: InP.CDV.20.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.20.AllAg.Endocardial_cells hg19 Input control Cardiovascular Endocardial ce...lls http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.20.AllAg.Endocardial_cells.bed ...

  15. File list: Pol.CDV.50.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.50.AllAg.Endocardial_cells hg19 RNA polymerase Cardiovascular Endocardial c...ells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.50.AllAg.Endocardial_cells.bed ...

  16. File list: InP.CDV.50.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.50.AllAg.Endocardial_cells hg19 Input control Cardiovascular Endocardial ce...lls http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.50.AllAg.Endocardial_cells.bed ...

  17. File list: Oth.CDV.20.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.20.AllAg.Endocardial_cells hg19 TFs and others Cardiovascular Endocardial c...ells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.20.AllAg.Endocardial_cells.bed ...

  18. File list: DNS.CDV.50.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.50.AllAg.Brachiocephalic_endothelial_cells hg19 DNase-seq Cardiovascular Brachiocephalic endot...helial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.50.AllAg.Brachiocephalic_endothelial_cells.bed ...

  19. File list: ALL.CDV.50.AllAg.Heart_Atria [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.50.AllAg.Heart_Atria mm9 All antigens Cardiovascular Heart Atria SRX272830,...SRX272831 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/ALL.CDV.50.AllAg.Heart_Atria.bed ...

  20. File list: ALL.CDV.20.AllAg.Heart_Atria [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.Heart_Atria mm9 All antigens Cardiovascular Heart Atria SRX272830,...SRX272831 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/ALL.CDV.20.AllAg.Heart_Atria.bed ...

  1. File list: His.CDV.10.AllAg.Wharton_Jelly [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.10.AllAg.Wharton_Jelly hg19 Histone Cardiovascular Wharton Jelly SRX1548210...,SRX1548226,SRX1548220 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.10.AllAg.Wharton_Jelly.bed ...

  2. File list: ALL.CDV.10.AllAg.Wharton_Jelly [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.Wharton_Jelly hg19 All antigens Cardiovascular Wharton Jelly SRX15...1548228,SRX1548216,SRX1548226,SRX1548220,SRX1548208 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.10.AllAg.Wharton_Jelly.bed ...

  3. File list: InP.CDV.20.Input_control.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.20.Input_control.AllCell mm9 Input control Input control Cardiovascular SRX...75,SRX373609,SRX373610,SRX373590,SRX320036,SRX275461,SRX275462,SRX066549,SRX1121694 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.20.Input_control.AllCell.bed ...

  4. File list: InP.CDV.05.Input_control.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.05.Input_control.AllCell hg19 Input control Input control Cardiovascular SR...SRX190068,SRX220067,SRX190094,SRX080409,SRX190090,SRX699736 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.05.Input_control.AllCell.bed ...

  5. File list: InP.CDV.10.Input_control.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.10.Input_control.AllCell hg19 Input control Input control Cardiovascular SR...SRX190094,SRX190090,SRX189947,SRX080435,DRX021454,SRX699736 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.10.Input_control.AllCell.bed ...

  6. File list: InP.CDV.50.Input_control.AllCell [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.50.Input_control.AllCell mm9 Input control Input control Cardiovascular SRX...74,SRX517514,SRX373580,SRX320036,SRX320037,SRX1121694,SRX275462,SRX275461,SRX066549 http://dbarchive.biosciencedbc.jp/kyushu-u/mm9/assembled/InP.CDV.50.Input_control.AllCell.bed ...

  7. File list: NoD.CDV.10.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.10.AllAg.Endocardial_cells hg19 No description Cardiovascular Endocardial c...ells DRX014674 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.10.AllAg.Endocardial_cells.bed ...

  8. File list: NoD.CDV.50.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.50.AllAg.Endocardial_cells hg19 No description Cardiovascular Endocardial c...ells DRX014674 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.50.AllAg.Endocardial_cells.bed ...

  9. File list: Oth.CDV.50.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.50.AllAg.Endocardial_cells hg19 TFs and others Cardiovascular Endocardial c...ells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.50.AllAg.Endocardial_cells.bed ...

  10. File list: InP.CDV.10.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.10.AllAg.Endocardial_cells hg19 Input control Cardiovascular Endocardial ce...lls http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.10.AllAg.Endocardial_cells.bed ...

  11. File list: ALL.CDV.10.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.Endocardial_cells hg19 All antigens Cardiovascular Endocardial cel...ls DRX014674 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.10.AllAg.Endocardial_cells.bed ...

  12. File list: NoD.CDV.05.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.05.AllAg.Endocardial_cells hg19 No description Cardiovascular Endocardial c...ells DRX014674 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.05.AllAg.Endocardial_cells.bed ...

  13. File list: ALL.CDV.50.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.50.AllAg.Endocardial_cells hg19 All antigens Cardiovascular Endocardial cel...ls DRX014674 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.50.AllAg.Endocardial_cells.bed ...

  14. File list: ALL.CDV.05.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.Endocardial_cells hg19 All antigens Cardiovascular Endocardial cel...ls DRX014674 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.05.AllAg.Endocardial_cells.bed ...

  15. File list: Oth.CDV.10.AllAg.Endocardial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

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  1. File list: Pol.CDV.20.AllAg.Atrioventicular_canals [Chip-atlas[Archive

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  10. File list: DNS.CDV.05.AllAg.Heart_Ventricles [Chip-atlas[Archive

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  11. Distributed fiber temperature and strain sensor using coherent radio-frequency detection of spontaneous Brillouin scattering

    Science.gov (United States)

    Geng, Jihong; Staines, Sean; Blake, Mike; Jiang, Shibin

    2007-08-01

    A novel technique that enables coherent detection of spontaneous Brillouin scattering in the radio-frequency (<500 MHz) region with excellent long-term stability has been demonstrated for distributed measurements of temperature and strain in long fiber. An actively stabilized single-frequency Brillouin fiber laser with extremely low phase noise and intensity noise is used as a well-defined, frequency-shifted local oscillator for the heterodyne detection, yielding measurements of spontaneous Brillouin scattering with high frequency stability. Based on this approach, a highly stable real-time fiber sensor for distributed measurements of both temperature and strain over long fiber has been developed utilizing advanced digital signal processing techniques.

  12. Exposure of pampas fox (Pseudalopex gymnocercus and crab-eating fox (Cerdocyon thous from the Southern region of Brazil to Canine distemper virus (CDV, Canine parvovirus (CPV and Canine coronavirus (CCoV

    Directory of Open Access Journals (Sweden)

    Silvia de Oliveira Hübner

    2010-06-01

    Full Text Available The exposure of 13 Brazilian free-ranging nondomestic canids (five pampas fox - Pseudalopex gymnocercus and eight crab-eating fox -Cerdocyon thous from Southern region of Brazil, to Canine distemper virus (CDV, canine parvovirus (CPV and Canine coronavirus (CCoV was investigated. Antibodies against CDV were detected in 38.5% (5/13 of the samples. There were anti-CDV antibodies in 60% (3/5 of P. gymnocercus and in 25% (2/8 of C. thous. The frequency was higher among the adults and males. Eleven canids (84.6% presented antibodies against CPV, 80% (4/5 were from P. gymnocercus and 87.5% (7/8 were from C. thous. There was no difference in positivity rate against CPV between gender and age. Antibodies against CCoV were detected in 38.5% (5/13 of the samples, with 60% (3/5 of positivity in P. gymnocercus and 25% (2/8 in C. thous. The frequency of antibodies against CCoV was higher among the adults and males. The study showed that these canids were exposed to CDV, CPV and CCoV.Foi investigada a ocorrência de exposição em 13 canídeos não domésticos de vida livre (cinco graxains-do-campo - Pseudalopex gymnocercus e oito graxains-do-mato - Cerdocyon thous da região sul do Brasil ao vírus da cinomose canina (CDV, parvovírus canino (CPV e coronavírus canino (CCoV. Anticorpos contra o CDV foram detectados em 38,5% (5/13 das amostras. Haviam anticorpos anti-CDV em 60% (3/5 dos P. gymnocercus e em 25% (2/8 dos C. thous. A freqüência foi maior entre machos e adultos. Para CPV, 11 canídeos (84,6% apresentaram anticorpos, 80% (4/5 eram da espécie P. gymnocercus e 87,5% (7/8 eram C. thous. Não houve diferença de positividade para o CPV entre sexos e idades. Anticorpos contra o CCoV foram detectados em 38,5% (5/13 das amostras, sendo 60% (3/5 de positividade entre os P. gymnocercus e 25% (2/8 entre os C. thous. A freqüência de anticorpos para CCoV foi maior entre os machos e adultos. O estudo revelou que estes canídeos foram expostos ao CDV, CPV

  13. [Construction of an Escherichia coli strain for sensitive detection of arsenite ion in water].

    Science.gov (United States)

    Wang, Wu; Ji, Songjun; Huang, Zhaozhu; Lu, Binbin; Lv, Jianxin

    2016-08-25

    In order to construct an Escherichia coli strain with high sensitivity and specificity to detect arsenic ion using fluorescence as reporter, a sensitive strain to arsenic ion was obtained by knocking out the gene arsB that acts as an arsenic efflux pump. The pET28b vector containing arsenite detecting cassette Pars-arsR-egfp was constructed and then transformed into arsB deleted mutant. Measuring conditions of this constructed whole-cell biosensor were optimized and its linear concentration range, limit of detection and specificity were determined. This modified biosensor was much more sensitive than that using wild-type strain as host. The optimal detection range of As³⁺ concentration was 0.013 to 42.71 μmol/L, and the limit concentration of detection was as low as 5.13 nmol/L. Thus we successfully improved the sensitivity of arsenite detecting biosensor by modification of E. coli genome, which may provide useful strategies for development and optimization of microbial sensors to detect heavy metals.

  14. Biomarkers for detecting nitrogen deficiency during alcoholic fermentation in different commercial wine yeast strains.

    Science.gov (United States)

    Gutiérrez, Alicia; Chiva, Rosana; Beltran, Gemma; Mas, Albert; Guillamon, José Manuel

    2013-05-01

    Nitrogen deficiencies in grape musts are one of the main causes of stuck or sluggish wine fermentations. Several putative biomarkers were tested in order to analyze their appropriateness to detect nitrogen stress in the yeast. To this aim, four commercial wine strains (PDM, ARM, RVA and TTA) were grown in a synthetic grape must with different nitrogen concentrations. Trehalose accumulation, arginase activity and the expression of eleven genes were tested in these wine strains, known to have different nitrogen requirements. The overall response of the four strains was similar, with differences in response intensity (PDM and RVA with higher intensity) and response time (which was also related with nitrogen consumption time). Trehalose response was mostly related to entry into the stationary phase, whereas arginase activity was responsive to nitrogen depletion, although its measurement is too complicated to be used for routine monitoring during winemaking. The expression of the genes DAL4, DAL5, DUR3 and GAP1 was clearly related to nitrogen depletion and thus, GAP1 and DAL4 were selected as markers of nitrogen deficiency. In order to adapt expression analysis to winemaking conditions, the original strains were transformed into reporter strains based on the expression of green fluorescent protein (GFP) under control of the promoters for GAP1 and DAL4. The transformants had a similar fermentative capacity to the parental strains and were able to detect alterations in yeast physiological status due to nitrogen limitations. Copyright © 2013 Elsevier Ltd. All rights reserved.

  15. Coherent Thz Frequency Radiation from Shock Waves: a New Ultrafast Strain Wave Detection Mechanism

    Science.gov (United States)

    Reed, Evan J.; Armstrong, Michael R.; Kim, Ki-Yong; Glownia, James H.

    2007-12-01

    We discover that strain waves of THz frequencies can coherently generate radiation when they propagate past an interface between materials with different piezoelectric coefficients. By considering AlN/GaN heterostructures, we show that the radiation is of detectable amplitude and contains sufficient information to determine the time-dependence of the strain wave with potentially unprecedented nearly atomic time and space resolution. We demonstrate this phenomenon within the context of high amplitude THz frequency strain waves that spontaneously form at the front of shock waves in GaN crystals. We have performed proof of principle experiments that demonstrate THz signals that correlate with strain wave propagation times across Al thin films.

  16. Detection and characterization of a human G9P[4] rotavirus strain in Japan.

    Science.gov (United States)

    Yamamoto, Seiji P; Kaida, Atsushi; Ono, Atsushi; Kubo, Hideyuki; Iritani, Nobuhiro

    2015-08-01

    In a surveillance system in Osaka City, Japan, 48 sporadic rotavirus A (RVA) infections were detected during 2008/2009-2011/2012 seasons. The G/P-genotypes of detected RVAs were G1P[8], G2P[4], G3P[8], G9P[4], and G9P[8]. Although G9P[4] is a rare genotype that had not been reported in Japan, it was the second most prevalent genotype, following G1P[8], and accounted for 35.3% of RVA cases in the 2011/2012 season. Further genotyping revealed that the G9P[4] strain had genotype 2 internal protein genes except for NSP3: G9-P[4]-I2-R2-C2-M2-A2-N2-T1-E2-H2. Among detected RVA strains, G9P[4] and some G9P[8] strains shared high nucleotide identity in VP7 and NSP3 genes. Phylogenetic and BLAST search analyses showed that the G9P[4] strain in Japan shared high nucleotide identity in genotype 2 genes with common G2P[4] strains circulating globally, but was distinct from other G9P[4] strains circulating worldwide. These results suggest that the G9P[4] strain in Japan may have emerged through an independent reassortment between G9P[8] and G2P[4]. Finally, the role of NSP3 protein in the circulating RVA from an amino acid comparison between T1- and T2-type NSP3 is discussed. These findings provide an important insight into less problematic combinations of circulating RVA genes derived from different genotypes. © 2015 Wiley Periodicals, Inc.

  17. A diagnostic PCR assay for the detection of an Australian epidemic strain of Pseudomonas aeruginosa

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    Murphy Anna

    2010-07-01

    Full Text Available Abstract Background Chronic lung infection with the bacterium Pseudomonas aeruginosa is one of the hallmarks of cystic fibrosis (CF and is associated with worsening lung function, increased hospitalisation and reduced life expectancy. A virulent clonal strain of P. aeruginosa (Australian epidemic strain I; AES-I has been found to be widespread in CF patients in eastern Australia. Methods Suppression subtractive hybridization (SSH was employed to identify genetic sequences that are present in the AES-I strain but absent from the sequenced reference strain PAO1. We used PCR to evaluate the distribution of several of the AES-I loci amongst a collection of 188 P. aeruginosa isolates which was comprised of 35 AES-I isolates (as determined by PFGE, 78 non-AES-I CF isolates including other epidemic CF strains as well as 69 P. aeruginosa isolates from other clinical and environmental sources. Results We have identified a unique AES-I genetic locus that is present in all 35 AES-I isolates tested and not present in any of the other 153 P. aeruginosa strains examined. We have used this unique AES-I locus to develop a diagnostic PCR and a real-time PCR assay to detect the presence of P. aeruginosa and AES-I in patient sputum samples. Conclusions We have developed diagnostic PCR assays that are 100% sensitive and 100% specific for the P. aeruginosa strain AES-I. We have also shown that Whatman FTA® Elute cards may be used with PCR-based assays to rapidly detect the presence of P. aeruginosa strains in CF sputum.

  18. Comparison of detection methods for extended-spectrum beta-lactamases in Escherichia coli strains

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    Ewelina Kałużna

    2014-06-01

    Full Text Available Introduction: Detection of extended-spectrum beta-lactamases (ESBLs could be a major challenge for microbiologists – the difficulties arise mainly from the phenotypic differences among strains.Materials and Methods: Evaluation of ESBLs was performed on 42 strains of E. coli by: 1 DDST on MHA, 2 DDST on MHA with cloxacillin, 3 CT on MHA, according to CLSI, 4 CT on MHA with cloxacillin, 5 Etest ESBL (AB Biodisk, 6 CHROMagarTM ESBL (GRASO, 7 ChromID® ESBL (bioMérieux, and 8 automatic system VITEK2 ESBL test (bioMérieux.Result: Positive results were obtained for 20 strains using method 1, for 18 strains using method 2, 17 by method 3, 14 by method 4, 11 by method 5, 39 by method 6, 40 by method 7, and 15 by method 8. Using Etest ESBL 6.0 non-determinable results were obtained. The most consistent results were obtained when comparing the results of method 3 with results of method 2 (97.6%, and comparing the results obtained using methods 3 and 8 (95.2%.Conclusions: Based on our study we conclude that the chromogenic media can only be used as a screening method for the detection of ESBLs in E. coli rods. Etest is less useful compared to other phenotype methods, due to the impossibility of obtaining results for all the tested strains. Adding cloxacillin to MHA does not increase the frequency of detection of ESBLs in E. coli strains. DDST seems to be the most reliable among phenotypic methods for the detection of ESBLs in E. coli rods.

  19. Phylogenetic analysis of Austrian canine distemper virus strains from clinical samples from dogs and wild carnivores.

    Science.gov (United States)

    Benetka, V; Leschnik, M; Affenzeller, N; Möstl, K

    2011-04-09

    Austrian field cases of canine distemper (14 dogs, one badger [Meles meles] and one stone marten [Martes foina]) from 2002 to 2007 were investigated and the case histories were summarised briefly. Phylogenetic analysis of fusion (F) and haemagglutinin (H) gene sequences revealed different canine distemper virus (CDV) lineages circulating in Austria. The majority of CDV strains detected from 2002 to 2004 were well embedded in the European lineage. One Austrian canine sample detected in 2003, with a high similarity to Hungarian sequences from 2005 to 2006, could be assigned to the Arctic group (phocine distemper virus type 2-like). The two canine sequences from 2007 formed a clearly distinct group flanked by sequences detected previously in China and the USA on an intermediate position between the European wildlife and the Asia-1 cluster. The Austrian wildlife strains (2006 and 2007) could be assigned to the European wildlife group and were most closely related to, yet clearly different from, the 2007 canine samples. To elucidate the epidemiological role of Austrian wildlife in the transmission of the disease to dogs and vice versa, H protein residues related to receptor and host specificity (residues 530 and 549) were analysed. All samples showed the amino acids expected for their host of origin, with the exception of a canine sequence from 2007, which had an intermediate position between wildlife and canine viral strains. In the period investigated, canine strains circulating in Austria could be assigned to four different lineages reflecting both a high diversity and probably different origins of virus introduction to Austria in different years.

  20. Molecular characterization of genotype G6 human rotavirus strains detected in Italy from 1986 to 2009.

    Science.gov (United States)

    De Grazia, Simona; Martella, Vito; Rotolo, Valentina; Bonura, Floriana; Matthijnssens, Jelle; Bányai, Krisztián; Ciarlet, Max; Giammanco, Giovanni M

    2011-08-01

    Group A human rotavirus (HRV) strains with a bovine-like (G6) major outer capsid protein VP7 were first detected in Palermo, Italy, in the late 1980s, and subsequently worldwide. During a 25-year rotavirus surveillance period, additional HRV G6 strains, associated with either a P[9] or P[14] VP4 genotype, have been detected sporadically, but repeatedly, in Palermo. Whether these G6 HRVs were transmitted to humans directly from an animal reservoir or could have circulated at low prevalence in susceptible individuals is uncertain. Upon sequence analyses of the VP7, VP4, VP6, NSP4 and NSP5 gene segments, all the Italian HRV strains displayed a conserved genotype constellation, G6-P[9]/[14]-I2-E2-H3. Intra-genotypic lineages and/or sub-lineages were observed among the various HRV strains, with some lineage/sublineage combinations being retained over time. Interestingly, two epidemiologically unrelated G6P[9] viruses, collected in the same rotavirus season, were found to have a clonal origin. In conclusion, our results indicate not only diverse origin of animal derived G6 HRVs in Palermo but also suggest human-to-human transmission of certain strains. Copyright © 2011 Elsevier B.V. All rights reserved.

  1. Detection of Steel Fatigue Cracks with Strain Sensing Sheets Based on Large Area Electronics

    Directory of Open Access Journals (Sweden)

    Yao Yao

    2015-04-01

    Full Text Available Reliable early-stage damage detection requires continuous monitoring over large areas of structure, and with sensors of high spatial resolution. Technologies based on Large Area Electronics (LAE can enable direct sensing and can be scaled to the level required for Structural Health Monitoring (SHM of civil structures and infrastructure. Sensing sheets based on LAE contain dense arrangements of thin-film strain sensors, associated electronics and various control circuits deposited and integrated on a flexible polyimide substrate that can cover large areas of structures. This paper presents the development stage of a prototype strain sensing sheet based on LAE for crack detection and localization. Two types of sensing-sheet arrangements with size 6 × 6 inch (152 × 152 mm were designed and manufactured, one with a very dense arrangement of sensors and the other with a less dense arrangement of sensors. The sensing sheets were bonded to steel plates, which had a notch on the boundary, so the fatigue cracks could be generated under cyclic loading. The sensors within the sensing sheet that were close to the notch tip successfully detected the initialization of fatigue crack and localized the damage on the plate. The sensors that were away from the crack successfully detected the propagation of fatigue cracks based on the time history of the measured strain. The results of the tests have validated the general principles of the proposed sensing sheets for crack detection and identified advantages and challenges of the two tested designs.

  2. Indicator cell lines for detection of primary strains of human and simian immunodeficiency viruses.

    Science.gov (United States)

    Vodicka, M A; Goh, W C; Wu, L I; Rogel, M E; Bartz, S R; Schweickart, V L; Raport, C J; Emerman, M

    1997-06-23

    CCR5 and CXCR4 are the two major coreceptors that have been identified for human immunodeficiency virus (HIV) entry. We have modified several beta-galactosidase-based HIV indicator cell lines to express CCR5 and/or CXCR4. Using these new reagents, we have been able to detect all primary isolates tested using one or both of these cell lines. However, there is large variation in the absolute viral infectivity among primary strains. Furthermore, all HIV strains are capable of causing syncytia in the indicator cells when the coreceptor is present regardless of whether they had previously been characterized as "syncytia-inducing" or "non-syncytium-inducing."

  3. Dual Recognition Element Lateral Flow Assay Toward Multiplex Strain Specific Influenza Virus Detection.

    Science.gov (United States)

    Le, Thao T; Chang, Pengxiang; Benton, Donald J; McCauley, John W; Iqbal, Munir; Cass, Anthony E G

    2017-06-20

    Different influenza virus strains have caused a number of recent outbreaks killing scores of people and causing significant losses in animal farming. Simple, rapid, sensitive, and specific detection of particular strains, such as a pandemic strain versus a previous seasonal influenza, plays a crucial role in the monitoring, controlling, and management of outbreaks. In this paper we describe a dual recognition element lateral flow assay (DRELFA) which pairs a nucleic acid aptamer with an antibody for use as a point-of-care platform which can detect particular strains of interest. The combination is used to overcome the individual limitations of antibodies' cross-reactivity and aptamers' slow binding kinetics. In the detection of influenza viruses, we show that DRELFA can discriminate a particular virus strain against others of the same subtype or common respiratory diseases while still exhibiting fast binding kinetic of the antibody-based lateral flow assay (LFA). The improvement in specificity that DRELFA exhibits is an advantage over the currently available antibody-based LFA systems for influenza viruses, which offer discrimination between influenza virus types and subtypes. Using quantitative real-time PCR (qRT-PCR), it showed that the DRELFA is very effective in localizing the analyte to the test line (consistently over 90%) and this is crucial for the sensitivity of the device. In addition, color intensities of the test lines showed a good correlation between the DRELFA and the qRT-PCR over a 50-fold concentration range. Finally, lateral flow strips with a streptavidin capture test line and an anti-antibody control line are universally applicable to specific detection of a wide range of different analytes.

  4. Detection of Shiga Toxin-Producing Escherichia coli from Nonhuman Sources and Strain Typing.

    Science.gov (United States)

    Beutin, Lothar; Fach, Patrick

    2014-06-01

    Shiga toxin-producing Escherichia coli (STEC) strains are commonly found in the intestine of ruminant species of wild and domestic animals. Excretion of STEC with animal feces results in a broad contamination of food and the environment. Humans get infected with STEC through ingestion of contaminated food, by contact with the environment, and from STEC-excreting animals and humans. STEC strains can behave as human pathogens, and some of them, called enterohemorrhagic E. coli (EHEC), may cause hemorrhagic colitis (HC) and hemolytic-uremic syndrome (HUS). Because of the diversity of STEC types, detection strategies for STEC and EHEC are based on the identification of Shiga toxins or the underlying genes. Cultural enrichment of STEC from test samples is needed for identification, and different protocols were developed for this purpose. Multiplex real-time PCR protocols (ISO/CEN TS13136 and USDA/FSIS MLG5B.01) have been developed to specifically identify EHEC by targeting the LEE (locus of enterocyte effacement)-encoded eae gene and genes for EHEC-associated O groups. The employment of more genetic markers (nle and CRISPR) is a future challenge for better identification of EHEC from any kinds of samples. The isolation of STEC or EHEC from a sample is required for confirmation, and different cultivation protocols and media for this purpose have been developed. Most STEC strains present in food, animals, and the environment are eae negative, but some of these strains can cause HC and HUS in humans as well. Phenotypic assays and molecular tools for typing EHEC and STEC strains are used to detect and characterize human pathogenic strains among members of the STEC group.

  5. Detection and Characterization of Histamine-Producing Strains of Photobacterium damselae subsp. damselae Isolated from Mullets

    Directory of Open Access Journals (Sweden)

    Marcello Trevisani

    2017-06-01

    Full Text Available Photobacterium damselae subsp. damselae (Pdd is considered to be an emerging pathogen of marine fish and has also been implicated in cases of histamine food poisoning. In this study, eight strains isolated from mullets of the genera Mugil and Liza captured in the Ligurian Sea were characterized, and a method to detect histamine-producing Pdd from fish samples was developed. The histamine-producing potential of the strains was evaluated in culture media (TSB+ using a histamine biosensor. Subsequently, two strains were used to contaminate mackerel fillets (4 or 40 CFU/g, simulating a cross-contamination on the selling fish stalls. Sample homogenates were enriched in TSB+. The cultures were then inoculated on thiosulfate-citrate-bile salts-sucrose agar (TCBS and the dark green colonies were cultured on Niven agar. The violet isolates were characterized using specific biochemical and PCR based tests. All Pdd strains were histamine producers, yielding concentration varying from 167 and 8977 µg/mL in TSB+ cultures incubated at 30 °C for 24 h. Pdd colonies were detected from the inoculated mackerel samples and their histidine decarboxylase gene was amplified using species-specific primer pairs designed for this study. The results indicate that mullets can be source of Pdd and the fish retailers needs to evaluate the risk posed by cross-contamination on the selling fish stalls.

  6. Feasibility of Detecting Natural Frequencies of Hydraulic Turbines While in Operation, Using Strain Gauges.

    Science.gov (United States)

    Valentín, David; Presas, Alexandre; Bossio, Matias; Egusquiza, Mònica; Egusquiza, Eduard; Valero, Carme

    2018-01-10

    Nowadays, hydropower plays an essential role in the energy market. Due to their fast response and regulation capacity, hydraulic turbines operate at off-design conditions with a high number of starts and stops. In this situation, dynamic loads and stresses over the structure are high, registering some failures over time, especially in the runner. Therefore, it is important to know the dynamic response of the runner while in operation, i.e., the natural frequencies, damping and mode shapes, in order to avoid resonance and fatigue problems. Detecting the natural frequencies of hydraulic turbine runners while in operation is challenging, because they are inaccessible structures strongly affected by their confinement in water. Strain gauges are used to measure the stresses of hydraulic turbine runners in operation during commissioning. However, in this paper, the feasibility of using them to detect the natural frequencies of hydraulic turbines runners while in operation is studied. For this purpose, a large Francis turbine runner (444 MW) was instrumented with several strain gauges at different positions. First, a complete experimental strain modal testing (SMT) of the runner in air was performed using the strain gauges and accelerometers. Then, the natural frequencies of the runner were estimated during operation by means of analyzing accurately transient events or rough operating conditions.

  7. Exon and junction microarrays detect widespread mouse strain- and sex-bias expression differences

    Directory of Open Access Journals (Sweden)

    Schadt Eric E

    2008-06-01

    Full Text Available Abstract Background Studies have shown that genetic and sex differences strongly influence gene expression in mice. Given the diversity and complexity of transcripts produced by alternative splicing, we sought to use microarrays to establish the extent of variation found in mouse strains and genders. Here, we surveyed the effect of strain and sex on liver gene and exon expression using male and female mice from three different inbred strains. Results 71 liver RNA samples from three mouse strains – DBA/2J, C57BL/6J and C3H/HeJ – were profiled using a custom-designed microarray monitoring exon and exon-junction expression of 1,020 genes representing 9,406 exons. Gene expression was calculated via two different methods, using the 3'-most exon probe ("3' gene expression profiling" and using all probes associated with the gene ("whole-transcript gene expression profiling", while exon expression was determined using exon probes and flanking junction probes that spanned across the neighboring exons ("exon expression profiling". Widespread strain and sex influences were detected using a two-way Analysis of Variance (ANOVA regardless of the profiling method used. However, over 90% of the genes identified in 3' gene expression profiling or whole transcript profiling were identified in exon profiling, along with 75% and 38% more genes, respectively, showing evidence of differential isoform expression. Overall, 55% and 32% of genes, respectively, exhibited strain- and sex-bias differential gene or exon expression. Conclusion Exon expression profiling identifies significantly more variation than both 3' gene expression profiling and whole-transcript gene expression profiling. A large percentage of genes that are not differentially expressed at the gene level demonstrate exon expression variation suggesting an influence of strain and sex on alternative splicing and a need to profile expression changes at sub-gene resolution.

  8. Surface Crack Detection in Prestressed Concrete Cylinder Pipes Using BOTDA Strain Sensors

    Directory of Open Access Journals (Sweden)

    Zhigang Xu

    2017-01-01

    Full Text Available Structural deterioration after a period of service can induce the failure of prestressed concrete cylinder pipes (PCCPs, with microcracks in the coating leading to the corrosion of the prestressed wires. In this paper, we propose the use of Brillouin optical time-domain analysis (BOTDA strain sensors for detecting the onset of microcracking in PCCP coating: the BOTDA strain sensors are mounted on the surface of the PCCP, and distributed strain measurements are employed to assess the cracks in the mortar coating and the structural state of the pipe. To validate the feasibility of the proposed approach, experimental investigations were conducted on a prototype PCCP segment, wherein the inner pressure was gradually increased to 1.6 MPa. Two types of BOTDA strain sensors—the steel wire packaged fiber optic sensor and the polyelastic packaged fiber optic sensor—were employed in the experiments. The experimental distributed measurements agreed well with the finite element computations, evidencing that the investigated strain sensors are sensitive to localized deterioration behaviors such as PCCP microcracking.

  9. Detection of enterotoxins and genotyping of Staphylococcus aureus strains isolated from Isfahan Educational Hospital, Iran

    Directory of Open Access Journals (Sweden)

    Seyed Asghar Havaei

    2017-10-01

    Full Text Available Background and aims: Staphylococcus aureus is known as one of the most important nosocomial pathogens, which may lead to several infections. The aim of this study was determining the enterotoxins A, C, and TSST-1 and molecular characterization of S. aureus strains with PFGE and MLST typing methods. Materials and methods: In the present study during the sixmonths sampling, fifty S. aureus strains were isolated from patients admitted to Al-Zahra university hospital. Antimicrobial susceptibility testing, Multiplex PCR for detection of enterotoxin A, C and TSST-1, pulse field gel electrophoresis (PFGE and multilocus sequence typing (MLST were used for molecular typing. Results: In antibiogram the highest and lowest percentage of resistance was belonged to tetracycline and rifampin respectively. Multiplex PCR indicated that 30% of the strains harbored sea and 34% harbored sec genes. However, only 4% of our collected isolates had tsst gene. In PFGE method analysis on all S. aureus strains, a total of 19 different patterns were identified. Nine various sequence types in 27 selected S. aureus isolates were identified by MLST. Conclusions: Present study indicates a possible higher variability among our S. aureus strains by two different molecular typing methods; nevertheless four main common types (CT1, CT7, CT9, and CT11 with at least one toxin genes were determined.

  10. A multiplex ligation detection assay for the characterization of Salmonella enterica strains

    DEFF Research Database (Denmark)

    Aarts, Henk J.M.; Vos, Pieter; Larsson, Jonas T.

    2011-01-01

    of four serovars each serovar was characterized by a unique virulence associated gene repertoire. The LDR microarray platform proved to be a convenient, rapid and easy to use tool with potential in tracing a Salmonella contamination in the food chain, for outbreak studies, and to provide data for risk....... The feasibility of the developed assay was verified in a method comparison study with conventional PCR using 16 Salmonella ‘test’ strains comprising eight serovars. Subsequently, the feasibility of the LDR microarray assay was also tested by analyzing 41 strains belonging to 23 serovars. With the exception......A proof of principle of a multi-target assay for genotyping Salmonella has been developed targeting 62 genomic marker sequences of Salmonella related to pathogenicity. The assay is based on multiplex ligation detection reaction (LDR) followed by customized ArrayTube® microarray detection...

  11. Integration of fiber Bragg grating optic sensors for strain detection in structures composed of CFRP composite

    Science.gov (United States)

    Harris, Jason; Barjasteh, Ehsan

    2017-04-01

    The study focuses on the formation of artificial neural pathways for the use of structural health monitoring in prosthesis by means of Fiber Bragg Grating (FBG) optic sensors to detect shifts in strain. Implementation of these fibers are embedded into carbon fiber reinforced polymer (CFRP) based structures. CFRP was considered for its wide use application in ankle-foot prosthesis, which undergoes high loads of stress and wear.. This method acts as a system of early detection which could prevent the prosthesis from critical failure due to previously undetected interior defects, further improving the patient's well being.

  12. Optical fiber strain sensor for application in intelligent intruder detection systems

    Science.gov (United States)

    Stańczyk, Tomasz; Tenderenda, Tadeusz; Szostkiewicz, Lukasz; Bienkowska, Beata; Kunicki, Daniel; Murawski, Michal; Mergo, Pawel; Nasilowski, Tomasz

    2017-10-01

    Nowadays technology allows to create highly effective Intruder Detection Systems (IDS), that are able to detect the presence of an intruder within a defined area. In such systems the best performance can be achieved by combining different detection techniques in one system. One group of devices that can be applied in an IDS, are devices based on Fiber Optic Sensors (FOS). The FOS benefits from numerous advantages of optical fibers like: small size, light weight or high sensitivity. In this work we present a novel Microstructured Optical Fiber (MOF) characterized by increased strain sensitivity dedicated to distributed acoustic sensing for intelligent intruder detection systems. By designing the MOF with large air holes in close proximity to a fiber core, we increased the effective refractive index sensitivity to longitudinal strain. The presented fiber can be easily integrated in a floor system in order to detect any movement in the investigated area. We believe that sensors, based on the presented MOF, due to its numerous advantages, can find application in intelligent IDS.

  13. Damage Detection Based on Static Strain Responses Using FBG in a Wind Turbine Blade.

    Science.gov (United States)

    Tian, Shaohua; Yang, Zhibo; Chen, Xuefeng; Xie, Yong

    2015-08-14

    The damage detection of a wind turbine blade enables better operation of the turbines, and provides an early alert to the destroyed events of the blade in order to avoid catastrophic losses. A new non-baseline damage detection method based on the Fiber Bragg grating (FBG) in a wind turbine blade is developed in this paper. Firstly, the Chi-square distribution is proven to be an effective damage-sensitive feature which is adopted as the individual information source for the local decision. In order to obtain the global and optimal decision for the damage detection, the feature information fusion (FIF) method is proposed to fuse and optimize information in above individual information sources, and the damage is detected accurately through of the global decision. Then a 13.2 m wind turbine blade with the distributed strain sensor system is adopted to describe the feasibility of the proposed method, and the strain energy method (SEM) is used to describe the advantage of the proposed method. Finally results show that the proposed method can deliver encouraging results of the damage detection in the wind turbine blade.

  14. Sequence variability, recombination analysis, and specific detection of the W strain of Plum pox virus.

    Science.gov (United States)

    Glasa, Miroslav; Malinowski, Tadeusz; Predajňa, Lukáš; Pupola, Neda; Dekena, Dzintra; Michalczuk, Lech; Candresse, Thierry

    2011-08-01

    Plum pox virus (PPV), a member of the genus Potyvirus, is the causal agent of Sharka, the most detrimental disease of stone-fruit trees worldwide. PPV isolates are grouped into seven distinct strains. The minor PPV-W strain was established recently for the divergent W3174 isolate found in Canada. Here, the partial or complete genomic sequences of four PPV-W isolates from Latvia have been determined. The completely sequenced isolates LV-141pl and LV-145bt share 93.1 and 92.1% nucleotide identity, respectively, with isolate W3174, with two regions of higher (>20%) divergence in the P1/HC-Pro and NIa (VPg) regions. Further analyses demonstrated that these two regions correspond to two independent recombination events in the W3174 genome, one involving PPV-M (approximate genome positions 692 to 1424) and the other PPV-D (nucleotides 5672 to 5789). The LV-141pl and LV-145bt isolates appear to be representatives of the "ancestral" PPV-W strain, not affected by recombination. The PPV-W intrastrain variability is substantially higher than that of all other PPV strains, with potential implications for the serological detection of PPV-W isolates. A PPV-W-specific primer pair has been developed, allowing the specific reverse-transcription polymerase chain reaction detection of all five presently available W isolates. The characterization of these new PPV-W isolates sheds light on PPV-W evolutionary history, further supports the hypothesis of its East-European origin, and opens the way for the biological and epidemiological characterization of this poorly known PPV strain.

  15. Smart bricks for strain sensing and crack detection in masonry structures

    Science.gov (United States)

    Downey, Austin; D’Alessandro, Antonella; Laflamme, Simon; Ubertini, Filippo

    2018-01-01

    The paper proposes the novel concept of smart bricks as a durable sensing solution for structural health monitoring of masonry structures. The term smart bricks denotes piezoresistive clay bricks with suitable electronics capable of outputting measurable changes in their electrical properties under changes in their state of strain. This feature can be exploited to evaluate stress at critical locations inside a masonry wall and to detect changes in loading paths associated with structural damage, for instance following an earthquake. Results from an experimental campaign show that normal clay bricks, fabricated in the laboratory with embedded electrodes made of a special steel for resisting the high baking temperature, exhibit a quite linear and repeatable piezoresistive behavior. That is a change in electrical resistance proportional to a change in axial strain. In order to be able to exploit this feature for strain sensing, high-resolution electronics are used with a biphasic DC measurement approach to eliminate any resistance drift due to material polarization. Then, an enhanced nanocomposite smart brick is proposed, where titania is mixed with clay before baking, in order to enhance the brick’s mechanical properties, improve its noise rejection, and increase its electrical conductivity. Titania was selected among other possible conductive nanofillers due to its resistance to high temperatures and its ability to improve the durability of construction materials while maintaining the aesthetic appearance of clay bricks. An application of smart bricks for crack detection in masonry walls is demonstrated by laboratory testing of a small-scale wall specimen under different loading conditions and controlled damage. Overall, it is demonstrated that a few strategically placed smart bricks enable monitoring of the state of strain within the wall and provide information that is capable of crack detection.

  16. File list: NoD.CDV.50.AllAg.HUVEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

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    Lifescience Database Archive (English)

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  18. File list: NoD.CDV.10.AllAg.HAoEC [Chip-atlas[Archive

    Lifescience Database Archive (English)

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  19. Molecular Detection of Aflatoxin Producing Strains of Aspergillus Flavus from Peanut (Arachis Hypogaea

    Directory of Open Access Journals (Sweden)

    Adeela Hussain

    2015-02-01

    Full Text Available Aflatoxins are the potential carcinogens produced as secondary metabolites by Aspergillus flavus. They have the ability to contaminate large number of food which ultimately affect the human population. Malt extract agar was selected for the growth of control stains of fungus. The aim of the study was to develop a reliable and quick method for the detection of aflatoxin producing strains in peanuts by using molecular approaches. Total 80 samples of infected peanuts were collected from four different cities of Punjab and checked for their aflatoxin contamination. For aflatoxin detection, three target genes nor1, ver1 and aflR were selected which was involved in the aflatoxin biosynthesis. In all examined cases, 24 out of 80 (30% samples successfully amplified all three genes indicating aflatoxigenic activity. Discrimination between aflatoxigenic and non-aflatoxigenic strains were also determined on the basis of amplification of these three target DNA fragments. In this study, it was also demonstrated that only specific strains were able to produce the aflatoxin contamination in peanuts.

  20. An evaluation of PCR methods to detect strains of Mycoplasma fermentans.

    Science.gov (United States)

    Afshar, Baharak; Pitcher, David; Nicholas, Robin A J; Miles, Roger J

    2008-03-01

    A panel of 30 putative Mycoplasma fermentans strains, isolated from various sources including human, ovine and cell lines, were tested by a previously described polymerase chain reaction (PCR) to confirm their identity by amplification of a conserved 206 bp region of the insertion sequence IS1550. In addition, the application of another PCR based on the major part of the IS1550 element showed one or two products of different length (1144 and 1341 bp) enabling M. fermentans strains to be divided into two types designated as Type A and Type B. A PCR, which amplifies the macrophage activating lipopeptide gene (malp), supported the identification of all the strains as M. fermentans. Thirteen other species of Mycoplasma from human sources gave negative results in these tests, with the exception of Mycoplasma orale, which was detected by both IS1550-PCRs based on the major part and the conserved 206 bp region of the IS1550 element. This study suggests that all M. fermentans isolates possess both the IS1550 element and the malp gene. In contrast to the IS1550, the malp gene is shown to be species-specific and the use of a malp PCR described here could prove to be a useful adjunct to IS1550 detection as confirmation of the presence of M. fermentans in clinical material.

  1. Strain-encoded CMR for the detection of inducible ischemia during intermediate stress.

    Science.gov (United States)

    Korosoglou, Grigorios; Lehrke, Stephanie; Wochele, Angela; Hoerig, Birgit; Lossnitzer, Dirk; Steen, Henning; Giannitsis, Evangelos; Osman, Nael F; Katus, Hugo A

    2010-04-01

    This study sought to evaluate the diagnostic accuracy of strain-encoded cardiac magnetic resonance (SENC) for the detection of inducible ischemia during intermediate stress. High-dose dobutamine stress cardiac magnetic resonance (DS-CMR) is a well-established modality for the noninvasive detection of coronary artery disease (CAD). However, the assessment of cine scans relies on the visual interpretation of wall motion, which is subjective, and modalities that can objectively and quantitatively assess the time course of myocardial strain response during stress are lacking. Stress-induced ischemia was assessed by wall motion analysis and by SENC in 80 patients with suspected or known CAD and in 18 healthy volunteers who underwent DS-CMR in a clinical 1.5-T scanner. Quantitative coronary angiography was used as the standard reference for the presence of CAD (> or =50% diameter stenosis). On a patient level, 46 of 80 patients (58%) had CAD, including 20 with single-vessel, 18 with 2-vessel, and 8 with 3-vessel disease. During peak stress, SENC correctly detected ischemia in 45 versus 38 of 46 patients with CAD (7 additional correct findings for SENC), yielding significantly higher sensitivity than cine (98% vs. 83%, p intermediate stress, SENC showed diagnostic value similar to that provided by cine imaging only during peak dobutamine stress (sensitivity of 76% vs. 83%, specificity of 88% vs. 91%, and accuracy of 81% vs. 86%; p = NS for all). Quantification analysis demonstrated that strain rate response is a highly sensitive marker for the detection of inducible ischemia (area under the curve = 0.96; SE = 0.01; 95% confidence interval: 0.93 to 0.99) that precedes the development of inducible wall motion abnormalities and already significantly decreases with moderate 40% to 60% coronary lesions. Using SENC, CAD can be detected during intermediate stress with similar accuracy to that provided by cine only during peak stress. By this approach, patient safety may be

  2. Genetic diversity of Hungarian canine distemper virus strains.

    Science.gov (United States)

    Demeter, Zoltán; Lakatos, Béla; Palade, Elena Alina; Kozma, Tamás; Forgách, Petra; Rusvai, Miklós

    2007-06-21

    To achieve proper diagnosis of dogs based on acute clinical symptoms and poorly preserved field samples taken from animals that died due to canine distemper (CD), a new differential diagnostic test has been developed based on polymerase chain reaction (PCR). In this study, more than 150 samples collected from dogs showing respiratory, gastrointestinal and neurological signs suggesting canine distemper virus (CDV) infection were examined. The samples consisted of urine, blood and nasal swabs collected from clinically ill patients, sent to our laboratory by clinicians from various veterinary clinics throughout Hungary. Various organs collected during the necropsy of dogs with pathological changes that suggested CDV infection were also included. Three distinct PCRs were designed. For diagnostic purposes, a primer pair specific to a 409 bases-long segment within the conservative part of the large polymerase region (L) of the CDV genome was designed. Using this test, out of the 150 analyzed samples, 46 (30.66%) proved to be positive for CDV, indicating that CDV still represents a high risk to the canine population in Hungary. For the phylogenetical analysis, a primer pair that completely encompasses the hemagglutinin (H) gene of the CDV genome was designed. The amplicons of this region were sequenced in both directions using the appropriate primers. Our results indicate that several different CDV genotypes are currently present in Hungary. Nine of the analyzed Hungarian strains turned out to belong to the so-called Arctic group of CDVs, and were most closely related to non-European strains from North America, China and Greenland, as well as to the phocine distemper virus 2 (PDV-2) isolated from Baikal seals (Phoca sibirica). One of the Hungarian strains showed high similarity to other European isolates from Denmark, Germany, Italy and Turkey, as well as to other isolates from geographically more distant regions, such as the USA. Three Hungarian strains seem to join a

  3. Brillouin optical time domain reflectometry for fast detection of dynamic strain incorporating double-edge technique

    Science.gov (United States)

    Shangguan, Mingjia; Wang, Chong; Xia, Haiyun; Shentu, Guoliang; Dou, Xiankang; Zhang, Qiang; Pan, Jian-wei

    2017-09-01

    For the first time, to the best of our knowledge, a direct detection Brillouin optical time-domain reflectometry (BOTDR) is demonstrated for fast distributed dynamic strain sensing incorporating double-edge technique, time-division multiplexing technique and upconversion technique. In order to guarantee the robust stability of the system, the double-edge technique is implemented by using a convert single-channel FPI and a fiber-coupled upconversion single-photon detector, incorporating a time-division multiplexing method. The upconversion single-photon detector is adopted to upconvert the backscattering photons from 1548.1 nm to 863 nm, which is subsequently detected by a Silicon avalanche photodiode (Si-APD). In the experiment, dynamic strain disturbance up to 1.9 mε over 1.5 km of a polarization maintaining fiber is detected at a sampling rate of 30 Hz. An accuracy of ± 30 με and spatial resolution of 0.6 m are realized.

  4. Detection of highly and minimally leukotoxic Actinobacillus actinomycetemcomitans strains in patients with periodontal disease

    Directory of Open Access Journals (Sweden)

    Cortelli Sheila Cavalca

    2003-01-01

    Full Text Available This study examined the prevalence of highly and minimally leukotoxic Actinobacillus actinomycetemcomitans in patients with periodontal disease. Pooled subgingival plaque samples from 136 patients with some form of periodontal disease were examined. Subjects were between 14 and 76 years of age. Clinical examinations included periodontal pocket depth (PD, plaque index (PI and bleeding index (BI. The obtained plaque samples were examined for the presence of highly or minimally leukotoxic A. actinomycetemcomitans strains by the polymerase chain reaction (PCR. Chi-square and logistic regression were performed to evaluate the results. Forty-seven subjects were diagnosed with gingivitis, 70 with chronic periodontitis and 19 with aggressive periodontitis. According to chi-square there was no significant correlation detected between PD (chi2 = 0.73, PI (chi2 = 0.35, BI (chi2 = 0.09 and the presence of the highly leukotoxic A. actinomycetemcomitans. The highly leukotoxic A. actinomycetemcomitans strains were correlated with subjects that were 28 years of age and younger (chi2 = 7.41. There was a significant correlation between highly leukotoxic A. actinomycetemcomitans and aggressive periodontitis (chi2 = 22.06. This study of a Brazilian cohort confirms the strong association between highly leukotoxic A. actinomycetemcomitans strains and the presence of aggressive periodontitis.

  5. Evaluation of Rapid Molecular Detection Assays for Salmonella in Challenging Food Matrices at Low Inoculation Levels and Using Difficult-to-Detect Strains.

    Science.gov (United States)

    Ryan, Gina; Roof, Sherry; Post, Laurie; Wiedmann, Martin

    2015-09-01

    Assays for detection of foodborne pathogens are generally initially evaluated for performance in validation studies carried out according to guidelines provided by validation schemes (e.g., AOAC International or the International Organization for Standardization). End users often perform additional validation studies to evaluate the performance of assays in specific matrices (e.g., specific foods or raw material streams of interest) and with specific pathogen strains. However, these types of end-user validations are typically not well defined. This study was conducted to evaluate a secondary end user validation of four AOAC-validated commercial rapid detection assays (an isothermal nucleic acid amplification, an immunoassay, and two PCR-based assays) for their ability to detect Salmonella in two challenging matrices (dry pet food and dark chocolate). Inclusivity was evaluated with 68 diverse Salmonella strains at low population levels representing the limit of detection (LOD) for each assay. One assay detected all strains at the LOD, two assays detected multiple strains only at 10 times the LOD, and the fourth assay failed to detect two strains (Salmonella bongori and S. enterica subsp. houtenae) even at 1,000 times the LOD; this assay was not further evaluated. The three remaining assays were subsequently evaluated for their ability to detect five selected Salmonella strains in food samples contaminated at fractional levels. Unpaired comparisons revealed no significant difference between the results for each given assay and the results obtained with the reference assay. However, analysis of paired culture-confirmed results revealed assay false-negative rates of 4 to 26% for dry pet food and 12 to 16% for dark chocolate. Overall, our data indicate that rapid assays may have high false-negative rates when performance is evaluated under challenging conditions, including low-moisture matrices, strains that are difficult to detect, injured cells, and low inoculum

  6. Pathogenesis and phylogenetic analyses of canine distemper virus strain ZJ7 isolate from domestic dogs in China

    Directory of Open Access Journals (Sweden)

    Tan Bin

    2011-11-01

    Full Text Available Abstract A new isolate of canine distemper virus (CDV, named ZJ7, was isolated from lung tissues of a dog suspected with CDV infection using MDCK cells. The ZJ7 isolate induced cytopathogenic effects of syncytia in MDCK cell after six passages. In order to evaluate pathogenesis of ZJ7 strain, three CDV sero-negative dogs were intranasally inoculated with its virus suspension. All infected dogs developed clinical signs of severe bloody diarrhea, conjunctivitis, ocular discharge, nasal discharge and coughing, fever and weight loss at 21 dpi, whereas the mock group infected with DMEM were normal. The results demonstrated that CDV-ZJ7 strain isolated by MDCK cell was virulent, and the nucleotide and amino acid sequences of strain ZJ7 had no change after isolation by MDCK cell when compared with the original virus from the fresh tissues. Molecular and phylogenetic analyses for the nucleocapsid (N, phosphoprotein (P and receptor binding haemagglutinin (H gene of the ZJ7 isolate clearly showed it is joins to the Asia 1 group cluster of CDV strains, the predominant genotype in China.

  7. Designing and comparison study of rapid detection methods of resistance to injectable drugs in clinical strains of Mycobacterium tuberculosis

    Directory of Open Access Journals (Sweden)

    Fatemeh Salehi

    2012-01-01

    Full Text Available Introduction: In this study, some molecular methods were designed for rapid detection of resistance to kanamycin and amikacin.Materials and methods: Among 120 clinical isolates of mycobacterium tuberculosis, 70 strains were selected for evaluation of possible mutations. A PCR-RFLP method was designed for detection of wild type (using enzyme ajii and mutant from (BstFNI enzyme of the isolates. Furthermore, allele specific method (as PCR was designed for detection mutations in codons 1401 and 1402 gene rrs. Some selected isolates were sequenced.Results: In PCR-RFLP method, among the 70 strains examined by BstFNI enzyme, could detect 17 mutant strains among 24 phenotypicaly resistant and 44 non-mutant isolates from 46 susceptible isolates. The sensitivity of this method was %70.83 and specificity was %95.65 on the other hand, 12 mutant from 20 resistant strains and 29 non-mutant strains from 32 susceptible strains were detected by AjiI enzyme. The sensitivity and specificity of this method was 60 and %90.62, respectively. In MAS PCR, 3 mutants from 6 resistant strains and 12 non-mutants from 17 resistant strains were detected. The sensitivity of this method was 50 and specificity was 70.58. Results of sequencing method confirmed the results of molecular methods.Discussion and conclusion: PCR-RFLP method by BstFNI enzyme was the best method for rapid detection of Mycobacterium tuberculosis resistant to second-line injectable drugs and was recommended for routine use.

  8. Detection of virulence genes in Uropathogenic E. coli (UPEC strains by Multiplex-PCR method

    Directory of Open Access Journals (Sweden)

    Javad Mohammadi

    2017-06-01

    Full Text Available Background & Objectives: Urinary tract infection caused by E. coli is one of the most common illnesses in all age groups worldwide. Presence of virulence genes is a key factor in bacterial pathogens in uroepithelial cells. The present study was performed to detect iha, iroN, ompT genes in the Uropathogenic E.coli isolates from clinical samples using multiplex-PCR method in Kerman. Materials & Methods: In this descriptive cross-sectional study, 200 samples of patients with urinary tract infections in Kerman hospitals were collected. After biochemical and microbiological tests, all strains were tested with regard to the presence of iha, iroN, and ompT genes using multiplex-PCR method. Results: The results of Multiplex-PCR showed that all specimens had one, two, or three virulence genes simultaneously. The highest and lowest frequency distribution of genes was related to iha (56.7% and iroN (20% respectively. Conclusion: According to the prevalence of urinary tract infection in the community and distribution of resistance and virulence factors, the fast and accurate detection of the strains and virulence genes is necessary

  9. Bioavailable nitrate detection in water by an immobilized luminescent cyanobacterial reporter strain.

    Science.gov (United States)

    Mbeunkui, F; Richaud, C; Etienne, A-L; Schmid, R D; Bachmann, T T

    2002-11-01

    Cyanobacteria are a major group of photosynthetic bacteria that can accumulate in surface water as so-called "blooms" in response to environmental factors such as temperature, light and certain nutrients such as N, P, and Fe. Some species of cyanobacteria produce toxins, causing a considerable danger for human and livestock health. As a consequence, monitoring of bloom formation and toxin production of drinking water supplies has become a major concern. To enable prediction and monitoring of cyanobacterial blooms, tools to detect nutrient bioavailability in water would be advantageous. A whole-cell biosensor was developed for monitoring nitrate (NO(3-)) bioavailability in aquatic ecosystems using the recombinant bioluminescent cyanobacterial strain Synechocystis PCC 6803 harboring an insertion of a luxAB-kmr fusion with nblA1 in its chromosomal DNA, leading to PnblA::luxAB-kmr. This reporter strain was designated N1LuxKm. Cells were immobilized in microtiter plates and showed a dose-dependent response to nitrate deprivation. The resultant CyanoSensor could detect nitrate in the 4-100 micro M concentration range after a sample incubation time of 10 h under continuous illumination (50 micro E m(-2) s(-1)). The optimal temperature for sensor operation was 29 degrees C and the immobilized biosensor could be stored at 4 degrees C in dark for about 1 month without significant loss of sensitivity.

  10. Bioavailable nitrate detection in water by an immobilized luminescent cyanobacterial reporter strain

    Energy Technology Data Exchange (ETDEWEB)

    Mbeunkui, F.; Schmid, R.D.; Bachmann, T.T. [Inst. of Technical Biochemistry, Univ. of Stuttgart, Stuttgart (Germany); Richaud, C.; Etienne, A.L. [UMR 8543, Centre National de la Recherche Scientifique, Ecole Normale Superieure, Paris (France)

    2003-07-01

    Cyanobacteria are a major group of photosynthetic bacteria that can accumulate in surface water as so-called ''blooms'' in response to environmental factors such as temperature, light and certain nutrients such as N, P, and Fe. Some species of cyanobacteria produce toxins, causing a considerable danger for human and livestock health. As a consequence, monitoring of bloom formation and toxin production of drinking water supplies has become a major concern. To enable prediction and monitoring of cyanobacterial blooms, tools to detect nutrient bioavailability in water would be advantageous. A whole-cell biosensor was developed for monitoring nitrate (NO{sup 3-}) bioavailability in aquatic ecosystems using the recombinant bioluminescent cyanobacterial strain Synechocystis PCC 6803 harboring an insertion of a luxAB-kmr fusion with nblA1 in its chromosomal DNA, leading to PnblA::luxAB-kmr. This reporter strain was designated N1LuxKm. Cells were immobilized in microtiter plates and showed a dose-dependent response to nitrate deprivation. The resultant CyanoSensor could detect nitrate in the 4-100 {mu}M concentration range after a sample incubation time of 10 h under continuous illumination (50 {mu}E m{sup -2} s{sup -1}). The optimal temperature for sensor operation was 29 C and the immobilized biosensor could be stored at 4 C in dark for about 1 month without significant loss of sensitivity. (orig.)

  11. Two novel Ehrlichia strains detected in Amblyomma tigrinum ticks associated to dogs in peri-urban areas of Argentina.

    Science.gov (United States)

    Cicuttin, Gabriel L; De Salvo, M Nazarena; Nava, Santiago

    2017-08-01

    The aim of this work was to describe two novel strains of Ehrlichia associated to Amblyomma tigrinum from Argentina. Molecular detection of agents belonging to the family Anaplasmataceae was performed targeting three different loci: 16S rRNA gene, dsb gene and a fragment of groESL heat shock operon. The results have shown that two different strains of Ehrlichia sp. associated to A. tigrinum are circulating in peri-urban areas of Argentina. The Ehrlichia strain detected in ticks from San Luis Province, named as Ehrlichia sp. strain San Luis, is closely related to the Ehrlichia chaffeensis. The novel Ehrlichia strain detected in Córdoba Province, named as Ehrlichia sp. strain Córdoba, is phylogenetically related to three Ehrlichia strains from Brazil, two of them isolated from wild carnivorous and the third one isolated from horse. Even though Ehrlichia sp. strain Córdoba was clustered with the three Ehrlichia strains from Brazil, the genetic similarity was too low to consider them as the same taxonomic entity. Blood samples of dogs were positive to Anaplasma platys. The association of these two novel strains with A. tigrinum has epidemiological relevance because adult stages of this tick species are common parasite of dogs in rural and peri-urban areas and they are aggressive to humans. The presence of these two novel Ehrlichia strains implies a potential epidemiological risk in Argentina because the species of the genus Ehrlichia are known to be pathogenic to both domestic mammals and humans. Copyright © 2017 Elsevier Ltd. All rights reserved.

  12. Differentiation of UK endemic strains of Salmonella enterica serovar Newport from epidemic North American strains by PCR detection of a truncated bapA chromosomal gene.

    Science.gov (United States)

    Horton, R A; Card, R; Randall, L P; Teale, C J

    2016-02-01

    The aim of this study was to develop a PCR test to detect chromosomal differences between epidemic multidrug resistant (epi-MDR) strains of Salmonella enterica serovar Newport (S. Newport) and non-epi-MDR strains of S. Newport that are endemic to the United Kingdom (UK). Sequence analysis of the biofilm-associated protein A gene (bapA) showed that epi-MDR strains of S. Newport from the United States of America (USA) had a deletion of 309 bp, which was not present in non-epi-MDR strains of S. Newport from the UK. A PCR test was developed using primers designed to target this difference and was applied to a panel of S. Newport isolates comprising of strains from the UK (n=20, non-epi-MDR), from the USA (n=10, epi-MDR) and from Canada (n=7). A second panel of isolates (n=73) was used to assess the test specificity, and these isolates consisted of non-Newport Salmonella serovars (n=25), and other epidemic serovars (n=48). Epi-MDR S. Newport isolates produced a characteristic 505 bp amplicon, whereas non-epi-MDR S. Newport isolates produced an 814 bp amplicon. The bapA PCR has potential to discriminate between these S. Newport strains irrespective of their carrying resistance genes. Crown Copyright © 2015. Published by Elsevier Ltd. All rights reserved.

  13. Development of a multiplex Q-PCR to detect Trichoderma harzianum Rifai strain T22 in plant roots.

    Science.gov (United States)

    Horn, Ivo R; van Rijn, Menno; Zwetsloot, Tom J J; Basmagi, Said; Dirks-Mulder, Anita; van Leeuwen, Willem B; Ravensberg, Willem J; Gravendeel, Barbara

    2016-02-01

    The fungal species Trichoderma harzianum is widely used as a biological agent in crop protection. To verify the continued presence of this fungus on plant roots manually inoculated with T. harzianum strain T22, a Q-PCR was designed using specific probes for this particular strain. To develop these molecular diagnostic tools, genome mining was first carried out to retrieve putative new regions by which different strains of T. harzianum could be distinguished. Subsequently, Sanger sequencing of the L-aminoacid oxidase gene (aox1) in T. harzianum was applied to determine the mutations differing between various strains isolated from the Trichoderma collection of Koppert Biological Systems. Based on the sequence information obtained, a set of hydrolysis probes was subsequently developed which discriminated T. harzianum T22 strains varying in only a single nucleotide. Probes designed for two strains uniquely recognized the respective strains in Q-PCR with a detection limit of 12,5ng DNA. Titration assays in which T. harzianum DNA from distinct strains was varied further underscored the specificity of the probes. Lastly, fungal DNA extracted from roots of greenhouse cultured tomato plants was analyzed using the probe-based assay. DNA from T. harzianum strain T22 could readily be identified on roots of greenhouse reared tomato plants inoculated with varying concentrations up to one week after treatment with a detection limit of 3e6 colony forming units of T. harzianum T22. We conclude that the Q-PCR method is a reliable and robust method for assessing the presence and quantity of T. harzianum strain T22 in manually inoculated plant material. Our method provides scope for the development of DNA based strain specific identification of additional strains of Trichoderma and other fungal biological control agents. Copyright © 2015 Elsevier B.V. All rights reserved.

  14. File list: NoD.CDV.10.AllAg.Brachiocephalic_endothelial_cells [Chip-atlas[Archive

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  18. File list: Oth.CDV.10.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

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  2. File list: Pol.CDV.20.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.20.AllAg.Coronary_artery_endothelial_cells hg19 RNA polymerase Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.20.AllAg.Coronary_artery_endothelial_cells.bed ...

  3. File list: InP.CDV.50.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.50.AllAg.Coronary_artery_endothelial_cells hg19 Input control Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.50.AllAg.Coronary_artery_endothelial_cells.bed ...

  4. File list: His.CDV.50.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.50.AllAg.Coronary_artery_smooth_muscle hg19 Histone Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.50.AllAg.Coronary_artery_smooth_muscle.bed ...

  5. File list: DNS.CDV.10.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.10.AllAg.Coronary_artery_endothelial_cells hg19 DNase-seq Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.10.AllAg.Coronary_artery_endothelial_cells.bed ...

  6. File list: NoD.CDV.10.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.10.AllAg.Coronary_artery_smooth_muscle hg19 No description Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.10.AllAg.Coronary_artery_smooth_muscle.bed ...

  7. File list: Unc.CDV.10.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.10.AllAg.Coronary_artery_smooth_muscle hg19 Unclassified Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.10.AllAg.Coronary_artery_smooth_muscle.bed ...

  8. File list: Unc.CDV.20.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.20.AllAg.Coronary_artery_smooth_muscle hg19 Unclassified Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.20.AllAg.Coronary_artery_smooth_muscle.bed ...

  9. File list: His.CDV.10.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.10.AllAg.Coronary_artery_smooth_muscle hg19 Histone Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.10.AllAg.Coronary_artery_smooth_muscle.bed ...

  10. File list: ALL.CDV.50.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.50.AllAg.Coronary_artery_endothelial_cells hg19 All antigens Cardiovascular Coronary arte...RX014592,DRX014602,DRX014641,DRX014600 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.50.AllAg.Coronary_artery_endothelial_cells.bed ...

  11. File list: Pol.CDV.50.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.50.AllAg.Coronary_artery_smooth_muscle hg19 RNA polymerase Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.50.AllAg.Coronary_artery_smooth_muscle.bed ...

  12. File list: Unc.CDV.20.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.20.AllAg.Coronary_artery_endothelial_cells hg19 Unclassified Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.20.AllAg.Coronary_artery_endothelial_cells.bed ...

  13. File list: DNS.CDV.05.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.05.AllAg.Coronary_artery_endothelial_cells hg19 DNase-seq Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.05.AllAg.Coronary_artery_endothelial_cells.bed ...

  14. File list: NoD.CDV.50.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.50.AllAg.Coronary_artery_endothelial_cells hg19 No description Cardiovascular Coronary arte...,DRX014592,DRX014602,DRX014641,DRX014600 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.50.AllAg.Coronary_artery_endothelial_cells.bed ...

  15. File list: Pol.CDV.10.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.10.AllAg.Coronary_artery_endothelial_cells hg19 RNA polymerase Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.10.AllAg.Coronary_artery_endothelial_cells.bed ...

  16. File list: DNS.CDV.10.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.10.AllAg.Coronary_artery_smooth_muscle hg19 DNase-seq Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.10.AllAg.Coronary_artery_smooth_muscle.bed ...

  17. File list: Oth.CDV.20.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.20.AllAg.Coronary_artery_smooth_muscle hg19 TFs and others Cardiovascular Coronary arte...osciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.20.AllAg.Coronary_artery_smooth_muscle.bed ...

  18. File list: Unc.CDV.05.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.05.AllAg.Coronary_artery_endothelial_cells hg19 Unclassified Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.05.AllAg.Coronary_artery_endothelial_cells.bed ...

  19. File list: NoD.CDV.50.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.50.AllAg.Coronary_artery_smooth_muscle hg19 No description Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.50.AllAg.Coronary_artery_smooth_muscle.bed ...

  20. File list: ALL.CDV.05.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.Coronary_artery_endothelial_cells hg19 All antigens Cardiovascular Coronary arte...RX014636,DRX014602,DRX014641,DRX014600 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.05.AllAg.Coronary_artery_endothelial_cells.bed ...

  1. File list: ALL.CDV.10.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.Coronary_artery_smooth_muscle hg19 All antigens Cardiovascular Coronary arte...ttp://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.10.AllAg.Coronary_artery_smooth_muscle.bed ...

  2. File list: ALL.CDV.10.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.10.AllAg.Coronary_artery_endothelial_cells hg19 All antigens Cardiovascular Coronary arte...RX014602,DRX014587,DRX014600,DRX014639 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.10.AllAg.Coronary_artery_endothelial_cells.bed ...

  3. File list: InP.CDV.50.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.50.AllAg.Coronary_artery_smooth_muscle hg19 Input control Cardiovascular Coronary arte...ry smooth muscle SRX699739,SRX699736 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.50.AllAg.Coronary_artery_smooth_muscle.bed ...

  4. File list: DNS.CDV.50.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.50.AllAg.Coronary_artery_endothelial_cells hg19 DNase-seq Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.50.AllAg.Coronary_artery_endothelial_cells.bed ...

  5. File list: Unc.CDV.50.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.50.AllAg.Coronary_artery_smooth_muscle hg19 Unclassified Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.50.AllAg.Coronary_artery_smooth_muscle.bed ...

  6. File list: NoD.CDV.10.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available NoD.CDV.10.AllAg.Coronary_artery_endothelial_cells hg19 No description Cardiovascular Coronary arte...,DRX014602,DRX014587,DRX014600,DRX014639 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/NoD.CDV.10.AllAg.Coronary_artery_endothelial_cells.bed ...

  7. File list: Oth.CDV.05.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.05.AllAg.Coronary_artery_endothelial_cells hg19 TFs and others Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.05.AllAg.Coronary_artery_endothelial_cells.bed ...

  8. File list: Pol.CDV.05.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.05.AllAg.Coronary_artery_endothelial_cells hg19 RNA polymerase Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.05.AllAg.Coronary_artery_endothelial_cells.bed ...

  9. File list: ALL.CDV.20.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.Coronary_artery_smooth_muscle hg19 All antigens Cardiovascular Coronary arte...ttp://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.20.AllAg.Coronary_artery_smooth_muscle.bed ...

  10. File list: Unc.CDV.10.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Unc.CDV.10.AllAg.Coronary_artery_endothelial_cells hg19 Unclassified Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Unc.CDV.10.AllAg.Coronary_artery_endothelial_cells.bed ...

  11. File list: Pol.CDV.50.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Pol.CDV.50.AllAg.Coronary_artery_endothelial_cells hg19 RNA polymerase Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Pol.CDV.50.AllAg.Coronary_artery_endothelial_cells.bed ...

  12. File list: Oth.CDV.50.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available Oth.CDV.50.AllAg.Coronary_artery_endothelial_cells hg19 TFs and others Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/Oth.CDV.50.AllAg.Coronary_artery_endothelial_cells.bed ...

  13. File list: ALL.CDV.20.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.20.AllAg.Coronary_artery_endothelial_cells hg19 All antigens Cardiovascular Coronary arte...RX014587,DRX014639,DRX014600,DRX014602 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.20.AllAg.Coronary_artery_endothelial_cells.bed ...

  14. File list: InP.CDV.05.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available InP.CDV.05.AllAg.Coronary_artery_smooth_muscle hg19 Input control Cardiovascular Coronary arte...ry smooth muscle SRX699739,SRX699736 http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/InP.CDV.05.AllAg.Coronary_artery_smooth_muscle.bed ...

  15. File list: DNS.CDV.50.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.50.AllAg.Coronary_artery_smooth_muscle hg19 DNase-seq Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.50.AllAg.Coronary_artery_smooth_muscle.bed ...

  16. File list: His.CDV.20.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.20.AllAg.Coronary_artery_smooth_muscle hg19 Histone Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.20.AllAg.Coronary_artery_smooth_muscle.bed ...

  17. File list: His.CDV.20.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.20.AllAg.Coronary_artery_endothelial_cells hg19 Histone Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.20.AllAg.Coronary_artery_endothelial_cells.bed ...

  18. File list: ALL.CDV.05.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available ALL.CDV.05.AllAg.Coronary_artery_smooth_muscle hg19 All antigens Cardiovascular Coronary arte...ttp://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/ALL.CDV.05.AllAg.Coronary_artery_smooth_muscle.bed ...

  19. File list: DNS.CDV.20.AllAg.Coronary_artery_endothelial_cells [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available DNS.CDV.20.AllAg.Coronary_artery_endothelial_cells hg19 DNase-seq Cardiovascular Coronary arte...ry endothelial cells http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/DNS.CDV.20.AllAg.Coronary_artery_endothelial_cells.bed ...

  20. File list: His.CDV.05.AllAg.Coronary_artery_smooth_muscle [Chip-atlas[Archive

    Lifescience Database Archive (English)

    Full Text Available His.CDV.05.AllAg.Coronary_artery_smooth_muscle hg19 Histone Cardiovascular Coronary arte...ry smooth muscle http://dbarchive.biosciencedbc.jp/kyushu-u/hg19/assembled/His.CDV.05.AllAg.Coronary_artery_smooth_muscle.bed ...