نتایج جستجو برای: genetic locus

تعداد نتایج: 656620  

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2009
Brian J Bennett Susanna S Wang Xuping Wang Xiaohui Wu Aldons J Lusis

OBJECTIVE We sought to determine the genetic factors contributing to atherosclerotic plaque size and cellular composition in the innominate artery, a murine model of advanced atherosclerosis. METHODS AND RESULTS We examined genetic contributions to innominate atherosclerotic plaque size and cellular composition in an intercross between C57BL/6J.Apoe(-/-), a strain susceptible to aortic lesion...

Journal: :Current Biology 2005
Annabelle Lewis Lisa Redrup

The imprinted Dlk1-Gtl2 region of the mammalian genome - which in sheep encompasses the Callipyge locus, known for its unusual mode of inheritance - encodes a number of maternally expressed miRNAs. Five of these miRNAs, hosted by the antisense transcript antiPeg11, have now been shown to target degradation of the paternally expressed Peg11 mRNA by an RNAi-mediated mechanism.

2013
I. C. McManus Angus Davison John A. L. Armour

Rightand left-handedness run in families, show greater concordance in monozygotic than dizygotic twins, and are well described by single-locus Mendelian models. Here we summarize a large genome-wide association study (GWAS) that finds no significant associations with handedness and is consistent with a meta-analysis of GWASs. The GWAS had 99% power to detect a single locus using the conventiona...

2018
S. Manna B.D. Ortika E.M. Dunne K.E. Holt M. Kama F.M. Russell J. Hinds C. Satzke

OBJECTIVES As part of annual cross-sectional Streptococcus pneumoniae carriage surveys in Fiji (2012-2015), we detected pneumococci in over 100 nasopharyngeal swabs that serotyped as '11F-like' by microarray. We examined the genetic basis of this divergence in the 11F-like capsular polysaccharide (cps) locus compared to the reference 11F cps sequence. The impact of this diversity on capsule phe...

2011
Carl Vangestel Joachim Mergeay Deborah A. Dawson Viki Vandomme Luc Lens

Fluctuating asymmetry (FA), a measure of developmental instability, has been hypothesized to increase with genetic stress. Despite numerous studies providing empirical evidence for associations between FA and genome-wide properties such as multi-locus heterozygosity, support for single-locus effects remains scant. Here we test if, and to what extent, FA co-varies with single- and multilocus mar...

2013
I C McManus Angus Davison John A L Armour

Right- and left-handedness run in families, show greater concordance in monozygotic than dizygotic twins, and are well described by single-locus Mendelian models. Here we summarize a large genome-wide association study (GWAS) that finds no significant associations with handedness and is consistent with a meta-analysis of GWASs. The GWAS had 99% power to detect a single locus using the conventio...

Journal: :پژوهش های علوم دامی ایران 0
سریرا بهروزی‎نیا سید ضیاءالدین میرحسینی فضل‎الله افراز علیرضا سهرابی سید ابوالقاسم محمدی صالح شهبازی سید بنیامین دلیرصفت

this study compares diversity patterns of five microsatellite (ssr) markers in two iranian native horse populations (turkoman sahra and turkoman jergelan) to infer relationships between them and to compare levels of their polymorphism for use in conservation efforts. two populations across microsatellite loci had significant deviations from hardy-weinberg equilibrium. average number of alleles ...

2015
Jie Zhang Qixiang Zhang Tangren Cheng Weiru Yang Huitang Pan Junjun Zhong Long Huang Enze Liu

High-density genetic map is a valuable tool for fine mapping locus controlling a specific trait especially for perennial woody plants. In this study, we firstly constructed a high-density genetic map of mei (Prunus mume) using SLAF markers, developed by specific locus amplified fragment sequencing (SLAF-seq). The linkage map contains 8,007 markers, with a mean marker distance of 0.195 cM, makin...

Journal: :American journal of human genetics 2006
V Anttila M Kallela G Oswell M A Kaunisto D R Nyholt E Hamalainen H Havanka M Ilmavirta J Terwilliger E Sobel L Peltonen J Kaprio M Farkkila M Wessman A Palotie

The commonly used "end diagnosis" phenotype that is adopted in linkage and association studies of complex traits is likely to represent an oversimplified model of the genetic background of a disease. This is also likely to be the case for common types of migraine, for which no convincingly associated genetic variants have been reported. In headache disorders, most genetic studies have used end ...

E. Hamedmonfared Gh. Nikbakht Brujeni, H. Mahmoudzadeh H. Rezaei M. Emam R. Talebnia Jahromi

Several studies have focused on polymorphisms of major histocompatibility complex (MHC) in sheep, Ovar-MHC. This molecule plays a pivotal role in antigen presentation for eliciting immune responses against invading pathogens. The best-characterized genetic control of disease resistance and immune response in animals is associated with MHC. Numerous molecular genetic investigations have been und...

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