نتایج جستجو برای: ovar drb1 gene

تعداد نتایج: 1143501  

2010
Judith Field Sharon R. Browning Laura J. Johnson Patrick Danoy Michael D. Varney Brian D. Tait Kaushal S. Gandhi Jac C. Charlesworth Robert N. Heard Graeme J. Stewart Trevor J. Kilpatrick Simon J. Foote Melanie Bahlo Helmut Butzkueven James Wiley David R. Booth Bruce V. Taylor Matthew A. Brown Justin P. Rubio Jim Stankovich

We conducted an association study across the human leukocyte antigen (HLA) complex to identify loci associated with multiple sclerosis (MS). Comparing 1927 SNPs in 1618 MS cases and 3413 controls of European ancestry, we identified seven SNPs that were independently associated with MS conditional on the others (each P ≤ 4 x 10(-6)). All associations were significant in an independent replicatio...

Journal: :Annals of hepatology 2009
Genaro Vázquez-Elizondo Guadalupe Ponciano-Rodríguez Misael Uribe Nahum Méndez-Sánchez

BACKGROUND AND AIM Primary biliary cirrhosis (PBC) is a chronic cholestatic disease of autoimmune origin and has a genetic component. Although it has been reported that the prevalence of the HLA-DRB1*08 allele is high in various populations, the prevalence of HLA alleles in Mexican PBC patients has not been described. The aim of this study was to quantify the prevalence of HLA-B/-DR alleles in ...

2010
Caroline Brorsson Niclas Tue Hansen Regine Bergholdt Søren Brunak Flemming Pociot

BACKGROUND The individual contribution of genes in the HLA region to the risk of developing type 1 diabetes (T1D) is confounded by the high linkage disequilibrium (LD) in this region. Using a novel approach we have combined genetic association data with information on functional protein-protein interactions to elucidate risk independent of LD and to place the genetic association into a function...

2015
Hao Sun Zhaoqing Yang Keqin Lin Shuyuan Liu Kai Huang Xiuyun Wang Jiayou Chu Xiaoqin Huang Francesc Calafell

Pathogen-driven balancing selection determines the richness of human leukocyte antigen (HLA) alleles. Changes in the pathogen spectrum may cause corresponding changes in HLA loci. Approximately 700 years ago, a Mongolian population moved from the north of China to the Yunnan region in the south of China. The pathogen spectrum in the south of China differs from that in the north. In this study, ...

Journal: :cell journal 0

objective: type 1 diabetes mellitus (t1d) is an autoimmune and multifactorial disorder. subsequent analysis on human leukocyte antigen ( hla) region shows that hla-drb1 and -dqb1 genes have the strongest association with t1d. in this study, for the first time, we investigated the influence of gender on the hla-drb1 and -dqb1 association with type 1 diabetes mellitus in iranian patients in order...

2011
Qinqin Pan Su Fan Xiaoyan Wang Xing Zhao Meng Pan Chengya Wang Jie Shen

The present study was aimed to analyze the frequencies of human leukocyte antigen (HLA)-A, -B, and -DRB1 alleles and A-B-DRB1, A-B, A-DRB1 and B-DRB1 haplotypes in inhabitants of Guizhou province, China. All samples were typed in the HLA-A,-B, and -DRB1 loci using the polymerase chain reaction-reverse sequence specific oligonucleotide probe (PCR-rSSOP) method and HLA polymorphisms were analyzed...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم پزشکی 1389

مقدمه :یکی از انواع شایع آلرژی رینیت آلرژی است .عامل اصلی این نوع آلرژی گرده گل ها، درختان و علف های هرز است .این گیاهان به طور عمده در بهار و تابستان گرده افشانی می کنند . یکی از این گیاهان آرتمیسیا ولگاریس است که در اواخر تابستان گرده افشانی می کند و از شیوع با?یی در سراسر جهان از جمله ایران برخوردار است . ارتباط مهمی بین آلل های hla-drb1 و آلرژی به گیاه آرتمیسیا ولگاریس در شهرستان سبزوار واق...

2013
Inger-Lise Mero Marte W. Gustavsen Hanne S. Sæther Siri T. Flåm Pål Berg-Hansen Helle B. Søndergaard Poul Erik H. Jensen Tone Berge Anja Bjølgerud Aslaug Muggerud Jan H. Aarseth Kjell-Morten Myhr Elisabeth G. Celius Finn Sellebjerg Jan Hillert Lars Alfredsson Tomas Olsson Annette Bang Oturai Ingrid Kockum Benedicte A. Lie Bettina Kulle Andreassen Hanne F. Harbo

The presence of oligoclonal bands (OCB) in cerebrospinal fluid (CSF) is a typical finding in multiple sclerosis (MS). We applied data from Norwegian, Swedish and Danish (i.e. Scandinavian) MS patients from a genome-wide association study (GWAS) to search for genetic differences in MS relating to OCB status. GWAS data was compared in 1367 OCB positive and 161 OCB negative Scandinavian MS patient...

2014
Nathali Kaushansky Avraham Ben-Nun

Susceptibility to multiple sclerosis (MS) has been linked mainly to the HLA-DRB1 locus, with the HLA-DR15 haplotype (DRB1*1501-DQA1*0102-DQB1*0602-DRB5*0101) dominating MS risk in Caucasians. Although genes in the HLA-II region, particularly DRB1*1501, DQA1*0102-DQB1*0602, are in tight linkage disequilibrium, genome-wide-association, and gene candidate studies identified the DRB1*15:01 allele a...

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