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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Tissue Antigensarrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Tissue Antigens
Article . 2014 . Peer-reviewed
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Data sources: Crossref
Tissue Antigens
Article . 2014
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Association of HLA‐B27 and ERAP1 with ankylosing spondylitis susceptibility in Beijing Han Chinese

Authors: Z, Zhang; D, Dai; K, Yu; F, Yuan; J, Jin; L, Ding; Y, Hao; +6 Authors

Association of HLA‐B27 and ERAP1 with ankylosing spondylitis susceptibility in Beijing Han Chinese

Abstract

AbstractThis study investigated the genetic polymorphisms of HLA‐B27, together with polymorphisms on endoplasmic reticulum aminopeptidase 1 (ERAP1), and susceptibility for ankylosing spondylitis (AS) in the Beijing Han population. A case‐control study was carried out for 602 AS patient samples and 619 matched controls of Han Chinese. HLA‐B27 genotyping was performed by polymerase chain reaction‐sequence specific primers (PCR‐SSP), and four ERAP1 SNPs (rs27037, rs27980, rs27582, and rs27434) were selected and genotyped on the Sequenom iPlex platform (Sequenom, San Diego, CA). Association analysis was performed using the likelihood ratio χ2 test. This study identified four HLA‐B27 alleles in Beijing Han AS patients, B*27:02, B*27:04, B*27:05, and B*27:07, of which B*27:05 was the most significant geographical different subtype among AS patients in Chinese. Our results confirmed that HLA‐B27 was strongly associated with AS (P = 1.9 × 10−150), and the most strongly associated alleles were B*27:04, B*27:05, and B*27:02. Our study also confirmed a weak association between ERAP1 (rs27434) and AS. We also observed that for HLA‐B*27:02 and HLA‐B*27:04 positive AS patients, rs27434 and rs27582 were associated with AS. In contrast, for HLA‐B27‐negative and HLA‐B*27:05‐positive AS patients, this association was not observed. This is the first study to show that both B27 and ERAP1 are AS genetic susceptibility genes in Beijing Han. Interactions between ERAP1 and HLA‐B*27:02 and B*27:04 may play an important role in the AS pathogenesis.

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Keywords

Adult, Male, Genetic Linkage, Gene Expression, Aminopeptidases, Polymorphism, Single Nucleotide, Minor Histocompatibility Antigens, Asian People, Gene Frequency, Case-Control Studies, Humans, Female, Genetic Predisposition to Disease, Spondylitis, Ankylosing, Alleles, HLA-B27 Antigen

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
26
Top 10%
Top 10%
Top 10%
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