The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus.
about
Genome-Wide Analysis in Brazilians Reveals Highly Differentiated Native American Genome RegionsPolymorphisms in the inflammatory genes CIITA, CLEC16A and IFNG influence BMD, bone loss and fracture in elderly women.CIITA rs4774 and rs6498122 polymorphisms are associated with oral lichen planus in Chinese people: a case-control study.Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus.Association of EVI5 rs11808092, CD58 rs2300747, and CIITA rs3087456 polymorphisms with multiple sclerosis risk: A meta-analysisFunctions of NOD-Like Receptors in Human Diseases.From Identification to Characterization of the Multiple Sclerosis Susceptibility Gene CLEC16A.MHC2TA and FCRL3 genes are not associated with rheumatoid arthritis in Mexican patients.Effects of C2ta genetic polymorphisms on MHC class II expression and autoimmune diseases.Genotypic and phenotypic predictors of inflammation in patients with chronic kidney disease.
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P2860
The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
The rs4774 CIITA missense vari ...... systemic lupus erythematosus.
@ast
The rs4774 CIITA missense vari ...... systemic lupus erythematosus.
@en
type
label
The rs4774 CIITA missense vari ...... systemic lupus erythematosus.
@ast
The rs4774 CIITA missense vari ...... systemic lupus erythematosus.
@en
prefLabel
The rs4774 CIITA missense vari ...... systemic lupus erythematosus.
@ast
The rs4774 CIITA missense vari ...... systemic lupus erythematosus.
@en
P2093
P2860
P356
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P1476
The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus
@en
P2093
B A Goldstein
J B Harley
K B Beckman
L A Criswell
L F Barcellos
M F Seldin
P G Bronson
P2860
P2888
P304
P356
10.1038/GENE.2011.36
P577
2011-05-26T00:00:00Z