Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.
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Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitisRecent Insights Into the Genetics of Inflammatory Bowel DiseaseGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseA candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritisA human type 1 diabetes susceptibility locus maps to chromosome 21q22.3The CD40, CTLA-4, thyroglobulin, TSH receptor, and PTPN22 gene quintet and its contribution to thyroid autoimmunity: back to the futureRheumatoid arthritis seropositive for the rheumatoid factor is linked to the protein tyrosine phosphatase nonreceptor 22-620W alleleAutoimmune diseases - connecting risk alleles with molecular traits of the immune system.PTPN22 R620W Polymorphism is Associated with Myasthenia Gravis Risk: A Systematic Review and Meta-AnalysisClinical perspectives on lupus genetics: advances and opportunitiesCurrent aspects of vitiligo geneticsSolving the puzzle of autoimmunity: critical questionsAnalysis of interleukin-23 receptor (IL23R) gene polymorphisms in systemic lupus erythematosusRecent advances in the genetics of autoimmune diseaseGenetic variants of CC chemokine genes in experimental autoimmune encephalomyelitis, multiple sclerosis and rheumatoid arthritisHigh basal activity of the PTPN22 gain-of-function variant blunts leukocyte responsiveness negatively affecting IL-10 production in ANCA vasculitisPTPN22 R620W polymorphism and ANCA disease risk in white populations: a metaanalysisPleiotropy in complex traits: challenges and strategiesThe contribution of genetic variation and infection to the pathogenesis of ANCA-associated systemic vasculitisTYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traitsApplying semantic web technologies for phenome-wide scan using an electronic health record linked BiobankNovel associations for hypothyroidism include known autoimmune risk lociGenome-wide analysis of haplotype interaction for the data from the North American Rheumatoid Arthritis ConsortiumNetwork biology concepts in complex disease comorbiditiesA genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis.The R620W C/T polymorphism of the gene PTPN22 is associated with SLE independently of the association of PDCD1.A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseasesPervasive sharing of genetic effects in autoimmune disease.rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype.Overview of the Type I Diabetes Genetics Consortium.Genetics of Autoimmune Thyroiditis in Type 1 Diabetes Reveals a Novel Association With DPB1*0201: Data From the Type 1 Diabetes Genetics Consortium.On the Wegener granulomatosis associated region on chromosome 6p21.3.A functional PTPN22 polymorphism associated with several autoimmune diseases is not associated with IgA deficiency in the Spanish population.The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes.Modeling the effect of PTPN22 in rheumatoid arthritis.Specificity of the STAT4 genetic association for severe disease manifestations of systemic lupus erythematosusIL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor production.Systems biology of lupus: mapping the impact of genomic and environmental factors on gene expression signatures, cellular signaling, metabolic pathways, hormonal and cytokine imbalance, and selecting targets for treatment.Lymphoid tyrosine phosphatase R620W variant and inflammatory bowel disease in Tunisia.Psoriasis and multiple sclerosis: is there a link?
P2860
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P2860
Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.
description
2005 nî lūn-bûn
@nan
2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Analysis of families in the mu ...... ultiple autoimmune phenotypes.
@ast
Analysis of families in the mu ...... ultiple autoimmune phenotypes.
@en
type
label
Analysis of families in the mu ...... ultiple autoimmune phenotypes.
@ast
Analysis of families in the mu ...... ultiple autoimmune phenotypes.
@en
prefLabel
Analysis of families in the mu ...... ultiple autoimmune phenotypes.
@ast
Analysis of families in the mu ...... ultiple autoimmune phenotypes.
@en
P2093
P2860
P356
P1476
Analysis of families in the mu ...... multiple autoimmune phenotypes
@en
P2093
Ann B Begovich
Annette T Lee
Bonnie Gonzales
Jill Novitzke
Kathy L Moser
Kirsten A Pfeiffer
Lindsey A Criswell
Marlena Kern
Raymond F Lum
Timothy W Behrens
P2860
P304
P356
10.1086/429096
P407
P577
2005-02-17T00:00:00Z