about
Substrate specificity of lymphoid-specific tyrosine phosphatase (Lyp) and identification of Src kinase-associated protein of 55 kDa homolog (SKAP-HOM) as a Lyp substrateRheumatoid arthritis seropositive for the rheumatoid factor is linked to the protein tyrosine phosphatase nonreceptor 22-620W alleleFamilial aggregation of autoimmune disease in juvenile dermatomyositisDifferential association of the PTPN22 coding variant with autoimmune diseases in a Dutch populationAutoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variantA functional PTPN22 polymorphism associated with several autoimmune diseases is not associated with IgA deficiency in the Spanish population.A functional variant of PTPN22 confers risk for Vogt-Koyanagi-Harada syndrome but not for ankylosing spondylitis.PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritisNo association of PTPN22 polymorphisms with susceptibility to ocular Behcet's disease in two Chinese Han populationsPTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes.Association of PTPN22 1858T/T genotype with type 1 diabetes, Graves' disease but not with rheumatoid arthritis in Russian population.Study of the role of functional variants of SLC22A4, RUNX1 and SUMO4 in systemic lupus erythematosus.Association of FCRL3 Genetic Polymorphisms With Endometriosis-Related Infertility Risk: An Independent Study in Han Chinese.Update on the genetics characterization of vitiligo.Disease-promoting and -protective genomic loci on mouse chromosomes 3 and 19 control the incidence and severity of autoimmune arthritis.Intersection of population variation and autoimmunity genetics in human T cell activationGene network analysis of small molecules with autoimmune disease associated genes predicts a novel strategy for drug efficacy.Genetics of autoimmune diseases--disorders of immune homeostasis.Genetic Basis of Type 1 Diabetes: Similarities and Differences between East and West.Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.The balancing act of autoimmunity: central and peripheral tolerance versus infection control.Protein tyrosine phosphatase inhibitors: a patent review (2002 - 2011).Meta-analysis reveals PTPN22 1858C/T polymorphism confers susceptibility to rheumatoid arthritis in Caucasian but not in Asian population.Association analyses identifying two common susceptibility loci shared by psoriasis and systemic lupus erythematosus in the Chinese Han population.Can your genes make you more prone to pneumococcal disease?Lack of association between ankylosing spondylitis and a functional polymorphism of PTPN22 proposed as a general susceptibility marker for autoimmunity.The CTLA-4 +49 A/G, CT60 A/G and PTPN22 1858 C/T polymorphisms and susceptibility to vitiligo: a meta-analysis.A novel single nucleotide polymorphism in the protein tyrosine phosphatase N22 gene (PTPN22) is associated with Type 1 diabetes in a Chinese population.Finnish case-control and family studies support PTPN22 R620W polymorphism as a risk factor in rheumatoid arthritis, but suggest only minimal or no effect in juvenile idiopathic arthritis.Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease.Gaining insight into PTPN22 and autoimmunity.Meta-analysis of the correlation between PTPN22 gene polymorphisms and susceptibility to systemic lupus erythematosus.The Protein Tyrosine Phosphatase Nonreceptor 22 (PTPN22) R620W Functional Polymorphism in Psoriasis.Cross-Phenotype Association Analysis Using Summary Statistics from GWAS.Autoimmune polyglandular syndrome type 2 shows the same HLA class II pattern as type 1 diabetes.Protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene R620W variant and sporadic idiopathic hypoparathyroidism in Asian Indians.A variant within intron 1 of the PTPN22 gene decreases the genetic susceptibility of ankylosing spondylitis in a central south Chinese Han population.Molecular scanning of the gene for programmed cell death-1 (PDCD-1) as a candidate for type 1 diabetes susceptibility.The PTPN22 C1858T polymorphism and rheumatoid arthritis: a meta-analysis.The role of inflammatory bowel disease susceptibility loci in multiple sclerosis and systemic lupus erythematosus
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
PTPN22 and autoimmune disease.
@en
PTPN22 and autoimmune disease.
@nl
type
label
PTPN22 and autoimmune disease.
@en
PTPN22 and autoimmune disease.
@nl
prefLabel
PTPN22 and autoimmune disease.
@en
PTPN22 and autoimmune disease.
@nl
P2860
P356
P1433
P1476
PTPN22 and autoimmune disease.
@en
P2093
Katherine A Siminovitch
P2860
P2888
P304
P356
10.1038/NG1204-1248
P407
P577
2004-12-01T00:00:00Z