Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations.
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Protein tyrosine phosphatase PTPN22 in human autoimmunityHigh 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 metaanalysisSusceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population.Meta-analysis reveals an association of PTPN22 C1858T with autoimmune diseases, which depends on the localization of the affected tissue.Lymphoid tyrosine phosphatase R620W variant and inflammatory bowel disease in Tunisia.Single nucleotide polymorphisms at the TRAF1/C5 locus are associated with rheumatoid arthritis in a Han Chinese population.Lymphoid tyrosine phosphatase and autoimmunity: human genetics rediscovers tyrosine phosphatases.PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritisPTPN22 polymorphism and anti-cyclic citrullinated peptide antibodies in combination strongly predicts future onset of rheumatoid arthritis and has a specificity of 100% for the disease.Association of PTPN22 1858 single-nucleotide polymorphism with rheumatoid arthritis in a German cohort: higher frequency of the risk allele in male compared to female patients.Association of PTPN22 1858T/T genotype with type 1 diabetes, Graves' disease but not with rheumatoid arthritis in Russian population.PTPN22: the archetypal non-HLA autoimmunity gene.Cells of the synovium in rheumatoid arthritis. T lymphocytes.Associations between the PTPN22 1858C->T polymorphism and radiographic joint destruction in patients with rheumatoid arthritis: results from a 10-year longitudinal studyThe PTPN22 1858C/T polymorphism is associated with anti-cyclic citrullinated peptide antibody-positive early rheumatoid arthritis in northern Sweden.Functional single nucleotide polymorphism-based association studies.Genetics of autoimmune diseases--disorders of immune homeostasis.Genetic analysis of the Trichuris muris-induced model of colitis reveals QTL overlap and a novel gene cluster for establishing colonic inflammationCo-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives.Advances in the genetics of rheumatoid arthritis point to subclassification into distinct disease subsets.Developments in the scientific understanding of rheumatoid arthritis.Family case of achalasia cardia: case report and review of literaturers2476601 polymorphism in PTPN22 is associated with Crohn's disease but not with ulcerative colitis: a meta-analysis of 16,838 cases and 13,356 controls.Update on the genetic risk factors for rheumatoid arthritis.What does the immunogenetic basis of rheumatoid arthritis teach us about the immunobiology of the disease?Pathogenesis of achalasia cardia.How far are we from understanding the genetic basis of Hashimoto's thyroiditis?Meta-analysis reveals PTPN22 1858C/T polymorphism confers susceptibility to rheumatoid arthritis in Caucasian but not in Asian population.Clinical characteristics and PTPN22 1858C/T variant analysis in Jordanian Arab vitiligo patients.Association of PTPN22 rs2476601 and EGFR rs17337023 Gene polymorphisms and rheumatoid arthritis in Zahedan, Southeast Iran.Differential association of two PTPN22 coding variants with Crohn's disease and ulcerative colitis.High-density SNP analysis of 642 Caucasian families with rheumatoid arthritis identifies two new linkage regions on 11p12 and 2q33.Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn's disease in the Czech population: high frequency of the CARD15 1007fs.A general autoimmunity gene (PTPN22) is not associated with inflammatory bowel disease in a British population.Gaining insight into PTPN22 and autoimmunity.Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosis.The association of PTPN22 with rheumatoid arthritis and juvenile idiopathic arthritis.Multiplex family-based study in systemic lupus erythematosus: association between the R620W polymorphism of PTPN22 and the FcgammaRIIa (CD32A) R131 allele.The PTPN22 C1858T polymorphism and rheumatoid arthritis: a meta-analysis.
P2860
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P2860
Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations.
description
2005 nî lūn-bûn
@nan
2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հուլիսին 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
Association of the lymphoid ty ...... ease, in Canadian populations.
@ast
Association of the lymphoid ty ...... ease, in Canadian populations.
@en
type
label
Association of the lymphoid ty ...... ease, in Canadian populations.
@ast
Association of the lymphoid ty ...... ease, in Canadian populations.
@en
prefLabel
Association of the lymphoid ty ...... ease, in Canadian populations.
@ast
Association of the lymphoid ty ...... ease, in Canadian populations.
@en
P2093
P50
P356
P1476
Association of the lymphoid ty ...... ease, in Canadian populations.
@en
P2093
Albert Kwan
Benjamin Johnson
Bill Newman
Dianne Mosher
Ed Keystone
Julie Owen
Katherine A Siminovitch
Laurence A Rubin
Mark van Oene
Mehrdad Yazdanpanah
P304
P356
10.1002/ART.21123
P577
2005-07-01T00:00:00Z