The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis.
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Systematic analysis, comparison, and integration of disease based human genetic association data and mouse genetic phenotypic informationInterleukin-23R rs7517847 T/G Polymorphism Contributes to the Risk of Crohn's Disease in Caucasians: A Meta-AnalysisAssembly of inflammation-related genes for pathway-focused genetic analysisNovel associations for hypothyroidism include known autoimmune risk lociDiscovery of a novel series of inhibitors of lymphoid tyrosine phosphatase with activity in human T cells.Modeling of PTPN22 and HLA-DRB1 susceptibility to rheumatoid arthritisA functional variant of PTPN22 confers risk for Vogt-Koyanagi-Harada syndrome but not for ankylosing spondylitis.Genetic regulation of serum cytokines in systemic lupus erythematosusThe PTPN22 locus and rheumatoid arthritis: no evidence for an effect on risk independent of Arg620Trp.Genetic factors predisposing to systemic lupus erythematosus and lupus nephritis.Prevalence of unprotected anal intercourse in men who have sex with men recruited online versus offline: a meta-analysisLymphoid tyrosine phosphatase and autoimmunity: human genetics rediscovers tyrosine phosphatases.Evaluation of the rheumatoid arthritis susceptibility loci HLA-DRB1, PTPN22, OLIG3/TNFAIP3, STAT4 and TRAF1/C5 in an inception cohort.Recent advances in the genetics of systemic lupus erythematosus.Protein Tyrosine Phosphatase Non-receptor 22 Gene C1858T Polymorphism in Patients with Coexistent Type 2 Diabetes and Hashimoto's Thyroiditis.Non-synonymous variant (Gly307Ser) in CD226 is associated with susceptibility to multiple autoimmune diseases.Only one independent genetic association with rheumatoid arthritis within the KIAA1109-TENR-IL2-IL21 locus in Caucasian sample sets: confirmation of association of rs6822844 with rheumatoid arthritis at a genome-wide level of significanceThe association of PTPN22 R620W polymorphism is stronger with late-onset AChR-myasthenia gravis in Turkey.A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis.PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical resultsAssociations between human leukocyte antigen, PTPN22, CTLA4 genotypes and rheumatoid arthritis phenotypes of autoantibody status, age at diagnosis and erosions in a large cohort study.No association of PTPN22 polymorphisms with susceptibility to ocular Behcet's disease in two Chinese Han populationsAssociation of the IL2RA/CD25 gene with juvenile idiopathic arthritisPTGDR polymorphisms and susceptibility to asthma: a meta-analysis.Meta-analysis of genome-wide linkage studies across autoimmune diseases.The association between the PTPN22 1858C>T variant and type 1 diabetes depends on HLA risk and GAD65 autoantibodies.PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes.Maternal methyl-donor supplementation induces prolonged murine offspring colitis susceptibility in association with mucosal epigenetic and microbiomic changes.Assessment of type 1 diabetes risk conferred by HLA-DRB1, INS-VNTR and PTPN22 genes using the Bayesian network approach.Association of PTPN22 polymorphsims and ankylosing spondylitis susceptibility.STAT4 rs7574865 G/T and PTPN22 rs2488457 G/C polymorphisms influence the risk of developing juvenile idiopathic arthritis in Han Chinese patients.Evidence for gene-gene epistatic interactions among susceptibility loci for systemic lupus erythematosusThe genetic basis of graves' disease.Meta-analysis of genetic polymorphisms in granulomatosis with polyangiitis (Wegener's) reveals shared susceptibility loci with rheumatoid arthritisIdentification of new SLE-associated genes with a two-step Bayesian study design.The genetics of human autoimmune disease: A perspective on progress in the field and future directions.Immunogenetics of systemic lupus erythematosus: A comprehensive review.Genetic associations of FCRL3 polymorphisms with the susceptibility of Graves ophthalmopathy in a Chinese population.Current status of lupus geneticsCell damage and autoimmunity: a critical appraisal
P2860
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P2860
The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis.
@ast
The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis.
@en
type
label
The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis.
@ast
The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis.
@en
prefLabel
The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis.
@ast
The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis.
@en
P2093
P31
P356
P1433
P1476
The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis.
@en
P2093
P356
10.1093/RHEUMATOLOGY/KEL170
P577
2006-06-07T00:00:00Z