The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis.
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Recent advances in the genetics of autoimmune diseasePathways to gene identification in rheumatoid arthritis: PTPN22 and beyondProtein tyrosine phosphatase PTPN22 in human autoimmunityDifferential association of the PTPN22 coding variant with autoimmune diseases in a Dutch populationGenetic 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 metaanalysisThe R620W C/T polymorphism of the gene PTPN22 is associated with SLE independently of the association of PDCD1.Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population.IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor production.Meta-analysis reveals an association of PTPN22 C1858T with autoimmune diseases, which depends on the localization of the affected tissue.Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritisAssociation of PTPN22 1858T/T genotype with type 1 diabetes, Graves' disease but not with rheumatoid arthritis in Russian population.Lack of association between the protein tyrosine phosphatase non-receptor 22 (PTPN22)*620W allele and systemic sclerosis in the French Caucasian population.Genetic basis of autoimmunity.The balance of expression of PTPN22 splice forms is significantly different in rheumatoid arthritis patients compared with controls.Role of PTPN22 and CSK gene polymorphisms as predictors of susceptibility and clinical heterogeneity in patients with Henoch-Schönlein purpura (IgA vasculitis).Multiple sclerosis genetics: leaving no stone unturned.Targeting the PTPome in human disease.Gene 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.Recent advances in genetic analysis of multiple sclerosis: genetic associations and therapeutic implications.PTPN22: its role in SLE and autoimmunity.Rheumatoid arthritis: a view of the current genetic landscape.General and Specific Genetic Polymorphism of Cytokines-Related Gene in AITD.Update on the genetic risk factors for rheumatoid arthritis.How far are we from understanding the genetic basis of Hashimoto's thyroiditis?Lack of association between ankylosing spondylitis and a functional polymorphism of PTPN22 proposed as a general susceptibility marker for autoimmunity.Influence of protein tyrosine phosphatase gene (PTPN22) polymorphisms on rheumatic heart disease susceptibility in North Indian population.Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases.No evidence for association between 1858 C/T single-nucleotide polymorphism of PTPN22 gene and primary Sjögren's syndrome.Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves' disease in a Polish population: association and gene dose-dependent correlation with age of onset.Protein tyrosine phosphatase gene PTPN22 polymorphism in psoriasis: lack of evidence for association.A case-control study of tyrosine phosphatase (PTPN22) confirms the lack of association with Crohn's disease.The functional genetic variation in the PTPN22 gene has a negligible effect on the susceptibility to develop inflammatory bowel disease.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.
P2860
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P2860
The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis.
description
2005 nî lūn-bûn
@nan
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
2005年论文
@zh
2005年论文
@zh-cn
name
The R620W polymorphism of the ...... iated with multiple sclerosis.
@en
The R620W polymorphism of the ...... iated with multiple sclerosis.
@nl
type
label
The R620W polymorphism of the ...... iated with multiple sclerosis.
@en
The R620W polymorphism of the ...... iated with multiple sclerosis.
@nl
prefLabel
The R620W polymorphism of the ...... iated with multiple sclerosis.
@en
The R620W polymorphism of the ...... iated with multiple sclerosis.
@nl
P2093
P2860
P356
P1476
The R620W polymorphism of the ...... iated with multiple sclerosis.
@en
P2093
Ann B Begovich
Heather C Alexander
Joanne M Penko
Jorge R Oksenberg
Lisa F Barcellos
Stacy J Caillier
Stephen L Hauser
P2860
P304
P356
10.1086/427244
P407
P577
2005-01-01T00:00:00Z