Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus - Wikidata - awgldk - TriplyDB

Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus

Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus

http://www.wikidata.org/entity/Q28301821

about

The interferon induced with helicase domain 1 A946T polymorphism is not associated with rheumatoid arthritis Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4 Identification of Cd101 as a susceptibility gene for Novosphingobium aromaticivorans-induced liver autoimmunity Rheumatoid arthritis seropositive for the rheumatoid factor is linked to the protein tyrosine phosphatase nonreceptor 22-620W allele Knowledge-based analysis of genetic associations of rheumatoid arthritis to inform studies searching for pleiotropic genes: a literature review and network analysis Analysis of interleukin-23 receptor (IL23R) gene polymorphisms in systemic lupus erythematosus Protein tyrosine phosphatase PTPN22 in human autoimmunity High basal activity of the PTPN22 gain-of-function variant blunts leukocyte responsiveness negatively affecting IL-10 production in ANCA vasculitis PTPN22 R620W polymorphism and ANCA disease risk in white populations: a metaanalysis The R620W C/T polymorphism of the gene PTPN22 is associated with SLE independently of the association of PDCD1.Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analyses Susceptibility 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.Identification of the PTPN22 functional variant R620W as susceptibility genetic factor for giant cell arteritis.The CD45 77C/G allele is not associated with myasthenia gravis - a reassessment of the potential role of CD45 in autoimmunity Single nucleotide polymorphisms at the TRAF1/C5 locus are associated with rheumatoid arthritis in a Han Chinese population.Autoimmune diseases and autoantibodies in the first degree relatives of patients with systemic sclerosis.Lymphoid tyrosine phosphatase and autoimmunity: human genetics rediscovers tyrosine phosphatases.Why is PTPN22 a good candidate susceptibility gene for autoimmune disease?PTPN22 1858C>T polymorphism distribution in Europe and association with rheumatoid arthritis: case-control study and meta-analysis.Major histocompatibility complex (MHC) class II alleles, haplotypes and epitopes which confer susceptibility or protection in systemic sclerosis: analyses in 1300 Caucasian, African-American and Hispanic cases and 1000 controls.PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical results Association of TNFSF4 (OX40L) polymorphisms with susceptibility to systemic sclerosis.PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis Associations between human leukocyte antigen, PTPN22, CTLA4 genotypes and rheumatoid arthritis phenotypes of autoantibody status, age at diagnosis and erosions in a large cohort study.Genes and Sjögren's syndrome.Altered B cell homeostasis and toll-like receptor 9-driven response in type 1 diabetes carriers of the C1858T PTPN22 allelic variant: implications in the disease pathogenesis The TT genotype of the STAT4 rs7574865 polymorphism is associated with high disease activity and disability in patients with early arthritis.PTPN22 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.PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes.Regulation of lymphoid tyrosine phosphatase activity: inhibition of the catalytic domain by the proximal interdomain 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.Towards systemic sclerosis and away from primary biliary cirrhosis: the case of PTPN22.Association of the PTPN22 R620W polymorphism with increased risk for SLE in the genetically homogeneous population of Crete.Role of PTPN22 and CSK gene polymorphisms as predictors of susceptibility and clinical heterogeneity in patients with Henoch-Schönlein purpura (IgA vasculitis).Associations between the PTPN22 1858C->T polymorphism and radiographic joint destruction in patients with rheumatoid arthritis: results from a 10-year longitudinal study The vitamin D3 transcriptomic response in skin cells derived from the Atlantic bottlenose dolphin.Targeting the PTPome in human disease.

P2860

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P2860

Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus

http://www.wikidata.org/entity/Q28301821

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Arthritis & Rheumatology

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Association of a functional si ...... d systemic lupus erythematosus

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Alejandro Balsa

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Antonio Nuñez-Roldan

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Belén Torres

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Dora Pascual-Salcedo

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Elena Sánchez

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Juan Jiménez-Alonso

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Maria Francisca González-Escribano

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Miguel A González-Gay

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Miguel A López-Nevot

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Rafael Cáliz

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P2860

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

Protein tyrosine phosphatases in the human genome

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.

Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.

A genome-wide search for susceptibility genes in human systemic lupus erythematosus sib-pair families

Evolving concepts of rheumatoid arthritis

Cooperative inhibition of T-cell antigen receptor signaling by a complex between a kinase and a phosphatase.

Immune cell signaling in lupus.

Autoimmune diseases.

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219-24

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147362

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10.1002/ART.20771

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1

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