Association of the C8orf13-BLK region with systemic sclerosis in North-American and European populations - Wikidata - wikimedia - TriplyDB

Association of the C8orf13-BLK region with systemic sclerosis in North-American and European populations

Association of the C8orf13-BLK region with systemic sclerosis in North-American and European populations

http://www.wikidata.org/entity/Q33653276

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Contribution of Genetic Factors to Sjögren's Syndrome and Sjögren's Syndrome Related Lymphomagenesis Genetics of systemic sclerosis: recent advances Genetics, Epigenetics, and Genomics of Systemic Sclerosis Recent advances in the genetics of systemic sclerosis: toward biological and clinical significance Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy The SLE variant Ala71Thr of BLK severely decreases protein abundance and binding to BANK1 through impairment of the SH3 domain function.Meta-analysis reveals an association of PTPN22 C1858T with autoimmune diseases, which depends on the localization of the affected tissue.Autoimmune diseases and autoantibodies in the first degree relatives of patients with systemic sclerosis.Association of EBF1, FAM167A(C8orf13)-BLK and TNFSF4 gene variants with primary Sjögren's syndrome.C8orf13-BLK is a genetic risk locus for systemic sclerosis and has additive effects with BANK1: results from a large french cohort and meta-analysis.Recent findings on genetics of systemic autoimmune diseases Genetics of scleroderma: implications for personalized medicine?Possible single-nucleotide polymorphism loci associated with systemic sclerosis susceptibility: a genetic association study in a Chinese Han population.Epistatic interaction between BANK1 and BLK in rheumatoid arthritis: results from a large trans-ethnic meta-analysis.The effect of inversion at 8p23 on BLK association with lupus in Caucasian population Systems level analysis of systemic sclerosis shows a network of immune and profibrotic pathways connected with genetic polymorphisms.The epigenetics of autoimmunity.Association between a C8orf13-BLK polymorphism and polymyositis/dermatomyositis in the Japanese population: an additive effect with STAT4 on disease susceptibility.Reduced B lymphoid kinase (Blk) expression enhances proinflammatory cytokine production and induces nephrosis in C57BL/6-lpr/lpr mice.Towards systemic sclerosis and away from primary biliary cirrhosis: the case of PTPN22.Primary biliary cirrhosis associated with systemic sclerosis: diagnostic and clinical challenges.Environmental pathways to autoimmune diseases: the cases of primary biliary cirrhosis and multiple sclerosis.Concordance of increased B1 cell subset and lupus phenotypes in mice and humans is dependent on BLK expression levels.Pathogenesis of Systemic Sclerosis.Association study of ITGAM, ITGAX, and CD58 autoimmune risk loci in systemic sclerosis: results from 2 large European Caucasian cohorts The autoimmunity-associated BLK haplotype exhibits cis-regulatory effects on mRNA and protein expression that are prominently observed in B cells early in development.A multicenter study confirms CD226 gene association with systemic sclerosis-related pulmonary fibrosis Identification of an Association of TNFAIP3 Polymorphisms With Matrix Metalloproteinase Expression in Fibroblasts in an Integrative Study of Systemic Sclerosis-Associated Genetic and Environmental Factors Genetic Susceptibility to Interstitial Lung Disease Associated with Systemic Sclerosis.The genetics of scleroderma: looking into the postgenomic era The role of type 1 interferon in systemic sclerosis.8p22-23-rs2254546 as a susceptibility locus for Kawasaki disease: a case-control study and a meta-analysis.Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription.Gene-gene interaction of BLK, TNFSF4, TRAF1, TNFAIP3, and REL in systemic lupus erythematosus Deciphering the genetic background of systemic sclerosis.Genetics of systemic sclerosis: an update.The therapeutic potential of epigenetics in autoimmune diseases.Unraveling the genetic component of systemic sclerosis.Genetic, genomic and epigenetic studies as tools for elucidating disease pathogenesis in primary Sjögren's syndrome.

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Association of the C8orf13-BLK region with systemic sclerosis in North-American and European populations

http://www.wikidata.org/entity/Q33653276

description

2009 nî lūn-bûn

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2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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Association of the C8orf13-BLK ...... rican and European populations

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Association of the C8orf13-BLK ...... rican and European populations

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Association of the C8orf13-BLK ...... rican and European populations

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Association of the C8orf13-BLK ...... rican and European populations

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Association of the C8orf13-BLK ...... rican and European populations

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Association of the C8orf13-BLK ...... rican and European populations

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P356

J.JAUT.2009.08.014

P1433

Journal of Autoimmunity

P1476

Association of the C8orf13-BLK ...... rican and European populations

@en

P2093

Blanca Rueda

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Carmen P Simeon

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Dipal Divecha

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Esther Vicente

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Ezequiel Martin

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Filemon K Tan

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Frank C Arnett

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Gene Paz

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Haley Bunting

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Hilda Draeger

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P2860

Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci

Molecular cloning and chromosomal localization of the human homologue of a B-lymphocyte specific protein tyrosine kinase (blk)

Specific expression of a tyrosine kinase gene, blk, in B lymphoid cells

Essential role of Src-family protein tyrosine kinases in NF-kappaB activation during B cell development

Interferon-inducible gene expression signature in peripheral blood cells of patients with severe lupus

Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX

Association of the PTPN22 R620W polymorphism with anti-topoisomerase I- and anticentromere antibody-positive systemic sclerosis

Abnormalities in the regulators of angiogenesis in patients with scleroderma

HLA haplotypes and microsatellite polymorphisms in and around the major histocompatibility complex region in a Native American population with a high prevalence of scleroderma (systemic sclerosis).

Molecular cloning, characterization, and chromosomal localization of a human lymphoid tyrosine kinase related to murine Blk.

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155-162

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scholarly article

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10.1016/J.JAUT.2009.08.014

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2

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34

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John D Reveille

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2009-09-30T00:00:00Z

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19796918

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2821978

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