Association of EBF1, FAM167A(C8orf13)-BLK and TNFSF4 gene variants with primary Sjögren's syndrome. - Wikidata - awgldk - TriplyDB

Association of EBF1, FAM167A(C8orf13)-BLK and TNFSF4 gene variants with primary Sjögren's syndrome.

Association of EBF1, FAM167A(C8orf13)-BLK and TNFSF4 gene variants with primary Sjögren's syndrome.

http://www.wikidata.org/entity/Q34139580

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Contribution of Genetic Factors to Sjögren's Syndrome and Sjögren's Syndrome Related Lymphomagenesis Immune-regulatory mechanisms in systemic autoimmune and rheumatic diseases Interferons in Sjögren's Syndrome: Genes, Mechanisms, and Effects Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients The SLE variant Ala71Thr of BLK severely decreases protein abundance and binding to BANK1 through impairment of the SH3 domain function.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.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.Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4.Immune checkpoint receptors in regulating immune reactivity in rheumatic disease.Genetics and genomics of Sjögren's syndrome: research provides clues to pathogenesis and novel therapies.Reduced B lymphoid kinase (Blk) expression enhances proinflammatory cytokine production and induces nephrosis in C57BL/6-lpr/lpr mice.Single nucleotide polymorphisms in the FAM167A-BLK gene are associated with polymyositis/dermatomyositis in the Han Chinese population.Concordance of increased B1 cell subset and lupus phenotypes in mice and humans is dependent on BLK expression levels.An in silico Approach Reveals Associations between Genetic and Epigenetic Factors within Regulatory Elements in B Cells from Primary Sjögren's Syndrome Patients.The origin, global distribution, and functional impact of the human 8p23 inversion polymorphism.OX40 Ligand Contributes to Human Lupus Pathogenesis by Promoting T Follicular Helper Response The autoimmunity-associated BLK haplotype exhibits cis-regulatory effects on mRNA and protein expression that are prominently observed in B cells early in development.Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.Association between NF-κB Pathway Gene Variants and sICAM1 Levels in Taiwanese Independent replication and meta analysis of association studies establish TNFSF4 as a susceptibility gene preferentially associated with the subset of anticentromere-positive patients with systemic sclerosis Possible Mechanisms of Lymphoma Development in Sjögren's Syndrome.Genome-wide DNA methylation analysis in multiple tissues in primary Sjögren's syndrome reveals regulatory effects at interferon-induced genes.Association of TNFSF4 Polymorphisms with Vogt-Koyanagi-Harada and Behcet's Disease in Han Chinese.Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders.Unraveling the genetic component of systemic sclerosis.The role of viruses in autoreactive B cell activation within tertiary lymphoid structures in autoimmune diseases.The value of animal models to study immunopathology of primary human Sjögren's syndrome symptoms.B-cell hyperactivity in primary Sjögren's syndrome.Genetic, genomic and epigenetic studies as tools for elucidating disease pathogenesis in primary Sjögren's syndrome.OX40, OX40L and Autoimmunity: a Comprehensive Review.Update on Pathogenesis of Sjögren's syndrome.B cell OX40L supports T follicular helper cell development and contributes to SLE pathogenesis.The Ox40/Ox40 Ligand Pathway Promotes Pathogenic Th Cell Responses, Plasmablast Accumulation, and Lupus Nephritis in NZB/W F1 Mice.Beyond TNF: TNF superfamily cytokines as targets for the treatment of rheumatic diseases.Omics studies: their use in diagnosis and reclassification of SLE and other systemic autoimmune diseases.A possible genetic association with chronic fatigue in primary Sjögren's syndrome: a candidate gene study.Host mechanisms involved in cattle Escherichia coli O157 shedding: a fundamental understanding for reducing foodborne pathogen in food animal production.Fine mapping and conditional analysis identify a new mutation in the autoimmunity susceptibility gene BLK that leads to reduced half-life of the BLK protein.Severe dental caries as the first presenting clinical feature in primary Sjögren's syndrome.

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Association of EBF1, FAM167A(C8orf13)-BLK and TNFSF4 gene variants with primary Sjögren's syndrome.

http://www.wikidata.org/entity/Q34139580

description

2010 nî lūn-bûn

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2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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Association of EBF1, FAM167A(C ...... th primary Sjögren's syndrome.

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Association of EBF1, FAM167A(C ...... th primary Sjögren's syndrome.

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Association of EBF1, FAM167A(C ...... th primary Sjögren's syndrome.

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Association of EBF1, FAM167A(C ...... th primary Sjögren's syndrome.

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Association of EBF1, FAM167A(C ...... th primary Sjögren's syndrome.

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Association of EBF1, FAM167A(C ...... th primary Sjögren's syndrome.

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Association of EBF1, FAM167A(C ...... th primary Sjögren's syndrome.

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Association of EBF1, FAM167A(C ...... th primary Sjögren's syndrome.

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Association of EBF1, FAM167A(C ...... th primary Sjögren's syndrome.

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Genes and Immunity

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Association of EBF1, FAM167A(C ...... ith primary Sjögren's syndrome

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A Lundmark

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P2860

Early B-cell Factor gene association with multiple sclerosis in the Spanish population.

CD40 AND CD154 IN CELL-MEDIATED IMMUNITY

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

Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus

A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus

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

Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

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

Association of BANK1 and TNFSF4 with systemic lupus erythematosus in Hong Kong Chinese

Association of TNFSF4 (OX40L) polymorphisms with susceptibility to systemic sclerosis.

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10.1038/GENE.2010.44

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