STAT4: genetics, mechanisms, and implications for autoimmunity. - Wikidata - awgldk - TriplyDB

STAT4: genetics, mechanisms, and implications for autoimmunity.

STAT4: genetics, mechanisms, and implications for autoimmunity.

http://www.wikidata.org/entity/Q34804543

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The oncoprotein HBXIP uses two pathways to up-regulate S100A4 in promotion of growth and migration of breast cancer cells Association of STAT4 gene rs7574865G > T polymorphism with ulcerative colitis risk: evidence from 1532 cases and 3786 controls The effects of TLR activation on T-cell development and differentiation Pharmacogenomics of adverse drug reactions Protein kinase C θ regulates the phenotype of murine CD4+ Th17 cells 12- and 15-lipoxygenases in adipose tissue inflammation Association of STAT4 polymorphisms with susceptibility to type-1 autoimmune hepatitis in the Japanese population Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma Temporal dynamics of host molecular responses differentiate symptomatic and asymptomatic influenza a infection.Human mucosal in vivo transcriptome responses to three lactobacilli indicate how probiotics may modulate human cellular pathways.Evaluation of a DLA-79 allele associated with multiple immune-mediated diseases in dogs.A single-nucleotide polymorphism of the STAT4 gene is associated with systemic lupus erythematosus (SLE) in female Chinese population.Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.STAT4 is a genetic risk factor for systemic sclerosis in a Chinese population.Association between STAT4 gene polymorphisms and autoimmune thyroid diseases in a Chinese population Plasmacytoid dendritic cells in multiple sclerosis: chemokine and chemokine receptor modulation by interferon-beta.The TT genotype of the STAT4 rs7574865 polymorphism is associated with high disease activity and disability in patients with early arthritis.A multilocus genetic study in a cohort of Italian SLE patients confirms the association with STAT4 gene and describes a new association with HCP5 gene.Interferon-β inhibits toll-like receptor 9 processing in multiple sclerosis.An autoimmune-associated variant in PTPN2 reveals an impairment of IL-2R signaling in CD4(+) T cells.Cell type and gender-dependent differential regulation of the p202 and Aim2 proteins: implications for the regulation of innate immune responses in SLE.Type I interferon and systemic lupus erythematosus.Interleukin-12 (IL-12)/STAT4 Axis Is an Important Element for β-Cell Dysfunction Induced by Inflammatory Cytokines.The Minor Allele of rs7574865 in the STAT4 Gene Is Associated with Increased mRNA and Protein Expression.STAT4 regulates antiviral gamma interferon responses and recurrent disease during herpes simplex virus 2 infection.Progesterone and autoimmune disease.Immunogenetics of systemic lupus erythematosus: A comprehensive review.Polymorphisms in STAT4, PTPN2, PSORS1C1 and TRAF3IP2 Genes Are Associated with the Response to TNF Inhibitors in Patients with Rheumatoid Arthritis.Genetics of SLE: functional relevance for monocytes/macrophages in disease Comparison of probiotic lactobacilli and bifidobacteria effects, immune responses and rotavirus vaccines and infection in different host species Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs.The search for lupus biomarkers.Stronger inflammatory/cytotoxic T-cell response in women identified by microarray analysis.Genetics of rheumatoid arthritis: GWAS and beyond.Polymorphisms of STAT4 and the risk of inflammatory bowel disease: A case-control study in Chinese Han population Beyond gene discovery in inflammatory bowel disease: the emerging role of epigenetics.The pro-inflammatory signalling regulator Stat4 promotes vasculogenesis of great vessels derived from endothelial precursors.Genome-Wide Identification of Target Genes for the Key B Cell Transcription Factor Ets1 Deciphering the genetic background of systemic sclerosis.Psoriasis: new insight about pathogenesis, role of barrier organ integrity, NLR / CATERPILLER family genes and microbial flora.

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STAT4: genetics, mechanisms, and implications for autoimmunity.

http://www.wikidata.org/entity/Q34804543

description

2008 nî lūn-bûn

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2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

STAT4: genetics, mechanisms, and implications for autoimmunity.

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STAT4: genetics, mechanisms, and implications for autoimmunity.

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STAT4: genetics, mechanisms, and implications for autoimmunity.

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STAT4: genetics, mechanisms, and implications for autoimmunity.

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STAT4: genetics, mechanisms, and implications for autoimmunity.

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STAT4: genetics, mechanisms, and implications for autoimmunity.

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STAT4: genetics, mechanisms, and implications for autoimmunity.

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STAT4: genetics, mechanisms, and implications for autoimmunity.

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Current Allergy and Asthma Reports

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STAT4: genetics, mechanisms, and implications for autoimmunity.

@en

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Benjamin D Korman

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Daniel L Kastner

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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

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study

Protein tyrosine phosphatase PTPN22 in human autoimmunity

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

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

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 candidate gene approach identifies the TRAF1/C5 region as a risk factor for rheumatoid arthritis

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398-403

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10.1007/S11882-008-0077-8

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5

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Elaine F. Remmers

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