Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease. - Wikidata - wikimedia - TriplyDB

Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.

Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.

http://www.wikidata.org/entity/Q34073780

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Recent Insights Into the Genetics of Inflammatory Bowel Disease T helper 17 cell heterogeneity and pathogenicity in autoimmune disease The emerging role of IL-17 in the pathogenesis of psoriasis: preclinical and clinical findings Genomic views of STAT function in CD4+ T helper cell differentiation Intestinal Behçet's Disease: A True Inflammatory Bowel Disease or Merely an Intestinal Complication of Systemic Vasculitis?Adalimumab in the management of Behçet's disease Skewed Helper T-Cell Responses to IL-12 Family Cytokines Produced by Antigen-Presenting Cells and the Genetic Background in Behcet's Disease Advances in the genetically complex autoinflammatory diseases An update on the genetics of HLA B27-associated acute anterior uveitis.Current concepts and future directions in the pathogenesis and treatment of non-infectious intraocular inflammation.Behçet's disease in children, an overview The immunogenetics of Behçet's disease: A comprehensive review Genome-Wide Association of Heroin Dependence in Han Chinese The composition and signaling of the IL-35 receptor are unconventional Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1 Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease Pathological implications of Th1/Th2 cytokine genetic variants in Behçet's disease: Data from a pilot study in a Sicilian population.Identification of possible pathogenic pathways in Behçet's disease using genome-wide association study data from two different populations Intestinal Behçet and Crohn's disease: two sides of the same coin.Enriched protein screening of human bone marrow mesenchymal stromal cell secretions reveals MFAP5 and PENK as novel IL-10 modulators.Gender Differences in Behçet's Disease Associated Uveitis.Comprehensive analysis of the association between UBAC2 polymorphisms and Behçet's disease in a Japanese population Diagnosis and management of intestinal Behçet's disease.Investigation of a possible extended risk haplotype in the IL23R region associated with ankylosing spondylitis.Determination of Genes Related to Uveitis by Utilization of the Random Walk with Restart Algorithm on a Protein-Protein Interaction Network.Behçet disease-associated MHC class I residues implicate antigen binding and regulation of cell-mediated cytotoxicity HLA-B*51 the primary risk in Behçet disease.Proinflammatory cytokines and C-reactive protein in uveitis associated with Behçet's disease Epistatic interaction of ERAP1 and HLA-B in Behçet disease: a replication study in the Spanish population Genetic polymorphisms of C-type lectin receptors in Behcet's disease in a Chinese Han population.Biological treatments in Behçet's disease: beyond anti-TNF therapy.Immunopathogenesis of ocular Behçet's disease Association study of genes controlling IL-12-dependent IFN-γ immunity: STAT4 alleles increase risk of pulmonary tuberculosis in Morocco.Cytokine gene variation is associated with depressive symptom trajectories in oncology patients and family caregivers.Psoriasis regression analysis of MHC loci identifies shared genetic variants with vitiligo.Genetics, genomics, and their relevance to pathology and therapy.Principal component analysis characterizes shared pathogenetics from genome-wide association studies.No association of PTPN22 polymorphisms with susceptibility to ocular Behcet's disease in two Chinese Han populations

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Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.

http://www.wikidata.org/entity/Q34073780

description

2010 nî lūn-bûn

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2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2010 թվականի հուլիսին 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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name

Genome-wide association study ...... ociated with Behçet's disease.

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Genome-wide association study ...... ociated with Behçet's disease.

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Genome-wide association study ...... ociated with Behçet's disease.

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Genome-wide association study ...... ociated with Behçet's disease.

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Genome-wide association study ...... ociated with Behçet's disease.

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Genome-wide association study ...... ociated with Behçet's disease.

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Genome-wide association study ...... ociated with Behçet's disease.

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Nature Genetics

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Afet Akdag Kose

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Ahmet Gül

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Aris Cakiris

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Barbara Yang

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Benjamin D Korman

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Burak Erer

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Colleen Satorius

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Daniel L Kastner

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Dongsik Bang

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Eldad Ben-Chetrit

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P2860

Interleukin-10 and the interleukin-10 receptor

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

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

PLINK: a tool set for whole-genome association and population-based linkage analyses

A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

Haploview: Visualization and analysis of SNP genotype data.

Familial aggregation of Behçet's disease in Turkey.

HLA-B51/B5 and the risk of Behçet's disease: a systematic review and meta-analysis of case-control genetic association studies.

P2888

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698-702

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10.1038/NG.625

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8

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42

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Elaine F. Remmers

Graham R. Wallace

Michael J. Ombrello

Christopher Amos

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2010-07-11T00:00:00Z

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45151838

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1032813793

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20622878

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genome-wide association study

Behcet's disease

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2923807

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