Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. - Wikidata - awgldk - TriplyDB

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

http://www.wikidata.org/entity/Q34459129

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Systematic association mapping identifies NELL1 as a novel IBD disease gene Matrix-assisted laser desorption/ionisation, time-of-flight mass spectrometry in genomics research Inflammatory bowel disease in Asia: A systematic review Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease Recent Insights Into the Genetics of Inflammatory Bowel Disease Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci TNFSF15 is an ethnic-specific IBD gene IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci Association study of TNFSF15 polymorphisms in Japanese patients with inflammatory bowel disease Pooled DNA genotyping on Affymetrix SNP genotyping arrays The TNF-family cytokine TL1A: from lymphocyte costimulator to disease co-conspirator Immunopathology of inflammatory bowel disease Biochemical and Structural Characterization of the Human TL1A Ectodomain ,Contribution of the novel inflammatory bowel disease gene IL23R to disease susceptibility and phenotype Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4 Functional studies on the IBD susceptibility gene IL23R implicate reduced receptor function in the protective genetic variant R381Q Genetic predictors of medically refractory ulcerative colitis Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease Inflammatory bowel disease Inflammatory bowel disease Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility Candidate loci for insulin sensitivity and disposition index from a genome-wide association analysis of Hispanic participants in the Insulin Resistance Atherosclerosis (IRAS) Family Study.Role of TL1A and its receptor DR3 in two models of chronic murine ileitis.Variant detection and runs of homozygosity in next generation sequencing data elucidate the genetic background of Lundehund syndrome IBD-associated TL1A gene (TNFSF15) haplotypes determine increased expression of TL1A protein.Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis Genome-wide association study and follow-up analysis of adiposity traits in Hispanic Americans: the IRAS Family Study.TLR8-mediated activation of human monocytes inhibits TL1A expression.Non-synonymous and synonymous coding SNPs show similar likelihood and effect size of human disease association.SLCO3A1, A novel crohn's disease-associated gene, regulates nf-κB activity and associates with intestinal perforation An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.Tumour necrosis factor superfamily members in the pathogenesis of inflammatory bowel disease Evaluation of 22 genetic variants with Crohn's disease risk in the Ashkenazi Jewish population: a case-control study.Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease

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P2860

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

http://www.wikidata.org/entity/Q34459129

description

2005 nî lūn-bûn

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2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2005 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

@ast

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

@en

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

@nl

type

label

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

@ast

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

@en

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

@nl

prefLabel

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

@ast

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

@en

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

@nl

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Human Molecular Genetics

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Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.

@en

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Akihiro Sekine

http://www.w3.org/2001/XMLSchema#string

Aritoshi Iida

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Atsushi Takahashi

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Derek Jewell

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Dermot McGovern

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Helen Butler

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Jiannis Ragoussis

http://www.w3.org/2001/XMLSchema#string

Keiko Yamazaki

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Lon Cardon

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Marta Paolucci

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P2860

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

TL1A is a TNF-like ligand for DR3 and TR6/DcR3 and functions as a T cell costimulator

Association of the gene encoding wingless-type mammary tumor virus integration-site family member 5B (WNT5B) with type 2 diabetes

The structure of haplotype blocks in the human genome

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibilit

Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease.

Deficient host-bacteria interactions in inflammatory bowel disease? The toll-like receptor (TLR)-4 Asp299gly polymorphism is associated with Crohn's disease and ulcerative colitis

Inflammatory bowel disease gene hunting by linkage analysis: rationale, methodology, and present status of the field.

Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: evidence for epistasis between 1p and IBD1.

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3499-3506

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scholarly article

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10.1093/HMG/DDI379

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22

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14

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2005-10-12T00:00:00Z

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7544016

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16221758

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Crohn's disease

single-nucleotide polymorphism