rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants
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Intestinal DMBT1 expression is modulated by Crohn's disease-associated IL23R variants and by a DMBT1 variant which influences binding of the transcription factors CREB1 and ATF-2Interaction of Crohn's disease susceptibility genes in an Australian paediatric cohortThe differentiation of human T(H)-17 cells requires transforming growth factor-beta and induction of the nuclear receptor RORgammatGenetic Influences on the Development of Fibrosis in Crohn's DiseaseRole of genetics in the diagnosis and prognosis of Crohn's diseaseCEACAM6 gene variants in inflammatory bowel diseaseThe NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variantsLack of evidence for association of primary sclerosing cholangitis and primary biliary cirrhosis with risk alleles for Crohn's disease in Polish patients.IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac diseaseThe cannabinoid 1 receptor (CNR1) 1359 G/A polymorphism modulates susceptibility to ulcerative colitis and the phenotype in Crohn's disease.Interaction of the major inflammatory bowel disease susceptibility alleles in Crohn's disease patients.NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.Replication and meta-analysis of 13,000 cases defines the risk for interleukin-23 receptor and autophagy-related 16-like 1 variants in Crohn's disease.The role of osteopontin (OPN/SPP1) haplotypes in the susceptibility to Crohn's diseasePTPN2 gene variants are associated with susceptibility to both Crohn's disease and ulcerative colitis supporting a common genetic disease backgroundAnalysis of IL12B gene variants in inflammatory bowel disease.Polymorphisms of IL23R and Fuchs' syndrome in a Chinese Han population.Association of single nucleotide polymorphisms of IL23R and IL17 with ulcerative colitis risk in a Chinese Han population.PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sitesIRGM variants and susceptibility to inflammatory bowel disease in the German population.Association between polymorphisms of the IL-23R gene and allergic rhinitis in a Chinese Han population.Role of genetics in the diagnosis and prognosis of Crohn's diseaseRole of ATG16L, NOD2 and IL23R in Crohn's disease pathogenesisInterleukin-23 receptor (IL-23R) gene polymorphisms in acquired aplastic anemia.Association of Interleukin-23 receptor gene polymorphisms with susceptibility to Crohn's disease: A meta-analysisRetrospective Binary-Trait Association Test Elucidates Genetic Architecture of Crohn Disease.Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAP.New global map of Crohn's disease: Genetic, environmental, and socioeconomic correlations.Association of polymorphisms in the Interleukin 23 receptor gene with osteonecrosis of femoral head in Korean populationRole of mucosal dendritic cells in inflammatory bowel disease.Replication of interleukin 23 receptor and autophagy-related 16-like 1 association in adult- and pediatric-onset inflammatory bowel disease in Italy.From interleukin-23 to T-helper 17 cells: human T-helper cell differentiation revisited.Genome-wide association studies--a summary for the clinical gastroenterologist.Susceptibility to ulcerative colitis in Hungarian patients determined by gene-gene interactions.Polymorphisms of STAT4 and the risk of inflammatory bowel disease: A case-control study in Chinese Han populationIL23R single nucleotide polymorphisms could be either beneficial or harmful in ulcerative colitis.IL-23R mutation is associated with ulcerative colitis: A systemic review and meta-analysis.Genetics of childhood-onset inflammatory bowel disease.Genetics of ulcerative colitis.
P2860
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P2860
rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants
description
2007 nî lūn-bûn
@nan
2007 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
rs1004819 is the main disease- ...... , CARD15, and OCTN1/2 variants
@ast
rs1004819 is the main disease- ...... , CARD15, and OCTN1/2 variants
@en
type
label
rs1004819 is the main disease- ...... , CARD15, and OCTN1/2 variants
@ast
rs1004819 is the main disease- ...... , CARD15, and OCTN1/2 variants
@en
prefLabel
rs1004819 is the main disease- ...... , CARD15, and OCTN1/2 variants
@ast
rs1004819 is the main disease- ...... , CARD15, and OCTN1/2 variants
@en
P2093
P2860
P1433
P1476
rs1004819 is the main disease- ...... , CARD15, and OCTN1/2 variants
@en
P2093
Astrid Konrad
Burkhard Göke
Christian Folwaczny
Christine Grassl
Helga-Paula Török
Julia Dambacher
Julia Seiderer
Jörg T Epplen
Jürgen Glas
Kerstin Maier
P2860
P356
10.1371/JOURNAL.PONE.0000819
P407
P577
2007-09-05T00:00:00Z