Systematic association mapping identifies NELL1 as a novel IBD disease gene
about
Interaction of Crohn's disease susceptibility genes in an Australian paediatric cohortCrohn's disease risk alleles on the NOD2 locus have been maintained by natural selection on standing variationXBP1 links ER stress to intestinal inflammation and confers genetic risk for human inflammatory bowel diseaseGenome-wide association identifies multiple ulcerative colitis susceptibility lociProliferation and osteogenic differentiation of mesenchymal stem cells induced by a short isoform of NELL-1Functional studies on the IBD susceptibility gene IL23R implicate reduced receptor function in the protective genetic variant R381QA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility lociA genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North IndiansVariant detection and runs of homozygosity in next generation sequencing data elucidate the genetic background of Lundehund syndromeA genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale.Increased susceptibility to dextran sulfate sodium induced colitis in the T cell protein tyrosine phosphatase heterozygous mouseMicrobiota regulate intestinal epithelial gene expression by suppressing the transcription factor Hepatocyte nuclear factor 4 alphaEvaluation of 22 genetic variants with Crohn's disease risk in the Ashkenazi Jewish population: a case-control study.Genetic evidence supporting the association of protease and protease inhibitor genes with inflammatory bowel disease: a systematic reviewAdvances and challenges in biomarker development for type 1 diabetes prediction and prevention using omic technologiesGenotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sitesInvestigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait lociInvestigating the Role of Gene-Gene Interactions in TB Susceptibility.Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohn's disease risk in a population-based case-control study: evidence of gene-gene interactions.Prevalence of genetic variants associated with inflammatory bowel disease in a healthy First Nations cohortGenome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.Retrospective Binary-Trait Association Test Elucidates Genetic Architecture of Crohn Disease.MAST3: a novel IBD risk factor that modulates TLR4 signaling.Apical junction complex proteins and ulcerative colitis: a focus on the PTPRS gene.Replication of interleukin 23 receptor and autophagy-related 16-like 1 association in adult- and pediatric-onset inflammatory bowel disease in Italy.An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29.Family-based genome-wide association studies.Genome-wide association studies--a summary for the clinical gastroenterologist.Association between type 1 diabetes and GWAS SNPs in the southeast US Caucasian populationAutophagy-related gene LRRK2 is likely a susceptibility gene for systemic lupus erythematosus in northern Han Chinese.Meta-analysis of published studies identified eight additional common susceptibility loci for Crohn's disease and ulcerative colitis.Is there evidence to claim or deny association between variants of the multidrug resistance gene (MDR1 or ABCB1) and inflammatory bowel disease?Genetic studies of Crohn's disease: past, present and future.The genetics of Crohn's disease and ulcerative colitis--status quo and beyond.The genetic burden of inflammatory bowel diseases: implications for the clinic?Genetic risk variants as therapeutic targets for Crohn's disease.Genetic susceptibility and genotype-phenotype association in 588 Danish children with inflammatory bowel disease.T300A polymorphism of ATG16L1 and susceptibility to inflammatory bowel diseases: a meta-analysis.
P2860
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P2860
Systematic association mapping identifies NELL1 as a novel IBD disease gene
description
2007 nî lūn-bûn
@nan
2007 թուականին հրատարակուած գիտական յօդուած
@hyw
2007 թվականին 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
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@ast
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@en
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@en-gb
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@nl
type
label
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@ast
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@en
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@en-gb
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@nl
prefLabel
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@ast
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@en
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@en-gb
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@nl
P2093
P2860
P50
P3181
P1433
P1476
Systematic association mapping identifies NELL1 as a novel IBD disease gene
@en
P2093
Andre Franke
Andreas Ruether
Christian Becker
Clive M Onnie
Florian Wagner
Gabriele Mayr
Hélène Fournier
Mario Albrecht
Michael Wittig
Monika Stoll
P2860
P3181
P356
10.1371/JOURNAL.PONE.0000691
P407
P50
P577
2007-01-01T00:00:00Z