Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.
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Evidence for significant overlap between common risk variants for Crohn's disease and ankylosing spondylitisGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseProtein characterization of a candidate mechanism SNP for Crohn's disease: the macrophage stimulating protein R689C substitutionStructural basis for the binding specificity of human Recepteur d'Origine Nantais (RON) receptor tyrosine kinase to macrophage-stimulating proteinRon receptor tyrosine kinase signaling as a therapeutic targetCrystal Structure of the Sema-PSI Extracellular Domain of Human RON Receptor Tyrosine KinaseGenome-wide association identifies multiple ulcerative colitis susceptibility lociFunctional consequences of the macrophage stimulating protein 689C inflammatory bowel disease risk alleleGenome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility lociGenetic Basis of Common Human Disease: Insight into the Role of Missense SNPs from Genome-Wide Association StudiesGene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder.Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.Application of Zebrafish Models in Inflammatory Bowel DiseaseRon receptor signaling is protective against DSS-induced colitis in mice.Genetic evidence supporting the association of protease and protease inhibitor genes with inflammatory bowel disease: a systematic reviewVariants at the 3p21 locus influence susceptibility and phenotype both in adults and early-onset patients with inflammatory bowel disease.Crohn disease: a current perspective on genetics, autophagy and immunityDeep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis.Oxidant stress regulatory genetic variation in recipients and donors contributes to risk of primary graft dysfunction after lung transplantation.Distinct and overlapping genetic loci in Crohn's disease and ulcerative colitis: correlations with pathogenesis.Opportunities and challenges of whole-genome and -exome sequencing.Genome-wide association studies: a new window into immune-mediated diseases.Autoimmune diseases: insights from genome-wide association studiesGenome-wide association studies--a summary for the clinical gastroenterologist.Prediction of candidate primary immunodeficiency disease genes using a support vector machine learning approach.Genetics of childhood-onset inflammatory bowel disease.Ulcerative colitis: immune function, tissue fibrosis and current therapeutic considerations.TGR5 sequence variation in primary sclerosing cholangitis.Genetics in PSC: what do the "risk genes" teach us?Differences between adults and children: genetics and beyond.Membrane-bound serine protease inhibitor HAI-1 is required for maintenance of intestinal epithelial integrity.Strategies of targeting the extracellular domain of RON tyrosine kinase receptor for cancer therapy and drug delivery.Sequencing and analysis of an Irish human genome.The history of genetics in inflammatory bowel disease.Effect of BSN-MST1 locus on inflammatory bowel disease and multiple sclerosis susceptibility.Phenotype-genotype profiles in Crohn's disease predicted by genetic markers in autophagy-related genes (GOIA study II).Cutting edge issues in primary sclerosing cholangitis.The impact of ulcerative colitis on the long-term outcome of patients with primary sclerosing cholangitis.Nutrigenomics and inflammatory bowel diseases.Macrophage-stimulating protein polymorphism rs3197999 is associated with a gain of function: implications for inflammatory bowel disease.
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P2860
Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.
@ast
Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.
@en
type
label
Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.
@ast
Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.
@en
prefLabel
Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.
@ast
Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.
@en
P2093
P2860
P356
P1433
P1476
Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.
@en
P2093
C Deslandres
C Lefebvre
K D Taylor
M S Silverberg
P2860
P2888
P304
P356
10.1038/MI.2007.15
P577
2008-01-16T00:00:00Z
P5875
P6179
1024892825