CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.
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Genetic Influences on the Development of Fibrosis in Crohn's DiseaseHost-microbiome interaction in Crohn's disease: A familiar or familial issue?Role of genetics in the diagnosis and prognosis of Crohn's diseaseNOD2: ethnic and geographic differencesAssociations between NOD2/CARD15 genotype and phenotype in Crohn's disease--Are we there yet?Genotypes and phenotypes in Crohn's disease: do they help in clinical management?Assessment of heterogeneity between European Populations: a Baltic and Danish replication case-control study of SNPs from a recent European ulcerative colitis genome wide association study.Common NOD2/CARD15 variants are not associated with susceptibility or the clinicopathologic characteristics of sporadic colorectal cancer in Hungarian patients.Inflammatory response gene polymorphisms and their relationship with colorectal cancer risk.Prediction of Crohn's disease aggression through NOD2/CARD15 gene sequencing in an Australian cohort.Contribution of genetics to a new vision in the understanding of inflammatory bowel disease.Family and twin studies in inflammatory bowel diseaseCombination of genetic and quantitative serological immune markers are associated with complicated Crohn's disease behaviorNOD2/CARD15 gene polymorphism in patients with inflammatory bowel disease: is Hungary different?Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.Influence of a nucleotide oligomerization domain 1 (NOD1) polymorphism and NOD2 mutant alleles on Crohn's disease phenotypeToll-like receptor 4 and NOD2/CARD15 mutations in Hungarian patients with Crohn's disease: phenotype-genotype correlationsFamilial aggregation in inflammatory bowel disease: is it genes or environment?Current and future role of biomarkers in Crohn's disease risk assessment and treatment.CARD15 gene polymorphisms in patients with spondyloarthropathies identify a specific phenotype previously related to Crohn's diseaseAnti-Saccharomyces cerevisiae antibodies in twins with inflammatory bowel diseaseDLG5 variants do not influence susceptibility to inflammatory bowel disease in the Scottish population.Role of genetics in the diagnosis and prognosis of Crohn's diseaseNOD2/CARD15 mutations in Polish and Bosnian populations with and without Crohn's disease: prevalence and genotype-phenotype analysis.Unravelling the complex genetics of inflammatory bowel diseaseInhibitory effect of enterohepatic Helicobacter hepaticus on innate immune responses of mouse intestinal epithelial cells.NOD2 mutations and anti-Saccharomyces cerevisiae antibodies are risk factors for Crohn's disease in African AmericansUsefulness of faecal calprotectin measurement in children with various types of inflammatory bowel disease.Long-term Outcomes and Risk Factors for Reoperation After Surgical Treatment for Gastrointestinal Crohn Disease According to Anti-tumor Necrosis Factor-α Antibody Use: 35 Years of Experience at a Single Institute in Korea.Mutations in pattern recognition receptor genes modulate seroreactivity to microbial antigens in patients with inflammatory bowel diseaseNo evidence of association between NOD2/CARD15 gene polymorphism and atherosclerotic events after renal transplantationLactase persistence, NOD2 status and Mycobacterium avium subsp. paratuberculosis infection associations to Inflammatory Bowel Disease.Current status of genetics research in inflammatory bowel disease.Current concept on the pathogenesis of inflammatory bowel disease-crosstalk between genetic and microbial factors: pathogenic bacteria and altered bacterial sensing or changes in mucosal integrity take "toll" ?Analysis of TLR4 and TLR2 polymorphisms in inflammatory bowel disease in a Guangxi Zhuang population.Review article: genetic susceptibility and application of genetic testing in clinical management of inflammatory bowel disease.Genetics of inflammatory bowel disease: current status and future directions.Wound healing and fibrosis in intestinal disease.Long-term natural history of Crohn's diseaseA protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.
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P2860
CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
CARD15/NOD2 gene variants are ...... ated forms of Crohn's disease.
@ast
CARD15/NOD2 gene variants are ...... ated forms of Crohn's disease.
@en
type
label
CARD15/NOD2 gene variants are ...... ated forms of Crohn's disease.
@ast
CARD15/NOD2 gene variants are ...... ated forms of Crohn's disease.
@en
prefLabel
CARD15/NOD2 gene variants are ...... ated forms of Crohn's disease.
@ast
CARD15/NOD2 gene variants are ...... ated forms of Crohn's disease.
@en
P2093
P2860
P356
P1433
P1476
CARD15/NOD2 gene variants are ...... cated forms of Crohn's disease
@en
P2093
M Lappalainen
P Paavola-Sakki
P2860
P304
P356
10.1136/GUT.52.4.558
P407
P577
2003-04-01T00:00:00Z