The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease - Wikidata - awgldk - TriplyDB

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

http://www.wikidata.org/entity/Q22250943

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Molecular reclassification of Crohn's disease by cluster analysis of genetic variants Mycobacteria in Crohn’s disease: how innate immune deficiency may result in chronic inflammation Crohn's disease: an immune deficiency state Innate immunity in inflammatory bowel disease: a disease hypothesis Interventions for prevention of post-operative recurrence of Crohn's disease Epidemiological evidence for Mycobacterium avium subspecies paratuberculosis as a cause of Crohn's disease Genetic Influences on the Development of Fibrosis in Crohn's Disease miRNAs as new molecular insights into inflammatory bowel disease: Crucial regulators in autoimmunity and inflammation Mechanisms of Microbe-Host Interaction in Crohn's Disease: Dysbiosis vs. Pathobiont Selection Association of DLG5 R30Q variant with inflammatory bowel disease CARD15/NOD2 mutations in Crohn's disease Associations between NOD2/CARD15 genotype and phenotype in Crohn's disease--Are we there yet?NOD2 is a negative regulator of Toll-like receptor 2-mediated T helper type 1 responses Molecular reclassification of Crohn's disease: a cautionary note on population stratification Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility Altered epithelial cell lineage allocation and global expansion of the crypt epithelial stem cell population are associated with ileitis in SAMP1/YitFc mice.Genotypes and phenotypes in Crohn's disease: do they help in clinical management?The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants Functional characterization of two novel 5' untranslated exons reveals a complex regulation of NOD2 protein expression.Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer.Prediction of Crohn's disease aggression through NOD2/CARD15 gene sequencing in an Australian cohort.Some aspects of molecular diagnostics in Lynch syndrome.Absence of Mycobacterium avium subspecies paratuberculosis components from Crohn's disease intestinal biopsy tissues Polymorphisms in interleukin-10 gene according to mutations of NOD2/CARD15 gene and relation to phenotype in Spanish patients with Crohn's disease.Genetic predisposition to fracture non-union: a case control study of a preliminary single nucleotide polymorphisms analysis of the BMP pathway Vitamin D deficiency in mice impairs colonic antibacterial activity and predisposes to colitis A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease.IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis.Cigarette smoke extract (CSE) delays NOD2 expression and affects NOD2/RIPK2 interactions in intestinal epithelial cells.ASCA IgG and CBir antibodies are associated with the development of Crohn's disease and fistulae following ileal pouch-anal anastomosis.Inflammatory bowel diseases phenotype, C. difficile and NOD2 genotype are associated with shifts in human ileum associated microbial composition.Host genes related to paneth cells and xenobiotic metabolism are associated with shifts in human ileum-associated microbial composition.Inflammatory bowel disease: an impaired barrier disease.IBD1 and IBD3 determine location of Crohn's disease in the Spanish population.NOD2/CARD15 gene polymorphism in patients with inflammatory bowel disease: is Hungary different?Bacterial interactions with cells of the intestinal mucosa: Toll-like receptors and NOD2 SMAD3 gene variant is a risk factor for recurrent surgery in patients with Crohn's disease Role of the NFKB1 -94ins/delATTG promoter polymorphism in IBD and potential interactions with polymorphisms in the CARD15/NOD2, IKBL, and IL-1RN genes.Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

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The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

http://www.wikidata.org/entity/Q22250943

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The contribution of NOD2 gene ...... in inflammatory bowel disease

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Andrew P. Cuthbert

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Jeremy Sanderson

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inflammatory bowel diseases