Single nucleotide polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with Crohn's disease (Q28293850)

2

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Athanassios J Archimandritis

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George Nasioulas

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Nicholas P Anagnou

World Journal of Gastroenterology

5

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language of work or name

English

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publication date

21 December 2005

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published in

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volume

11

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issue

47

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page(s)

7525-30

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cites work

A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease

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Genetic variation in DLG5 is associated with inflammatory bowel disease

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Functional variants of OCTN cation transporter genes are associated with Crohn disease

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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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Mapping of a susceptibility locus for Crohn's disease on chromosome 16

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A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn's disease locus (IBD5)

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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

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DLG5 variants do not influence susceptibility to inflammatory bowel disease in the Scottish population

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Association between polymorphisms in the Toll-like receptor 4, CD14, and CARD15/NOD2 and inflammatory bowel disease in the Greek population

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Genome scan analyses and positional cloning strategy in IBD: successes and limitations

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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

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International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16.

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Genetics of inflammatory bowel disease: a reappraisal.

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Metabolic induction of experimental ulcerative colitis by inhibition of fatty acid oxidation

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Inflammatory bowel disease (1)

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Further evidence of IBD5/CARD15 (NOD2) epistasis in the susceptibility to ulcerative colitis

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Characterization of genotype-phenotype relationships and stratification by the CARD15 variant genotype for inflammatory bowel disease susceptibility loci using multiple short tandem repeat genetic markers

21 January 2018

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Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

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Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

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Linkage heterogeneity for the IBD1 locus in Crohn's disease pedigrees by disease onset and severity

21 January 2018

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12 December 2020

Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease

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12 December 2020

The genetics of inflammatory bowel disease

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12 December 2020

Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel disease

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12 December 2020

Association of NOD2/CARD15 variants with Crohn's disease in a Greek population

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12 December 2020