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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2003-3-12
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pubmed:abstractText |
Variants of the caspase activating recruitment domain 15/nucleotide oligomerisation domain 2 (CARD15/NOD2) gene have been associated with susceptibility to Crohn's disease (CD). Aim: Our aim was to evaluate the allele frequencies of the CARD15 variants R702W, G908R, and 1007fs in Finnish inflammatory bowel disease (IBD) patients and to search for possible associations between CARD15 variants and occurrence of familial forms of IBD or complicated forms of CD.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-10053016,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-10439963,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-10469845,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-10701144,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-10888861,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11058605,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11087742,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11216980,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11309682,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11378820,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11385576,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11385577,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11425413,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11585102,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11607846,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11709511,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11875755,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11910336,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-11910337,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-12020527,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-12105836,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-12126248,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-8587604,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-8894707,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-9616307,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-9679041,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-9797357,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-9797359,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12631669-9924607
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0017-5749
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
52
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
558-62
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:12631669-Adolescent,
pubmed-meshheading:12631669-Adult,
pubmed-meshheading:12631669-Age of Onset,
pubmed-meshheading:12631669-Aged,
pubmed-meshheading:12631669-Carrier Proteins,
pubmed-meshheading:12631669-Child,
pubmed-meshheading:12631669-Colitis, Ulcerative,
pubmed-meshheading:12631669-Crohn Disease,
pubmed-meshheading:12631669-Female,
pubmed-meshheading:12631669-Gene Frequency,
pubmed-meshheading:12631669-Genetic Predisposition to Disease,
pubmed-meshheading:12631669-Genetic Variation,
pubmed-meshheading:12631669-Heterozygote,
pubmed-meshheading:12631669-Homozygote,
pubmed-meshheading:12631669-Humans,
pubmed-meshheading:12631669-Intracellular Signaling Peptides and Proteins,
pubmed-meshheading:12631669-Male,
pubmed-meshheading:12631669-Middle Aged,
pubmed-meshheading:12631669-Nod2 Signaling Adaptor Protein,
pubmed-meshheading:12631669-Phenotype,
pubmed-meshheading:12631669-Retrospective Studies
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pubmed:year |
2003
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pubmed:articleTitle |
CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.
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pubmed:affiliation |
Department of Medicine, Helsinki University Hospital, Helsinki, Finland. tiina.helio@hus.fi
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Multicenter Study
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