16002353

Source:http://linkedlifedata.com/resource/pubmed/id/16002353

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010346, umls-concept:C0041432, umls-concept:C0680240, umls-concept:C1710263, umls-concept:C1826449, umls-concept:C1882417, umls-concept:C2698415
pubmed:issue	10
pubmed:dateCreated	2005-9-13
pubmed:abstractText	CARD15/NOD2 polymorphisms are associated with Crohn's disease. There is a high concordance for disease and disease phenotype in monozygotic twin pairs with Crohn's disease.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100958385
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Arginine, http://linkedlifedata.com/resource/pubmed/chemical/Glycine, http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/Leucine, http://linkedlifedata.com/resource/pubmed/chemical/NOD2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Nod2 Signaling Adaptor Protein, http://linkedlifedata.com/resource/pubmed/chemical/Tryptophan
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1590-8658
pubmed:author	pubmed-author:BresseLL, pubmed-author:D'AmateCC, pubmed-author:HalfvarsonJJ, pubmed-author:JärnerotGG, pubmed-author:PetterssonSS, pubmed-author:TyskCC
pubmed:issnType	Print
pubmed:volume	37
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	768-72
pubmed:dateRevised	2008-5-13
pubmed:meshHeading	pubmed-meshheading:16002353-Adolescent, pubmed-meshheading:16002353-Adult, pubmed-meshheading:16002353-Arginine, pubmed-meshheading:16002353-Case-Control Studies, pubmed-meshheading:16002353-Child, pubmed-meshheading:16002353-Crohn Disease, pubmed-meshheading:16002353-Female, pubmed-meshheading:16002353-Frameshift Mutation, pubmed-meshheading:16002353-Gene Frequency, pubmed-meshheading:16002353-Genetic Predisposition to Disease, pubmed-meshheading:16002353-Genotype, pubmed-meshheading:16002353-Glycine, pubmed-meshheading:16002353-Humans, pubmed-meshheading:16002353-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:16002353-Leucine, pubmed-meshheading:16002353-Male, pubmed-meshheading:16002353-Middle Aged, pubmed-meshheading:16002353-Nod2 Signaling Adaptor Protein, pubmed-meshheading:16002353-Polymorphism, Genetic, pubmed-meshheading:16002353-Sweden, pubmed-meshheading:16002353-Tryptophan, pubmed-meshheading:16002353-Twins, Monozygotic
pubmed:year	2005
pubmed:articleTitle	CARD15/NOD2 polymorphisms do not explain concordance of Crohn's disease in Swedish monozygotic twins.
pubmed:affiliation	Division of Gastroenterology, Department of Internal Medicine, Orebro University Hospital, 701 85 Orebro, Sweden. jonas.halfvarson@orebroll.se
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't