UNIGE document Scientific Article
previous document  unige:25737  next document
add to browser collection
Title

Association of a common vitamin D-binding protein polymorphism with inflammatory bowel disease
Authors
Eloranta, Jyrki J
Wenger, Christa
Mwinyi, Jessica
Hiller, Christian
Gubler, Christoph
Vavricka, Stephan R
Fried, Michael
Kullak-Ublick, Gerd A
CollaborationWith : Tempia-Caliera Schaeppi, Michela
Published in Pharmacogenetics and genomics. 2011, vol. 21, no. 9, p. 559-64
Abstract Inflammatory bowel diseases (IBDs), Crohn's disease, and ulcerative colitis (UC), are multifactorial disorders, characterized by chronic inflammation of the intestine. A number of genetic components have been proposed to contribute to IBD pathogenesis. In this case-control study, we investigated the association between two common vitamin D-binding protein (DBP) genetic variants and IBD susceptibility. These two single nucleotide polymorphisms (SNPs) in exon 11 of the DBP gene, at codons 416 (GAT>GAG; Asp>Glu) and 420 (ACG>AAG; Thr>Lys), have been previously suggested to play roles in the etiology of other autoimmune diseases.
Keywords Adolescent — Adult — Aged — Aged, 80 and over — Case-Control Studies — Female — Gene Frequency — Genetic Association Studies — Genetic Predisposition to Disease — Genotype — Haplotypes — Humans — Inflammatory Bowel Diseases/genetics — Male — Middle Aged — Polymorphism, Genetic — Polymorphism, Single Nucleotide — Vitamin D-Binding Protein/genetics
Identifiers
PMID: 21832969
Full text
Article (Published version) (123 Kb) - document accessible for UNIGE members only Limited access to UNIGE
Structures
Faculté de médecine / Section de médecine fondamentale / Département de pathologie et immunologie
Faculté de médecine / Section de médecine clinique / Département de pédiatrie, gynécologie et obstétrique
Research group Gastroentérologie et transplantation (pédiatrie) (181)
Citation
(ISO format) 		ELORANTA, Jyrki J et al. Association of a common vitamin D-binding protein polymorphism with inflammatory bowel disease. In: Pharmacogenetics and genomics, 2011, vol. 21, n° 9, p. 559-64. doi: 10.1097/FPC.0b013e328348f70c https://archive-ouverte.unige.ch/unige:25737

536 hits

0 download

Contact an author

Update request

Update

Deposited on : 2013-01-18

Export document
Format :
Citation style :