Investigation of associations between the pregnane-X receptor gene (NR1I2) and Crohnʼs disease in Canadian children using a gene-wide haplotype-based approach-Reference-Cited by-同舟云学术

Investigation of associations between the pregnane-X receptor gene (NR1I2) and Crohnʼs disease in Canadian children using a gene-wide haplotype-based approach

Published:2008-09 Issue:9 Volume:14 Page:1214-1218
ISSN:1078-0998
Container-title:Inflammatory Bowel Diseases
language:en
Short-container-title:Inflammatory Bowel Diseases

Author:

Amre Devendra K.,Mack David R.,Israel David,Morgan Kenneth,Krupoves Alfreda,Costea Irina,Lambrette Philippe,Grimard Guy,Deslandres Colette,Levy Emile,Seidman Ernest G.

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

Reference25 articles.

1. The Epidemiology of Inflammatory Bowel Disease in Canada: A Population-Based Study

2. Inflammatory bowel diseases in pediatric and adolescent patients: Clinical, therapeutic, and psychosocial considerations

3. Inflammatory bowel disease in early childhood and adolescence: special considerations

4. Genetic susceptibility has a more important role in pediatric-onset Crohnʼs disease than in adult-onset Crohnʼs disease

5. Is Age of Onset of Crohn's Disease Governed by Mutations in NOD2/Caspase Recruitment Domains 15 and Toll-Like Receptor 4? Evaluation of a Pediatric Cohort

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4. Effect of Single Nucleotide Polymorphisms in the Xenobiotic-sensing Receptors NR1I2 and NR1I3 on the Pharmacokinetics and Toxicity of Irinotecan in Colorectal Cancer Patients;Clinical Pharmacokinetics;2016-04-26

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