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Inflammatory Bowel Diseases|January 20, 2023
Serum Lipidomic Screen Identifies Key Metabolites, Pathways, and Disease Classifiers in Crohn's DiseaseRomain Ferru-Clément, Gabrielle Boucher, Anik Forest, et al.Journal of Crohn'S & Colitis|October 10, 2015
Ocular Manifestations in Inflammatory Bowel Disease Are Associated with Other Extra-intestinal Manifestations, Gender, and Genes Implicated in Other Immune-related TraitsSasha Taleban, Dalin Li, Stephan R Targan, et al.Gut|May 20, 2016
Appendectomy does not decrease the risk of future colectomy in UC: results from a large cohort and meta-analysisAlyssa Parian, Berkeley Limketkai, Joyce Koh, et al.Nature Genetics|January 24, 2009
Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's diseaseSteven A McCarroll, Alan Huett, Petric Kuballa, et al.Science (New York, N.Y.)|February 9, 2018
<i>C1orf106</i> is a colitis risk gene that regulates stability of epithelial adherens junctionsVishnu Mohanan, Toru Nakata, A Nicole Desch, et al.Plos Genetics|February 8, 2011
A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac diseaseEleonora A M Festen, Philippe Goyette, Todd Green, et al.American Journal of Epidemiology|June 5, 2010
Variation within DNA repair pathway genes and risk of multiple sclerosisFarren B S Briggs, Benjamin A Goldstein, Jacob L McCauley, et al.Human Molecular Genetics|March 10, 2010
CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosisPaola G Bronson, Stacy Caillier, Patricia P Ramsay, et al.Nature Genetics|December 23, 2008
Common variants in the NLRP3 region contribute to Crohn's disease susceptibilityAlexandra-Chloé Villani, Mathieu Lemire, Geneviève Fortin, et al.Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|December 28, 2020
Life-threatening arrhythmias with autosomal recessive TECRL variantsGregory Webster, Elhadi H Aburawi, Marie A Chaix, et al.Pageof 19