Showing results (371-380 of 432) with videos related to

Sort By:
Pageof 44
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|March 3, 2016
Single nucleotide polymorphism in IL1B is associated with infection risk in paediatric acute myeloid leukaemiaL Sung, D Dix, S Cellot, et al.
Inflammatory Bowel Diseases|June 29, 2019
Analysis of Genetic Association of Intestinal Permeability in Healthy First-degree Relatives of Patients with Crohn's DiseaseWilliams Turpin, Osvaldo Espin-Garcia, Larbi Bedrani, et al.
Translational Psychiatry|February 3, 2021
Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorderChristie L Burton, Mathieu Lemire, Bowei Xiao, et al.
JCI Insight|October 22, 2024
Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplicationRabiat Adele, Rowaida Hussein, Erika Tavares, et al.
Brain : a Journal of Neurology|March 27, 2015
PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxiaRebekah K Jobling, Mirna Assoum, Oleksandr Gakh, et al.
Gastroenterology|August 14, 2020
Increased Intestinal Permeability Is Associated With Later Development of Crohn's DiseaseWilliams Turpin, Sun-Ho Lee, Juan Antonio Raygoza Garay, et al.
Human Genetics|November 30, 2014
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genesMarc Woodbury-Smith, Andrew D Paterson, Bhooma Thiruvahindrapduram, et al.
Gastroenterology|July 22, 2021
Anti-Microbial Antibody Response is Associated With Future Onset of Crohn's Disease Independent of Biomarkers of Altered Gut Barrier Function, Subclinical Inflammation, and Genetic RiskSun-Ho Lee, Williams Turpin, Osvaldo Espin-Garcia, et al.
Plos One|October 23, 2010
Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancerMiralem Mrkonjic, Nicole M Roslin, Celia M Greenwood, et al.
Gut|September 9, 2011
NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2Aleixo M Muise, Wei Xu, Cong-Hui Guo, et al.
Pageof 44