Showing results (851-860 of 1,326) with videos related to

Sort By:
Pageof 133
CMAJ Open|October 24, 2022
Determinants of SARS-CoV-2 vaccine willingness among people incarcerated in 3 Canadian federal prisons: a cross-sectional studyKathryn Romanchuk, Blake Linthwaite, Joseph Cox, et al.
BMC Public Health|February 2, 2021
Feasibility of implementation of CARD™ for school-based immunizations in Calgary, Alberta: a cluster trialAnna Taddio, Joanne Coldham, Charlotte Logeman, et al.
Endocrinology|December 15, 2015
Research-Focused Isolation of Human Islets From Donors With and Without Diabetes at the Alberta Diabetes Institute IsletCoreJames Lyon, Jocelyn E Manning Fox, Aliya F Spigelman, et al.
Bipolar Disorders|March 3, 2015
Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorderEliana Marisa Ramos, Tammy Gillis, Jayalakshmi S Mysore, et al.
Vaccine|May 20, 2016
Contributions and challenges for worldwide vaccine safety: The Global Advisory Committee on Vaccine Safety at 15 yearsEdwin J Asturias, Melinda Wharton, Robert Pless, et al.
The Journal of Biological Chemistry|February 6, 2008
Investigation of transport mechanisms and regulation of intracellular Zn2+ in pancreatic alpha-cellsArmen V Gyulkhandanyan, Hongfang Lu, Simon C Lee, et al.
Molecular Metabolism|March 22, 2025
Peptidylglycine alpha-amidating monooxygenase is important in mice for beta-cell cilia formation and insulin secretion but promotes diabetes risk through beta-cell independent mechanismsYi-Chun Chen, Nils E Bäck, Jenicia Zhen, et al.
Journal of Autoimmunity|October 18, 2016
In vivo effector functions of high-affinity mouse IgG receptor FcγRI in disease and therapy modelsCaitlin M Gillis, Priscila P Zenatti, David A Mancardi, et al.
Neurobiology of Disease|October 22, 2008
Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genesElla Dragileva, Audrey Hendricks, Allison Teed, et al.
Nature Genetics|October 1, 1993
De novo expansion of a (CAG)n repeat in sporadic Huntington's diseaseR H Myers, M E MacDonald, W J Koroshetz, et al.
Pageof 133