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Nature Medicine|May 28, 2021
Loss-of-function mutations in the melanocortin 4 receptor in a UK birth cohortKaitlin H Wade, Brian Y H Lam, Audrey Melvin, et al.Nature Medicine|March 5, 2024
Multi-ancestry polygenic mechanisms of type 2 diabetesKirk Smith, Aaron J Deutsch, Carolyn McGrail, et al.Molecular Metabolism|December 12, 2025
Cross-species studies implicate the melanocortin 3 receptor more strongly in the control of pubertal development than energy balanceKatie Duckett, Alyce McClellan, Laura J Corbin, et al.Nature|April 22, 2026
Glycerol-driven TNAP activation in thermogenesis and mineralizationMohammed Faiz Hussain, Shreya S Krishnan, Brittany L Carroll, et al.Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controlsSam Hodgson, Vi Bui, Siqi Hu, et al.The Journal of Clinical Endocrinology and Metabolism|June 20, 2023
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and PubertyKatie Duckett, Alice Williamson, John W R Kincaid, et al.American Journal of Human Genetics|January 24, 2023
Loci for insulin processing and secretion provide insight into type 2 diabetes riskK Alaine Broadaway, Xianyong Yin, Alice Williamson, et al.Nature Genetics|June 8, 2023
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptakeAlice Williamson, Dougall M Norris, Xianyong Yin, et al.Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complicationsKen Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, et al.Nature|February 19, 2024
Genetic drivers of heterogeneity in type 2 diabetes pathophysiologyKen Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, et al.Pageof 2