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Nature Metabolism|January 27, 2026
Unravelling the molecular mechanisms causal to type 2 diabetes across global populations and disease-relevant tissuesOzvan Bocher, Ana Luiza Arruda, Satoshi Yoshiji, et al.Nature Communications|November 20, 2021
Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant complex traitsMatthew C Pahl, Claudia A Doege, Kenyaita M Hodge, et al.Journal of Medicinal Chemistry|May 19, 2026
Discovery of Fosigotifator, a Potent eIF2B Activator with Desired Properties for Human StudiesJennifer M Frost, Yunsong Tong, Xiangdong Xu, et al.Nature Communications|November 3, 2025
Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese populationNobuyuki Enzan, Kazuo Miyazawa, Satoshi Koyama, et al.Plos Genetics|June 2, 2022
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran ProgramSridharan Raghavan, Jie Huang, Catherine Tcheandjieu, et al.American Journal of Epidemiology|July 16, 2009
Underlying genetic models of inheritance in established type 2 diabetes associationsGeorgia Salanti, Lorraine Southam, David Altshuler, et al.Plos One|August 26, 2020
Validating a non-invasive, ALT-based non-alcoholic fatty liver phenotype in the million veteran programMarina Serper, Marijana Vujkovic, David E Kaplan, et al.Medrxiv : the Preprint Server for Health Sciences|July 29, 2024
Multi-omics characterization of type 2 diabetes associated genetic variationRavi Mandla, Kim Lorenz, Xianyong Yin, et al.Diabetes Care|December 18, 2019
Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHCRajashree Mishra, Mikael Åkerlund, Diana L Cousminer, et al.Nature|April 25, 2014
Guidelines for investigating causality of sequence variants in human diseaseD G MacArthur, T A Manolio, D P Dimmock, et al.Pageof 42