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Nature Genetics|June 2, 2026
Integrative analyses elucidate transcriptional regulatory functions of risk alleles for metabolic liver diseaseBiying Zhu, Na He, Yang Xiao, et al.Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Epigenetics in Abdominal Aortic Aneurysm: Mechanisms and Risk PredictionShuai Yuan, Gabrielle Shakt, Michael G Levin, et al.Nature Communications|May 22, 2026
Genetic variants affect diurnal glucose levels throughout the dayNasa Sinnott-Armstrong, Satu Strausz, Lea Urpa, et al.Journal of Pineal Research|February 17, 2016
Melatonin prevents cisplatin-induced primordial follicle loss via suppression of PTEN/AKT/FOXO3a pathway activation in the mouse ovaryHoon Jang, Ok-Hee Lee, Youngeun Lee, et al.Clinical Pharmacology and Therapeutics|January 27, 2025
Investigation of Genomic and Transcriptomic Risk Factors of Clopidogrel Response in African AmericansGuang Yang, Cristina Alarcon, Catherine Chanfreau, et al.Journal of the American Heart Association|June 29, 2021
Genetic Evidence for Repurposing of GLP1R (Glucagon-Like Peptide-1 Receptor) Agonists to Prevent Heart FailureIyas Daghlas, Ville Karhunen, Devleena Ray, et al.Circulation. Genomic and Precision Medicine|February 10, 2022
Coronary Artery Disease Risk of Familial Hypercholesterolemia Genetic Variants Independent of Clinically Observed Longitudinal Cholesterol ExposureShoa L Clarke, Catherine Tcheandjieu, Austin T Hilliard, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 25, 2009
Collapse of the CD27+ B-cell compartment associated with systemic plasmacytosis in patients with advanced melanoma and other cancersErica L Carpenter, Rosemarie Mick, Andrew J Rech, et al.Plos One|May 30, 2013
A randomized, double-blind, placebo-controlled assessment of BMS-936558, a fully human monoclonal antibody to programmed death-1 (PD-1), in patients with chronic hepatitis C virus infectionDavid Gardiner, Jay Lalezari, Eric Lawitz, et al.American Journal of Human Genetics|July 1, 2026
Linkage disequilibrium and allelic heterogeneity explain variation in coronary artery disease risk at 9p21 across populations and reduced effect in AfricansHasan Alkhairo, Satoshi Koyama, Kruthika Iyer, et al.Pageof 23