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Science Advances|May 28, 2019
HspB1 phosphorylation regulates its intramolecular dynamics and mechanosensitive molecular chaperone interaction with filamin CMiranda P Collier, T Reid Alderson, Carin P de Villiers, et al.American Journal of Human Genetics|January 9, 2008
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemiaChris Wallace, Stephen J Newhouse, Peter Braund, et al.Plos Genetics|June 9, 2009
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrationsMelanie Kolz, Toby Johnson, Serena Sanna, et al.Journal of the American College of Cardiology|February 18, 2026
Cardiomyopathy Gene Variants and Polygenic Risk Scores in Atrial Fibrillation: Evidence for an Atrial-First PhenotypeGuilherme L da Rocha, James Feiner, Julieta Lazarte, et al.Plos One|March 25, 2009
Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformationHelen R Griffin, Darroch H Hall, Ana Topf, et al.Diabetes|July 18, 2008
G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetesDavid-Alexandre Trégouet, Per-Henrik Groop, Steven McGinn, et al.The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.Plos Genetics|June 30, 2010
A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathyHouman Ashrafian, Louise Docherty, Vincenzo Leo, et al.European Heart Journal. Digital Health|July 31, 2024
Hypertrophic cardiomyopathy detection with artificial intelligence electrocardiography in international cohorts: an external validation studyKonstantinos C Siontis, Mikolaj A Wieczorek, Maren Maanja, et al.The New England Journal of Medicine|April 9, 2015
Genetically determined height and coronary artery diseaseChristopher P Nelson, Stephen E Hamby, Danish Saleheen, et al.Pageof 43