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BMJ Open|May 7, 2013
Dabigatran use in Danish atrial fibrillation patients in 2011: a nationwide studyRikke Sørensen, Gunnar Gislason, Christian Torp-Pedersen, et al.
Nature Communications|April 26, 2016
Identifying genetically driven clinical phenotypes using linear mixed modelsJonathan D Mosley, John S Witte, Emma K Larkin, et al.
Thrombosis and Haemostasis|February 17, 2017
Identification of unique venous thromboembolism-susceptibility variants in African-AmericansJohn A Heit, Sebastian M Armasu, Bryan M McCauley, et al.
American Journal of Physiology. Cell Physiology|November 21, 2019
Real-time visualization of titin dynamics reveals extensive reversible photobleaching in human induced pluripotent stem cell-derived cardiomyocytesAdrian G Cadar, Tromondae K Feaster, Kevin R Bersell, et al.
Circulation. Arrhythmia and Electrophysiology|October 8, 2009
Biophysical properties of 9 KCNQ1 mutations associated with long-QT syndromeTao Yang, Seo-Kyung Chung, Wei Zhang, et al.
Blood|June 7, 2008
A genome-wide scan for common genetic variants with a large influence on warfarin maintenance doseGregory M Cooper, Julie A Johnson, Taimour Y Langaee, et al.
The Journal of Clinical Investigation|August 26, 2006
Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardiaBjörn C Knollmann, Nagesh Chopra, Thinn Hlaing, et al.
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