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Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 31, 2023
Evidence of recent and ongoing admixture in the U.S. and influences on health and disparitiesHannah M Seagle, Jacklyn N Hellwege, Brian S Mautz, et al.
European Heart Journal. Cardiovascular Pharmacotherapy|December 28, 2016
Non-steroidal anti-inflammatory drug use is associated with increased risk of out-of-hospital cardiac arrest: a nationwide case-time-control studyKathrine B Sondergaard, Peter Weeke, Mads Wissenberg, et al.
Pharmacogenomics|December 11, 2014
Genetic variation in the UGT1A locus is associated with simvastatin efficacy in a clinical practice settingOtito F Iwuchukwu, QiPing Feng, Wei-Qi Wei, et al.
Archives of Cardiovascular Diseases|November 6, 2019
Heart failure and atrial tachyarrhythmia on abiraterone: A pharmacovigilance studyMarie Bretagne, Bénédicte Lebrun-Vignes, Antoine Pariente, et al.
Circulation. Genomic and Precision Medicine|January 28, 2026
Unbiased Characterization of Atrial Fibrillation Phenotypic Architecture Provides Insight Into Genetic Liability and Clinically Relevant OutcomesGiovanni Davogustto, Shilin Zhao, Yajing Li, et al.
Circulation|January 7, 2022
Common Ancestry-Specific Ion Channel Variants Predispose to Drug-Induced ArrhythmiasYuko Wada, Tao Yang, Christian M Shaffer, et al.
Medrxiv : the Preprint Server for Health Sciences|February 26, 2024
Unbiased characterization of atrial fibrillation phenotypic architecture provides insight to genetic liability and clinically relevant outcomesGiovanni Davogustto, Shilin Zhao, Yajing Li, et al.
Plos Computational Biology|June 18, 2015
Deciphering Signaling Pathway Networks to Understand the Molecular Mechanisms of Metformin ActionJingchun Sun, Min Zhao, Peilin Jia, et al.
Heart Rhythm|September 1, 2009
Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)Pieter G Postema, Christian Wolpert, Ahmad S Amin, et al.
Cardiovascular Research|February 19, 2015
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative studyElijah R Behr, Eleonora Savio-Galimberti, Julien Barc, et al.
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