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International Journal of Molecular Sciences|July 29, 2025
Transmembrane Protein 43: Molecular and Pathogenetic Implications in Arrhythmogenic Cardiomyopathy and Various Other DiseasesBuyan-Ochir Orgil, Mekaea S Spaulding, Harrison P Smith, et al.Pediatric Cardiology|July 1, 2016
The Impact of Concomitant Left Ventricular Non-compaction with Congenital Heart Disease on Perioperative OutcomesPreeti Ramachandran, Jessica G Woo, Thomas D Ryan, et al.American Journal of Physiology. Heart and Circulatory Physiology|November 8, 2015
Accelerated cardiac remodeling in desmoplakin transgenic mice in response to endurance exercise is associated with perturbed Wnt/β-catenin signalingRuben Martherus, Rahul Jain, Ken Takagi, et al.Molecular Genetics and Metabolism|June 8, 2002
Novel mutations in domain I of SCN5A cause Brugada syndromeMatteo Vatta, Robert Dumaine, Charles Antzelevitch, et al.Journal of Cardiac Failure|October 16, 2013
Characteristics and outcomes of heart failure-related intensive care unit admissions in children with cardiomyopathyPirouz Shamszad, Matthew Hall, Joseph W Rossano, et al.Reviews in Cardiovascular Medicine|September 10, 2025
Left Ventricular Noncompaction Cardiomyopathy in Children: A Focus on Genetic and Molecular MechanismsMonica B Lehman, Buyan-Ochir Orgil, Karine Guerrier, et al.Journal of the American College of Cardiology|March 5, 2004
Molecular normalization of dystrophin in the failing left and right ventricle of patients treated with either pulsatile or continuous flow-type ventricular assist devicesMatteo Vatta, Sonny J Stetson, Shinawe Jimenez, et al.Research Square|May 5, 2025
Unraveling the Genetic Blueprint of Doxorubicin-Induced Cardiotoxicity Through Systems Genetics ApproachesBuyan-Ochir Orgil, Akhilesh K Bajpai, Neely Alberson, et al.Pediatric Cardiology|November 19, 2004
Left ventricular noncompaction cardiomyopathy in association with trisomy 13C J McMahon, A C Chang, R H Pignatelli, et al.Cell|March 10, 1995
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndromeQ Wang, J Shen, I Splawski, et al.Pageof 44