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Jonathan M Cordeiro

Showing results (41-50 of 62) with videos related to

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Stem Cells International|September 21, 2020
Susceptibility to Ventricular Arrhythmias Resulting from Mutations in <i>FKBP1B</i>, <i>PXDNL</i>, and <i>SCN9A</i> Evaluated in hiPSC CardiomyocytesHector Barajas-Martinez, Maya Smith, Dan Hu, et al.
Canadian Journal of Physiology and Pharmacology|December 18, 2010
Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2Jonathan M Cordeiro, Guillermo J Perez, Nicole Schmitt, et al.
Journal of Cardiovascular Electrophysiology|July 28, 2007
A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndromeYoshiyasu Aizawa, Kazuo Ueda, Fabiana Scornik, et al.
Circulation Research|July 5, 2008
Lidocaine-induced Brugada syndrome phenotype linked to a novel double mutation in the cardiac sodium channelHector M Barajas-Martínez, Dan Hu, Jonathan M Cordeiro, et al.
Circulation. Heart Failure|May 31, 2014
Ranolazine effectively suppresses atrial fibrillation in the setting of heart failureAlexander Burashnikov, José M Di Diego, Hector Barajas-Martínez, et al.
Journal of Molecular and Cellular Cardiology|April 2, 2013
Identification and characterization of a transient outward K+ current in human induced pluripotent stem cell-derived cardiomyocytesJonathan M Cordeiro, Vladislav V Nesterenko, Serge Sicouri, et al.
Pacing and Clinical Electrophysiology : PACE|December 23, 2009
Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndromeDan Hu, Hector Barajas-Martinez, Vladislav V Nesterenko, et al.
Journal of Veterinary Cardiology : the Official Journal of the European Society of Veterinary Cardiology|February 26, 2013
Cardiomyocyte calcium cycling in a naturally occurring German shepherd dog model of inherited ventricular arrhythmia and sudden cardiac deathSophy A Jesty, Seung Woo Jung, Jonathan M Cordeiro, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotypeDan Hu, Hector Barajas-Martinez, Elena Burashnikov, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|June 21, 2022
The G213D variant in Nav1.5 alters sodium current and causes an arrhythmogenic phenotype resulting in a multifocal ectopic Purkinje-related premature contraction phenotype in human-induced pluripotent stem cell-derived cardiomyocytesKirstine Calloe, Michelle Geryk, Kristine Freude, et al.
Pageof 7

Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
Stem Cells International|September 21, 2020
Susceptibility to Ventricular Arrhythmias Resulting from Mutations in <i>FKBP1B</i>, <i>PXDNL</i>, and <i>SCN9A</i> Evaluated in hiPSC CardiomyocytesHector Barajas-Martinez, Maya Smith, Dan Hu, et al.
Canadian Journal of Physiology and Pharmacology|December 18, 2010
Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2Jonathan M Cordeiro, Guillermo J Perez, Nicole Schmitt, et al.
Journal of Cardiovascular Electrophysiology|July 28, 2007
A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndromeYoshiyasu Aizawa, Kazuo Ueda, Fabiana Scornik, et al.
Circulation Research|July 5, 2008
Lidocaine-induced Brugada syndrome phenotype linked to a novel double mutation in the cardiac sodium channelHector M Barajas-Martínez, Dan Hu, Jonathan M Cordeiro, et al.
Circulation. Heart Failure|May 31, 2014
Ranolazine effectively suppresses atrial fibrillation in the setting of heart failureAlexander Burashnikov, José M Di Diego, Hector Barajas-Martínez, et al.
Journal of Molecular and Cellular Cardiology|April 2, 2013
Identification and characterization of a transient outward K+ current in human induced pluripotent stem cell-derived cardiomyocytesJonathan M Cordeiro, Vladislav V Nesterenko, Serge Sicouri, et al.
Pacing and Clinical Electrophysiology : PACE|December 23, 2009
Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndromeDan Hu, Hector Barajas-Martinez, Vladislav V Nesterenko, et al.
Journal of Veterinary Cardiology : the Official Journal of the European Society of Veterinary Cardiology|February 26, 2013
Cardiomyocyte calcium cycling in a naturally occurring German shepherd dog model of inherited ventricular arrhythmia and sudden cardiac deathSophy A Jesty, Seung Woo Jung, Jonathan M Cordeiro, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotypeDan Hu, Hector Barajas-Martinez, Elena Burashnikov, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|June 21, 2022
The G213D variant in Nav1.5 alters sodium current and causes an arrhythmogenic phenotype resulting in a multifocal ectopic Purkinje-related premature contraction phenotype in human-induced pluripotent stem cell-derived cardiomyocytesKirstine Calloe, Michelle Geryk, Kristine Freude, et al.
Pageof 7