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Mohamed Chahine

Showing results (1-10 of 171) with videos related to

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Frontiers in Pharmacology|July 23, 2011
New insights into cardiac and brain sodium channels modulation by Beta blockersMohamed Chahine
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 15, 2025
AAV-mediated DMPK silencing: A defining moment in myotonic dystrophy type 1 therapeuticsMohamed Chahine
The Journal of General Physiology|February 23, 2018
Improving the characterization of calcium channel gating pore currents with Stac3Mohamed Chahine
Journal of Cardiovascular Electrophysiology|December 18, 2003
Pathophysiology of Brugada syndromeMohamed Chahine
Future Cardiology|May 30, 2015
Gating pore current is a novel biophysical defect of Nav1.5 mutations associated with unusual cardiac arrhythmias and dilationMohamed Chahine
Circulation Research|October 10, 2009
Cardiac metabolic state and Brugada syndrome: a link revealedMohamed Chahine
Frontiers in Cellular Neuroscience|October 7, 2014
Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neuronsOlivier Thériault, Mohamed Chahine
Frontiers in Cardiovascular Medicine|October 26, 2018
A New Cardiac Channelopathy: From Clinical Phenotypes to Molecular Mechanisms Associated With Na<sub>v</sub>1.5 Gating PoresAdrien Moreau, Mohamed Chahine
The Journal of Membrane Biology|June 15, 2007
Accessibility of four arginine residues on the S4 segment of the Bacillus halodurans sodium channelJonathan Blanchet, Mohamed Chahine
The Journal of Physiology|January 14, 2021
R1617Q epilepsy mutation slows Na<sub>V</sub> 1.6 sodium channel inactivation and increases the persistent current and neuronal firingHugo Poulin, Mohamed Chahine
Pageof 18

Showing results (1-10 of 171) with videos related to

Sort By:
Pageof 18
Frontiers in Pharmacology|July 23, 2011
New insights into cardiac and brain sodium channels modulation by Beta blockersMohamed Chahine
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 15, 2025
AAV-mediated DMPK silencing: A defining moment in myotonic dystrophy type 1 therapeuticsMohamed Chahine
The Journal of General Physiology|February 23, 2018
Improving the characterization of calcium channel gating pore currents with Stac3Mohamed Chahine
Journal of Cardiovascular Electrophysiology|December 18, 2003
Pathophysiology of Brugada syndromeMohamed Chahine
Future Cardiology|May 30, 2015
Gating pore current is a novel biophysical defect of Nav1.5 mutations associated with unusual cardiac arrhythmias and dilationMohamed Chahine
Circulation Research|October 10, 2009
Cardiac metabolic state and Brugada syndrome: a link revealedMohamed Chahine
Frontiers in Cellular Neuroscience|October 7, 2014
Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neuronsOlivier Thériault, Mohamed Chahine
Frontiers in Cardiovascular Medicine|October 26, 2018
A New Cardiac Channelopathy: From Clinical Phenotypes to Molecular Mechanisms Associated With Na<sub>v</sub>1.5 Gating PoresAdrien Moreau, Mohamed Chahine
The Journal of Membrane Biology|June 15, 2007
Accessibility of four arginine residues on the S4 segment of the Bacillus halodurans sodium channelJonathan Blanchet, Mohamed Chahine
The Journal of Physiology|January 14, 2021
R1617Q epilepsy mutation slows Na<sub>V</sub> 1.6 sodium channel inactivation and increases the persistent current and neuronal firingHugo Poulin, Mohamed Chahine
Pageof 18