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S Kass

Showing results (281-290 of 321) with videos related to

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Circulation Research|April 17, 2001
Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channelH Abriel, C Cabo, X H Wehrens, et al.
The Journal of Physiology|October 26, 2011
Biophysical properties of slow potassium channels in human embryonic stem cell derived cardiomyocytes implicate subunit stoichiometryKai Wang, Cecile Terrenoire, Kevin J Sampson, et al.
Nature Communications|January 20, 2016
Autonomous beating rate adaptation in human stem cell-derived cardiomyocytesGeorge Eng, Benjamin W Lee, Lev Protas, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|July 21, 2005
Clinical, genetic, and electrophysiologic characteristics of a new PAS-domain HERG mutation (M124R) causing Long QT syndromeLiat Shushi, Batsheva Kerem, Maya Goldmit, et al.
Journal of Behavioral Medicine|December 11, 2012
Improving secondary stroke self-care among underserved ethnic minority individuals: a randomized clinical trial of a pilot interventionGina L Evans-Hudnall, Melinda A Stanley, Allison N Clark, et al.
Circulation|March 10, 2001
Characterization of sodium channel alpha- and beta-subunits in rat and mouse cardiac myocytesJ Dhar Malhotra, C Chen, I Rivolta, et al.
Heart Rhythm|April 27, 2005
Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac deathTom Rossenbacker, Sheila J Carroll, Huajun Liu, et al.
Bioorganic & Medicinal Chemistry Letters|June 1, 2021
Human iPSC-derived cardiomyocytes and pyridyl-phenyl mexiletine analogsMark Johnson, Jorge Gomez-Galeno, Daniel Ryan, et al.
The Journal of General Physiology|January 18, 2012
Characterization of KCNQ1 atrial fibrillation mutations reveals distinct dependence on KCNE1Priscilla J Chan, Jeremiah D Osteen, Dazhi Xiong, et al.
The Journal of Clinical Investigation|September 1, 1995
Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3C A MacRae, N Ghaisas, S Kass, et al.
Pageof 33

Showing results (281-290 of 321) with videos related to

Sort By:
Pageof 33
Circulation Research|April 17, 2001
Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channelH Abriel, C Cabo, X H Wehrens, et al.
The Journal of Physiology|October 26, 2011
Biophysical properties of slow potassium channels in human embryonic stem cell derived cardiomyocytes implicate subunit stoichiometryKai Wang, Cecile Terrenoire, Kevin J Sampson, et al.
Nature Communications|January 20, 2016
Autonomous beating rate adaptation in human stem cell-derived cardiomyocytesGeorge Eng, Benjamin W Lee, Lev Protas, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|July 21, 2005
Clinical, genetic, and electrophysiologic characteristics of a new PAS-domain HERG mutation (M124R) causing Long QT syndromeLiat Shushi, Batsheva Kerem, Maya Goldmit, et al.
Journal of Behavioral Medicine|December 11, 2012
Improving secondary stroke self-care among underserved ethnic minority individuals: a randomized clinical trial of a pilot interventionGina L Evans-Hudnall, Melinda A Stanley, Allison N Clark, et al.
Circulation|March 10, 2001
Characterization of sodium channel alpha- and beta-subunits in rat and mouse cardiac myocytesJ Dhar Malhotra, C Chen, I Rivolta, et al.
Heart Rhythm|April 27, 2005
Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac deathTom Rossenbacker, Sheila J Carroll, Huajun Liu, et al.
Bioorganic & Medicinal Chemistry Letters|June 1, 2021
Human iPSC-derived cardiomyocytes and pyridyl-phenyl mexiletine analogsMark Johnson, Jorge Gomez-Galeno, Daniel Ryan, et al.
The Journal of General Physiology|January 18, 2012
Characterization of KCNQ1 atrial fibrillation mutations reveals distinct dependence on KCNE1Priscilla J Chan, Jeremiah D Osteen, Dazhi Xiong, et al.
The Journal of Clinical Investigation|September 1, 1995
Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3C A MacRae, N Ghaisas, S Kass, et al.
Pageof 33