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Alfred L George

Showing results (51-60 of 296) with videos related to

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Molecular Pharmacology|September 17, 2020
GS-967 and Eleclazine Block Sodium Channels in Human Induced Pluripotent Stem Cell-Derived CardiomyocytesFranck Potet, Defne E Egecioglu, Paul W Burridge, et al.
Circulation. Arrhythmia and Electrophysiology|May 30, 2015
Intracellular calcium attenuates late current conducted by mutant human cardiac sodium channelsFranck Potet, Thomas M Beckermann, Jennifer D Kunic, et al.
The Journal of General Physiology|December 29, 2005
Single-channel properties of human NaV1.1 and mechanism of channel dysfunction in SCN1A-associated epilepsyCarlos G Vanoye, Christoph Lossin, Thomas H Rhodes, et al.
The Journal of Clinical Investigation|December 19, 2002
Functional repair of a mutant chloride channel using a trans-splicing ribozymeChristopher S Rogers, Carlos G Vanoye, Bruce A Sullenger, et al.
The Journal of Physiology|November 26, 2008
KCNE4 domains required for inhibition of KCNQ1Lauren J Manderfield, Melissa A Daniels, Carlos G Vanoye, et al.
Heart Rhythm|May 13, 2014
Novel SCN5A mutation in amiodarone-responsive multifocal ventricular ectopy-associated cardiomyopathyThomas M Beckermann, Karen McLeod, Victoria Murday, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2017
CaMKII modulates sodium current in neurons from epileptic <i>Scn2a</i> mutant miceChristopher H Thompson, Nicole A Hawkins, Jennifer A Kearney, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Epilepsy-associated Variants of a Single SCN1A Codon exhibit Divergent Functional PropertiesLanie N Liebovitz, Christopher H Thompson, Linda L Laux, et al.
The Journal of General Physiology|January 30, 2020
Alternative splicing potentiates dysfunction of early-onset epileptic encephalopathy SCN2A variantsChristopher H Thompson, Roy Ben-Shalom, Kevin J Bender, et al.
Neurobiology of Disease|November 27, 2024
Novel mouse model of alternating hemiplegia of childhood exhibits prominent motor and seizure phenotypesNicole A Hawkins, Jean-Marc DeKeyser, Jennifer A Kearney, et al.
Pageof 30

Showing results (51-60 of 296) with videos related to

Sort By:
Pageof 30
Molecular Pharmacology|September 17, 2020
GS-967 and Eleclazine Block Sodium Channels in Human Induced Pluripotent Stem Cell-Derived CardiomyocytesFranck Potet, Defne E Egecioglu, Paul W Burridge, et al.
Circulation. Arrhythmia and Electrophysiology|May 30, 2015
Intracellular calcium attenuates late current conducted by mutant human cardiac sodium channelsFranck Potet, Thomas M Beckermann, Jennifer D Kunic, et al.
The Journal of General Physiology|December 29, 2005
Single-channel properties of human NaV1.1 and mechanism of channel dysfunction in SCN1A-associated epilepsyCarlos G Vanoye, Christoph Lossin, Thomas H Rhodes, et al.
The Journal of Clinical Investigation|December 19, 2002
Functional repair of a mutant chloride channel using a trans-splicing ribozymeChristopher S Rogers, Carlos G Vanoye, Bruce A Sullenger, et al.
The Journal of Physiology|November 26, 2008
KCNE4 domains required for inhibition of KCNQ1Lauren J Manderfield, Melissa A Daniels, Carlos G Vanoye, et al.
Heart Rhythm|May 13, 2014
Novel SCN5A mutation in amiodarone-responsive multifocal ventricular ectopy-associated cardiomyopathyThomas M Beckermann, Karen McLeod, Victoria Murday, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2017
CaMKII modulates sodium current in neurons from epileptic <i>Scn2a</i> mutant miceChristopher H Thompson, Nicole A Hawkins, Jennifer A Kearney, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Epilepsy-associated Variants of a Single SCN1A Codon exhibit Divergent Functional PropertiesLanie N Liebovitz, Christopher H Thompson, Linda L Laux, et al.
The Journal of General Physiology|January 30, 2020
Alternative splicing potentiates dysfunction of early-onset epileptic encephalopathy SCN2A variantsChristopher H Thompson, Roy Ben-Shalom, Kevin J Bender, et al.
Neurobiology of Disease|November 27, 2024
Novel mouse model of alternating hemiplegia of childhood exhibits prominent motor and seizure phenotypesNicole A Hawkins, Jean-Marc DeKeyser, Jennifer A Kearney, et al.
Pageof 30