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Alfred L George

Showing results (151-160 of 296) with videos related to

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The Journal of General Physiology|August 14, 2023
Epilepsy-associated SCN2A (NaV1.2) variants exhibit diverse and complex functional propertiesChristopher H Thompson, Franck Potet, Tatiana V Abramova, et al.
The Journal of Clinical Investigation|May 23, 2017
Sodium channel NaV1.9 mutations associated with insensitivity to pain dampen neuronal excitabilityJianying Huang, Carlos G Vanoye, Alison Cutts, et al.
Circulation|October 14, 2009
NOS1AP is a genetic modifier of the long-QT syndromeLia Crotti, Maria Cristina Monti, Roberto Insolia, et al.
Forensic Science, Medicine, and Pathology|June 9, 2018
Long QT syndrome KCNH2 mutation with sequential fetal and maternal sudden deathJon M Tuveng, Britt-Marie Berling, Gabor Bunford, et al.
Circulation. Arrhythmia and Electrophysiology|August 17, 2023
Sex and Gene Influence Arrhythmia Susceptibility in Murine Models of CalmodulinopathyLisa M Wren, Jean-Marc DeKeyser, David Y Barefield, et al.
Plos One|September 14, 2019
Upgraded molecular models of the human KCNQ1 potassium channelGeorg Kuenze, Amanda M Duran, Hope Woods, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2011
Voltage-gated potassium channel KCNV2 (Kv8.2) contributes to epilepsy susceptibilityBenjamin S Jorge, Courtney M Campbell, Alison R Miller, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
An upstream open reading frame represses translation of the neuronal potassium channel KCNQ2Dalton J Huey, Eduardo Guadarrama, Jean-Marc DeKeyser, et al.
Circulation. Cardiovascular Genetics|February 18, 2011
SCN5A variation is associated with electrocardiographic traits in the Jackson Heart StudyJanina M Jeff, Kristin Brown-Gentry, Sarah G Buxbaum, et al.
Heart Rhythm|November 9, 2011
Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmiaLisa L Murphy, Anita J Moon-Grady, Bettina F Cuneo, et al.
Pageof 30

Showing results (151-160 of 296) with videos related to

Sort By:
Pageof 30
The Journal of General Physiology|August 14, 2023
Epilepsy-associated SCN2A (NaV1.2) variants exhibit diverse and complex functional propertiesChristopher H Thompson, Franck Potet, Tatiana V Abramova, et al.
The Journal of Clinical Investigation|May 23, 2017
Sodium channel NaV1.9 mutations associated with insensitivity to pain dampen neuronal excitabilityJianying Huang, Carlos G Vanoye, Alison Cutts, et al.
Circulation|October 14, 2009
NOS1AP is a genetic modifier of the long-QT syndromeLia Crotti, Maria Cristina Monti, Roberto Insolia, et al.
Forensic Science, Medicine, and Pathology|June 9, 2018
Long QT syndrome KCNH2 mutation with sequential fetal and maternal sudden deathJon M Tuveng, Britt-Marie Berling, Gabor Bunford, et al.
Circulation. Arrhythmia and Electrophysiology|August 17, 2023
Sex and Gene Influence Arrhythmia Susceptibility in Murine Models of CalmodulinopathyLisa M Wren, Jean-Marc DeKeyser, David Y Barefield, et al.
Plos One|September 14, 2019
Upgraded molecular models of the human KCNQ1 potassium channelGeorg Kuenze, Amanda M Duran, Hope Woods, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2011
Voltage-gated potassium channel KCNV2 (Kv8.2) contributes to epilepsy susceptibilityBenjamin S Jorge, Courtney M Campbell, Alison R Miller, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
An upstream open reading frame represses translation of the neuronal potassium channel KCNQ2Dalton J Huey, Eduardo Guadarrama, Jean-Marc DeKeyser, et al.
Circulation. Cardiovascular Genetics|February 18, 2011
SCN5A variation is associated with electrocardiographic traits in the Jackson Heart StudyJanina M Jeff, Kristin Brown-Gentry, Sarah G Buxbaum, et al.
Heart Rhythm|November 9, 2011
Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmiaLisa L Murphy, Anita J Moon-Grady, Bettina F Cuneo, et al.
Pageof 30