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Craig T January

Showing results (31-40 of 58) with videos related to

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Heart Rhythm|February 25, 2014
KCNJ2 mutation causes an adrenergic-dependent rectification abnormality with calcium sensitivity and ventricular arrhythmiaMatthew M Kalscheur, Ravi Vaidyanathan, Kate M Orland, et al.
American Journal of Physiology. Heart and Circulatory Physiology|September 6, 2011
High purity human-induced pluripotent stem cell-derived cardiomyocytes: electrophysiological properties of action potentials and ionic currentsJunyi Ma, Liang Guo, Steve J Fiene, et al.
Circulation|November 25, 2010
Novel chemical suppressors of long QT syndrome identified by an in vivo functional screenDavid S Peal, Robert W Mills, Stacey N Lynch, et al.
Journal of the American Heart Association|December 16, 2014
Mouse ERG K(+) channel clones reveal differences in protein trafficking and functionEric C Lin, Brooke M Moungey, Evi Lim, et al.
International Journal of Molecular Sciences|July 9, 2022
Mutation-Specific Differences in Kv7.1 (<i>KCNQ1</i>) and Kv11.1 (<i>KCNH2</i>) Channel Dysfunction and Long QT Syndrome PhenotypesPeter M Kekenes-Huskey, Don E Burgess, Bin Sun, et al.
Biomolecules|August 8, 2020
Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 <i>KCNH2</i> (<i>hERG</i>) Mutations and Identifying New PatientsMakoto Ono, Don E Burgess, Elizabeth A Schroder, et al.
Physiological Genomics|February 6, 2004
Molecular heterogeneity of calcium channel beta-subunits in canine and human heart: evidence for differential subcellular localizationJason D Foell, Ravi C Balijepalli, Brian P Delisle, et al.
Circulation|January 25, 2006
Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanismCorey L Anderson, Brian P Delisle, Blake D Anson, et al.
The Journal of Biological Chemistry|September 25, 2002
Interaction with GM130 during HERG ion channel trafficking. Disruption by type 2 congenital long QT syndrome mutations. Human Ether-à-go-go-Related GeneElon C Roti Roti, Cena D Myers, Rebecca A Ayers, et al.
Circulation|November 9, 2012
Mechanism of loss of Kv11.1 K+ current in mutant T421M-Kv11.1-expressing rat ventricular myocytes: interaction of trafficking and gatingSadguna Y Balijepalli, Evi Lim, Sarah P Concannon, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Heart Rhythm|February 25, 2014
KCNJ2 mutation causes an adrenergic-dependent rectification abnormality with calcium sensitivity and ventricular arrhythmiaMatthew M Kalscheur, Ravi Vaidyanathan, Kate M Orland, et al.
American Journal of Physiology. Heart and Circulatory Physiology|September 6, 2011
High purity human-induced pluripotent stem cell-derived cardiomyocytes: electrophysiological properties of action potentials and ionic currentsJunyi Ma, Liang Guo, Steve J Fiene, et al.
Circulation|November 25, 2010
Novel chemical suppressors of long QT syndrome identified by an in vivo functional screenDavid S Peal, Robert W Mills, Stacey N Lynch, et al.
Journal of the American Heart Association|December 16, 2014
Mouse ERG K(+) channel clones reveal differences in protein trafficking and functionEric C Lin, Brooke M Moungey, Evi Lim, et al.
International Journal of Molecular Sciences|July 9, 2022
Mutation-Specific Differences in Kv7.1 (<i>KCNQ1</i>) and Kv11.1 (<i>KCNH2</i>) Channel Dysfunction and Long QT Syndrome PhenotypesPeter M Kekenes-Huskey, Don E Burgess, Bin Sun, et al.
Biomolecules|August 8, 2020
Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 <i>KCNH2</i> (<i>hERG</i>) Mutations and Identifying New PatientsMakoto Ono, Don E Burgess, Elizabeth A Schroder, et al.
Physiological Genomics|February 6, 2004
Molecular heterogeneity of calcium channel beta-subunits in canine and human heart: evidence for differential subcellular localizationJason D Foell, Ravi C Balijepalli, Brian P Delisle, et al.
Circulation|January 25, 2006
Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanismCorey L Anderson, Brian P Delisle, Blake D Anson, et al.
The Journal of Biological Chemistry|September 25, 2002
Interaction with GM130 during HERG ion channel trafficking. Disruption by type 2 congenital long QT syndrome mutations. Human Ether-à-go-go-Related GeneElon C Roti Roti, Cena D Myers, Rebecca A Ayers, et al.
Circulation|November 9, 2012
Mechanism of loss of Kv11.1 K+ current in mutant T421M-Kv11.1-expressing rat ventricular myocytes: interaction of trafficking and gatingSadguna Y Balijepalli, Evi Lim, Sarah P Concannon, et al.
Pageof 6