Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Craig T January

Showing results (41-50 of 58) with videos related to

Pageof 6
Sort By:
American Journal of Physiology. Heart and Circulatory Physiology|October 18, 2005
Specific serine proteases selectively damage KCNH2 (hERG1) potassium channels and I(Kr)Sridharan Rajamani, Corey L Anderson, Carmen R Valdivia, et al.
American Journal of Physiology. Heart and Circulatory Physiology|April 6, 2010
Properties of WT and mutant hERG K(+) channels expressed in neonatal mouse cardiomyocytesEric C Lin, Katherine M Holzem, Blake D Anson, et al.
Molecular Pharmacology|April 27, 2005
Intragenic suppression of trafficking-defective KCNH2 channels associated with long QT syndromeBrian P Delisle, Jessica K Slind, Jennifer A Kilby, et al.
Journal of the American College of Cardiology|September 15, 2004
An intronic mutation causes long QT syndromeLi Zhang, G Michael Vincent, Marco Baralle, et al.
The Journal of Biological Chemistry|November 26, 2008
Small GTPase determinants for the Golgi processing and plasmalemmal expression of human ether-a-go-go related (hERG) K+ channelsBrian P Delisle, Heather A S Underkofler, Brooke M Moungey, et al.
Circulation. Genomic and Precision Medicine|April 18, 2023
Elucidation of <i>ALG10B</i> as a Novel Long-QT Syndrome-Susceptibility GeneWei Zhou, Dan Ye, David J Tester, et al.
American Journal of Physiology. Cell Physiology|July 19, 2013
Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulumJennifer L Smith, Allison R Reloj, Parvathi S Nataraj, et al.
Circulation. Arrhythmia and Electrophysiology|December 17, 2009
Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium currentJianding Cheng, David W Van Norstrand, Argelia Medeiros-Domingo, et al.
Heart Rhythm|September 21, 2010
R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillationDaniel C Bartos, Sabine Duchatelet, Don E Burgess, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|August 10, 2016
Identification of Drug-Drug Interactions In Vitro: A Case Study Evaluating the Effects of Sofosbuvir and Amiodarone on hiPSC-Derived CardiomyocytesDaniel C Millard, Christopher J Strock, Coby B Carlson, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
American Journal of Physiology. Heart and Circulatory Physiology|October 18, 2005
Specific serine proteases selectively damage KCNH2 (hERG1) potassium channels and I(Kr)Sridharan Rajamani, Corey L Anderson, Carmen R Valdivia, et al.
American Journal of Physiology. Heart and Circulatory Physiology|April 6, 2010
Properties of WT and mutant hERG K(+) channels expressed in neonatal mouse cardiomyocytesEric C Lin, Katherine M Holzem, Blake D Anson, et al.
Molecular Pharmacology|April 27, 2005
Intragenic suppression of trafficking-defective KCNH2 channels associated with long QT syndromeBrian P Delisle, Jessica K Slind, Jennifer A Kilby, et al.
Journal of the American College of Cardiology|September 15, 2004
An intronic mutation causes long QT syndromeLi Zhang, G Michael Vincent, Marco Baralle, et al.
The Journal of Biological Chemistry|November 26, 2008
Small GTPase determinants for the Golgi processing and plasmalemmal expression of human ether-a-go-go related (hERG) K+ channelsBrian P Delisle, Heather A S Underkofler, Brooke M Moungey, et al.
Circulation. Genomic and Precision Medicine|April 18, 2023
Elucidation of <i>ALG10B</i> as a Novel Long-QT Syndrome-Susceptibility GeneWei Zhou, Dan Ye, David J Tester, et al.
American Journal of Physiology. Cell Physiology|July 19, 2013
Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulumJennifer L Smith, Allison R Reloj, Parvathi S Nataraj, et al.
Circulation. Arrhythmia and Electrophysiology|December 17, 2009
Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium currentJianding Cheng, David W Van Norstrand, Argelia Medeiros-Domingo, et al.
Heart Rhythm|September 21, 2010
R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillationDaniel C Bartos, Sabine Duchatelet, Don E Burgess, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|August 10, 2016
Identification of Drug-Drug Interactions In Vitro: A Case Study Evaluating the Effects of Sofosbuvir and Amiodarone on hiPSC-Derived CardiomyocytesDaniel C Millard, Christopher J Strock, Coby B Carlson, et al.
Pageof 6