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

J Ackerman

Showing results (831-840 of 1,140) with videos related to

Pageof 114
Sort By:
Anesthesiology|September 26, 2007
Does low-dose droperidol administration increase the risk of drug-induced QT prolongation and torsade de pointes in the general surgical population?Gregory A Nuttall, Karen M Eckerman, Kelly A Jacob, et al.
Circulation. Genomic and Precision Medicine|March 27, 2023
Interpreting Incidentally Identified Variants in Genes Associated With Heritable Cardiovascular Disease: A Scientific Statement From the American Heart AssociationAndrew P Landstrom, Anwar A Chahal, Michael J Ackerman, 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 American Journal of Cardiology|August 15, 2015
Surgical Ventricular Septal Myectomy for Patients With Noonan Syndrome and Symptomatic Left Ventricular Outflow Tract ObstructionJoseph T Poterucha, Jonathan N Johnson, Patrick W O'Leary, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|December 6, 2008
Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathyYuri A Saito, Peter R Strege, David J Tester, et al.
Circulation. Cardiovascular Genetics|January 26, 2017
Genetic Insurance Discrimination in Sudden Arrhythmia Death Syndromes: Empirical Evidence From a Cross-Sectional Survey in North AmericaSaira Mohammed, Zaneta Lim, Paige H Dean, 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.
Journal of Cellular Biochemistry|January 12, 2012
TGFβ-inducible early gene-1 (TIEG1) mutations in hypertrophic cardiomyopathyJ Martijn Bos, Malayannan Subramaniam, John R Hawse, et al.
The Journal of Biological Chemistry|April 15, 2008
A mutation in telethonin alters Nav1.5 functionAmelia Mazzone, Peter R Strege, David J Tester, et al.
The American Journal of Cardiology|February 13, 2016
Impact of Genotype on the Occurrence of Atrial Fibrillation in Patients With Hypertrophic CardiomyopathyCarolina Bongini, Cecilia Ferrantini, Francesca Girolami, et al.
Pageof 114

Showing results (831-840 of 1,140) with videos related to

Sort By:
Pageof 114
Anesthesiology|September 26, 2007
Does low-dose droperidol administration increase the risk of drug-induced QT prolongation and torsade de pointes in the general surgical population?Gregory A Nuttall, Karen M Eckerman, Kelly A Jacob, et al.
Circulation. Genomic and Precision Medicine|March 27, 2023
Interpreting Incidentally Identified Variants in Genes Associated With Heritable Cardiovascular Disease: A Scientific Statement From the American Heart AssociationAndrew P Landstrom, Anwar A Chahal, Michael J Ackerman, 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 American Journal of Cardiology|August 15, 2015
Surgical Ventricular Septal Myectomy for Patients With Noonan Syndrome and Symptomatic Left Ventricular Outflow Tract ObstructionJoseph T Poterucha, Jonathan N Johnson, Patrick W O'Leary, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|December 6, 2008
Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathyYuri A Saito, Peter R Strege, David J Tester, et al.
Circulation. Cardiovascular Genetics|January 26, 2017
Genetic Insurance Discrimination in Sudden Arrhythmia Death Syndromes: Empirical Evidence From a Cross-Sectional Survey in North AmericaSaira Mohammed, Zaneta Lim, Paige H Dean, 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.
Journal of Cellular Biochemistry|January 12, 2012
TGFβ-inducible early gene-1 (TIEG1) mutations in hypertrophic cardiomyopathyJ Martijn Bos, Malayannan Subramaniam, John R Hawse, et al.
The Journal of Biological Chemistry|April 15, 2008
A mutation in telethonin alters Nav1.5 functionAmelia Mazzone, Peter R Strege, David J Tester, et al.
The American Journal of Cardiology|February 13, 2016
Impact of Genotype on the Occurrence of Atrial Fibrillation in Patients With Hypertrophic CardiomyopathyCarolina Bongini, Cecilia Ferrantini, Francesca Girolami, et al.
Pageof 114