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

David J Tester

Showing results (171-180 of 212) with videos related to

Pageof 22
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2021
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca<sup>2+</sup> regulationMatthew Halvorsen, Laura Gould, Xiaohan Wang, et al.
Plos One|September 4, 2014
A CACNA1C variant associated with reduced voltage-dependent inactivation, increased CaV1.2 channel window current, and arrhythmogenesisJessica A Hennessey, Nicole J Boczek, Yong-Hui Jiang, et al.
Circulation. Arrhythmia and Electrophysiology|August 13, 2016
Novel CPVT-Associated Calmodulin Mutation in CALM3 (CALM3-A103V) Activates Arrhythmogenic Ca Waves and SparksNieves Gomez-Hurtado, Nicole J Boczek, Dmytro O Kryshtal, et al.
Circulation Research|October 22, 2016
A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT SyndromeWorawan B Limpitikul, Ivy E Dick, David J Tester, et al.
The Journal of Pediatrics|October 1, 2018
Exome-Wide Rare Variant Analyses in Sudden Infant Death SyndromeDavid J Tester, Leonie C H Wong, Pritha Chanana, et al.
Journal of Molecular and Cellular Cardiology|May 19, 2007
Mutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humansAndrew P Landstrom, Noah Weisleder, Karin B Batalden, et al.
Biorxiv : the Preprint Server for Biology|March 11, 2024
A Multi-Omics Atlas of Sex-Specific Differences in Obstructive Hypertrophic CardiomyopathyRamin Garmany, Surendra Dasari, J Martijn Bos, et al.
Heart Rhythm|April 27, 2005
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testingMichael J Ackerman, Igor Splawski, Jonathan C Makielski, et al.
Biochemistry|October 25, 2012
High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeationDon E Burgess, Daniel C Bartos, Allison R Reloj, et al.
Circulation. Arrhythmia and Electrophysiology|October 16, 2012
A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5Taisuke Ishikawa, Akinori Sato, Cherisse A Marcou, et al.
Pageof 22

Showing results (171-180 of 212) with videos related to

Sort By:
Pageof 22
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2021
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca<sup>2+</sup> regulationMatthew Halvorsen, Laura Gould, Xiaohan Wang, et al.
Plos One|September 4, 2014
A CACNA1C variant associated with reduced voltage-dependent inactivation, increased CaV1.2 channel window current, and arrhythmogenesisJessica A Hennessey, Nicole J Boczek, Yong-Hui Jiang, et al.
Circulation. Arrhythmia and Electrophysiology|August 13, 2016
Novel CPVT-Associated Calmodulin Mutation in CALM3 (CALM3-A103V) Activates Arrhythmogenic Ca Waves and SparksNieves Gomez-Hurtado, Nicole J Boczek, Dmytro O Kryshtal, et al.
Circulation Research|October 22, 2016
A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT SyndromeWorawan B Limpitikul, Ivy E Dick, David J Tester, et al.
The Journal of Pediatrics|October 1, 2018
Exome-Wide Rare Variant Analyses in Sudden Infant Death SyndromeDavid J Tester, Leonie C H Wong, Pritha Chanana, et al.
Journal of Molecular and Cellular Cardiology|May 19, 2007
Mutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humansAndrew P Landstrom, Noah Weisleder, Karin B Batalden, et al.
Biorxiv : the Preprint Server for Biology|March 11, 2024
A Multi-Omics Atlas of Sex-Specific Differences in Obstructive Hypertrophic CardiomyopathyRamin Garmany, Surendra Dasari, J Martijn Bos, et al.
Heart Rhythm|April 27, 2005
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testingMichael J Ackerman, Igor Splawski, Jonathan C Makielski, et al.
Biochemistry|October 25, 2012
High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeationDon E Burgess, Daniel C Bartos, Allison R Reloj, et al.
Circulation. Arrhythmia and Electrophysiology|October 16, 2012
A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5Taisuke Ishikawa, Akinori Sato, Cherisse A Marcou, et al.
Pageof 22