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S Kass

Showing results (291-300 of 321) with videos related to

Pageof 33
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Cardiovascular Research|April 9, 2008
IKs response to protein kinase A-dependent KCNQ1 phosphorylation requires direct interaction with microtubulesCéline S Nicolas, Kyu-Ho Park, Aziza El Harchi, et al.
Neuroscience Letters|February 5, 2008
Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsyKatherine D Holland, Jennifer A Kearney, Tracy A Glauser, et al.
Human Mutation|April 4, 2003
A novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gatingXander H T Wehrens, Tom Rossenbacker, Roselie J Jongbloed, et al.
Cancer Research|September 5, 2002
Carcinoembryonic antigen as a target for specific antitumor immunotherapy of head and neck cancerErik S Kass, John W Greiner, Judith A Kantor, et al.
Biorxiv : the Preprint Server for Biology|June 10, 2024
Ion channel inhibition by targeted recruitment of NEDD4-2 with divalent nanobodiesTravis J Morgenstern, Arden Darko-Boateng, Emmanuel Afriyie, et al.
Nature Genetics|August 1, 1994
A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1S Kass, C MacRae, H L Graber, et al.
Circulation Research|June 26, 2004
Cardiac voltage-gated sodium channel Nav1.5 is regulated by Nedd4-2 mediated ubiquitinationMiguel X van Bemmelen, Jean-Sébastien Rougier, Bruno Gavillet, et al.
Science (New York, N.Y.)|August 24, 2002
Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmiaIgor Splawski, Katherine W Timothy, Michihiro Tateyama, et al.
Journal of Medicinal Chemistry|May 4, 2021
Antiarrhythmic Hit to Lead Refinement in a Dish Using Patient-Derived iPSC CardiomyocytesJohn R Cashman, Daniel Ryan, Wesley L McKeithan, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|February 15, 2002
Variable expression of long QT syndrome among gene carriers from families with five different HERG mutationsJesaia Benhorin, Arthur J Moss, Matthew Bak, et al.
Pageof 33

Showing results (291-300 of 321) with videos related to

Sort By:
Pageof 33
Cardiovascular Research|April 9, 2008
IKs response to protein kinase A-dependent KCNQ1 phosphorylation requires direct interaction with microtubulesCéline S Nicolas, Kyu-Ho Park, Aziza El Harchi, et al.
Neuroscience Letters|February 5, 2008
Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsyKatherine D Holland, Jennifer A Kearney, Tracy A Glauser, et al.
Human Mutation|April 4, 2003
A novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gatingXander H T Wehrens, Tom Rossenbacker, Roselie J Jongbloed, et al.
Cancer Research|September 5, 2002
Carcinoembryonic antigen as a target for specific antitumor immunotherapy of head and neck cancerErik S Kass, John W Greiner, Judith A Kantor, et al.
Biorxiv : the Preprint Server for Biology|June 10, 2024
Ion channel inhibition by targeted recruitment of NEDD4-2 with divalent nanobodiesTravis J Morgenstern, Arden Darko-Boateng, Emmanuel Afriyie, et al.
Nature Genetics|August 1, 1994
A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1S Kass, C MacRae, H L Graber, et al.
Circulation Research|June 26, 2004
Cardiac voltage-gated sodium channel Nav1.5 is regulated by Nedd4-2 mediated ubiquitinationMiguel X van Bemmelen, Jean-Sébastien Rougier, Bruno Gavillet, et al.
Science (New York, N.Y.)|August 24, 2002
Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmiaIgor Splawski, Katherine W Timothy, Michihiro Tateyama, et al.
Journal of Medicinal Chemistry|May 4, 2021
Antiarrhythmic Hit to Lead Refinement in a Dish Using Patient-Derived iPSC CardiomyocytesJohn R Cashman, Daniel Ryan, Wesley L McKeithan, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|February 15, 2002
Variable expression of long QT syndrome among gene carriers from families with five different HERG mutationsJesaia Benhorin, Arthur J Moss, Matthew Bak, et al.
Pageof 33