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 (801-810 of 1,140) with videos related to

Pageof 114
Sort By:
Plos One|June 29, 2017
MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathyJames W McNamara, Amy Li, Sean Lal, et al.
Circulation. Cardiovascular Genetics|April 24, 2015
Enhanced Classification of Brugada Syndrome-Associated and Long-QT Syndrome-Associated Genetic Variants in the SCN5A-Encoded Na(v)1.5 Cardiac Sodium ChannelJamie D Kapplinger, John R Giudicessi, Dan Ye, et al.
The American Journal of Cardiology|December 12, 2022
Cardiopulmonary Exercise Testing in Athletes With Hypertrophic CardiomyopathyDarrell B Newman, Ramin Garmany, Alejandra Meza Contreras, et al.
Journal of Medical Genetics|March 8, 2017
KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1Jamie D Kapplinger, Anders Erickson, Sirisha Asuri, et al.
Cardiovascular Research|September 28, 2007
A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardiaBi-Hua Tan, Pedro Iturralde-Torres, Argelia Medeiros-Domingo, et al.
Nucleic Acids Research|April 14, 2010
Functional capacity of XRCC1 protein variants identified in DNA repair-deficient Chinese hamster ovary cell lines and the human populationBrian R Berquist, Dharmendra Kumar Singh, Jinshui Fan, et al.
Acta Cardiologica|March 8, 2018
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathySalma I Patel, Michael J Ackerman, Fadi E Shamoun, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 15, 1993
Molecular cloning and characterization of human eosinophil Charcot-Leyden crystal protein (lysophospholipase). Similarities to IgE binding proteins and the S-type animal lectin superfamilyS J Ackerman, S E Corrette, H F Rosenberg, et al.
Journal of Molecular and Cellular Cardiology|June 24, 2008
Molecular and functional characterization of novel hypertrophic cardiomyopathy susceptibility mutations in TNNC1-encoded troponin CAndrew P Landstrom, Michelle S Parvatiyar, Jose R Pinto, et al.
Stem Cell Reports|May 10, 2023
Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytesDaniel J Clemens, Dan Ye, Lili Wang, et al.
Pageof 114

Showing results (801-810 of 1,140) with videos related to

Sort By:
Pageof 114
Plos One|June 29, 2017
MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathyJames W McNamara, Amy Li, Sean Lal, et al.
Circulation. Cardiovascular Genetics|April 24, 2015
Enhanced Classification of Brugada Syndrome-Associated and Long-QT Syndrome-Associated Genetic Variants in the SCN5A-Encoded Na(v)1.5 Cardiac Sodium ChannelJamie D Kapplinger, John R Giudicessi, Dan Ye, et al.
The American Journal of Cardiology|December 12, 2022
Cardiopulmonary Exercise Testing in Athletes With Hypertrophic CardiomyopathyDarrell B Newman, Ramin Garmany, Alejandra Meza Contreras, et al.
Journal of Medical Genetics|March 8, 2017
KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1Jamie D Kapplinger, Anders Erickson, Sirisha Asuri, et al.
Cardiovascular Research|September 28, 2007
A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardiaBi-Hua Tan, Pedro Iturralde-Torres, Argelia Medeiros-Domingo, et al.
Nucleic Acids Research|April 14, 2010
Functional capacity of XRCC1 protein variants identified in DNA repair-deficient Chinese hamster ovary cell lines and the human populationBrian R Berquist, Dharmendra Kumar Singh, Jinshui Fan, et al.
Acta Cardiologica|March 8, 2018
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathySalma I Patel, Michael J Ackerman, Fadi E Shamoun, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 15, 1993
Molecular cloning and characterization of human eosinophil Charcot-Leyden crystal protein (lysophospholipase). Similarities to IgE binding proteins and the S-type animal lectin superfamilyS J Ackerman, S E Corrette, H F Rosenberg, et al.
Journal of Molecular and Cellular Cardiology|June 24, 2008
Molecular and functional characterization of novel hypertrophic cardiomyopathy susceptibility mutations in TNNC1-encoded troponin CAndrew P Landstrom, Michelle S Parvatiyar, Jose R Pinto, et al.
Stem Cell Reports|May 10, 2023
Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytesDaniel J Clemens, Dan Ye, Lili Wang, et al.
Pageof 114