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Plos One
|
June 29, 2017
MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathy
James 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 Channel
Jamie D Kapplinger, John R Giudicessi, Dan Ye, et al.
The American Journal of Cardiology
|
December 12, 2022
Cardiopulmonary Exercise Testing in Athletes With Hypertrophic Cardiomyopathy
Darrell 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 1
Jamie 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 tachycardia
Bi-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 population
Brian R Berquist, Dharmendra Kumar Singh, Jinshui Fan, et al.
Acta Cardiologica
|
March 8, 2018
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy
Salma 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 superfamily
S 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 C
Andrew 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 cardiomyocytes
Daniel J Clemens, Dan Ye, Lili Wang, et al.
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of 114
Search research articles
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Showing results (801-810 of 1,140) with videos related to
Sort By:
Page
of 114
Plos One
|
June 29, 2017
MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathy
James 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 Channel
Jamie D Kapplinger, John R Giudicessi, Dan Ye, et al.
The American Journal of Cardiology
|
December 12, 2022
Cardiopulmonary Exercise Testing in Athletes With Hypertrophic Cardiomyopathy
Darrell 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 1
Jamie 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 tachycardia
Bi-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 population
Brian R Berquist, Dharmendra Kumar Singh, Jinshui Fan, et al.
Acta Cardiologica
|
March 8, 2018
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy
Salma 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 superfamily
S 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 C
Andrew 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 cardiomyocytes
Daniel J Clemens, Dan Ye, Lili Wang, et al.
Page
of 114