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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.
AANA Journal
|
February 13, 2025
Critical Events in Patients With Alternating Hemiplegia of Childhood: A Cohort Study Subgroup Analysis
Emily M Funk, Guy de L Dear, Mary E Moya-Mendez, et al.
Journal of Personalized Medicine
|
May 28, 2022
Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric Cardiomyopathy
Leonie M Kurzlechner, Edward G Jones, Amy M Berkman, et al.
Heart Rhythm
|
October 23, 2025
Disease penetrance and phenotypic spectrum of desmoplakin variant carriers in the population
Manasa Gurumoorthi, Ghaith Sharaf Dabbagh, Rachel Wolfe, et al.
Science Advances
|
March 20, 2026
Regulation of sodium/calcium homeostasis by BacNa<sub>v</sub> gene therapy rescues cardiac dysfunction in chronic heart failure
Tianyu Wu, Yongwu Li, Robin M Perelli, 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 Association
Andrew P Landstrom, Anwar A Chahal, Michael J Ackerman, et al.
Frontiers in Physiology
|
May 6, 2017
Hypertrophic Cardiomyopathy Cardiac Troponin C Mutations Differentially Affect Slow Skeletal and Cardiac Muscle Regulation
Tiago Veltri, Maicon Landim-Vieira, Michelle S Parvatiyar, et al.
Scientific Reports
|
June 23, 2019
Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathy
Edward G Jones, Neda Mazaheri, Reza Maroofian, et al.
Cardiovascular Research
|
May 30, 2013
Junctophilin-2 is necessary for T-tubule maturation during mouse heart development
Julia O Reynolds, David Y Chiang, Wei Wang, et al.
Epilepsia
|
January 11, 2025
Progressive central cardiorespiratory rate downregulation and intensifying epilepsy lead to sudden unexpected death in epilepsy in mouse model of the most common human ATP1A3 mutation
Arsen S Hunanyan, Amitesh Verma, Minu-Tshyeto Bidzimou, et al.
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of 12
Search research articles
Search
Showing results (51-60 of 113) with videos related to
Sort By:
Page
of 12
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.
AANA Journal
|
February 13, 2025
Critical Events in Patients With Alternating Hemiplegia of Childhood: A Cohort Study Subgroup Analysis
Emily M Funk, Guy de L Dear, Mary E Moya-Mendez, et al.
Journal of Personalized Medicine
|
May 28, 2022
Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric Cardiomyopathy
Leonie M Kurzlechner, Edward G Jones, Amy M Berkman, et al.
Heart Rhythm
|
October 23, 2025
Disease penetrance and phenotypic spectrum of desmoplakin variant carriers in the population
Manasa Gurumoorthi, Ghaith Sharaf Dabbagh, Rachel Wolfe, et al.
Science Advances
|
March 20, 2026
Regulation of sodium/calcium homeostasis by BacNa<sub>v</sub> gene therapy rescues cardiac dysfunction in chronic heart failure
Tianyu Wu, Yongwu Li, Robin M Perelli, 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 Association
Andrew P Landstrom, Anwar A Chahal, Michael J Ackerman, et al.
Frontiers in Physiology
|
May 6, 2017
Hypertrophic Cardiomyopathy Cardiac Troponin C Mutations Differentially Affect Slow Skeletal and Cardiac Muscle Regulation
Tiago Veltri, Maicon Landim-Vieira, Michelle S Parvatiyar, et al.
Scientific Reports
|
June 23, 2019
Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathy
Edward G Jones, Neda Mazaheri, Reza Maroofian, et al.
Cardiovascular Research
|
May 30, 2013
Junctophilin-2 is necessary for T-tubule maturation during mouse heart development
Julia O Reynolds, David Y Chiang, Wei Wang, et al.
Epilepsia
|
January 11, 2025
Progressive central cardiorespiratory rate downregulation and intensifying epilepsy lead to sudden unexpected death in epilepsy in mouse model of the most common human ATP1A3 mutation
Arsen S Hunanyan, Amitesh Verma, Minu-Tshyeto Bidzimou, et al.
Page
of 12