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Nature Communications
|
February 3, 2022
Engineered bacterial voltage-gated sodium channel platform for cardiac gene therapy
Hung X Nguyen, Tianyu Wu, Daniel Needs, et al.
The Journal of Pediatrics
|
September 3, 2018
Copy Number Variants of Undetermined Significance Are Not Associated with Worse Clinical Outcomes in Hypoplastic Left Heart Syndrome
Andrew L Dailey-Schwartz, Hanna J Tadros, Mahshid Sababi Azamian, et al.
Frontiers in Pediatrics
|
December 27, 2021
Risk Factors for Sudden Infant Death in North Carolina
Merick M Yamada, Michael B Rosamilia, Karen E Chiswell, et al.
Circulation. Genomic and Precision Medicine
|
August 20, 2021
Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association
Andrew P Landstrom, Jeffrey J Kim, Bruce D Gelb, et al.
Heart Rhythm
|
March 5, 2018
Amino acid-level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noise
Andrew P Landstrom, Ernesto Fernandez, Jill A Rosenfeld, et al.
Circulation. Heart Failure
|
January 11, 2011
Junctophilin-2 expression silencing causes cardiocyte hypertrophy and abnormal intracellular calcium-handling
Andrew P Landstrom, Cherisse A Kellen, Sayali S Dixit, et al.
Scientific Reports
|
March 6, 2020
Cardiac dysregulation following intrahippocampal kainate-induced status epilepticus
Amber T Levine, Heather A Born, Andrew P Landstrom, et al.
Journal of Muscle Research and Cell Motility
|
November 12, 2020
A comprehensive guide to genetic variants and post-translational modifications of cardiac troponin C
Tyler R Reinoso, Maicon Landim-Vieira, Yun Shi, et al.
Circulation. Arrhythmia and Electrophysiology
|
March 31, 2022
GENESIS: Gene-Specific Machine Learning Models for Variants of Uncertain Significance Found in Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome-Associated Genes
Rachel L Draelos, Jordan E Ezekian, Farica Zhuang, et al.
Journal of Personalized Medicine
|
November 24, 2022
Rapid Whole Genome Sequencing in Critically Ill Neonates Enables Precision Medicine Pipeline
Makenzie Beaman, Kimberley Fisher, Marie McDonald, et al.
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Search research articles
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Showing results (41-50 of 113) with videos related to
Sort By:
Page
of 12
Nature Communications
|
February 3, 2022
Engineered bacterial voltage-gated sodium channel platform for cardiac gene therapy
Hung X Nguyen, Tianyu Wu, Daniel Needs, et al.
The Journal of Pediatrics
|
September 3, 2018
Copy Number Variants of Undetermined Significance Are Not Associated with Worse Clinical Outcomes in Hypoplastic Left Heart Syndrome
Andrew L Dailey-Schwartz, Hanna J Tadros, Mahshid Sababi Azamian, et al.
Frontiers in Pediatrics
|
December 27, 2021
Risk Factors for Sudden Infant Death in North Carolina
Merick M Yamada, Michael B Rosamilia, Karen E Chiswell, et al.
Circulation. Genomic and Precision Medicine
|
August 20, 2021
Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association
Andrew P Landstrom, Jeffrey J Kim, Bruce D Gelb, et al.
Heart Rhythm
|
March 5, 2018
Amino acid-level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noise
Andrew P Landstrom, Ernesto Fernandez, Jill A Rosenfeld, et al.
Circulation. Heart Failure
|
January 11, 2011
Junctophilin-2 expression silencing causes cardiocyte hypertrophy and abnormal intracellular calcium-handling
Andrew P Landstrom, Cherisse A Kellen, Sayali S Dixit, et al.
Scientific Reports
|
March 6, 2020
Cardiac dysregulation following intrahippocampal kainate-induced status epilepticus
Amber T Levine, Heather A Born, Andrew P Landstrom, et al.
Journal of Muscle Research and Cell Motility
|
November 12, 2020
A comprehensive guide to genetic variants and post-translational modifications of cardiac troponin C
Tyler R Reinoso, Maicon Landim-Vieira, Yun Shi, et al.
Circulation. Arrhythmia and Electrophysiology
|
March 31, 2022
GENESIS: Gene-Specific Machine Learning Models for Variants of Uncertain Significance Found in Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome-Associated Genes
Rachel L Draelos, Jordan E Ezekian, Farica Zhuang, et al.
Journal of Personalized Medicine
|
November 24, 2022
Rapid Whole Genome Sequencing in Critically Ill Neonates Enables Precision Medicine Pipeline
Makenzie Beaman, Kimberley Fisher, Marie McDonald, et al.
Page
of 12