Disease modeling of cardiac arrhythmias using human induced pluripotent stem cells
Author:
Affiliation:
1. Division of Cardiology, Department of Medicine, University of Ottawa Heart Institute, Ottawa, Canada
2. Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Canada
Funder
Institute of Circulatory and Respiratory Health
Publisher
Informa UK Limited
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology
Link
https://www.tandfonline.com/doi/pdf/10.1080/14712598.2019.1575359
Reference178 articles.
1. Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden death
2. Systematic Assessment of Patients With Unexplained Cardiac Arrest
3. Interplay Between Genetic Substrate, QTc Duration, and Arrhythmia Risk in Patients With Long QT Syndrome
4. Genetics of cardiac arrhythmias
5. Genotype- and Phenotype-Guided Management of Congenital Long QT Syndrome
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2. “Betwixt Mine Eye and Heart a League Is Took”: The Progress of Induced Pluripotent Stem-Cell-Based Models of Dystrophin-Associated Cardiomyopathy;International Journal of Molecular Sciences;2020-09-23
3. BEaTS-α an open access 3D printed device for in vitro electromechanical stimulation of human induced pluripotent stem cells;Scientific Reports;2020-07-09
4. Disease Modelling and Precision Medicine Using Canadian Cardiomyocytes;Canadian Journal of Cardiology;2020-04
5. The Emergence of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes (hiPSC-CMs) as a Platform to Model Arrhythmogenic Diseases;International Journal of Molecular Sciences;2020-01-19
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