Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference5 articles.
1. Identification of a targeted and testable antiarrhythmic therapy for long-QT syndrome type 2 using a patient-specific cellular model;Mehta;Eur. Heart J.,2018
2. Induced pluripotent stem cell technology: toward the future of cardiac arrhythmias;Gnecchi;Int. J. Cardiol.,2017
3. The KCNH2-IVS9-28A/G mutation causes aberrant isoform expression and hERG trafficking defect in cardiomyocytes derived from patients affected by long QT syndrome type 2;Mura;Int. J. Cardiol.,2017
4. Long-QT syndrome: from genetics to management;Schwartz;Circ. Arrhythm Electrophysiol.,2012
5. The role of the sympathetic nervous system in the long qt syndrome: the long road from pathophysiology to therapy;Schwartz;Card Electrophysiol. Clin.,2012
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1. Deciphering Common Long QT Syndrome Using CRISPR/Cas9 in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes;Frontiers in Cardiovascular Medicine;2022-05-13
2. Quantum Biology Research Meets Pathophysiology and Therapeutic Mechanisms: A Biomedical Perspective;Quantum Reports;2022-04-04
3. Cardiac transmembrane ion channels and action potentials: cellular physiology and arrhythmogenic behavior;Physiological Reviews;2021-07-01
4. Patient-specific induced pluripotent stem cells as “disease-in-a-dish” models for inherited cardiomyopathies and channelopathies – 15 years of research;World Journal of Stem Cells;2021-04-26
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