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Stem Cells International, ISSN 1687-966X, 2016, Volume 2016, pp. 1684792 - 16
Hypertrophic cardiomyopathy (HCM) is a genetic cardiac disease, which affects the structure of heart muscle tissue. The clinical symptoms include arrhythmias,... 
PLURIPOTENT STEM-CELLS | EXPRESSION PATTERNS | SARCOMERIC CARDIOMYOPATHIES | GENE | LONG-QT SYNDROME | DYSFUNCTION | FOUNDER MUTATIONS | EASTERN FINLAND | CULTURE | HAPLOINSUFFICIENCY | CELL & TISSUE ENGINEERING
Journal Article
Circulation Research, ISSN 0009-7330, 06/2017, Volume 121, Issue 5, pp. 525 - 536
RATIONALE:Mutations in the cardiac Ryanodine Receptor gene (RYR2) cause dominant Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT), a leading cause... 
Cardiac arrhythmia | Ryanodine receptor calcium channel | Cardiac sudden death | Cathecholaminergic polymorphic ventricular tachycardia | Transgenic mice | Genetics | Gene therapy | POLYMORPHIC VENTRICULAR-TACHYCARDIA | CARDIAC & CARDIOVASCULAR SYSTEMS | cardiac arrhythmia | cardiac sudden death | gene therapy | IN MOUSE MODEL | RELEASE | cathecholaminergic polymorphic ventricular tachycardia | KNOCK | genetics | transgenic mice | CARDIAC CALSEQUESTRIN | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | Animals, Newborn | Arrhythmias, Cardiac - prevention & control | Humans | Mice, Inbred C57BL | RNA, Messenger - genetics | Cells, Cultured | Male | Mice, Transgenic | Ryanodine Receptor Calcium Release Channel - ultrastructure | Mutation - genetics | RNA, Messenger - ultrastructure | Arrhythmias, Cardiac - pathology | Phenotype | Animals | Ryanodine Receptor Calcium Release Channel - deficiency | Ryanodine Receptor Calcium Release Channel - genetics | Alleles | HEK293 Cells | Heterozygote | Mice | Gene Silencing - physiology | Arrhythmias, Cardiac - genetics | Neonates | Phenotypes | Transcription | Cardiac muscle | RNA-mediated interference | Ryanodine receptors | Tubules | Isoproterenol | Proteins | Gene silencing | Mitochondria | Tachycardia | Sarcoplasmic reticulum | Rodents | Mutation | Ventricle | Heart diseases | Index Medicus
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 03/2018, Volume 24, Issue 5, pp. 1038 - 1047
Journal Article
2016, ISBN 0128044691, ix, 180 pages
Nonsense Mutation Correction in Human Diseases: An Approach for Targeted Medicine provides an introduction on genetic diseases, discusses the prevalence of... 
Genetic Diseases, Inborn | Mutation (Biology) | Genetic disorders | Nonsense mutation | Biology, life sciences
Book
Circulation, ISSN 0009-7322, 2012, Volume 125, Issue 16, pp. 1988 - +
Journal Article
Journal of Thoracic Oncology, ISSN 1556-0864, 06/2011, Volume 6, Issue 6, pp. 1006 - 1015
Journal Article
2015, Volume 7, 4
Reference
Clinical Cancer Research, ISSN 1078-0432, 11/2006, Volume 12, Issue 21, pp. 6494 - 6501
Journal Article
Circulation, ISSN 0009-7322, 11/2007, Volume 116, Issue 20, pp. 2260 - 2268
Journal Article
Journal Article