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Circulation, ISSN 0009-7322, 2015, Volume 131, Issue 8, pp. 695 - 708
Background-The cardiac cytoskeleton plays key roles in maintaining myocyte structural integrity in health and disease. In fact, human mutations in cardiac... 
Cardiac | Cytoskeleton | Ventricular tachycardia | Ion channels | Catecholaminergic polymorphic ventricular arrhythmia | Protein transport | Arrhythmias | protein transport | CARDIAC & CARDIOVASCULAR SYSTEMS | COMPLEX PROTEINS | cytoskeleton | VENTRICULAR-TACHYCARDIA | HEART-FAILURE | arrhythmias, cardiac | CELL-ADHESION | DIFFERENTIAL REGULATION | ion channels | ALPHA-SPECTRIN | catecholaminergic polymorphic ventricular arrhythmia | ANKYRIN-B SYNDROME | ventricular tachycardia | NEONATAL CARDIOMYOCYTES | SUDDEN CARDIAC DEATH | PERIPHERAL VASCULAR DISEASE | RYANODINE RECEPTOR DISTRIBUTION | Humans | Heart Failure - physiopathology | Microfilament Proteins - physiology | Molecular Sequence Data | Arrhythmias, Cardiac - physiopathology | Arrhythmias, Cardiac - pathology | Membrane Proteins - physiology | Spectrin - physiology | Microfilament Proteins - genetics | Arrhythmias, Cardiac - genetics | Disease Models, Animal | Carrier Proteins - physiology | Spectrin - chemistry | Amino Acid Sequence | Microfilament Proteins - deficiency | Microtubules - physiology | Heart Failure - genetics | Ankyrins - physiology | Heart Failure - pathology | Mutation - genetics | Spectrin - analysis | Mice, Knockout | Carrier Proteins - genetics | Myocytes, Cardiac - pathology | Phenotype | Animals | Myocytes, Cardiac - physiology | Ankyrins - genetics | Cytoskeleton - physiology | Mice | cytoskeletal dynamics | cardiovascular physiology | protein trafficking arrhythmia | catecholaminergic polymorphic ventricular tachycardia | arrhythmia (heart rhythm disorders)
Journal Article
2018, ISBN 2889456439
A well-adjusted expression of cardiac ion channels at the sarcolemma is of crucial importance for normal action potential formation and thus cardiac function.... 
Connexin43 (Cx43) | Kv11 | Glycosylation | NaV1 | Autophagy | Protein complexes | ion channel | arrhythmia | TRPM4 channel | trafficking | 5 channels | Kir2 | 1 channels
eBook
Circulation Research: Journal of the American Heart Association, ISSN 0009-7330, 06/2004, Volume 94, Issue 11, pp. 1418 - 1428
The mechanisms underlying normal and abnormal cardiac rhythms are complex and incompletely understood. Through the study of uncommon inheritable arrhythmia... 
Cell biology | Ion channels | Arrhythmia | Protein trafficking | POLYMORPHIC VENTRICULAR-TACHYCARDIA | CARDIAC & CARDIOVASCULAR SYSTEMS | protein trafficking | MARIE-TOOTH-DISEASE | INFANT-DEATH-SYNDROME | ion channels | TRANSMEMBRANE CONDUCTANCE REGULATOR | cell biology | arrhythmia | PERIPHERAL VASCULAR DISEASE | LONG-QT-SYNDROME | FAMILIAL ATRIAL-FIBRILLATION | HERG POTASSIUM CHANNEL | CYSTIC-FIBROSIS | NEPHROGENIC DIABETES-INSIPIDUS | HEMATOLOGY | X-LINKED FORM | Phosphorylation | Potassium Channels, Voltage-Gated - physiology | Protein Sorting Signals - physiology | Humans | Genetic Diseases, Inborn - genetics | Ion Channels - genetics | Protein Transport - physiology | Ion Channels - physiology | ERG1 Potassium Channel | Arrhythmias, Cardiac - physiopathology | Long QT Syndrome - physiopathology | Ion Channel Gating - physiology | Ion Channels - chemistry | Arrhythmias, Cardiac - genetics | Potassium Channels, Voltage-Gated - genetics | Arrhythmias, Cardiac - metabolism | Genetic Predisposition to Disease | Potassium Channels, Voltage-Gated - chemistry | Endoplasmic Reticulum - physiology | Ether-A-Go-Go Potassium Channels | Protein Folding | Protein Processing, Post-Translational - physiology | Long QT Syndrome - genetics | Protein Conformation | Signal Transduction - physiology | Genetic Diseases, Inborn - physiopathology
Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 04/2017, Volume 7, Issue 1, p. 46259
Journal Article
Circulation, ISSN 0009-7322, 05/1999, Volume 99, Issue 17, pp. 2290 - 2294
Background-The congenital long-QT syndrome (LQTS) is an inherited disorder characterized by a prolonged cardiac action potential and a QT interval that leads... 
Arrhythmia | Genes | Long-QT syndrome | CELLS | CARDIAC & CARDIOVASCULAR SYSTEMS | GENE | genes | RECTIFIER K+ CURRENT | arrhythmia | PERIPHERAL VASCULAR DISEASE | MUTATIONS | DYSFUNCTION | HEMATOLOGY | MOLECULAR-BASIS | long-QT syndrome
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 01/2016, Volume 126, Issue 1, p. 239
  In this paper, the authors have described a homozygous missense variant (c.602C>T, p.S201F) in POPDC1, identified by wholeexome sequencing, in a family of 4... 
Heart | Cardiac arrhythmia | Medical research | Medical imaging | Cardiomyopathy | Genes | Kinases | Muscular dystrophy | Proteins | Studies | Musculoskeletal system | Biopsy | Mutation | Age | Binding sites
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 06/2004, Volume 279, Issue 26, pp. 27194 - 27198
Journal Article
Frontiers in Physiology, ISSN 1664-042X, 10/2017, Volume 8, p. 808
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2008, Volume 105, Issue 40, pp. 15617 - 15622
Journal Article