Intracellular Calcium Handling Dysfunction and Arrhythmogenesis

This publication has 18 references indexed in Scilit:

• Enhanced Store Overload–Induced Ca ²⁺ Release and Channel Sensitivity to Luminal Ca ²⁺ Activation Are Common Defects of RyR2 Mutations Linked to Ventricular Tachycardia and Sudden Death
  Circulation Research, 2005
• Cardiac and skeletal muscle disorders caused by mutations in the intracellular Ca2+ release channels
  Journal of Clinical Investigation, 2005
• Genetics of Right Ventricular Cardiomyopathy
  Journal of Cardiovascular Electrophysiology, 2005
• Bidirectional Ventricular Tachycardia and Fibrillation Elicited in a Knock-In Mouse Model Carrier of a Mutation in the Cardiac Ryanodine Receptor
  Circulation Research, 2005
• Cellular Mechanism of Calcium-Mediated Triggered Activity in the Heart
  Circulation Research, 2005
• Functional heterogeneity of ryanodine receptor mutations associated with sudden cardiac death
  Cardiovascular Research, 2004
• Calstabin deficiency, ryanodine receptors, and sudden cardiac death
  Biochemical and Biophysical Research Communications, 2004
• Protection from Cardiac Arrhythmia Through Ryanodine Receptor-Stabilizing Protein Calstabin2
  Science, 2004
• Ryanodine Receptor Mutations Associated With Stress-Induced Ventricular Tachycardia Mediate Increased Calcium Release in Stimulated Cardiomyocytes
  Circulation Research, 2003
• A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from Israel
  American Journal of Human Genetics, 2001