Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia

[1]  C. H. George,et al.  Ryanodine receptor mutations in arrhythmias: advances in understanding the mechanisms of channel dysfunction. , 2007, Biochemical Society transactions.

[2]  A. Wilde,et al.  Expanding Spectrum of Human RYR2-Related Disease: New Electrocardiographic, Structural, and Genetic Features , 2007, Circulation.

[3]  M. Fishman,et al.  Calcium extrusion is critical for cardiac morphogenesis and rhythm in embryonic zebrafish hearts. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[4]  D. Nicoll,et al.  Mutation in sodium-calcium exchanger 1 (NCX1) causes cardiac fibrillation in zebrafish. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[5]  Huihui Kong,et al.  Enhanced Store Overload–Induced Ca2+ Release and Channel Sensitivity to Luminal Ca2+ Activation Are Common Defects of RyR2 Mutations Linked to Ventricular Tachycardia and Sudden Death , 2005, Circulation research.

[6]  S. Viskin,et al.  The cardiologists' worst nightmare sudden death from "benign" ventricular arrhythmias. , 2005, Journal of the American College of Cardiology.

[7]  C. Wahl-Schott,et al.  Increased SR Ca2+ cycling contributes to improved contractile performance in SERCA2a-overexpressing transgenic rats. , 2005, Cardiovascular research.

[8]  M. Viitasalo,et al.  Catecholaminergic polymorphic ventricular tachycardia: recent mechanistic insights. , 2005, Cardiovascular research.

[9]  R. Haworth,et al.  Increased Nitration of Sarcoplasmic Reticulum Ca2+-ATPase in Human Heart Failure , 2005, Circulation.

[10]  S. Reiken,et al.  Sudden Death in Familial Polymorphic Ventricular Tachycardia Associated With Calcium Release Channel (Ryanodine Receptor) Leak , 2004, Circulation.

[11]  Shi-Xian Deng,et al.  Protection from Cardiac Arrhythmia Through Ryanodine Receptor-Stabilizing Protein Calstabin2 , 2004, Science.

[12]  K. Kontula,et al.  Molecular genetics of exercise-induced polymorphic ventricular tachycardia: identification of three novel cardiac ryanodine receptor mutations and two common calsequestrin 2 amino-acid polymorphisms , 2003, European Journal of Human Genetics.

[13]  Donald M Bers,et al.  Sarcoplasmic reticulum Ca2+ and heart failure: roles of diastolic leak and Ca2+ transport. , 2003, Circulation research.

[14]  G. Dorn,et al.  Polymorphic SERCA2a variants do not account for inter-individual differences in phospholamban-SERCA2a interactions in human heart failure. , 2003, Journal of molecular and cellular cardiology.

[15]  S. Priori,et al.  FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death , 2003, Cell.

[16]  B. Xiao,et al.  Enhanced Basal Activity of a Cardiac Ca2+ Release Channel (Ryanodine Receptor) Mutant Associated With Ventricular Tachycardia and Sudden Death , 2002, Circulation research.

[17]  Carlo Napolitano,et al.  Clinical and Molecular Characterization of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia , 2002, Circulation.

[18]  K. Brown,et al.  Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia , 2001, Circulation.

[19]  S. Priori,et al.  Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia , 2001, Circulation.

[20]  J. Kere,et al.  Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts. , 1999, Journal of the American College of Cardiology.