Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
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Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart StudyRYR2 sequencing reveals novel missense mutations in a Kazakh idiopathic ventricular tachycardia study cohortArrhythmogenic right ventricular cardiomyopathy/dysplasiaHeart Disease and Stroke Statistics--2013 Update: A Report From the American Heart AssociationMutations in calmodulin cause ventricular tachycardia and sudden cardiac deathCalsequestrin 2 and arrhythmiasThe Ser96Ala variant in histidine-rich calcium-binding protein is associated with life-threatening ventricular arrhythmias in idiopathic dilated cardiomyopathyIn situ modulation of the human cardiac ryanodine receptor (hRyR2) by FKBP12.6Dysfunctional ryanodine receptors in the heart: new insights into complex cardiovascular diseasesMany roads lead to a broken heart: the genetics of dilated cardiomyopathy.Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humansCatecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden deathElectrophysiological Mechanisms of Gastrointestinal Arrhythmogenesis: Lessons from the HeartNext-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death CasesCatecholaminergic polymorphic ventricular tachycardia: An exciting new eraMechanisms of cardiac arrhythmiasCardiovascular Disease Modeling Using Patient-Specific Induced Pluripotent Stem CellsMolecular and genetic basis of sudden cardiac deathInduced pluripotent stem cell-derived cardiomyocytes for cardiovascular disease modeling and drug screeningIon Channels in the HeartThe molecular autopsy: should the evaluation continue after the funeral?Defective interactions of protein partner with ion channels and transporters as alternative mechanisms of membrane channelopathiesClinical Potentials of Cardiomyocytes Derived from Patient-Specific Induced Pluripotent Stem CellsDeterminants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromesChannel Activity of Cardiac Ryanodine Receptors (RyR2) Determines Potency and Efficacy of Flecainide and R-Propafenone against Arrhythmogenic Calcium Waves in Ventricular CardiomyocytesCardiac innervation and sudden cardiac death.Role of sodium and calcium dysregulation in tachyarrhythmias in sudden cardiac death.Disease mutations in the ryanodine receptor N-terminal region couple to a mobile intersubunit interfaceCardiac disease and arrhythmogenesis: Mechanistic insights from mouse modelsPatient Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Development and Screening In Catecholaminergic Polymorphic Ventricular TachycardiaCurrent topics in catecholaminergic polymorphic ventricular tachycardiaA missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelLocalization of the 12.6-kDa FK506-binding protein (FKBP12.6) binding site to the NH2-terminal domain of the cardiac Ca2+ release channel (ryanodine receptor)Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardiaInherited conduction system abnormalities--one group of diseases, many genesGenetic bases of arrhythmogenic right ventricular CardiomyopathyCalsequestrin mutations and catecholaminergic polymorphic ventricular tachycardiaThe RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading framComprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy
P2860
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P2860
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
description
2001 nî lūn-bûn
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2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
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2001年の論文
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2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Mutations in the cardiac ryano ...... orphic ventricular tachycardia
@ast
Mutations in the cardiac ryano ...... orphic ventricular tachycardia
@en
Mutations in the cardiac ryano ...... orphic ventricular tachycardia
@nl
type
label
Mutations in the cardiac ryano ...... orphic ventricular tachycardia
@ast
Mutations in the cardiac ryano ...... orphic ventricular tachycardia
@en
Mutations in the cardiac ryano ...... orphic ventricular tachycardia
@nl
prefLabel
Mutations in the cardiac ryano ...... orphic ventricular tachycardia
@ast
Mutations in the cardiac ryano ...... orphic ventricular tachycardia
@en
Mutations in the cardiac ryano ...... orphic ventricular tachycardia
@nl
P2093
P3181
P356
P1433
P1476
Mutations in the cardiac ryano ...... orphic ventricular tachycardia
@en
P2093
C Napolitano
G A Danieli
S G Priori
V Sorrentino
P304
P3181
P356
10.1161/01.CIR.103.2.196
P407
P577
2001-01-16T00:00:00Z