Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
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Heart Disease and Stroke Statistics--2013 Update: A Report From the American Heart AssociationThe 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 FKBP12.6Many roads lead to a broken heart: the genetics of dilated cardiomyopathy.Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)Catecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden deathNext-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death CasesGenetics of channelopathies associated with sudden cardiac deathThe molecular autopsy: should the evaluation continue after the funeral?Defective interactions of protein partner with ion channels and transporters as alternative mechanisms of membrane channelopathiesPatient 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 IsraelInvolvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardiaGenetic bases of arrhythmogenic right ventricular CardiomyopathyThe 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 framRyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca2+ release (SOICR)Defective domain-domain interactions within the ryanodine receptor as a critical cause of diastolic Ca2+ leak in failing heartsMutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humansDoxapram hydrochloride aggravates adrenaline-induced arrhythmias accompanied by bidirectional ventricular tachycardiaThree-dimensional reconstruction of the recombinant type 2 ryanodine receptor and localization of its divergent region 1Antiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC ModelsStabilization of cardiac ryanodine receptor prevents intracellular calcium leak and arrhythmiasDynamic, inter-subunit interactions between the N-terminal and central mutation regions of cardiac ryanodine receptorTECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVTHeart disease and stroke statistics--2012 update: a report from the American Heart AssociationMonogenec Arrhythmic Syndromes: From Molecular and Genetic Aspects to Bedside.Mutation in sodium-calcium exchanger 1 (NCX1) causes cardiac fibrillation in zebrafishLeaky Ca2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice.Prevention of ventricular arrhythmia and calcium dysregulation in a catecholaminergic polymorphic ventricular tachycardia mouse model carrying calsequestrin-2 mutation.Exercise-induced bidirectional ventricular tachycardia with alternating right and left bundle branch block-type patterns--a case report.Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia.A missense mutation in CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.Identification of novel missense mutations of cardiac ryanodine receptor gene in exercise-induced sudden death at autopsy.The molecular basis of catecholaminergic polymorphic ventricular tachycardia: what are the different hypotheses regarding mechanisms?Catecholaminergic polymorphic ventricular tachycardia in a child: a case report.Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia.Catecholaminergic polymorphic ventricular tachycardia: a current overview.A case of catecholaminergic polymorphic ventricular tachycardia.Autosomal recessive catecholamine-induced polymorphic ventricular tachycardia.
P2860
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P2860
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
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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
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2001年論文
@zh-tw
2001年论文
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name
Mutations of the cardiac ryano ...... orphic ventricular tachycardia
@ast
Mutations of the cardiac ryano ...... orphic ventricular tachycardia
@en
Mutations of the cardiac ryano ...... orphic ventricular tachycardia
@nl
type
label
Mutations of the cardiac ryano ...... orphic ventricular tachycardia
@ast
Mutations of the cardiac ryano ...... orphic ventricular tachycardia
@en
Mutations of the cardiac ryano ...... orphic ventricular tachycardia
@nl
prefLabel
Mutations of the cardiac ryano ...... orphic ventricular tachycardia
@ast
Mutations of the cardiac ryano ...... orphic ventricular tachycardia
@en
Mutations of the cardiac ryano ...... orphic ventricular tachycardia
@nl
P2093
P3181
P356
P1433
P1476
Mutations of the cardiac ryano ...... orphic ventricular tachycardia
@en
P2093
Brahmbhatt B
Devaney JM
Donarum EA
Laitinen PJ
Stephan DA
P304
P3181
P356
10.1161/01.CIR.103.4.485
P407
P577
2001-01-01T00:00:00Z