scholarly article | Q13442814 |
P50 | author | Christine E. Seidman | Q30123970 |
P2093 | author name string | Libin Wang | |
Charles I. Berul | |||
Michael Arad | |||
Tetsuo Konno | |||
Ronny Alcalai | |||
David Planer | |||
Hiroko Wakimoto | |||
Jon G. Seidman | |||
P2860 | cites work | Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak | Q24296910 |
Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia | Q24299780 | ||
Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes | Q24315860 | ||
Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans | Q24608179 | ||
Catecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden death | Q24674590 | ||
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia | Q28142708 | ||
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia | Q28201561 | ||
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 | Q28204838 | ||
Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia | Q28235110 | ||
Abnormal calcium signaling and sudden cardiac death associated with mutation of calsequestrin | Q28237997 | ||
Quantitation of protein | Q28279026 | ||
Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia | Q28279395 | ||
Catecholaminergic polymorphic ventricular tachycardia | Q28287523 | ||
Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardia | Q28589230 | ||
Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21. | Q33146452 | ||
Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia. | Q33147854 | ||
Bidirectional ventricular tachycardia and fibrillation elicited in a knock-in mouse model carrier of a mutation in the cardiac ryanodine receptor. | Q33152686 | ||
Calcium channel blockers and beta-blockers versus beta-blockers alone for preventing exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia | Q33155477 | ||
Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardia | Q33157356 | ||
Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients | Q33173888 | ||
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Direct binding of verapamil to the ryanodine receptor channel of sarcoplasmic reticulum | Q34126333 | ||
Cellular mechanisms underlying the development of catecholaminergic ventricular tachycardia. | Q34661902 | ||
Modulation of SR Ca release by luminal Ca and calsequestrin in cardiac myocytes: effects of CASQ2 mutations linked to sudden cardiac death. | Q36791253 | ||
Video-assisted thoracoscopic cardiac denervation: a potential novel therapeutic option for children with intractable ventricular arrhythmias | Q37339393 | ||
Caffeine induces Ca2+ release by reducing the threshold for luminal Ca2+ activation of the ryanodine receptor | Q37355318 | ||
ATPase Activities, Ca2+ Transport and Phosphoprotein Formation in Sarcoplasmic Reticulum Subfractions of Fast and Slow Rabbit Muscles | Q39840965 | ||
Sarcoplasmic reticulum calsequestrins: structural and functional properties | Q40565740 | ||
Modified release verapamil induced cardiogenic shock | Q41990514 | ||
Calsequestrin: more than 'only' a luminal Ca2+ buffer inside the sarcoplasmic reticulum | Q42992388 | ||
Intra-sarcoplasmic reticulum Ca2+ oscillations are driven by dynamic regulation of ryanodine receptor function by luminal Ca2+ in cardiomyocytes | Q43286787 | ||
Quantitative assessment of the SR Ca2+ leak-load relationship | Q44167973 | ||
Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutations | Q45273441 | ||
Early changes in excitation-contraction coupling: transition from compensated hypertrophy to failure in Dahl salt-sensitive rat myocytes. | Q54135977 | ||
Hormonal control of Mg2+ transport in the heart | Q59095759 | ||
In vivo cardiac electrophysiology studies in the mouse | Q71785180 | ||
Impaired cell shortening and relengthening with increased pacing frequency are intrinsic to the senescent mouse cardiomyocyte | Q73098110 | ||
Magnesium inhibition of ryanodine-receptor calcium channels: evidence for two independent mechanisms | Q73207956 | ||
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia | Q78390804 | ||
Arrhythmogenesis in catecholaminergic polymorphic ventricular tachycardia: insights from a RyR2 R4496C knock-in mouse model | Q79851890 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | ventricular tachycardia | Q56002 |
heart arrhythmia | Q189331 | ||
tachycardia | Q209583 | ||
catecholaminergic polymorphic ventricular tachycardia | Q1649897 | ||
P304 | page(s) | 316-324 | |
P577 | publication date | 2010-08-30 | |
P1433 | published in | Journal of Cardiovascular Electrophysiology | Q4736917 |
P1476 | title | Prevention of ventricular arrhythmia and calcium dysregulation in a catecholaminergic polymorphic ventricular tachycardia mouse model carrying calsequestrin-2 mutation | |
Prevention of Ventricular Arrhythmia and Calcium Dysregulation in a Catecholaminergic Polymorphic Ventricular Tachycardia Mouse Model Carrying Calsequestrin-2 Mutation | |||
P478 | volume | 22 |
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Q36941532 | Calsequestrin 2 deletion shortens the refractoriness of Ca²⁺ release and reduces rate-dependent Ca²⁺-alternans in intact mouse hearts |
Q38125941 | Current perspectives in genetic cardiovascular disorders: from basic to clinical aspects |
Q28589538 | Dynamic, inter-subunit interactions between the N-terminal and central mutation regions of cardiac ryanodine receptor |
Q38602828 | Efficacy and potency of class I antiarrhythmic drugs for suppression of Ca2+ waves in permeabilized myocytes lacking calsequestrin. |
Q36559205 | L-Type Calcium Channels Do Not Play a Critical Role in Chest Blow Induced Ventricular Fibrillation: Commotio Cordis |
Q89961129 | Molecular and tissue mechanisms of catecholaminergic polymorphic ventricular tachycardia |
Q38494265 | Pharmacotherapy for inherited arrhythmia syndromes: mechanistic basis, clinical trial evidence and practical application. |
Q33160416 | Therapeutic approach for patients with catecholaminergic polymorphic ventricular tachycardia: state of the art and future developments |
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