Pages that link to "Q24294249"
Jump to navigation
Jump to search
The following pages link to Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features (Q24294249):
Displaying 50 items.
- Ryanodine receptor 2 (Q3415811) (← links)
- Genetics of Human and Canine Dilated Cardiomyopathy (Q26798712) (← links)
- Ion Channels in the Heart (Q26829681) (← links)
- A network-oriented perspective on cardiac calcium signaling (Q27023389) (← links)
- The amino-terminal disease hotspot of ryanodine receptors forms a cytoplasmic vestibule (Q27665591) (← links)
- Cardiac disease and arrhythmogenesis: Mechanistic insights from mouse models (Q28066019) (← links)
- The cardiac conduction system (Q28116242) (← links)
- The 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 [...] (Q28265202) (← links)
- Inherited dysfunction of sarcoplasmic reticulum Ca2+ handling and arrhythmogenesis (Q28308142) (← links)
- Calmodulin kinase II-mediated sarcoplasmic reticulum Ca2+ leak promotes atrial fibrillation in mice (Q30488460) (← links)
- Ca²⁺-dependent phosphorylation of Ca²⁺ cycling proteins generates robust rhythmic local Ca²⁺ releases in cardiac pacemaker cells (Q30659905) (← links)
- Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia. (Q33157114) (← links)
- Clinical characteristics and mutational analysis of the RyR2 gene in seven Czech families with catecholaminergic polymorphic ventricular tachycardia (Q33161218) (← links)
- A family with recurrent sudden death and no clinical clue. (Q33161934) (← links)
- Genetic analysis of Iranian family with hereditary cardiac arrhythmias by next generation sequencing. (Q33167089) (← links)
- Cardiac aging and heart disease in humans (Q33639771) (← links)
- A coupled SYSTEM of intracellular Ca2+ clocks and surface membrane voltage clocks controls the timekeeping mechanism of the heart's pacemaker. (Q33722486) (← links)
- Pharmacological changes in cellular Ca2+ homeostasis parallel initiation of atrial arrhythmogenesis in murine Langendorff-perfused hearts. (Q33739827) (← links)
- Mechanisms of sinoatrial node dysfunction in a canine model of pacing-induced atrial fibrillation (Q34079072) (← links)
- Tachybradycardia in the isolated canine right atrium induced by chronic sympathetic stimulation and pacemaker current inhibition. (Q34150582) (← links)
- Acute atrial arrhythmogenicity and altered Ca(2+) homeostasis in murine RyR2-P2328S hearts (Q34575281) (← links)
- The role of the calcium and the voltage clocks in sinoatrial node dysfunction (Q34635508) (← links)
- Potential effects of intrinsic heart pacemaker cell mechanisms on dysrhythmic cardiac action potential firing (Q35110428) (← links)
- Generation and characterization of a mouse model harboring the exon-3 deletion in the cardiac ryanodine receptor (Q35152139) (← links)
- Calsequestrin 2 deletion causes sinoatrial node dysfunction and atrial arrhythmias associated with altered sarcoplasmic reticulum calcium cycling and degenerative fibrosis within the mouse atrial pacemaker complex1. (Q35176492) (← links)
- Array comparative genomic hybridization identifies a heterozygous deletion of exon 3 of the RYR2 gene (Q35922149) (← links)
- Abnormal termination of Ca2+ release is a common defect of RyR2 mutations associated with cardiomyopathies (Q35936858) (← links)
- What keeps us ticking: a funny current, a calcium clock, or both? (Q36010630) (← links)
- Ryanodine receptor cluster fragmentation and redistribution in persistent atrial fibrillation enhance calcium release. (Q36287960) (← links)
- Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathy. (Q36452297) (← links)
- The RyR2-P2328S mutation downregulates Nav1.5 producing arrhythmic substrate in murine ventricles. (Q36688514) (← links)
- Accelerated sinus rhythm prevents catecholaminergic polymorphic ventricular tachycardia in mice and in patients. (Q36696236) (← links)
- Abnormal Ca(2+) homeostasis, atrial arrhythmogenesis, and sinus node dysfunction in murine hearts modeling RyR2 modification (Q36952000) (← links)
- The renin-angiotensin-aldosterone system (RAAS) and cardiac arrhythmias (Q37011175) (← links)
- Implantable cardioverter-defibrillator implantation in a patient with atrial standstill (Q37114030) (← links)
- Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all (Q37255253) (← links)
- Pacemaker gene mutations, bradycardia, arrhythmias and the coupled clock theory (Q37373390) (← links)
- Regulation of basal and reserve cardiac pacemaker function by interactions of cAMP-mediated PKA-dependent Ca2+ cycling with surface membrane channels (Q37377209) (← links)
- Early and comprehensive management of atrial fibrillation: proceedings from the 2nd AFNET/EHRA consensus conference on atrial fibrillation entitled 'research perspectives in atrial fibrillation'. (Q37521378) (← links)
- Mapping cardiac pacemaker circuits: methodological puzzles of the sinoatrial node optical mapping. (Q37687714) (← links)
- Genetic evaluation of familial cardiomyopathy (Q37766140) (← links)
- The genetic and clinical features of cardiac channelopathies. (Q37770572) (← links)
- Common variants for atrial fibrillation: results from genome-wide association studies (Q37898563) (← links)
- Treatment of asymptomatic catecholaminergic polymorphic ventricular tachycardia (Q38014115) (← links)
- Inherited calcium channelopathies in the pathophysiology of arrhythmias (Q38021673) (← links)
- Ryanodine receptors: structure and function. (Q38028455) (← links)
- Themes and variations in ER/SR calcium release channels: structure and function (Q38065938) (← links)
- New clinical molecular diagnostic methods for congenital and inherited heart disease (Q38088719) (← links)
- Murine Electrophysiological Models of Cardiac Arrhythmogenesis (Q39038606) (← links)
- The calcium and voltage clocks in sinoatrial node automaticity (Q41863534) (← links)