Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3 - Wikidata - awgldk - TriplyDB

Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3

Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3

http://www.wikidata.org/entity/Q33906850

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Propranolol blocks cardiac and neuronal voltage-gated sodium channels Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome A systematic review to investigate whether Angiotensin-(1-7) is a promising therapeutic target in human heart failure Late Sodium Current in Human Atrial Cardiomyocytes from Patients in Sinus Rhythm and Atrial Fibrillation Ranolazine for Congenital Long-QT Syndrome Type III: Experimental and Long-Term Clinical Data.Sudden cardiac death and inherited channelopathy: the basic electrophysiology of the myocyte and myocardium in ion channel disease.Light phase-restricted feeding slows basal heart rate to exaggerate the type-3 long QT syndrome phenotype in mice.Electrophysiologic basis for the antiarrhythmic actions of ranolazine.Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs.Temporal response of ectopic activity in guinea pig ventricular myocardium in response to isoproterenol and acetylcholine Propranolol prevents life-threatening arrhythmias in LQT3 transgenic mice: implications for the clinical management of LQT3 patients Mouse Models of SCN5A-Related Cardiac Arrhythmias Congenital long and short QT syndromes.Cardiac electrophysiology in mice: a matter of size.The effects of ageing and adrenergic challenge on electrocardiographic phenotypes in a murine model of long QT syndrome type 3 An automated system using spatial oversampling for optical mapping in murine atria. Development and validation with monophasic and transmembrane action potentials.Minimally invasive closed-chest ultrasound-guided substance delivery into the pericardial space in mice Effectiveness of beta-blockers depending on the genotype of congenital long-QT syndrome: A meta-analysis.Autonomic nervous system and cardiac channelopathies in sleep apnea-one more piece of a complex puzzle?

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Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3

http://www.wikidata.org/entity/Q33906850

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2010 թվականի հունվարին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3

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Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3

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Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3

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Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3

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Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3

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Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3

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Cardiovascular Research

P1476

Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3

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P2093

Andreas Blana

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Burkhard Riemann

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Daniela Volkery

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Dierk Damke

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Edward Carmeliet

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Elena Aleynichenko

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Johannes Steinfurt

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Kathrin Theis

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Lisa Fortmüller

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Markus Emmerich

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P2860

Molecular basis of ranolazine block of LQT-3 mutant sodium channels: evidence for site of action

Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD

Pronounced pharmacologic deficits in M2 muscarinic acetylcholine receptor knockout mice

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block.

Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers.

Implantable cardioverter defibrillator implantation in children in The Netherlands.

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

Differential effects of beta-adrenergic agonists and antagonists in LQT1, LQT2 and LQT3 models of the long QT syndrome.

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60-72

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scholarly article

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10.1093/CVR/CVQ029

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1

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87

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Peter Carmeliet

Paulus Kirchhof

Larissa Fabritz

Günter Breithardt

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2010-01-28T00:00:00Z

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41173638

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20110334

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2883895

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