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Genetics of sudden cardiac death syndromes

Genetics of sudden cardiac death syndromes

http://www.wikidata.org/entity/Q28307856

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AKAP9 is essential for spermatogenesis and sertoli cell maturation in mice SNP rs3825214 in TBX5 is associated with lone atrial fibrillation in Chinese Han population.Investigating the effects of resveratrol on chronically ischemic myocardium in a swine model of metabolic syndrome: a proteomics analysis.Calcium/calmodulin-dependent protein kinase II (CaMKII) inhibition ameliorates arrhythmias elicited by junctin ablation under stress conditions Genome-Wide Association Study Identifies Novel Susceptibility Genes Associated with Coronary Artery Aneurysm Formation in Kawasaki Disease Cardiac ion channelopathies and the sudden infant death syndrome Loss of the transcription factor Meis1 prevents sympathetic neurons target-field innervation and increases susceptibility to sudden cardiac death The link between abnormal calcium handling and electrical instability in acquired long QT syndrome--Does calcium precipitate arrhythmic storms?Immunohistochemical detection of S100A1 in the postmortem diagnosis of acute myocardial infarction.Genetic mutation in Korean patients of sudden cardiac arrest as a surrogating marker of idiopathic ventricular arrhythmia Divergent regulation of ryanodine receptor 2 calcium release channels by arrhythmogenic human calmodulin missense mutants.SK4 K+ channels are therapeutic targets for the treatment of cardiac arrhythmias Induced pluripotent stem cell-derived cardiomyocytes: boutique science or valuable arrhythmia model?The emerging role of calmodulin regulation of RyR2 in controlling heart rhythm, the progression of heart failure and the antiarrhythmic action of dantrolene.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.Non-targeted metabolomics identified a common metabolic signature of lethal ventricular tachyarrhythmia (LVTA) in two rat models.De Novo FGF12 (Fibroblast Growth Factor 12) Functional Variation Is Potentially Associated With Idiopathic Ventricular Tachycardia.Serum lipid feature and potential biomarkers of lethal ventricular tachyarrhythmia (LVTA) induced by myocardial ion channel diseases: a rat model study.

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Genetics of sudden cardiac death syndromes

http://www.wikidata.org/entity/Q28307856

description

2011 nî lūn-bûn

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2011 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2011 թվականի մայիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Genetics of sudden cardiac death syndromes

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Genetics of sudden cardiac death syndromes

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Genetics of sudden cardiac death syndromes

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type

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Genetics of sudden cardiac death syndromes

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Genetics of sudden cardiac death syndromes

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Genetics of sudden cardiac death syndromes

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prefLabel

Genetics of sudden cardiac death syndromes

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Genetics of sudden cardiac death syndromes

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Genetics of sudden cardiac death syndromes

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Current Opinion in Cardiology

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Genetics of sudden cardiac death syndromes

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Björn C Knollmann

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Nagesh Chopra

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P2860

Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy

Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias

Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosis

Expression and function of dipeptidyl-aminopeptidase-like protein 6 as a putative beta-subunit of human cardiac transient outward current encoded by Kv4.3

Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromes

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

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

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196-203

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scholarly article

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3145336

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