The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
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14-3-3 amplifies and prolongs adrenergic stimulation of HERG K+ channel activityMolecular genetics of coronary artery diseasePhobic memory and somatic vulnerabilities in anorexia nervosa: a necessary unity?Impact of New Genomic Technologies on Understanding Adverse Drug ReactionsMolecular and genetic basis of sudden cardiac deathSex differences in the mechanisms underlying long QT syndromeMolecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriersPAS domains: internal sensors of oxygen, redox potential, and lightDevelopment and maintenance of ear innervation and function: lessons from mutations in mouse and man.A near-fatal case of long QT syndrome in a teenaged male.KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.Long QT syndrome: first and fatal events provoked by hemodialysis.Effect of phenylephrine provocation on dispersion of repolarization in congenital long QT syndrome.Nav1.5/R1193Q polymorphism is associated with both long QT and Brugada syndromes.Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.Effect of beta-blockers on QT dynamics in the long QT syndrome: measuring the benefit.Iatrogenic QT Abnormalities and Fatal Arrhythmias: Mechanisms and Clinical SignificanceInherited disorders of voltage-gated sodium channels.Antiarrhythmics--from cell to clinic: past, present, and future.Stimulation of HERG channel activity by β-catenin.Incomplete penetrance and variable expressivity of a growth defect as a consequence of knocking out two K(+) transporters in the euascomycete fungus Podospora anserina.Congenital long-QT syndromes: a clinical and genetic update from infancy through adulthood.Selective knockout of mouse ERG1 B potassium channel eliminates I(Kr) in adult ventricular myocytes and elicits episodes of abrupt sinus bradycardia.Single-molecule detection of structural changes during Per-Arnt-Sim (PAS) domain activation.The antihistamine fexofenadine does not affect I(Kr) currents in a case report of drug-induced cardiac arrhythmiaGenome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy.LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.Characterization of a novel KCNQ1 mutation for type 1 long QT syndrome and assessment of the therapeutic potential of a novel IKs activator using patient-specific induced pluripotent stem cell-derived cardiomyocytes.Strategies for the prevention and treatment of sudden cardiac death.LQT4 gene: the "missing" ankyrin.Inherited arrhythmic disorders: long QT and Brugada syndromesGenetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of SingaporeRisk factors in sudden death in epilepsy (SUDEP): the quest for mechanisms.Methadone-associated long QT syndrome: improving pharmacotherapy for dependence on illegal opioids and lessons learned for pharmacology.Drug-induced Inhibition and Trafficking Disruption of ion Channels: Pathogenesis of QT Abnormalities and Drug-induced Fatal Arrhythmias.Up-regulation of hERG K⁺ channels by B-RAF.A fatal combination in a young lady: Long QT syndrome and coronary artery anomaly.Serum- and glucocorticoid-inducible kinase 1 in the regulation of renal and extrarenal potassium transport.AMP-activated protein kinase regulates hERG potassium channel.The long QT syndrome and torsade de pointes.
P2860
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P2860
The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
@ast
The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
@en
type
label
The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
@ast
The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
@en
prefLabel
The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
@ast
The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
@en
P1476
The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
@en
P2093
G M Vincent
P304
P356
10.1146/ANNUREV.MED.49.1.263
P577
1998-01-01T00:00:00Z