Identification of a Kir3.4 mutation in congenital long QT syndrome
about
RING finger protein RNF207, a novel regulator of cardiac excitationChannelopathiesGenetics of channelopathies associated with sudden cardiac deathGenetics of inherited primary arrhythmia disordersNeuronal and Cardiovascular Potassium Channels as Therapeutic Drug Targets: Promise and PitfallsLong-QT syndrome: from genetics to managementMolecular and genetic basis of sudden cardiac deathIon Channels in the HeartEssential role of the m2R-RGS6-IKACh pathway in controlling intrinsic heart rate variabilityCongenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.Pharmacological inhibition of IK1 by PA-6 in isolated rat hearts affects ventricular repolarization and refractorinessMutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.Patient with syncope and LQTS carrying a mutation in the PAS domain of the hERG1 channel.Genotype-phenotype analysis of three Chinese families with Jervell and Lange-Nielsen syndrome.Inherited long QT syndrome: clinical manifestation, genetic diagnostics, and therapy.Long QT syndrome in South Africa: the results of comprehensive genetic screening.Genetics of long QT syndrome.RNA interference-based therapeutics for inherited long QT syndromeDeleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT.Overview of the genetic determinants of primary aldosteronism.KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome.Clathrin-independent endocytosis: a cargo-centric viewHigh prevalence of genetic variants previously associated with LQT syndrome in new exome dataIon channel associated diseases: overview of molecular mechanismsMicroRNAs in cardiac arrhythmia: DNA sequence variation of MiR-1 and MiR-133A in long QT syndromeDrug-induced long QT syndromeOverview of Basic Mechanisms of Cardiac ArrhythmiaLQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.Paralogous annotation of disease-causing variants in long QT syndrome genes.Jacobsen Syndrome: Surgical Complications due to Unsuspected Diagnosis, the Importance of Molecular Studies in Patients with Craniosynostosis.The GIRK1 subunit potentiates G protein activation of cardiac GIRK1/4 hetero-tetramers.Gene mutations in cardiac arrhythmias: a review of recent evidence in ion channelopathies.Genetic testing in heritable cardiac arrhythmia syndromes: differentiating pathogenic mutations from background genetic noise.Quantitative PCR as an alternative in the diagnosis of long-QT syndromeKCNE genetics and pharmacogenomics in cardiac arrhythmias: much ado about nothing?Tissue-specific effects of acetylcholine in the canine heart.G-protein-coupled inward rectifier potassium current contributes to ventricular repolarizationRGS6, but not RGS4, is the dominant regulator of G protein signaling (RGS) modulator of the parasympathetic regulation of mouse heart rate.Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic AdvancesGenetics of sudden death: focus on inherited channelopathies.
P2860
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P248
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P2860
Identification of a Kir3.4 mutation in congenital long QT syndrome
description
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2010
@ast
im Juni 2010 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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vedecký článok (publikovaný 2010/06/11)
@sk
vědecký článek publikovaný v roce 2010
@cs
wetenschappelijk artikel (gepubliceerd op 2010/06/11)
@nl
наукова стаття, опублікована в червні 2010
@uk
مقالة علمية (نشرت في 11-6-2010)
@ar
name
Identification of a Kir3.4 mutation in congenital long QT syndrome
@ast
Identification of a Kir3.4 mutation in congenital long QT syndrome
@en
Identification of a Kir3.4 mutation in congenital long QT syndrome
@nl
type
label
Identification of a Kir3.4 mutation in congenital long QT syndrome
@ast
Identification of a Kir3.4 mutation in congenital long QT syndrome
@en
Identification of a Kir3.4 mutation in congenital long QT syndrome
@nl
prefLabel
Identification of a Kir3.4 mutation in congenital long QT syndrome
@ast
Identification of a Kir3.4 mutation in congenital long QT syndrome
@en
Identification of a Kir3.4 mutation in congenital long QT syndrome
@nl
P2093
P2860
P50
P921
P3181
P1476
Identification of a Kir3.4 mutation in congenital long QT syndrome
@en
P2093
Dandan Liang
Jinqiu Liu
Junjie Xiao
Lianjun Gao
Luying Peng
Patrick T. Ellinor
P2860
P304
P3181
P356
10.1016/J.AJHG.2010.04.017
P407
P577
2010-06-11T00:00:00Z