KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.
about
Structural insight into KCNQ (Kv7) channel assembly and channelopathyMolecular pathogenesis of long QT syndrome type 1Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.Identification of novel missense mutations of cardiac ryanodine receptor gene in exercise-induced sudden death at autopsy.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.Inherited long QT syndrome: clinical manifestation, genetic diagnostics, and therapy.Long QT syndrome in South Africa: the results of comprehensive genetic screening.Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.Transcription factor MEF2A mutations in patients with coronary artery disease.Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy.Arrhythmia formation in subclinical ("silent") long QT syndrome requires multiple insults: quantitative mechanistic study using the KCNQ1 mutation Q357R as exampleIntracellular ATP binding is required to activate the slowly activating K+ channel I(Ks)Prevalence of the congenital long-QT syndrome.Genetics and cardiac channelopathies.Arrhythmic risk biomarkers for the assessment of drug cardiotoxicity: from experiments to computer simulations.The voltage-gated channel accessory protein KCNE2: multiple ion channel partners, multiple ways to long QT syndrome.Modeling of the adrenergic response of the human IKs current (hKCNQ1/hKCNE1) stably expressed in HEK-293 cells.Pharmacological and non-pharmacological therapy for arrhythmias in the pediatric population: EHRA and AEPC-Arrhythmia Working Group joint consensus statement.Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome.Atrioventricular Block-induced Torsades de Pointes Associated with KCNQ1-G269S.Even pore-localizing missense variants at highly conserved sites in KCNQ1-encoded Kv7.1 channels may have wild-type function and not cause type 1 long QT syndrome: Do not rely solely on the genetic test company's interpretation.
P2860
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P2860
KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.
description
2003 nî lūn-bûn
@nan
2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
KCNQ1 mutations in patients wi ...... arrhythmias and sudden death.
@ast
KCNQ1 mutations in patients wi ...... arrhythmias and sudden death.
@en
type
label
KCNQ1 mutations in patients wi ...... arrhythmias and sudden death.
@ast
KCNQ1 mutations in patients wi ...... arrhythmias and sudden death.
@en
prefLabel
KCNQ1 mutations in patients wi ...... arrhythmias and sudden death.
@ast
KCNQ1 mutations in patients wi ...... arrhythmias and sudden death.
@en
P2093
P2860
P1433
P1476
KCNQ1 mutations in patients wi ...... arrhythmias and sudden death.
@en
P2093
F Zimmerman
G M Vincent
P2860
P304
P356
10.1034/J.1399-0004.2003.00048.X
P577
2003-04-01T00:00:00Z