Single nucleotide polymorphism map of five long-QT genes.
about
Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjectsDeterminants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromesRelationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart StudyPositive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes.Evolutionary analyses of KCNQ1 and HERG voltage-gated potassium channel sequences reveal location-specific susceptibility and augmented chemical severities of arrhythmogenic mutations.Several polymorphisms of KCNQ1 gene are associated with plasma lipid levels in general Chinese populations.AKAP9 is a genetic modifier of congenital long-QT syndrome type 1Possible interethnic differences in quinidine-induced QT prolongation between healthy Caucasian and Korean subjectsCommon genetic variants associated with sudden cardiac death: the FinSCDgen study.A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial InfarctionRisk factors in sudden death in epilepsy (SUDEP): the quest for mechanisms.The primary arrhythmia syndromes: same mutation, different manifestations. Are we starting to understand why?Common candidate gene variants are associated with QT interval duration in the general population.An Examination of KCNE1 Mutations and Common Variants in Chronic Tinnitus.The voltage-gated channel accessory protein KCNE2: multiple ion channel partners, multiple ways to long QT syndrome.Pharmacological and electrophysiological characterization of nine, single nucleotide polymorphisms of the hERG-encoded potassium channel.A novel missense mutation causing a G487R substitution in the S2-S3 loop of human ether-à-go-go-related gene channel.HealthTwiSt: the Berlin Twin Registry for health research.Mutation analysis for the detection of long QT-syndrome (LQTS) associated SNPs.Detection of genetic variation in KCNQ1 gene by high-resolution melting analysis in a prospective-based series of postmortem negative sudden death: comparison of results obtained in fresh frozen and formalin-fixed paraffin-embedded tissues.Screening for germline KCNQ1 and KCNE2 mutations in a set of somatotropinoma patients.Single Nucleotide Polymorphisms and Haplotype of Four Genes Encoding Cardiac Ion Channels in Chinese and their Association with Arrhythmia
P2860
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P2860
Single nucleotide polymorphism map of five long-QT genes.
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年學術文章
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name
Single nucleotide polymorphism map of five long-QT genes.
@en
Single nucleotide polymorphism map of five long-QT genes.
@nl
type
label
Single nucleotide polymorphism map of five long-QT genes.
@en
Single nucleotide polymorphism map of five long-QT genes.
@nl
prefLabel
Single nucleotide polymorphism map of five long-QT genes.
@en
Single nucleotide polymorphism map of five long-QT genes.
@nl
P2093
P1476
Single nucleotide polymorphism map of five long-QT genes.
@en
P2093
Atakan Aydin
Regina Uhlmann
Stefan Dahm
Sylvia Bähring
Ulf P Guenther
P2888
P304
P356
10.1007/S00109-004-0595-3
P577
2004-12-15T00:00:00Z