DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
about
Changes in channel trafficking and protein stability caused by LQT2 mutations in the PAS domain of the HERG channelUse of mutant-specific ion channel characteristics for risk stratification of long QT syndrome patients.Long QT syndrome in South Africa: the results of comprehensive genetic screening.Potassium channel gene mutations rarely cause atrial fibrillationLQTS gene LOVD databaseThe use of denaturing high-performance liquid chromatography (DHPLC) for the analysis of genetic variations: impact for diagnostics and pharmacogenetics.Genetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of SingaporePharmacogenetic issues in thorough QT trials.An Examination of KCNE1 Mutations and Common Variants in Chronic Tinnitus.HERG potassium channel regulation by the N-terminal eag domain.Pharmacological and electrophysiological characterization of nine, single nucleotide polymorphisms of the hERG-encoded potassium channel.Regions of KCNQ K(+) channels controlling functional expressionMolecular analysis of potassium ion channel genes in sudden death cases among patients administered psychotropic drug therapy: are polymorphisms in LQT genes a potential risk factor?Gain-of-function KCNH2 mutations in patients with Brugada syndrome.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.Whole blood RNA offers a rapid, comprehensive approach to genetic diagnosis of cardiovascular diseases.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
DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
@en
DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
@nl
type
label
DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
@en
DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
@nl
prefLabel
DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
@en
DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
@nl
P2093
P2860
P356
P1433
P1476
DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
@en
P2093
Carlo Marcelis
Crool Velter
Hubert Smeets
Joep Geraedts
Pieter Doevendans
Roselie Jongbloed
P2860
P304
P356
10.1002/HUMU.10131
P577
2002-11-01T00:00:00Z