IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome
about
Kcne2 deletion uncovers its crucial role in thyroid hormone biosynthesisDeep resequencing of the voltage-gated potassium channel subunit KCNE3 gene in chronic tinnitusDifferential association between HERG and KCNE1 or KCNE2KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channelRegulation of the Kv2.1 potassium channel by MinK and MiRP1Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafnessKCNE4 is an inhibitory subunit to the KCNQ1 channelGenetics of inherited primary arrhythmia disordersNeuronal and Cardiovascular Potassium Channels as Therapeutic Drug Targets: Promise and PitfallsFunctional significance of K+ channel β-subunit KCNE3 in auditory neuronsDisruption of the K+ channel beta-subunit KCNE3 reveals an important role in intestinal and tracheal Cl- transportEndogenous KCNE subunits govern Kv2.1 K+ channel activation kinetics in Xenopus oocyte studiesKCNE beta subunits determine pH sensitivity of KCNQ1 potassium channelsKCNQ1/KCNE1 channels during germ-cell differentiation in the rat: expression associated with testis pathologiesCurrent insights in noise-induced hearing loss: a literature review of the underlying mechanism, pathophysiology, asymmetry, and management options.Genetics of auditory mechano-electrical transduction.Working model for the structural basis for KCNE1 modulation of the KCNQ1 potassium channel.In silico analysis of 2085 clones from a normalized rat vestibular periphery 3' cDNA libraryA gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.Development and maintenance of ear innervation and function: lessons from mutations in mouse and man.At the speed of sound: gene discovery in the auditory systemA KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance.Long QT syndrome in South Africa: the results of comprehensive genetic screening.Ion channel genes and human neurological disease: recent progress, prospects, and challenges.Beginning of a molecular era in hearing and deafness.Mechanisms of disease pathogenesis in long QT syndrome type 5Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.Science, medicine, and the future: New interventions in hearing impairment.A new spontaneous mouse mutation in the Kcne1 geneThe genetics of cardiac arrhythmias.Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss.Pore- and state-dependent cadmium block of I(Ks) channels formed with MinK-55C and wild-type KCNQ1 subunitsMutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias.The KCNQ1 potassium channel: from gene to physiological function.The multifaceted phenotype of the knockout mouse for the KCNE1 potassium channel gene.KCNE1 D85N polymorphism--a sex-specific modifier in type 1 long QT syndrome?Genetic disorders of neuromuscular ion channels.Potassium channels in epithelial transport.KCNE Regulation of K(+) Channel Trafficking - a Sisyphean Task?Impact of ancillary subunits on ventricular repolarization.
P2860
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P2860
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome
description
1997 nî lūn-bûn
@nan
1997 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
IsK and KvLQT1: mutation in ei ...... ell and Lange-Nielsen syndrome
@ast
IsK and KvLQT1: mutation in ei ...... ell and Lange-Nielsen syndrome
@en
IsK and KvLQT1: mutation in ei ...... ell and Lange-Nielsen syndrome
@nl
type
label
IsK and KvLQT1: mutation in ei ...... ell and Lange-Nielsen syndrome
@ast
IsK and KvLQT1: mutation in ei ...... ell and Lange-Nielsen syndrome
@en
IsK and KvLQT1: mutation in ei ...... ell and Lange-Nielsen syndrome
@nl
prefLabel
IsK and KvLQT1: mutation in ei ...... ell and Lange-Nielsen syndrome
@ast
IsK and KvLQT1: mutation in ei ...... ell and Lange-Nielsen syndrome
@en
IsK and KvLQT1: mutation in ei ...... ell and Lange-Nielsen syndrome
@nl
P2093
P356
P1476
IsK and KvLQT1: mutation in ei ...... ell and Lange-Nielsen syndrome
@en
P2093
B Aslaksen
J F Taylor
L Tranebjaerg
M Bitner-Glindzicz
P304
P356
10.1093/HMG/6.12.2179
P407
P577
1997-11-01T00:00:00Z