Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
about
Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversityKCNE5 induces time- and voltage-dependent modulation of the KCNQ1 current.Cellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndromeInhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptorsSlow delayed rectifier current and repolarization in canine cardiac Purkinje cells.Age-dependent electrical and morphological remodeling of the Drosophila heart caused by hERG/seizure mutations.A dominant negative mutant of the KCC1 K-Cl cotransporter: both N- and C-terminal cytoplasmic domains are required for K-Cl cotransport activity.Ginseng gintonin activates the human cardiac delayed rectifier K+ channel: involvement of Ca2+/calmodulin binding sites.Safety pharmacology of DW-224a, a novel fluoroquinolone antibiotic agent.Stimulation of HERG channel activity by β-catenin.Cardiac channelopathies.Ranolazine: ion-channel-blocking actions and in vivo electrophysiological effects.Electrophysiological safety of novel fluoroquinolone antibiotic agents gemifloxacin and balofloxacin.In vivo analysis of a gain-of-function mutation in the Drosophila eag-encoded K+ channel.Prevention of Pazopanib-Induced Prolonged Cardiac Repolarization and Proarrhythmic EffectsMolecular impact of MinK on the enantiospecific block of I(Ks) by chromanols.Insensitivity of cardiac delayed-rectifier I(Kr) to tyrosine phosphorylation inhibitors and stimulatorsThe therapeutic potential of neuronal KCNQ channel modulators.Differential effects of ginsenoside metabolites on slowly activating delayed rectifier K(+) and KCNQ1 K(+) channel currents.Up-regulation of hERG K⁺ channels by B-RAF.QT prolongation in the intensive care unit: commonly used medications and the impact of drug-drug interactions.Molecular Pathophysiology of Congenital Long QT Syndrome.AMP-activated protein kinase regulates hERG potassium channel.Normal function of HERG K+ channels expressed in HEK293 cells requires basal protein kinase B activity.Nitric oxide-dependent modulation of the delayed rectifier K+ current and the L-type Ca2+ current by ginsenoside Re, an ingredient of Panax ginseng, in guinea-pig cardiomyocytes.Desensitization of chemical activation by auxiliary subunits: convergence of molecular determinants critical for augmenting KCNQ1 potassium channels.Impairment of human ether-à-go-go-related gene (HERG) K+ channel function by hypoglycemia and hyperglycemia. Similar phenotypes but different mechanisms.Modulating effect of ginseng saponins on heterologously expressed HERG currents in Xenopus oocytes.KCNE1 and KCNE3 modulate KCNQ1 channels by affecting different gating transitions.Klotho sensitivity of the hERG channel.Drosophila in the Heart of Understanding Cardiac Diseases: Modeling Channelopathies and Cardiomyopathies in the Fruitfly.Comparison of protein behavior between wild-type and G601S hERG in living cells by fluorescence correlation spectroscopy.The C-terminal HRET sequence of Kv1.3 regulates gating rather than targeting of Kv1.3 to the plasma membrane.
P2860
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P2860
Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
@ast
Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
@en
type
label
Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
@ast
Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
@en
prefLabel
Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
@ast
Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
@en
P2860
P1476
Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
@en
P2093
M C Sanguinetti
P2860
P304
P356
10.1111/J.1749-6632.1999.TB11302.X
P407
P577
1999-04-01T00:00:00Z