Modulation of HERG potassium channels by extracellular magnesium and quinidine.
about
The anti-addiction drug ibogaine and the heart: a delicate relationHuman gene SLC41A1 encodes for the Na+/Mg²+ exchangerFamilial and acquired long qt syndrome and the cardiac rapid delayed rectifier potassium current.Antiarrhythmics--from cell to clinic: past, present, and future.Reductions in external divalent cations evoke novel voltage-gated currents in sensory neurons.Enhancement of HERG K+ currents by Cd2+ destabilization of the inactivated state.Electrophysiologic properties and antiarrhythmic actions of a novel antianginal agent.Natural products modulating the hERG channel: heartaches and hope.Differences between ion binding to eag and HERG voltage sensors contribute to differential regulation of activation and deactivation gating.Saxitoxin is a gating modifier of HERG K+ channels.Inhibition of the current of heterologously expressed HERG potassium channels by flecainide and comparison with quinidine, propafenone and lignocaine.The binding site for channel blockers that rescue misprocessed human long QT syndrome type 2 ether-a-gogo-related gene (HERG) mutations.Inhibition of the current of heterologously expressed HERG potassium channels by imipramine and amitriptyline.Mode-dependent inhibition by quinidine of Na+-Ca2+ exchanger current from guinea-pig isolated ventricular myocytes.Acidification alters antiarrhythmic drug blockade of the ether-a-go-go-related Gene (HERG) Channels.Tailoring Mathematical Models to Stem-Cell Derived Cardiomyocyte Lines Can Improve Predictions of Drug-Induced Changes to Their Electrophysiology.Observations on conducting whole-cell patch clamping of the hERG cardiac K+ channel in pure human serum.Modulation of homomeric and heteromeric KCNQ1 channels by external acidification.Early afterdepolarisation tendency as a simulated pro-arrhythmic risk indicator† †Electronic supplementary information (ESI) available. See DOI: 10.1039/C7TX00141J.Early afterdepolarisation tendency as a simulated pro-arrhythmic risk indicator.Improving the assessment of heart toxicity for all new drugs through translational regulatory science.
P2860
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P2860
Modulation of HERG potassium channels by extracellular magnesium and quinidine.
description
1999 nî lūn-bûn
@nan
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
1999年论文
@zh
1999年论文
@zh-cn
name
Modulation of HERG potassium channels by extracellular magnesium and quinidine.
@en
type
label
Modulation of HERG potassium channels by extracellular magnesium and quinidine.
@en
prefLabel
Modulation of HERG potassium channels by extracellular magnesium and quinidine.
@en
P2093
P1476
Modulation of HERG potassium channels by extracellular magnesium and quinidine.
@en
P2093
P304
P356
10.1097/00005344-199902000-00002
P407
P577
1999-02-01T00:00:00Z