Single-channel analysis of KCNQ K+ channels reveals the mechanism of augmentation by a cysteine-modifying reagent.
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Inactivation as a new regulatory mechanism for neuronal Kv7 channelsKCNQ potassium channels in sensory system and neural circuitsDriving with no brakes: molecular pathophysiology of Kv7 potassium channelsStructure of a Ca2+/CaM:Kv7.4 (KCNQ4) B-Helix Complex Provides Insight into M Current ModulationIKs channels open slowly because KCNE1 accessory subunits slow the movement of S4 voltage sensors in KCNQ1 pore-forming subunitsThe acrylamide (S)-2 as a positive and negative modulator of Kv7 channels expressed in Xenopus laevis oocytesDual phosphorylations underlie modulation of unitary KCNQ K(+) channels by Src tyrosine kinasePhospholipase C in Living CellsCa2+/calmodulin disrupts AKAP79/150 interactions with KCNQ (M-Type) K+ channelsDeterminants within the turret and pore-loop domains of KCNQ3 K+ channels governing functional activity.Homomeric and heteromeric assembly of KCNQ (Kv7) K+ channels assayed by total internal reflection fluorescence/fluorescence resonance energy transfer and patch clamp analysis.Discovery of a novel activator of KCNQ1-KCNE1 K channel complexes.Depolarization increases phosphatidylinositol (PI) 4,5-bisphosphate level and KCNQ currents through PI 4-kinase mechanismsStructural requirements for differential sensitivity of KCNQ K+ channels to modulation by Ca2+/calmodulin.The KCNQ5 potassium channel mediates a component of the afterhyperpolarization current in mouse hippocampus.Specification of skeletal muscle differentiation by repressor element-1 silencing transcription factor (REST)-regulated Kv7.4 potassium channels.Effects of KCNQ2 gene truncation on M-type Kv7 potassium currentsRedox and nitric oxide-mediated regulation of sensory neuron ion channel functionOxidative modification of M-type K(+) channels as a mechanism of cytoprotective neuronal silencing.KCNQ5/K(v)7.5 potassium channel expression and subcellular localization in primate retinal pigment epithelium and neural retinaG-protein βγ subunits are positive regulators of Kv7.4 and native vascular Kv7 channel activity.Gating currents from Kv7 channels carrying neuronal hyperexcitability mutations in the voltage-sensing domain.Effects of KCNQ channel modulators on the M-type potassium current in primate retinal pigment epithelium.The Role of the Carboxyl Terminus Helix C-D Linker in Regulating KCNQ3 K+ Current Amplitudes by Controlling Channel TraffickingPore helix-S6 interactions are critical in governing current amplitudes of KCNQ3 K+ channels.Combinatorial augmentation of voltage-gated KCNQ potassium channels by chemical openers.The Sensorless Pore Module of Voltage-gated K+ Channel Family 7 Embodies the Target Site for the Anticonvulsant Retigabine.Target-specific PIP(2) signalling: how might it work?N-ethylmaleimide activates a Cl(-)-independent component of K(+) flux in mouse erythrocytesGating consequences of charge neutralization of arginine residues in the S4 segment of K(v)7.2, an epilepsy-linked K+ channel subunitA carboxy-terminal inter-helix linker as the site of phosphatidylinositol 4,5-bisphosphate action on Kv7 (M-type) K+ channels.Regulation of neural KCNQ channels: signalling pathways, structural motifs and functional implications.Potassium channels in peripheral pain pathways: expression, function and therapeutic potential.Affinity for phosphatidylinositol 4,5-bisphosphate determines muscarinic agonist sensitivity of Kv7 K+ channels.Mg²⁺ modulation of the single-channel properties of KCa3.1 in human erythroleukemia cells.Voltage dependence of the Ca(2+)-activated K(+) channel K(Ca)3.1 in human erythroleukemia cells.Zinc pyrithione-mediated activation of voltage-gated KCNQ potassium channels rescues epileptogenic mutants.The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants.Direct modulation of TRPM4 and TRPM3 channels by the phospholipase C inhibitor U73122.Regions of KCNQ K(+) channels controlling functional expression
P2860
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P2860
Single-channel analysis of KCNQ K+ channels reveals the mechanism of augmentation by a cysteine-modifying reagent.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh
2004年學術文章
@zh-hant
name
Single-channel analysis of KCN ...... a cysteine-modifying reagent.
@en
Single-channel analysis of KCN ...... a cysteine-modifying reagent.
@en-gb
Single-channel analysis of KCN ...... a cysteine-modifying reagent.
@nl
type
label
Single-channel analysis of KCN ...... a cysteine-modifying reagent.
@en
Single-channel analysis of KCN ...... a cysteine-modifying reagent.
@en-gb
Single-channel analysis of KCN ...... a cysteine-modifying reagent.
@nl
prefLabel
Single-channel analysis of KCN ...... a cysteine-modifying reagent.
@en
Single-channel analysis of KCN ...... a cysteine-modifying reagent.
@en-gb
Single-channel analysis of KCN ...... a cysteine-modifying reagent.
@nl
P1476
Single-channel analysis of KCN ...... y a cysteine-modifying reagent
@en
P2093
Mark S Shapiro
P304
P356
10.1523/JNEUROSCI.0882-04.2004
P407
P577
2004-06-01T00:00:00Z