Residue-specific effects on slow inactivation at V787 in D2-S6 of Na(v)1.4 sodium channels.
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A molecular switch between the outer and the inner vestibules of the voltage-gated Na+ channelA pharmacophore derived phenytoin analogue with increased affinity for slow inactivated sodium channels exhibits a desired anticonvulsant profileVoltage-gated Na+ channels in neuropathic pain.Tryptophan substitution of a putative D4S6 gating hinge alters slow inactivation in cardiac sodium channels.Molecular basis of differential sensitivity of insect sodium channels to DCJW, a bioactive metabolite of the oxadiazine insecticide indoxacarb.Clinical utility of eslicarbazepine: current evidence.Role of the local anesthetic receptor in the state-dependent inhibition of voltage-gated sodium channels by the insecticide metaflumizoneSodium channel inactivation: molecular determinants and modulation.Compound-specific effects of mutations at Val787 in DII-S6 of Nav 1.4 sodium channels on the action of sodium channel inhibitor insecticides.Slow inactivation does not block the aqueous accessibility to the outer pore of voltage-gated Na channels.Indoxacarb, Metaflumizone, and Other Sodium Channel Inhibitor Insecticides: Mechanism and Site of Action on Mammalian Voltage-Gated Sodium Channels.Comparative effects of halogenated inhaled anesthetics on voltage-gated Na+ channel functionThe outer vestibule of the Na+ channel-toxin receptor and modulator of permeation as well as gating.Molecular Mechanism of Action and Selectivity of Sodium Channel Blocker Insecticides.Cold-induced disruption of Na+ channel slow inactivation underlies paralysis in highly thermosensitive paramyotonia.Relative resistance to slow inactivation of human cardiac Na+ channel hNav1.5 is reversed by lysine or glutamine substitution at V930 in D2-S6.A quantitative and comparative study of the effects of a synthetic ciguatoxin CTX3C on the kinetic properties of voltage-dependent sodium channels.Sodium channel slow inactivation interferes with open channel block.Sodium channels: ionic model of slow inactivation and state-dependent drug binding.Mechanisms of Drug Binding to Voltage-Gated Sodium Channels.A conserved ring of charge in mammalian Na+ channels: a molecular regulator of the outer pore conformation during slow inactivation.Voltage-Gated Sodium Channels as Insecticide Targets.
P2860
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P2860
Residue-specific effects on slow inactivation at V787 in D2-S6 of Na(v)1.4 sodium channels.
description
2001 nî lūn-bûn
@nan
2001 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
name
Residue-specific effects on sl ...... S6 of Na(v)1.4 sodium channels
@nl
Residue-specific effects on sl ...... 6 of Na(v)1.4 sodium channels.
@ast
Residue-specific effects on sl ...... 6 of Na(v)1.4 sodium channels.
@en
type
label
Residue-specific effects on sl ...... S6 of Na(v)1.4 sodium channels
@nl
Residue-specific effects on sl ...... 6 of Na(v)1.4 sodium channels.
@ast
Residue-specific effects on sl ...... 6 of Na(v)1.4 sodium channels.
@en
prefLabel
Residue-specific effects on sl ...... S6 of Na(v)1.4 sodium channels
@nl
Residue-specific effects on sl ...... 6 of Na(v)1.4 sodium channels.
@ast
Residue-specific effects on sl ...... 6 of Na(v)1.4 sodium channels.
@en
P2093
P2860
P3181
P1433
P1476
Residue-specific effects on sl ...... 6 of Na(v)1.4 sodium channels.
@en
P2093
P2860
P304
P3181
P356
10.1016/S0006-3495(01)75858-4
P407
P577
2001-10-01T00:00:00Z