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A single residue differentiates between human cardiac and skeletal muscle Na+ channel slow inactivationMexiletine block of disease-associated mutations in S6 segments of the human skeletal muscle Na(+) channelRapid protein kinase C-dependent reduction of rat skeletal muscle voltage-gated sodium channels by ciliary neurotrophic factorStructural determinants of slow inactivation in human cardiac and skeletal muscle sodium channels.Effects of channel cytoplasmic regions on the activation mechanisms of cardiac versus skeletal muscle Na(+) channelsIsoform-specific lidocaine block of sodium channels explained by differences in gatingTryptophan substitution of a putative D4S6 gating hinge alters slow inactivation in cardiac sodium channels.A Literature Review of the Use of Sodium Bicarbonate for the Treatment of QRS Widening.Functional roles of cytoplasmic loops and pore lining transmembrane helices in the voltage-dependent inactivation of HVA calcium channels.Small molecule cardiogenol C upregulates cardiac markers and induces cardiac functional properties in lineage-committed progenitor cellsExtracellular proton modulation of the cardiac voltage-gated sodium channel, Nav1.5.Sodium channel inactivation: molecular determinants and modulation.Molecular motions of the outer ring of charge of the sodium channel: do they couple to slow inactivation?Post-partum variation in the expression of paternal care is unrelated to urinary steroid metabolites in marmoset fathersDIFFERENCES IN IONIC CURRENTS BETWEEN CANINE MYOCARDIAL AND PURKINJE CELLS.Persistent human cardiac Na+ currents in stably transfected mammalian cells: Robust expression and distinct open-channel selectivity among Class 1 antiarrhythmics.Block of human cardiac sodium channels by lacosamide: evidence for slow drug binding along the activation pathway.The outer vestibule of the Na+ channel-toxin receptor and modulator of permeation as well as gating.Differential thermosensitivity in mixed syndrome cardiac sodium channel mutants.Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel.Relative resistance to slow inactivation of human cardiac Na+ channel hNav1.5 is reversed by lysine or glutamine substitution at V930 in D2-S6.Flecainide sensitivity of a Na channel long QT mutation shows an open-channel blocking mechanism for use-dependent block.A quantitative and comparative study of the effects of a synthetic ciguatoxin CTX3C on the kinetic properties of voltage-dependent sodium channels.Lidocaine induces a slow inactivated state in rat skeletal muscle sodium channels.Comparison of slow inactivation in human heart and rat skeletal muscle Na+ channel chimaeras.Interaction of scorpion alpha-toxins with cardiac sodium channels: binding properties and enhancement of slow inactivation.Molecular determination of selectivity of the site 3 modulator (BmK I) to sodium channels in the CNS: a clue to the importance of Nav1.6 in BmK I-induced neuronal hyperexcitability.Nitric oxide blocks fast, slow, and persistent Na+ channels in C-type DRG neurons by S-nitrosylation.Patch-clamp analysis in canine cardiac Purkinje cells of a novel sodium component in the pacemaker range.Negatively charged residues adjacent to IFM motif in the DIII-DIV linker of hNa(V)1.4 differentially affect slow inactivation.The Structural Basis and Functional Consequences of Interactions Between Tetrodotoxin and Voltage-Gated Sodium Channels.Characterization of the slowly inactivating sodium current INa2 in canine cardiac single Purkinje cells.Mechanisms of Drug Binding to Voltage-Gated Sodium Channels.Mechanisms and models of cardiac sodium channel inactivation.Differential calcium sensitivity in NaV 1.5 mixed syndrome mutants.Interaction between fast and ultra-slow inactivation in the voltage-gated sodium channel. Does the inactivation gate stabilize the channel structure?A slowly inactivating sodium current (INa2) in the plateau range in canine cardiac Purkinje single cells.Hyperpolarized shifts in the voltage dependence of fast inactivation of Nav1.4 and Nav1.5 in a rat model of critical illness myopathy.A conserved ring of charge in mammalian Na+ channels: a molecular regulator of the outer pore conformation during slow inactivation.Lacosamide Inhibition of Nav1.7 Voltage-Gated Sodium Channels: Slow Binding to Fast-Inactivated States.
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Slow inactivation in human cardiac sodium channels
@ast
Slow inactivation in human cardiac sodium channels
@en
Slow inactivation in human cardiac sodium channels
@nl
type
label
Slow inactivation in human cardiac sodium channels
@ast
Slow inactivation in human cardiac sodium channels
@en
Slow inactivation in human cardiac sodium channels
@nl
prefLabel
Slow inactivation in human cardiac sodium channels
@ast
Slow inactivation in human cardiac sodium channels
@en
Slow inactivation in human cardiac sodium channels
@nl
P2093
P2860
P1433
P1476
Slow inactivation in human cardiac sodium channels
@en
P2093
D E Featherstone
H A Hartmann
J E Richmond
P2860
P304
P356
10.1016/S0006-3495(98)78001-4
P407
P577
1998-06-01T00:00:00Z