Inherited sodium channelopathies: a continuum of channel dysfunction
about
Role of Ca2+/calmodulin-dependent protein kinase (CaMK) in excitation-contraction coupling in the heartRole of sodium and calcium dysregulation in tachyarrhythmias in sudden cardiac death.Sodium channel mutations and susceptibility to heart failure and atrial fibrillationPathways affected by asbestos exposure in normal and tumour tissue of lung cancer patientsThe neonatal splice variant of Nav1.5 potentiates in vitro invasive behaviour of MDA-MB-231 human breast cancer cells.Relating form and function of EF-hand calcium binding proteins.Kinetic model of Nav1.5 channel provides a subtle insight into slow inactivation associated excitability in cardiac cells.Activation of protein kinase C alters the intracellular distribution and mobility of cardiac Na+ channels.Pharmacogenetics and anti-arrhythmic drug therapy: a theoretical investigation.Sudden cardiac death and inherited arrhythmia syndromes.Modulation of cardiac Na(+) and Ca(2+) currents by CaM and CaMKII.Psychosis genetics: modeling the relationship between schizophrenia, bipolar disorder, and mixed (or "schizoaffective") psychosesCardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects.Sodium channel haploinsufficiency and structural change in ventricular arrhythmogenesis.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.Multiple targets for flecainide action: implications for cardiac arrhythmogenesis.Diversity in cardiac sodium channel disease phenotype in transgenic mice carrying a single SCN5A mutation.A double tyrosine motif in the cardiac sodium channel domain III-IV linker couples calcium-dependent calmodulin binding to inactivation gatingFunctional Interactions between Distinct Sodium Channel Cytoplasmic Domains through the Action of Calmodulin.Relative resistance to slow inactivation of human cardiac Na+ channel hNav1.5 is reversed by lysine or glutamine substitution at V930 in D2-S6.SCN5A-linked disease syndromes: complex monogenic disorders of cardiac rhythm.The beat goes on--driven by a cardiac calcium clock?Molecular basis for class Ib anti-arrhythmic inhibition of cardiac sodium channels.Effects of external stimuli on the pacemaker function of the sinoatrial node in sodium channel gene mutations models.Inhibitory effects of hesperetin on Nav1.5 channels stably expressed in HEK 293 cells and on the voltage-gated cardiac sodium current in human atrial myocytes.Molecular determinants of prokaryotic voltage-gated sodium channels for recognition of local anesthetics.
P2860
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P2860
Inherited sodium channelopathies: a continuum of channel dysfunction
description
2004 nî lūn-bûn
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2004 թուականի Յունուարին հրատարակուած գիտական յօդուած
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2004 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2004年の論文
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2004年論文
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2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
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2004年论文
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name
Inherited sodium channelopathies: a continuum of channel dysfunction
@ast
Inherited sodium channelopathies: a continuum of channel dysfunction
@en
Inherited sodium channelopathies: a continuum of channel dysfunction
@nl
type
label
Inherited sodium channelopathies: a continuum of channel dysfunction
@ast
Inherited sodium channelopathies: a continuum of channel dysfunction
@en
Inherited sodium channelopathies: a continuum of channel dysfunction
@nl
prefLabel
Inherited sodium channelopathies: a continuum of channel dysfunction
@ast
Inherited sodium channelopathies: a continuum of channel dysfunction
@en
Inherited sodium channelopathies: a continuum of channel dysfunction
@nl
P1476
Inherited sodium channelopathies: a continuum of channel dysfunction
@en
P2093
Jeffrey R Balser
Prakash C Viswanathan
P356
10.1016/J.TCM.2003.10.001
P407
P577
2004-01-01T00:00:00Z