Leaky sodium channels from voltage sensor mutations in periodic paralysis, but not paramyotonia
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Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 ComparisonChannelopathies of skeletal muscle excitabilityThe divergence, actions, roles, and relatives of sodium-coupled bicarbonate transportersDisrupted coupling of gating charge displacement to Na+ current activation for DIIS4 mutations in hypokalemic periodic paralysisA sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis.Pathophysiological role of omega pore current in channelopathiesGating pore currents and the resting state of Nav1.4 voltage sensor domainsA calcium channel mutant mouse model of hypokalemic periodic paralysisA recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis.Mice with an NaV1.4 sodium channel null allele have latent myasthenia, without susceptibility to periodic paralysis.Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca(v)1.1 mutation.NaV1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recovery.Novel insights into the pathomechanisms of skeletal muscle channelopathies.Pathophysiologic and anesthetic considerations for patients with myotonia congenita or periodic paralyses.Biophysics, pathophysiology, and pharmacology of ion channel gating pores.Cardiac arrhythmias in hypokalemic periodic paralysis: Hypokalemia as only cause?Molecular biology and biophysical properties of ion channel gating pores.HCO(3)(-)-independent conductance with a mutant Na(+)/HCO(3)(-) cotransporter (SLC4A4) in a case of proximal renal tubular acidosis with hypokalaemic paralysis.Domain III S4 in closed-state fast inactivation: insights from a periodic paralysis mutationGender differences in penetrance and phenotype in hypokalemic periodic paralysis.Stac3 enhances expression of human CaV1.1 in Xenopus oocytes and reveals gating pore currents in HypoPP mutant channels.Sodium Channelopathies of Skeletal Muscle.Spider toxin inhibits gating pore currents underlying periodic paralysis.Hypokalaemic periodic paralysis and myotonia in a patient with homozygous mutation p.R1451L in NaV1.4.A New Cardiac Channelopathy: From Clinical Phenotypes to Molecular Mechanisms Associated With Na1.5 Gating PoresGating Pore Currents in Sodium ChannelsA leaky voltage sensor domain of cardiac sodium channels causes arrhythmias associated with dilated cardiomyopathy
P2860
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P2860
Leaky sodium channels from voltage sensor mutations in periodic paralysis, but not paramyotonia
description
2011 nî lūn-bûn
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2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
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2011 թվականի ապրիլին հրատարակված գիտական հոդված
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2011年の論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年论文
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Leaky sodium channels from vol ...... aralysis, but not paramyotonia
@ast
Leaky sodium channels from vol ...... aralysis, but not paramyotonia
@en
Leaky sodium channels from vol ...... aralysis, but not paramyotonia
@nl
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label
Leaky sodium channels from vol ...... aralysis, but not paramyotonia
@ast
Leaky sodium channels from vol ...... aralysis, but not paramyotonia
@en
Leaky sodium channels from vol ...... aralysis, but not paramyotonia
@nl
prefLabel
Leaky sodium channels from vol ...... aralysis, but not paramyotonia
@ast
Leaky sodium channels from vol ...... aralysis, but not paramyotonia
@en
Leaky sodium channels from vol ...... aralysis, but not paramyotonia
@nl
P2093
P2860
P1433
P1476
Leaky sodium channels from vol ...... aralysis, but not paramyotonia
@en
P2093
Arie Struyk
David G Francis
Volodymyr Rybalchenko
P2860
P304
P356
10.1212/WNL.0B013E318219FB57
P407
P50
P577
2011-04-13T00:00:00Z