Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis.
about
A1152D mutation of the Na+ channel causes paramyotonia congenita and emphasizes the role of DIII/S4-S5 linker in fast inactivationCharacterization of a new sodium channel mutation at arginine 1448 associated with moderate Paramyotonia congenita in humansFunctional characterization and cold sensitivity of T1313A, a new mutation of the skeletal muscle sodium channel causing paramyotonia congenita in humansChannelopathies of skeletal muscle excitabilityFamilial hemiplegic migraine mutations change alpha1A Ca2+ channel kineticsNav 1.4 slow-inactivation: is it a player in the warm-up phenomenon of myotonic disorders?Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysisResidue-specific effects on slow inactivation at V787 in D2-S6 of Na(v)1.4 sodium channels.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(+) channelClass A calcium channel variants in pancreatic islets and their role in insulin secretionTargeted mutation of mouse skeletal muscle sodium channel produces myotonia and potassium-sensitive weakness.Sodium channel biophysics, late sodium current and genetic arrhythmic syndromesCold-induced defects of sodium channel gating in atypical periodic paralysis plus myotonia.Slow inactivation in human cardiac sodium channelsEnhanced slow inactivation by V445M: a sodium channel mutation associated with myotoniaStructural determinants of slow inactivation in human cardiac and skeletal muscle sodium channels.A point mutation in domain 4-segment 6 of the skeletal muscle sodium channel produces an atypical inactivation state.Rapid and slow voltage-dependent conformational changes in segment IVS6 of voltage-gated Na(+) channelsTryptophan substitution of a putative D4S6 gating hinge alters slow inactivation in cardiac sodium channels.Structure and function of voltage-gated sodium channels.Molecular basis of differential sensitivity of insect sodium channels to DCJW, a bioactive metabolite of the oxadiazine insecticide indoxacarb.Genetic disorders of neuromuscular ion channels.A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation.A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis.Slow inactivation does not affect movement of the fast inactivation gate in voltage-gated Na+ channels.Sodium channel inactivation: molecular determinants and modulation.Effect of alkali metal cations on slow inactivation of cardiac Na+ channels.A structural rearrangement in the sodium channel pore linked to slow inactivation and use dependence.Role of domain 4 in sodium channel slow inactivationMolecular motions of the outer ring of charge of the sodium channel: do they couple to slow inactivation?Proton sensors in the pore domain of the cardiac voltage-gated sodium channel.Voltage-sensor movements describe slow inactivation of voltage-gated sodium channels I: wild-type skeletal muscle Na(V)1.4.Voltage-sensor movements describe slow inactivation of voltage-gated sodium channels II: a periodic paralysis mutation in Na(V)1.4 (L689I)Skeletal muscle na channel disorders.Slow recovery from inactivation regulates the availability of voltage-dependent Na(+) channels in hippocampal granule cells, hilar neurons and basket cells.Cold-induced disruption of Na+ channel slow inactivation underlies paralysis in highly thermosensitive paramyotonia.Theoretical investigation of the neuronal Na+ channel SCN1A: abnormal gating and epilepsy.T-type Ca2+ channels encode prior neuronal activity as modulated recovery rates.Fiber type conversion alters inactivation of voltage-dependent sodium currents in murine C2C12 skeletal muscle cells.
P2860
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P2860
Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis.
description
1997 nî lūn-bûn
@nan
1997 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի մարտին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Slow inactivation differs amon ...... otonia and periodic paralysis.
@ast
Slow inactivation differs amon ...... otonia and periodic paralysis.
@en
type
label
Slow inactivation differs amon ...... otonia and periodic paralysis.
@ast
Slow inactivation differs amon ...... otonia and periodic paralysis.
@en
prefLabel
Slow inactivation differs amon ...... otonia and periodic paralysis.
@ast
Slow inactivation differs amon ...... otonia and periodic paralysis.
@en
P2093
P2860
P1433
P1476
Slow inactivation differs amon ...... otonia and periodic paralysis.
@en
P2093
L J Hayward
S C Cannon
P2860
P304
P356
10.1016/S0006-3495(97)78768-X
P407
P577
1997-03-01T00:00:00Z