(Q48971130)

17 February 2018

title

The equine periodic paralysis Na+ channel mutation alters molecular transitions between the open and inactivated states. (English)

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17 February 2018

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Hanna WJ

1

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17 February 2018

Tsushima RG

2

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17 February 2018

Sah R

3

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17 February 2018

McCutcheon LJ

4

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17 February 2018

Marban E

5

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17 February 2018

Backx PH

6

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17 February 2018

language of work or name

English

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publication date

1 December 1996

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17 February 2018

published in

Journal of Physiology

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17 February 2018

volume

497 ( Pt 2)

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17 February 2018

page(s)

349-364

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17 February 2018

Restoration of inactivation in mutants of Shaker potassium channels by a peptide derived from ShB.

cites work

1 reference

12 December 2020

Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

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12 December 2020

Potassium channel inactivation peptide blocks cyclic nucleotide-gated channels by binding to the conserved pore domain.

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12 December 2020

Stochastic behavior of a many-channel membrane system

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12 December 2020

Structural parts involved in activation and inactivation of the sodium channel

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12 December 2020

Monte-Carlo-simulations of voltage fluctuations in biological membranes in the case of small numbers of transport units

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12 December 2020

Primary structure and functional expression of a mammalian skeletal muscle sodium channel

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12 December 2020

The skeletal muscle sodium and chloride channel diseases

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12 December 2020

Different effects on gating of three myotonia-causing mutations in the inactivation gate of the human muscle sodium channel

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12 December 2020

A mutation in segment IVS6 disrupts fast inactivation of sodium channels

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12 December 2020

Sodium channel inactivation from resting states in guinea-pig ventricular myocytes

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12 December 2020

K(+)-aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation

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12 December 2020

Modulation of brain Na+ channels by a G-protein-coupled pathway

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12 December 2020

Temperature-sensitive mutations in the III–IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita

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12 December 2020

Episodic muscle tremors in a quarter horse: resemblance to hyperkalemic periodic paralysis.

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12 December 2020

Destruction of sodium conductance inactivation in squid axons perfused with pronase

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12 December 2020

Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

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12 December 2020

Effect of N-bromoacetamide on single sodium channel currents in excised membrane patches

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12 December 2020

Rapid and efficient site-specific mutagenesis without phenotypic selection

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12 December 2020

Sodium channel mutations in paramyotonia congenita exhibit similar biophysical phenotypes in vitro

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12 December 2020

A peptide segment critical for sodium channel inactivation functions as an inactivation gate in a potassium channel

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12 December 2020

Ion-channel defects and aberrant excitability in myotonia and periodic paralysis

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12 December 2020

DNA sequencing with chain-terminating inhibitors

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12 December 2020

Functional messenger RNAs are produced by SP6in vitrotranscription of cloned cDNAs

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12 December 2020

Molecular model of the action potential sodium channel

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12 December 2020

Altered ionic permeability in skeletal muscle from horses with hyperkalemic periodic paralysis.

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12 December 2020

Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding

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12 December 2020

Molecular localization of an ion-binding site within the pore of mammalian sodium channels

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12 December 2020

A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation

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12 December 2020

Primary structure and functional expression of the beta 1 subunit of the rat brain sodium channel

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12 December 2020

Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker

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12 December 2020

Primary structure of Electrophorus electricus sodium channel deduced from cDNA sequence

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12 December 2020

A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation

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12 December 2020

Functional expression of sodium channel mutations identified in families with periodic paralysis

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12 December 2020

Functional consequences of a Na+ channel mutation causing hyperkalemic periodic paralysis

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12 December 2020

Identification of an intracellular peptide segment involved in sodium channel inactivation

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12 December 2020

Multiple gating modes and the effect of modulating factors on the μI sodium channel

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12 December 2020

Sodium channel inactivation is impaired in equine hyperkalemic periodic paralysis

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12 December 2020

Voltage-Dependent Gating of Ionic Channels

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12 December 2020

Modification of the Na+ current conducted by the rat skeletal muscle alpha subunit by coexpression with a human brain beta subunit

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12 December 2020

Voltage-dependent regulation of modal gating in the rat SkM1 sodium channel expressed in Xenopus oocytes

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12 December 2020

Na+ channels must deactivate to recover from inactivation

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12 December 2020

10.1113/JPHYSIOL.1996.SP021773

Identifiers

DOI

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17 February 2018

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17 February 2018