(Q48898598)

16 February 2018

title

Myopathic mutations affect differently the inactivation of the two gating modes of sodium channels. (English)

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16 February 2018

author name string

O Moran

series ordinal

1

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16 February 2018

M Nizzari

series ordinal

2

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16 February 2018

F Conti

series ordinal

3

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16 February 2018

publication date

1 December 1999

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16 February 2018

Journal of Bioenergetics and Biomembranes

published in

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16 February 2018

volume

31

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16 February 2018

issue

6

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16 February 2018

page(s)

591-608

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16 February 2018

https://scigraph.springernature.com/pub.10.1023/a:1005473129183

exact match

0 references

cites work

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

1 reference

12 December 2020

Na channel kinetics remain stable during perforated-patch recordings.

1 reference

12 December 2020

Fast and slow gating of sodium channels encoded by a single mRNA.

1 reference

12 December 2020

Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis

1 reference

12 December 2020

Subunit stoichiometry of a mammalian K+ channel determined by construction of multimeric cDNAs.

1 reference

12 December 2020

Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscle

1 reference

12 December 2020

Impaired slow inactivation in mutant sodium channels

1 reference

12 December 2020

Muscle sodium channel inactivation defect in paramyotonia congenita with the thr1313met mutation

1 reference

12 December 2020

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

1 reference

12 December 2020

A rat brain Na+ channel alpha subunit with novel gating properties

1 reference

12 December 2020

Molecular pathology of the skeletal muscle sodium channel

1 reference

12 December 2020

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

1 reference

12 December 2020

Sodium and calcium channels in bovine chromaffin cells

1 reference

12 December 2020

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

1 reference

12 December 2020

μl Na+ channels expressed transiently in human embryonic kidney cells: Biochemical and biophysical properties

1 reference

12 December 2020

Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

1 reference

12 December 2020

Phenotype variation and newcomers in ion channel disorders

1 reference

12 December 2020

Rapid and efficient site-specific mutagenesis without phenotypic selection

1 reference

12 December 2020

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

1 reference

12 December 2020

Modal behavior of the mu 1 Na+ channel and effects of coexpression of the beta 1-subunit

1 reference

12 December 2020

The adult rat brain beta 1 subunit modifies activation and inactivation gating of multiple sodium channel alpha subunits.

1 reference

12 December 2020

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

1 reference

12 December 2020

DNA sequencing with chain-terminating inhibitors

1 reference

12 December 2020

Sodium channel defects in myotonia and periodic paralysis

1 reference

12 December 2020

Altered gating and conductance of Na+ channels in hyperkalemic periodic paralysis.

1 reference

12 December 2020

Fast- and slow-gating modes of the sodium channel are altered by a paramyotonia congenita-linked mutation.

1 reference

12 December 2020

Human Na+ channel fast and slow inactivation in paramyotonia congenita mutants expressed in Xenopus laevis oocytes.

1 reference

12 December 2020

A defect in skeletal muscle sodium channel deactivation exacerbates hyperexcitability in human paramyotonia congenita

1 reference

12 December 2020

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

1 reference

12 December 2020

A quantitative description of membrane current and its application to conduction and excitation in nerve

1 reference

12 December 2020

Overexcited or inactive: ion channels in muscle disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Inactivation defects produced by a myopathic II-S6 mutation of the muscle sodium channel.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Paramyotonia congenita mutations reveal different roles for segments S3 and S4 of domain D4 in hSkM1 sodium channel gating

1 reference

12 December 2020

Molecular genetics of ion channel diseases

1 reference

12 December 2020

Human sodium channel gating defects caused by missense mutations in S6 segments associated with myotonia: S804F and V1293I.

1 reference

12 December 2020

Inactivation defects caused by myotonia-associated mutations in the sodium channel III-IV linker

1 reference

12 December 2020

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

1 reference

12 December 2020

Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels

1 reference

12 December 2020

A simple and efficient method for the oligonucleotide-directed mutagenesis using plasmid DNA template and phosphorothioate-modified nucleotide

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss of Na+ channel inactivation by anemone toxin (ATX II) mimics the myotonic state in hyperkalaemic periodic paralysis.

1 reference

12 December 2020

Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one family

1 reference

12 December 2020

Slow inactivation of the sodium conductance in squid giant axons. Pronase resistance

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1005473129183

1 reference

16 February 2018

Dimensions Publication ID

0 references

1 reference

16 February 2018