(Q34569783)

3 August 2017

Size matters: Erythromelalgia mutation S241T in Nav1.7 alters channel gating (English)

1 reference

3 August 2017

Angelika Lampert

1

1 reference

3 August 2017

Sulayman D Dib-Hajj

series ordinal

2

1 reference

3 August 2017

Lynda Tyrrell

series ordinal

3

1 reference

3 August 2017

Stephen G Waxman

series ordinal

4

1 reference

3 August 2017

language of work or name

English

0 references

publication date

28 September 2006

1 reference

Journal of Biological Chemistry

3 August 2017

1 reference

3 August 2017

281

1 reference

3 August 2017

47

1 reference

3 August 2017

36029-36035

1 reference

Sodium channel mutations in epilepsy and other neurological disorders

3 August 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Epilepsy and sodium channel gene mutations: gain or loss of function?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Inherited disorders of voltage-gated sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

An expanding view for the molecular basis of familial periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Human skeletal muscle sodium channelopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Erythermalgia: molecular basis for an inherited pain syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Autosomal dominant erythermalgia associated with a novel mutation in the voltage-gated sodium channel alpha subunit Nav1.7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Sporadic onset of erythermalgia: a gain-of-function mutation in Nav1.7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Sodium channel alpha-subunit mRNAs I, II, III, NaG, Na6 and hNE (PN1): different expression patterns in developing rat nervous system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Identification of PN1, a predominant voltage-dependent sodium channel expressed principally in peripheral neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

A novel tetrodotoxin-sensitive, voltage-gated sodium channel expressed in rat and human dorsal root ganglia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Electrophysiological properties of mutant Nav1.7 sodium channels in a painful inherited neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

A single sodium channel mutation produces hyper- or hypoexcitability in different types of neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Distinct repriming and closed-state inactivation kinetics of Nav1.6 and Nav1.7 sodium channels in mouse spinal sensory neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Myasthenic syndrome caused by mutation of the SCN4A sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

A mutation that causes ataxia shifts the voltage-dependence of the Scn8a sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Cold induces shifts of voltage dependence in mutant SCN4A, causing hypokalemic periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Defective fast inactivation recovery and deactivation account for sodium channel myotonia in the I1160V mutant

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Effects of temperature and mexiletine on the F1473S Na+ channel mutation causing paramyotonia congenita

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Cooperative effect of S4-S5 loops in domains D3 and D4 on fast inactivation of the Na+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Interaction between the sodium channel inactivation linker and domain III S4-S5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Interactions between S4-S5 linker and S6 transmembrane domain modulate gating of HERG K+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

The S4-S5 linker couples voltage sensing and activation of pacemaker channels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Crystal structure of a mammalian voltage-dependent Shaker family K+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Voltage sensor of Kv1.2: structural basis of electromechanical coupling

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Electron microscopic analysis of KvAP voltage-dependent K+ channels in an open conformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

X-ray structure of a voltage-dependent K+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

The principle of gating charge movement in a voltage-dependent K+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Structural biology. Voltage sensor meets lipid membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Molecular architecture of the KvAP voltage-dependent K+ channel in a lipid bilayer

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

The voltage-sensor structure in a voltage-gated channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

The voltage-sensitive sodium channel is a bell-shaped molecule with several cavities

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

The S4-S5 linker directly couples voltage sensor movement to the activation gate in the human ether-a'-go-go-related gene (hERG) K+ channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Voltage sensor conformations in the open and closed states in ROSETTA structural models of K(+) channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Modelling insecticide-binding sites in the voltage-gated sodium channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Role of an S4-S5 linker in sodium channel inactivation probed by mutagenesis and a peptide blocker

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Role in fast inactivation of the IV/S4-S5 loop of the human muscle Na+ channel probed by cysteine mutagenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Inactivation and secondary structure in the D4/S4-5 region of the SkM1 sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

A critical role for the S4-S5 intracellular loop in domain IV of the sodium channel alpha-subunit in fast inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

A1152D mutation of the Na+ channel causes paramyotonia congenita and emphasizes the role of DIII/S4-S5 linker in fast inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

Regulation of muscle sodium channel transcripts during development and in response to denervation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M607637200

21 January 2018

Identifiers

DOI

10.1074/JBC.M607637200

1 reference

3 August 2017

1 reference