(Q39287807)

10 September 2017

title

A new Nav1.7 sodium channel mutation I234T in a child with severe pain (English)

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10 September 2017

8

C Geoffrey Woods

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10 September 2017

Hye-Sook Ahn

1

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10 September 2017

Sulayman D Dib-Hajj

2

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10 September 2017

James J Cox

3

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10 September 2017

Lynda Tyrrell

4

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10 September 2017

Frances V Elmslie

5

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10 September 2017

Antonia A Clarke

6

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10 September 2017

Joost P H Drenth

7

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10 September 2017

Stephen G Waxman

9

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10 September 2017

publication date

10 April 2010

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10 September 2017

published in

European Journal of Pain

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10 September 2017

volume

14

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10 September 2017

issue

9

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10 September 2017

page(s)

944-950

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The voltage-sensor structure in a voltage-gated channel

10 September 2017

cites work

1 reference

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Spinal sensory neurons express multiple sodium channel alpha-subunit mRNAs.

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Biophysical properties of human Na v1.7 splice variants and their regulation by protein kinase A.

21 January 2018

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Mutation I136V alters electrophysiological properties of the Na(v)1.7 channel in a family with onset of erythromelalgia in the second decade

21 January 2018

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Inherited erythermalgia: limb pain from an S4 charge-neutral Na channelopathy

21 January 2018

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Mexiletine-responsive erythromelalgia due to a new Na(v)1.7 mutation showing use-dependent current fall-off.

21 January 2018

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An SCN9A channelopathy causes congenital inability to experience pain

21 January 2018

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

21 January 2018

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From genes to pain: Na v 1.7 and human pain disorders

21 January 2018

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

21 January 2018

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Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders

21 January 2018

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NaV1.7 gain-of-function mutations as a continuum: A1632E displays physiological changes associated with erythromelalgia and paroxysmal extreme pain disorder mutations and produces symptoms of both disorders.

21 January 2018

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SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes

21 January 2018

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Paroxysmal extreme pain disorder (previously familial rectal pain syndrome)

21 January 2018

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A novel Nav1.7 mutation producing carbamazepine-responsive erythromelalgia

21 January 2018

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Early- and late-onset inherited erythromelalgia: genotype-phenotype correlation

21 January 2018

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

21 January 2018

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Na(V)1.7 mutant A863P in erythromelalgia: effects of altered activation and steady-state inactivation on excitability of nociceptive dorsal root ganglion neurons.

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Structural biology. Voltage sensor meets lipid membrane

21 January 2018

1 reference

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

21 January 2018

1 reference

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Multiple sodium channels and their roles in electrogenesis within dorsal root ganglion neurons

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJPAIN.2010.03.007

A Nav1.7 channel mutation associated with hereditary erythromelalgia contributes to neuronal hyperexcitability and displays reduced lidocaine sensitivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJPAIN.2010.03.007

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJPAIN.2010.03.007

Modulation of Nav1.7 and Nav1.8 peripheral nerve sodium channels by protein kinase A and protein kinase C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJPAIN.2010.03.007

Neurobiology: a channel sets the gain on pain

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJPAIN.2010.03.007

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/10.1016%2FJ.EJPAIN.2010.03.007

10.1016/J.EJPAIN.2010.03.007

21 January 2018

Identifiers

DOI

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release_ttjv7pv3lfhvhkreuxothh5qum

10 September 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/ttjv7pv3lfhvhkreuxothh5qum

mapped directly with Wikidata item

24 November 2022

based on heuristic

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