(Q40114322)

17 September 2017

title

A stop codon mutation in SCN9A causes lack of pain sensation (English)

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17 September 2017

16

Guy A Rouleau

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Dennis Hellgren

4

object named as

Dennis Hellgren

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17 September 2017

Sultan Ahmad

1

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17 September 2017

Leif Dahllund

2

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17 September 2017

Anders B Eriksson

3

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17 September 2017

Urban Karlsson

5

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17 September 2017

Per-Eric Lund

6

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17 September 2017

Inge A Meijer

7

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17 September 2017

Luc Meury

8

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17 September 2017

Tracy Mills

9

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17 September 2017

Adrian Moody

10

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17 September 2017

Anne Morinville

11

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17 September 2017

John Morten

12

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17 September 2017

Dajan O'donnell

13

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17 September 2017

Carina Raynoschek

14

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17 September 2017

Hugh Salter

15

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17 September 2017

Johannes J Krupp

17

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17 September 2017

publication date

27 June 2007

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17 September 2017

published in

Human Molecular Genetics

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17 September 2017

volume

16

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17 September 2017

issue

17

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17 September 2017

page(s)

2114-2121

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Involvement of Na+ channels in pain pathways

17 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

The tetrodotoxin-resistant sodium channel SNS has a specialized function in pain pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

Nociceptor-specific gene deletion reveals a major role for Nav1.7 (PN1) in acute and inflammatory pain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

An SCN9A channelopathy causes congenital inability to experience pain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

Heterologous expression and functional analysis of rat Nav1.8 (SNS) voltage-gated sodium channels in the dorsal root ganglion neuroblastoma cell line ND7-23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

Inherited disorders of voltage-gated sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

Molecular genetics of infantile nervous system channelopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

A sodium channel pore mutation causing Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

Congenital insensitivity to pain: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

'Touchdown' PCR to circumvent spurious priming during gene amplification

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

Restricted distribution of galanin receptor 3 (GalR3) mRNA in the adult rat central nervous system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM160

21 January 2018

Identifiers

DOI

10.1093/HMG/DDM160

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17 September 2017

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