A SCN10A SNP biases human pain sensitivity. - Wikidata - wikimedia - TriplyDB

A SCN10A SNP biases human pain sensitivity.

A SCN10A SNP biases human pain sensitivity.

http://www.wikidata.org/entity/Q37232148

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SCN11A variants may influence postoperative pain sensitivity after gynecological surgery in Chinese Han female patients.Sodium channels in pain disorders: pathophysiology and prospects for treatment.[EXPRESS] A variant in the SCN10A enhancer may affect human mechanical pain sensitivity.

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A SCN10A SNP biases human pain sensitivity.

http://www.wikidata.org/entity/Q37232148

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 02 September 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

A SCN10A SNP biases human pain sensitivity.

@en

A SCN10A SNP biases human pain sensitivity.

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label

A SCN10A SNP biases human pain sensitivity.

@en

A SCN10A SNP biases human pain sensitivity.

@nl

prefLabel

A SCN10A SNP biases human pain sensitivity.

@en

A SCN10A SNP biases human pain sensitivity.

@nl

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A SCN10A SNP biases human pain sensitivity.

@en

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Chongyang Han

http://www.w3.org/2001/XMLSchema#string

Guangyou Duan

http://www.w3.org/2001/XMLSchema#string

Lawrence Macala

http://www.w3.org/2001/XMLSchema#string

Li Zhang

http://www.w3.org/2001/XMLSchema#string

Mi Zhang

http://www.w3.org/2001/XMLSchema#string

Ningbo Li

http://www.w3.org/2001/XMLSchema#string

Palak Shah

http://www.w3.org/2001/XMLSchema#string

Penghao Huang

http://www.w3.org/2001/XMLSchema#string

Qingli Wang

http://www.w3.org/2001/XMLSchema#string

Shanna Guo

http://www.w3.org/2001/XMLSchema#string

P2860

Genetic variation in SCN10A influences cardiac conduction

Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science

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

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

A tetrodotoxin-resistant voltage-gated sodium channel expressed by sensory neurons

Replicating genotype-phenotype associations

Gain of function NaV1.7 mutations in idiopathic small fiber neuropathy

Genome-wide association studies of the PR interval in African Americans

A gain-of-function voltage-gated sodium channel 1.8 mutation drives intense hyperexcitability of A- and C-fiber neurons.

Pain perception is altered by a nucleotide polymorphism in SCN9A

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scholarly article

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10.1177/1744806916666083

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