Functional modulation of the human voltage-gated sodium channel NaV1.8 by auxiliary β subunits-Reference-Cited by-同舟云学术

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Functional modulation of the human voltage-gated sodium channel NaV1.8 by auxiliary β subunits

Published:2020-12-29 Issue:1 Volume:15 Page:79-93
ISSN:1933-6950
Container-title:Channels
language:en
Short-container-title:Channels

Author:

Nevin S. T.¹,Lawrence N.²^ORCID,Nicke A.¹²^ORCID,Lewis R. J.²^ORCID,Adams D. J.¹³^ORCID

Affiliation:

1. School of Biomedical Sciences and the Institute for Molecular Bioscience, The University of Queensland, Brisbane, Australia

2. Institute for Molecular Bioscience, The University of Queensland, Brisbane, Australia

3. Illawarra Health and Medical Research Institute (IHMRI), University of Wollongong, Wollongong, Australia

Funder

Australian Research Council

National Health and Medical Research Council

Publisher

Informa UK Limited

Subject

Biochemistry,Biophysics

Link

https://www.tandfonline.com/doi/pdf/10.1080/19336950.2020.1860399

Reference65 articles.

1. The saxitoxin receptor of the sodium channel from rat brain. Evidence for two nonidentical beta subunits.

2. The sodium channel from rat brain. Purification and subunit composition.

3. beta 3: An additional auxiliary subunit of the voltage-sensitive sodium channel that modulates channel gating with distinct kinetics

4. Sodium Channel β4, a New Disulfide-Linked Auxiliary Subunit with Similarity to β2

5. β3, a novel auxiliary subunit for the voltage-gated sodium channel, is expressed preferentially in sensory neurons and is upregulated in the chronic constriction injury model of neuropathic pain

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