Isoform‐specific mechanisms of a3b4*‐nicotinic acetylcholine receptor modulation by the prototoxin lynx1-Reference-Cited by-同舟云学术

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Isoform‐specific mechanisms of a3b4*‐nicotinic acetylcholine receptor modulation by the prototoxin lynx1

Published:2017-01-18 Issue:4 Volume:31 Page:1398-1420
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

George Andrew A.¹,Bloy Abigail¹²,Miwa Julie M.³,Lindstrom Jon M.⁴,Lukas Ronald J.¹,Whiteaker Paul¹

Affiliation:

1. Division of Neurobiology, Barrow Neurological InstituteSt. Joseph's Hospital and Medical Center Phoenix Arizona USA

2. Leeds Institute of Cancer and PathologySt. James' University Hospital Leeds United Kingdom

3. Department of Biological SciencesLehigh University Bethlehem Pennsylvania USA

4. Department of NeuroscienceUniversity of Pennsylvania Medical School Philadelphia Pennsylvania USA

Funder

National Institutes of Health

National Institute on Drug Abuse

Barrow Neurological Foundation

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.201600733R

Reference96 articles.

1. Optimizing Cholinergic Tone Through Lynx Modulators of Nicotinic Receptors: Implications for Plasticity and Nicotine Addiction

2. lynx1, an Endogenous Toxin-like Modulator of Nicotinic Acetylcholine Receptors in the Mammalian CNS

3. Isolation and Characterization of a New Member of the HumanLy6Gene Family(LY6H)

4. Identification of lynx2, a novel member of the ly-6/neurotoxin superfamily, expressed in neuronal subpopulations during mouse development

5. Identification and characterization of human LYPD6, a new member of the Ly-6 superfamily

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