A pharmacological characterization of GABA, THIP and DS2 at binary α4β3 and β3δ receptors: GABA activates β3δ receptors via the β3(+)δ(−) interface-Reference-Cited by-同舟云学术

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A pharmacological characterization of GABA, THIP and DS2 at binary α4β3 and β3δ receptors: GABA activates β3δ receptors via the β3(+)δ(−) interface

Published:2016-08 Issue: Volume:1644 Page:222-230
ISSN:0006-8993
Container-title:Brain Research
language:en
Short-container-title:Brain Research

Author:

Lee H.J.,Absalom N.L.,Hanrahan J.R.,van Nieuwenhuijzen P.,Ahring P.K.,Chebib M.

Funder

University of Sydney

Australian Postgraduate Award Scheme

National Health and Medical Research Council of Australia

Imk Almene Fond

Publisher

Elsevier BV

Subject

Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience

Reference38 articles.

1. GABAA receptor needs two homologous domains of the beta -subunit for activation by GABA but not by pentobarbital;Amin;Nature,1993

2. Structure of alpha6beta3delta GABAA receptors and their lack of ethanol sensitivity;Baur;J. Neurochem.,2009

3. Extrasynaptic GABAA receptors: form, pharmacology, and function;Belelli;J. Neurosci.,2009

4. Mapping the agonist binding site of the GABAA receptor: evidence for a beta-strand;Boileau;J. Neurosci.,1999

5. Extrasynaptic GABAA receptors: their function in the CNS and implications for disease;Brickley;Neuron,2012

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