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RECORD NUMBER: 43 OF 51

OLS Field Name OLS Field Data
Main Title The GABA Receptors [electronic resource] /
Type EBOOK
Author Enna, S. J.
Other Authors
Author Title of a Work
Möhler, Hanns.
Publisher Humana Press,
Year Published 2007
Call Number RC321-580
ISBN 9781597454650
Subjects Medicine. ; Neurosciences. ; Toxicology. ; Psychiatry. ; Cytology.
Internet Access
Description Access URL
http://dx.doi.org/10.1007/978-1-59745-465-0
Edition Third Edition.
Collation X, 325 p. online resource.
Notes
Due to license restrictions, this resource is available to EPA employees and authorized contractors only
Contents Notes
The GABA Receptors -- Functional Relevance of GABAA-Receptor Subtypes -- Trafficking of Postsynaptic GABAA Receptors by Receptor-Associated Proteins -- Subunit Composition and Structure of GABAA-Receptor Subtypes -- Differential Activation of GABAA-Receptor Subtypes -- GABAA-Receptor Mutations Associated With Idiopathic Generalized Epilepsies and Febrile Seizures -- Abuse and Dependence Liability of GABAA-Receptor Modulators -- Mechanisms of GABAA and GABAB Receptor Gene Regulation and Cell Surface Expression -- Chemistry of GABAB Modulators -- The Unusual Functioning of the GABAB-Receptor Heterodimer -- Characteristics of GABAB Receptor Mutant Mice -- GABAB Receptor ad a Potential Therapeutic Target. This volume is the third edition of a monograph series that was first published in 1983. The demand for this work is a testament to the impact of studies on -aminobutyric acid (GABA) receptors on the basic understanding of synaptic transmission and on defining the clinical importance of the neurotransmitter system. Chronicled in The GABA Receptors, Third Edition, are the advances made in understanding the molecular and pharmacological properties of GABA A and GABA receptors since the topic was last reviewed in 1996. Particular B emphasis is placed on describing the assembly, structure, and function of GABA B sites, the first heterodimeric G protein-coupled receptors identified in vivo. In addition, there are reports dealing with the subunit composition, trafficking, and pharmacological selectivity of GABA receptors. Aside from providing A insights into the fundamental properties of ligand-gated ion channels and second messenger systems, the findings detailed in this work point the way for developing novel therapeutics capable of more selectively manipulating these transmitter sites.