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FROM BINDING-STUDIES TO THE MOLECULAR-BIOLOGY OF GABA RECEPTORS
被引:20
|
作者
:
KNAPP, RJ
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ARIZONA, COLL MED, DEPT PHARMACOL, TUCSON, AZ 85724 USA
KNAPP, RJ
MALATYNSKA, E
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ARIZONA, COLL MED, DEPT PHARMACOL, TUCSON, AZ 85724 USA
MALATYNSKA, E
YAMAMURA, HI
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ARIZONA, COLL MED, DEPT PHARMACOL, TUCSON, AZ 85724 USA
YAMAMURA, HI
机构
:
[1]
UNIV ARIZONA, COLL MED, DEPT PHARMACOL, TUCSON, AZ 85724 USA
[2]
OHIO STATE UNIV, DEPT PSYCHIAT, PSYCHOPHARMACOL PROGRAM, COLUMBUS, OH 43210 USA
来源
:
NEUROCHEMICAL RESEARCH
|
1990年
/ 15卷
/ 02期
关键词
:
D O I
:
10.1007/BF00972199
中图分类号
:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号
:
071010 ;
081704 ;
摘要
:
The GABAA-complex remains enigmatic despite the substantial amount of information that has been gathered. The work of Barnard's group on the structure of the complex and the relationship of the recognition sites for GABA and benzodiazepines to its protein subunits has raised as many questions as have been answered. The existence of multiple forms of the α subunit and the ability of various combinations of the subunits to mediate GABA-gated choloride conductance suggest that there may be many forms of the GABAA-complex. Thus, the identification of previously unsuspected drug interactions, and evidence for the existence of additional endogenous ligands beside GABA (e.g. benzodiazepine-binding inhibitor (68) and certain steroids (69), all suggest that the characterization of the GABAA-complex has only begun. © 1990 Plenum Publishing Corporation.
引用
收藏
页码:105 / 112
页数:8
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