EXCITATORY AMINO-ACID RECEPTORS - NMDA MODULATORY SITES, KAINATE CLONED AND A NEW ROLE IN AIDS

被引：5

作者：

LEHMANN, J ^{[1
]}

RANDLE, JCR ^{[1
]}

REYNOLDS, IJ ^{[1
]}

机构：

[1] UNIV PITTSBURGH,DEPT PHARMACOL,PITTSBURGH,PA 15260

来源：

TRENDS IN PHARMACOLOGICAL SCIENCES | 1990年 / 11卷 / 01期

关键词：

D O I：

10.1016/0165-6147(90)90031-3

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

收藏

页码：1 / 3

页数：3

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FADDA, E
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[J]. NEUROPHARMACOLOGY, 1988, 27 (11) : 1183 - 1185
[2] MOLECULAR TARGET SIZE OF NMDA ANTAGONIST BINDING-SITES
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[3] GLYCINE POTENTIATES THE NMDA RESPONSE IN CULTURED MOUSE-BRAIN NEURONS
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ASCHER, P
[J]. NATURE, 1987, 325 (6104) : 529 - 531
[4] ANTAGONISM OF RESPONSES TO EXCITATORY AMINO-ACIDS ON RAT CORTICAL-NEURONS BY THE SPIDER TOXIN, ARGIOTOXIN-636
PRIESTLEY, T
WOODRUFF, GN
KEMP, JA
[J]. BRITISH JOURNAL OF PHARMACOLOGY, 1989, 97 (04) : 1315 - 1323
[5] COOPERATIVE MODULATION OF [H-3] MK-801 BINDING TO THE N-METHYL-D-ASPARTATE RECEPTOR-ION CHANNEL COMPLEX BY L-GLUTAMATE, GLYCINE, AND POLYAMINES
RANSOM, RW
STEC, NL
[J]. JOURNAL OF NEUROCHEMISTRY, 1988, 51 (03) : 830 - 836