Novel Pharmacology of Substance K-Binding Sites: a Third Type of Tachykinin Receptor
Author:
Affiliation:
1. Section on Biochemical Pharmacology, National Heart, Lung, and Blood Institute, and Experimental Therapeutics Branch, National Institute for Neurological and Communicative Disorders and Stroke, Bethesda, Maryland 20205
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference29 articles.
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2. BURCHER, E, AUTORADIOGRAPHIC DISTRIBUTION OF SUBSTANCE-K BINDING-SITES IN RAT GASTROINTESTINAL-TRACT - A COMPARISON WITH SUBSTANCE-P, EUROPEAN JOURNAL OF PHARMACOLOGY 102: 561 (1984).
3. Cascieri, M. A., Journal of Biological Chemistry 260: 1501 (1985).
4. CASCIERI, M.A., CHARACTERIZATION OF THE SUBSTANCE-P RECEPTOR IN RAT-BRAIN CORTEX MEMBRANES AND THE INHIBITION OF RADIOLIGAND BINDING BY GUANINE-NUCLEOTIDES, JOURNAL OF BIOLOGICAL CHEMISTRY 258: 5158 (1983).
5. CASCIERI, M.A., BINDING OF [BOLTON-I-125 HUNTER CONJUGATED ELEDOISIN TO RAT-BRAIN CORTEX MEMBRANES - EVIDENCE FOR 2 CLASSES OF TACHYKININ RECEPTORS IN THE MAMMALIAN CENTRAL NERVOUS-SYSTEM, LIFE SCIENCES 35: 179 (1984).
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