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Volumn 295, Issue 2, 2000, Pages 552-562
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δ-Opioid receptors are more efficiently coupled to adenylyl cyclase than to L-type Ca2+ channels in transfected rat pituitary cells
a
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Author keywords
[No Author keywords available]
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Indexed keywords
ADENYLATE CYCLASE;
ALKYLATING AGENT;
COMPLEMENTARY DNA;
DELTA OPIATE RECEPTOR;
GUANINE NUCLEOTIDE BINDING PROTEIN;
MU OPIATE RECEPTOR;
ANIMAL CELL;
ARTICLE;
CALCIUM CHANNEL;
CALCIUM CURRENT;
CALCIUM SIGNALING;
CELL CLONE;
CELL STRAIN GH3;
CONTROLLED STUDY;
ENZYME INHIBITION;
GENETIC TRANSFECTION;
HYPOPHYSIS CELL;
NONHUMAN;
PRIORITY JOURNAL;
PROTEIN PROTEIN INTERACTION;
RAT;
RECEPTOR BINDING;
RECEPTOR DENSITY;
ADENYLATE CYCLASE;
ALKYLATING AGENTS;
ANALGESICS, OPIOID;
ANIMAL;
BARIUM;
CALCIUM CHANNELS, L-TYPE;
ENKEPHALIN, D-PENICILLAMINE (2,5)-;
FENTANYL;
HETEROTRIMERIC GTP-BINDING PROTEINS;
ION CHANNELS;
NALTREXONE;
PITUITARY GLAND;
RATS;
RECEPTORS, OPIOID, DELTA;
RECEPTORS, OPIOID, MU;
SUPPORT, NON-U.S. GOV'T;
SUPPORT, U.S. GOV'T, P.H.S.;
TRANSFECTION;
VIRULENCE FACTORS, BORDETELLA;
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EID: 0033780440
PISSN: 00223565
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (22)
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References (40)
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