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2. Low affinity of FMRFamide and four FaRPs (FMRFamide-related peptides), including the mammalian-derived FaRPs F-8-Famide (NPFF) and A-18-Famide, for opioid mu, delta, kappa 1, kappa 2a, or kappa 2b receptors. Raffa RB, Kim A, Rice KC, de Costa BR, Codd EE, Rothman RB. Peptides; 1994 Jul; 15(3):401-4. PubMed ID: 7937312 [Abstract] [Full Text] [Related]
3. FMRFamide: an endogenous peptide with marked inhibitory effects on opioid-induced feeding behavior. Kavaliers M, Hirst M. Brain Res Bull; 1986 Sep; 17(3):403-8. PubMed ID: 3533222 [Abstract] [Full Text] [Related]
4. The actions of FMRF-NH2 and FMRF-NH2 related peptides on mammals. Raffa RB. NIDA Res Monogr; 1990 Sep; 105():243-9. PubMed ID: 1678861 [Abstract] [Full Text] [Related]
5. The action of FMRFamide (Phe-Met-Arg-Phe-NH2) and related peptides on mammals. Raffa RB. Peptides; 1988 Sep; 9(4):915-22. PubMed ID: 3067224 [Abstract] [Full Text] [Related]
6. Characterization of [3H]Met-enkephalin-Arg6-Phe7 binding to opioid receptors in frog brain membrane preparations. Wollemann M, Farkas J, Tóth G, Benyhe S. J Neurochem; 1994 Oct; 63(4):1460-5. PubMed ID: 7931298 [Abstract] [Full Text] [Related]
7. Characterisation and visualisation of [3H]dermorphin binding to mu opioid receptors in the rat brain. Combined high selectivity and affinity in a natural peptide agonist for the morphine (mu) receptor. Amiche M, Sagan S, Mor A, Pelaprat D, Rostene W, Delfour A, Nicolas P. Eur J Biochem; 1990 May 20; 189(3):625-35. PubMed ID: 2161761 [Abstract] [Full Text] [Related]
8. Quantitative analysis of multiple kappa-opioid receptors by selective and nonselective ligand binding in guinea pig spinal cord: resolution of high and low affinity states of the kappa 2 receptors by a computerized model-fitting technique. Tiberi M, Magnan J. Mol Pharmacol; 1990 May 20; 37(5):694-703. PubMed ID: 2160061 [Abstract] [Full Text] [Related]
9. Differences of binding characteristics of non-selective opiates towards mu and delta receptor types. Delay-Goyet P, Roques BP, Zajac JM. Life Sci; 1987 Aug 10; 41(6):723-31. PubMed ID: 3039270 [Abstract] [Full Text] [Related]
10. Biochemical characterization of high-affinity 3H-opioid binding. Further evidence for Mu1 sites. Nishimura SL, Recht LD, Pasternak GW. Mol Pharmacol; 1984 Jan 10; 25(1):29-37. PubMed ID: 6323950 [Abstract] [Full Text] [Related]
11. Opiate receptor binding profile in the rabbit cerebellum and brain membranes. Ho CL, Hammonds RG, Li CH. Biochem Pharmacol; 1985 Apr 01; 34(7):925-31. PubMed ID: 2985086 [Abstract] [Full Text] [Related]
12. Tyr-D-Ala-Gly-(Me)Phe-chloromethyl ketone: a mu specific affinity label for the opioid receptor. Benyhe S, Hepp J, Simon J, Borsodi A, Medzihradszky K, Wollemann M. Neuropeptides; 1987 Apr 01; 9(3):225-35. PubMed ID: 3037428 [Abstract] [Full Text] [Related]
13. The effect of two different buffers on the high affinity 3H-ethylketocyclazocine and 3H-SKF10047 binding to guinea pig brain membranes. Grynne BH, Maurset AR, Holmen AT, Enger M. Acta Pharmacol Toxicol (Copenh); 1984 Mar 01; 54(3):195-200. PubMed ID: 6144235 [Abstract] [Full Text] [Related]
14. Nalbuphine: an autoradiographic opioid receptor binding profile in the central nervous system of an agonist/antagonist analgesic. De Souza EB, Schmidt WK, Kuhar MJ. J Pharmacol Exp Ther; 1988 Jan 01; 244(1):391-402. PubMed ID: 2826773 [Abstract] [Full Text] [Related]
15. Site-directed alkylation of multiple opioid receptors. I. Binding selectivity. James IF, Goldstein A. Mol Pharmacol; 1984 May 01; 25(3):337-42. PubMed ID: 6328259 [Abstract] [Full Text] [Related]
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