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Synapse (New York, N.Y.)|February 1, 1995
6 beta-[125iodo]-3, 14-dihydroxy-17-methyl-4, 5 alpha-epoxymorphinan ([125I]IOXY-AGO): a potent and selective radioligand for opioid mu receptorsH Xu, C B Goodman, J S Partilla, et al.Peptides|January 1, 1994
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 receptorsR B Raffa, A Kim, K C Rice, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 1, 1990
Characterization of benzodiazepine receptors with fluorescent ligandsR T McCabe, B R de Costa, R L Miller, et al.Journal of Medicinal Chemistry|March 1, 1979
Paradoxical effects of N-cyanoalkyl substituents upon the activities of several classes of opioidsA E Jacobson, K C Rice, J Reden, et al.Life Sciences|June 30, 1986
Is Metaphit a phencyclidine antagonist? Studies with ketamine, phencyclidine and N-methylaspartateS N Davies, J Church, J Blake, et al.Insect Molecular Biology|February 15, 2000
Systematic screening of Anopheles mosquito genomes yields evidence for a major clade of Pao-like retrotransposonsJ M Cook, J Martin, A Lewin, et al.Transplantation|June 1, 1987
Increased monocyte Fc-dependent chemiluminescence in renal transplant patientsD N Rush, J M Cook, D A Niven, et al.Biochimica Et Biophysica Acta|November 26, 1987
The beta-phosphoro[35S]thioate analogue of UDP-Glc is efficiently utilized by the glucose phosphotransferase and is relatively resistant to hydrolytic degradationR B Marchase, A M Saunders, A A Rivera, et al.Life Sciences|January 1, 1989
Behavioral effects of benzodiazepine antagonists in chlordiazepoxide tolerant and non-tolerant ratsK Takada, T Suzuki, T Hagen, et al.Pharmacology, Biochemistry, and Behavior|December 1, 1992
Cocaine and GBR12909 produce equivalent motoric responses at different occupancy of the dopamine transporterR B Rothman, N Grieg, A Kim, et al.Pageof 48