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Psychopharmacology|April 14, 1978
Narcotic cuing and analgesic activity of narcotic analgesics: associative and dissociative characteristicsF C Colpaert, C J Niemegeers, P A JanssenEuropean Journal of Pharmacology|June 12, 2001
In the formalin model of tonic nociceptive pain, 8-OH-DPAT produces 5-HT1A receptor-mediated, behaviorally specific analgesiaL Bardin, J P Tarayre, W Koek, et al.Life Sciences|July 5, 1982
Further evidence validating adjuvant arthritis as an experimental model of chronic pain in the ratF C Colpaert, T Meert, P De Witte, et al.Journal of Theoretical Biology|June 8, 2002
Sign-reversal during persistent activation in mu-opioid signal transductionL A Bruins Slot, P J Pauwels, F C ColpaertBrain Research Bulletin|April 1, 1991
Effects of an alpha 2 antagonist in a 20-year-old Java monkey with MPTP-induced parkinsonian signsF C Colpaert, A D Degryse, H V Van CraenendonckBehavioural Brain Research|June 1, 1983
Effects of dorsal raphe stimulation on escape induced by medial hypothalamic or central gray stimulationP Schmitt, G Sandner, F C Colpaert, et al.Naunyn-Schmiedeberg'S Archives of Pharmacology|December 24, 1997
Stimulated [35S]GTP gamma S binding by 5-HT1A receptor agonists in recombinant cell lines. Modulation of apparent efficacy by G-protein activation stateP J Pauwels, S Tardif, T Wurch, et al.The Journal of Pharmacology and Experimental Therapeutics|January 20, 2000
Facilitation of constitutive alpha(2A)-adrenoceptor activity by both single amino acid mutation (Thr(373)Lys) and g(alphao) protein coexpression: evidence for inverse agonismP J Pauwels, S Tardif, T Wurch, et al.Naunyn-Schmiedeberg'S Archives of Pharmacology|July 1, 1996
Promotion of cell growth by stimulation of cloned human 5-HT1D receptor sites in transfected C6-glial cells is highly sensitive to intrinsic activity at 5-HT1D receptorsP J Pauwels, T Wurch, C Palmier, et al.British Journal of Pharmacology|August 28, 2001
Real-time analysis of dopamine: antagonist interactions at recombinant human D2long receptor upon modulation of its activation stateP J Pauwels, S Tardif, T Wurch, et al.Pageof 24