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Journal of Pharmacological Methods|April 1, 1985
A timed intravenous pentylenetetrazol infusion seizure model for quantitating the anticonvulsant effect of valproic acid in the ratG M Pollack, D D ShenBiochemical Pharmacology|May 15, 1997
Effect of prior morphine-3-glucuronide exposure on morphine disposition and antinociceptionD M Ouellet, G M PollackBiopharmaceutics & Drug Disposition|May 30, 1998
Rationale for influx enhancement versus efflux blockade to increase drug exposure to the brainP L Golden, G M PollackBiopharmaceutics & Drug Disposition|January 1, 1991
Central nervous system uptake kinetics of pentylenetetrazol in the developing ratL J Haberer, G M PollackDrug Metabolism and Disposition: the Biological Fate of Chemicals|January 1, 1994
Disposition and protein binding of valproic acid in the developing ratL J Haberer, G M PollackJournal of Pharmaceutical Sciences|December 1, 1991
Enterohepatic recirculation and renal metabolism of morphine in the ratT L Horton, G M PollackPharmaceutical Research|January 5, 2002
Pharmacokinetics and pharmacodynamics of 7-nitroindazole, a selective nitric oxide synthase inhibitor, in the rat hippocampusM A Bush, G M PollackBiopharmaceutics & Drug Disposition|December 26, 2001
Nonstationary disposition of valproic acid during prolonged intravenous infusion: contributions of unbound clearance and protein bindingT L Arens, G M PollackBiopharmaceutics & Drug Disposition|April 17, 2001
Pharmacokinetics and protein binding of the selective neuronal nitric oxide synthase inhibitor 7-nitroindazoleM A Bush, G M PollackThe Journal of Pharmacology and Experimental Therapeutics|May 1, 1997
Pharmacodynamics and tolerance development during multiple intravenous bolus morphine administration in ratsD M Ouellet, G M PollackPageof 630