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Biochemical Pharmacology|February 9, 1993
Protein binding and hepatobiliary distribution of valproic acid and valproate glucuronide in ratsK L Brouwer, E S Hall, G M Pollack
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 1, 1994
Site-dependent intestinal hydrolysis of valproate and morphine glucuronide in the developing ratG M Pollack, A P Spencer, T L Horton, et al.
Biochemical Pharmacology|August 23, 1996
Evidence for reversible sequestration of morphine in rat liverC J Matheny, D R Taft, K L Brouwer, et al.
Pharmaceutical Research|May 20, 1998
Effect of GF120918, a potent P-glycoprotein inhibitor, on morphine pharmacokinetics and pharmacodynamics in the ratS P Letrent, G M Pollack, K R Brouwer, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 29, 1999
Effects of a potent and specific P-glycoprotein inhibitor on the blood-brain barrier distribution and antinociceptive effect of morphine in the ratS P Letrent, G M Pollack, K R Brouwer, et al.
Journal of Pharmaceutical Sciences|April 1, 1996
Age-related changes in valproic acid binding to rat serum proteins in vitroP W Slattum, A E Cato, G M Pollack, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|March 1, 1995
Age-dependent intestinal hydrolysis of valproate glucuronide in ratP W Slattum, A E Cato, G M Pollack, et al.
Life Sciences|February 9, 2000
Increased brain P-glycoprotein in morphine tolerant ratsC L Aquilante, S P Letrent, G M Pollack, et al.
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