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International Journal of Pharmaceutics|February 13, 2001
A rapid screening system to determine drug affinities for the intestinal dipeptide transporter 2: affinities of ACE inhibitorsV A Moore, W J Irwin, P Timmins, et al.
Pharmaceutical Research|July 1, 1996
Suitability of enalapril as a probe of the dipeptide transporter system: in vitro and in vivo studiesR A Morrison, S Chong, A M Marino, et al.
Biochemical and Biophysical Research Communications|October 1, 1998
Direct evidence for peptide transporter (PepT1)-mediated uptake of a nonpeptide prodrug, valacyclovirP V Balimane, I Tamai, A Guo, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|December 9, 2003
Application of structure-metabolism relationships in the identification of a selective endothelin A antagonist, BMS-193884, with favourable pharmacokinetic propertiesW G Humphreys, M T Obermeier, J C Barrish, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 1, 1984
Isosorbide dinitrate disposition in the rat: metabolite pharmacokinetics and interactionsR A Morrison, H L Fung
Pediatric Nursing|November 1, 1989
Pain management in the child with sickle cell diseaseR A Morrison, D A Vedro
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|January 10, 2003
Oxidative activation of acylguanidine prodrugs: intestinal presystemic activation in rats limits absorption and can be inhibited by co-administration of ketoconazoleW G Humphreys, M T Obermeier, S Chong, et al.
Journal of Pharmaceutical Sciences|August 1, 1996
Prodrugs of BMS-183920: metabolism and permeability considerationsM T Obermeier, S Chong, S A Dando, et al.
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