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Drug Metabolism and Disposition: the Biological Fate of Chemicals|April 17, 2001
In vitro metabolism of the COX-2 inhibitor DFU, including a novel glutathione adduct rearomatizationJ A Yergey, L A Trimble, J Silva, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 13, 2001
Application of rat hepatocyte culture to predict in vivo metabolic auto-induction: studies with DFP, a cyclooxygenase-2 inhibitorD A Nicoll-Griffith, J M Silva, N Chauret, et al.
The Journal of Biological Chemistry|July 1, 1994
Cloning of the NCX2 isoform of the plasma membrane Na(+)-Ca2+ exchangerZ Li, S Matsuoka, L V Hryshko, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 1, 1993
Characterization of verlukast metabolites arising from an epoxide intermediate produced with hepatic microsomes from beta-naphthoflavone-treated rodents (P-4501A1)D A Nicoll-Griffith, N Chauret, J A Yergey, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 20, 1998
Refinement of an in vitro cell model for cytochrome P450 inductionJ M Silva, P E Morin, S H Day, et al.
The Journal of Biological Chemistry|January 15, 1991
Identification of a peptide inhibitor of the cardiac sarcolemmal Na(+)-Ca2+ exchangerZ Li, D A Nicoll, A Collins, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 15, 2001
The use of 3-[2-(N,N-diethyl-N-methylammonium)ethyl]-7-methoxy-4-methylcoumarin (AMMC) as a specific CYP2D6 probe in human liver microsomesN Chauret, B Dobbs, R L Lackman, et al.
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