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Antimicrobial Agents and Chemotherapy|January 1, 1996
Cytochrome P-450 complex formation in rat liver by the antibiotic tiamulinR F Witkamp, S M Nijmeijer, A S van Miert
Journal of Veterinary Pharmacology and Therapeutics|August 1, 1994
Tiamulin selectively inhibits oxidative hepatic steroid and drug metabolism in vitro in the pigR F Witkamp, S M Nijmeijer, G Csikó, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 1, 1995
The antibiotic tiamulin is a potent inducer and inhibitor of cytochrome P4503A via the formation of a stable metabolic intermediate complex. Studies in primary hepatocyte cultures and liver microsomes of the pigR F Witkamp, S M Nijmeijer, M Monshouwer, et al.
Biochemical Pharmacology|September 7, 1995
Tiamulin inhibits human CYP3A4 activity in an NIH/3T3 cell line stably expressing CYP3A4 cDNAE M De Groene, S M Nijmeijer, G J Horbach, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 1, 1993
Sulfamethazine as a model compound to assess sex hormone-dependent cytochrome P-450 activity in ratsR F Witkamp, S M Nijmeijer, H Yun, et al.
Journal of Veterinary Pharmacology and Therapeutics|June 1, 1993
Effect of gonadal hormones on the plasma clearance and metabolite formation of antipyrine in the dwarf goatR F Witkamp, S M Nijmeijer, H J Kolker, et al.
Research in Veterinary Science|July 1, 1993
Selective changes in oxidative xenobiotic metabolism in vivo and in vitro after parenteral administration of recombinant bovine somatotrophin to ratsR F Witkamp, H J Kolker, S M Nijmeijer, et al.
The Veterinary Quarterly|March 1, 1994
Oral bioavailability of sulphamethoxydiazine, sulphathiazole and sulphamoxole in dwarf goatsK Weijkamp, S M Faghihi, S M Nijmeijer, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA|July 27, 2010
Characterization of cytochrome P450 isoenzymes in primary cultures of pig hepatocytesM Monshouwer, G A Van't Klooster, S M Nijmeijer, et al.
The Journal of Endocrinology|February 1, 1993
The regulation of oxidative drug metabolism by growth hormone in the dwarf goat: differences from and similarities to the mechanisms in ratsR F Witkamp, S M Nijmeijer, C T Van Duin, et al.
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