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European Journal of Clinical Pharmacology|July 10, 2007
Tolfenamic acid is a potent CYP1A2 inhibitor in vitro but does not interact in vivo: correction for protein binding is needed for data interpretationMarjo J Karjalainen, Pertti J Neuvonen, Janne T Backman
European Journal of Clinical Pharmacology|June 8, 2006
Rifampicin is only a weak inducer of CYP1A2-mediated presystemic and systemic metabolism: studies with tizanidine and caffeineJanne T Backman, Marika T Granfors, Pertti J Neuvonen
European Journal of Clinical Pharmacology|October 24, 2007
Effects of gender and moderate smoking on the pharmacokinetics and effects of the CYP1A2 substrate tizanidineJanne T Backman, Marika T Schröder, Pertti J Neuvonen
Biochimica Et Biophysica Acta|July 30, 1990
Two novel c-abl mRNAs are expressed in rat parotid salivary glands during in vivo beta-adrenergic receptor stimulationP M Mertz, T Backman, A Bernards, et al.
International Journal of Clinical Pharmacology and Therapeutics|June 1, 1995
Azithromycin does not increase plasma concentrations of oral midazolamJ T Backman, K T Olkkola, P J Neuvonen
Clinical Pharmacology and Therapeutics|January 1, 1996
Rifampin drastically reduces plasma concentrations and effects of oral midazolamJ T Backman, K T Olkkola, P J Neuvonen
Basic & Clinical Pharmacology & Toxicology|September 26, 2008
In vitro inhibition of CYP1A2 by model inhibitors, anti-inflammatory analgesics and female sex steroids: predictability of in vivo interactionsMarjo J Karjalainen, Pertti J Neuvonen, Janne T Backman
Basic & Clinical Pharmacology & Toxicology|December 21, 2005
Effect of itraconazole on the pharmacokinetics of atenololJari J Lilja, Janne T Backman, Pertti J Neuvonen
European Journal of Clinical Pharmacology|January 17, 2008
Celecoxib is a CYP1A2 inhibitor in vitro but not in vivoMarjo J Karjalainen, Pertti J Neuvonen, Janne T Backman
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