Urinary excretion of 6β-hydroxycortisol in women during treatment with different oral contraceptive formulations
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Clinical Biochemistry,Endocrinology,Molecular Biology,Molecular Medicine,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference18 articles.
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3. Mechanism-based inactivation of human liver microsomal cytochrome P-450 IIIA4 by gestodene;Guengerich;Chem. Res. Toxic.,1990
4. Effect of the progestogens, gestodene, 3-keto desogestrel, levonorgestre, norethisterone and norgestimate and other substrates by human liver microsomes;Back;J. Steroid Biochem. Molec. Biol.,1991
5. In vitro interaction of contraceptive steroids with human liver cytochrome P-450 enzymes;Böcker;Adv. Contraception,1991
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1. Use of endogenous cortisol 6β-hydroxylation clearance for phenotyping in vivo CYP3A activity in women after sequential administration of an oral contraceptive (OC) containing ethinylestradiol and levonorgestrel as weak CYP3A inhibitors;Steroids;2014-09
2. Illicit treatments in cattle and urinary 6beta-hydroxycortisol/cortisol ratio;Analytica Chimica Acta;2007-03
3. Development of a Validated Liquid Chromatography Method for the Simultaneous Determination of Ethinyl Estradiol, Cyproterone Acetate, and Norgestrel in Breast Milk Following Solid‐Phase Extraction;Journal of Liquid Chromatography & Related Technologies;2006-03
4. Urinary 6?-hydroxycortisol: a validated test for evaluating drug induction or drug inhibition mediated through CYP3A in humans and in animals;European Journal of Clinical Pharmacology;2003-12-01
5. Progestogens with Antiandrogenic Properties;Drugs;2003
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