Inactivation of human placental aromatase by 6α- and 6β-hydroperoxyandrostenedione
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference21 articles.
1. Synthesis and properties of the epimeric 6-hydroperoxyandrostenediones, new substrates/inhibitors of human placental aromatase
2. URINARY 6β-HYDROXYCORTISOL IN ADRENOCORTICAL HYPERFUNCTION*†
3. STUDIES ON THE METABOLISM OF C-21 STEROIDS IN THE HUMAN FOETO-PLANCENTAL UNIT
4. Studies on the Metabolism of C21 Steroids in Rat Liver. Hydroxylation of Progesterone in Rat Liver Microsomes
5. Genetic Aspects of Adrenal and Hepatic Cortisol 2α- and 6β-Hydroxylation in Guinea Pigs: Developmental Pattern and Effect of Substrate Concentration
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1. Probing the binding pocket of the active site of aromatase with 6-ether or 6-ester substituted androst-4-ene-3,17-diones and their diene and triene analogs;Steroids;2000-12
2. Aryltricyclospirodienones; novel steroid mimics as inhibitors of aromatase;Journal of the Chemical Society, Perkin Transactions 1;1997
3. Design and action of steroidal aromatase inhibitors;Journal of the American Oil Chemists' Society;1996-11
4. Expression of human placental G proteins during pregnancy,;Journal of the Society for Gynecologic Investigation;1995-10
5. Expression of Human Placental G Proteins During Pregnancy;Journal of the Society for Gynecologic Investigation;1995-09
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