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Steroids|October 1, 1980
The addition of hypobromous acid to 3 beta, 17 beta-diacetoxy-4-estrene and an equilibration study involving neighboring group participation by the A-ring acetoxy groupD F Covey, V D ParikhThe Journal of Membrane Biology|February 11, 2005
The enantiomer of cholesterolE J Westover, D F CoveyJournal of Steroid Biochemistry|April 1, 1984
Study of the role of Schiff base formation in the aromatization of 3-[18O]testosterone and 3,17-di-[18O]androstenedione by human placental aromataseD D Beusen, D F CoveyBiochemistry|November 18, 1986
Mechanism-based inactivation of 17 beta,20 alpha-hydroxysteroid dehydrogenase by an acetylenic secoestradiolR J Auchus, D F CoveyEndocrinology|April 1, 1981
Enzyme-generated intermediates derived from 4-androstene-3,6,17-trione and 1,4,6-androstatriene-3,17-dione cause a time-dependent decrease in human placental aromatase activityD F Covey, W F HoodCancer Research|August 1, 1982
A new hypothesis based on suicide substrate inhibitor studies for the mechanism of action of aromataseD F Covey, W F HoodJournal of Medicinal Chemistry|November 26, 1993
Neurosteroid analogues: structure-activity studies of benz[e]indene modulators of GABAA receptor function. 1. The effect of 6-methyl substitution on the electrophysiological activity of 7-substituted benz[e]indene-3-carbonitrilesY Hu, C F Zorumski, D F CoveyThe Journal of Biological Chemistry|January 10, 1981
Human placental 17 beta-estradiol dehydrogenase and 20 alpha-hydroxysteroid dehydrogenase. Two activities at a single enzyme active siteR C Strickler, B Tobias, D F CoveyJournal of Medicinal Chemistry|October 11, 1996
Neurosteroid analogues. 4. The effect of methyl substitution at the C-5 and C-10 positions of neurosteroids on electrophysiological activity at GABAA receptorsM Han, C F Zorumski, D F CoveyPageof 11