The lipoidal derivatives of steroids as biosynthetic intermediates.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference12 articles.
1. Detection in bovine adrenal cortex of a lipoidal substance that yields pregnenolone upon treatment with alkali.
2. Naturally occurring lipoidal derivatives of 3β-hydroxy-5-pregnen-20-one; 3β, 17α-dihydroxy-5-pregnen-20-one and 3β-hydroxy-5-androsten-17-one
3. The Endocrine Society Seventh Postgraduate Training Course on Radioligand Assay Techniques
4. Evidence that Steroid Sulfates Serve as Biosynthetic Intermediates.* IV. Conversion of Cholesterol Sulfate in vivo to Urinary C19 and C21 Steroidal Sulfates†
5. Bildung von 17α-Hydroxy-Δ5-pregnenolon und 3β-Hydroxy-17-keto-Δ5-androsten (DHA) in Nebennieren- und Testes-Gewebe
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1. Other conceivable renditions of some of the oxidative processes used in the biosynthesis of steroid hormones;The Journal of Steroid Biochemistry and Molecular Biology;2006-09
2. Aromatase and testosterone fatty acid esters: the search for a cryptic biosynthetic pathway to estradiol esters;Steroids;1992-10
3. Lipoprotein-incorporated pregnenolone fatty acid esters act as substrate for ovarian progestin synthesis;Biochemical and Biophysical Research Communications;1991-09
4. Steroidal fatty acid esters;The Journal of Steroid Biochemistry and Molecular Biology;1991-01
5. Wide spectrum of steroids serving as substrates for the formation of lipoidal derivatives in ZR-75-1 human breast cancer cells;Journal of Steroid Biochemistry;1990-02
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