Structure–function relationships in 3α-hydroxysteroid dehydrogenases: a comparison of the rat and human isoforms-Reference-Cited by-同舟云学术

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Structure–function relationships in 3α-hydroxysteroid dehydrogenases: a comparison of the rat and human isoforms

Published:2003-06 Issue:2-5 Volume:85 Page:247-255
ISSN:0960-0760
Container-title:The Journal of Steroid Biochemistry and Molecular Biology
language:en
Short-container-title:The Journal of Steroid Biochemistry and Molecular Biology

Author:

Penning Trevor M,Jin Yi,Heredia Vladi V,Lewis Mitchell

Publisher

Elsevier BV

Subject

Cell Biology,Clinical Biochemistry,Endocrinology,Molecular Biology,Molecular Medicine,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference29 articles.

1. Comparison of the metabolites formed in rat prostate following the in vivo administration of seven natural androgens;Bruchovsky;Endocrinology,1971

2. Steroid structure and androgenic activity. Specificities involved in the receptor binding and nuclear retention of various androgens;Liao;J. Biol. Chem.,1973

3. 5α-Reductase inhibitors in prostate cancer;Gormley;Endocr. Rel. Cancer,1996

4. Expression cloning and characterization of oxidative 17β- and 3α-hydroxysteroid dehydrogenases from rat and human prostate;Biswas;J. Biol. Chem.,1997

5. Steroid hormone metabolites are barbiturate-like modulators of the GABA receptor;Majewska;Science,1986

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