Clinical application of 5α-reductase inhibitors

Author:

Cilotti A.,Danza G.,Serio M.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference32 articles.

1. Jenkins E.P., Hsieh C.L., Milatovich A., Normington K., Berman D.M., Francke U., Russell D.W. Characterization and chromosomal mapping of a human steroid 5α-reductase gene and pseudogene and mapping of the mouse homologue. Genomics 1991, 11: 1102–1112.

2. Thigpen A.E., Silver R.I., Guileyardo J.M., Casey M.L., McConnell J.D., Russell D.W. Tissue distribution and ontogeny of steroid 5α-reductase isozyme expression. J. Clin. Invest. 1993, 92: 903–910.

3. Bonkhoff H., Stein U., Aumuller G., Remberger K. Differential expression of 5α-reductase isoenzymes in the human prostate and prostatic carcinomas. Prostate 1996, 629: 261–267.

4. Boudon C., Lobaccaro J.M., Lumbroso S., Lechevallier E., Mottet N., Gibelin B., Sultan C. 5α-reductase activity in cultured epithelial and stromal cells from normal and hyperplastic human prostates effect of finasteride (Proscar), a 5α-reductase inhibitor. Cell. Mol. Biol. 1995, 41: 1007–1015.

5. Smith C.M., Ballard S.A., Worman N., Buettner R., Masters J.R. 5α-reductase expression by prostate cancer cell lines and benign prostatic hyperplasia in vitro. J. Clin. Endocrinol. Metab. 1996, 81: 1361–1366.

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