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Finasteride Treatment Alters Tissue Specific Androgen Receptor Expression in Prostate Tissues
BACKGROUND: Normal and pathologic growth of the prostate is dependent on the synthesis of dihydrotestosterone (DHT) from testosterone by 5α-reductase. Finasteride is a selective inhibitor of 5α-reductase 2, one isozyme of 5α-reductase found in abundance in the human prostate. The objective of this s...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4137476/ https://ncbi.nlm.nih.gov/pubmed/24789081 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pros.22810 |
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