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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...
Gorde:
| Egile Nagusiak: | , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2014
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| Gaiak: | |
| Sarrera elektronikoa: | 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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