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Suppression of Δ(5)-androstenediol-induced androgen receptor transactivation by selective steroids in human prostate cancer cells
Our earlier report suggested that androst-5-ene-3β,7β-diol (Δ(5)-androstenediol or Adiol) is a natural hormone with androgenic activity and that two potent antiandrogens, hydroxyflutamide (Eulexin) and bicalutamide (Casodex), fail to block completely the Adiol-induced androgen receptor (AR) transact...
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| Autori principali: | , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The National Academy of Sciences
1999
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC18006/ https://ncbi.nlm.nih.gov/pubmed/10500149 |
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