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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| Publicado no: | Proc Natl Acad Sci U S A |
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| Principais autores: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
1999
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC18006/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10500149/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.96.20.11173 |
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