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Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells

Histone deacetylases (HDACs) play important roles in transcriptional regulation and pathogenesis of cancer. Thus, HDAC inhibitors are candidate drugs for differentiation therapy of cancer. Here, we show that the well-tolerated antiepileptic drug valproic acid is a powerful HDAC inhibitor. Valproic a...

詳細記述

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書誌詳細
主要な著者: Göttlicher, Martin, Minucci, Saverio, Zhu, Ping, Krämer, Oliver H., Schimpf, Annemarie, Giavara, Sabrina, Sleeman, Jonathan P., Lo Coco, Francesco, Nervi, Clara, Pelicci, Pier Giuseppe, Heinzel, Thorsten
フォーマット: Artigo
言語:Inglês
出版事項: Oxford University Press 2001
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC125788/
https://ncbi.nlm.nih.gov/pubmed/11742974
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/20.24.6969
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