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To further elucidate the therapeutic mechanisms underlying D-CuP’s multivalent interactions, comprehensive proteomic analysis revealed two pivotal transcriptional regulators, the tumor suppressor protein p53 and histone deacetylase 7 (HDAC7) to be potential mechanistic targets
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281:36369–36377 10.1074/jbc.M604935200 [DOI] [PubMed] [Google Scholar] Várnai P., Balla T
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