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For diabetes management (marketed as Victoza), the maximum dose is lower at 1.8 mg daily

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To further elucidate the therapeutic mechanisms underlying D-CuPs 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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doi: 10.1007/s11916-016-0583-7 32