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Disruption of this inhibitory interaction allows increased nitric oxide production, which is relevant to endothelial signaling and vascular responsiveness in experimental systems [3]
doi: 10.1016/j.parkreldis.2014.01.011 121 MuellerC.PinterB.ReiterE.SchockeM.ScherflerC.PoeweW.et al
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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J Immunol (Baltimore Md: 1950) (2017) 198(1):45260
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