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3277 of 30 December 2021, Italian Ministry of University, Award No

It is also necessary to confirm the safety of GHK-Cu on human subjects

A contemporary site-directed mutation and computational modeling analysis indicates that Asp206 of hDAT is also a key player in Tat binding where Asp206Leu mutation inhibits Tat binding without altering the basal DA uptake (Quizon et al., 2021)

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