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195 WangZ.HeW.YangG.WangJ.WangZ.NeslandJ

Mechanistically, DUSP22 dephosphorylates UBR2 at Ser1694 and Tyr1697 residues, leading to UBR2 proteasomal degradation and Lck inactivation [30]

Nevertheless, although these findings are encouraging, their applicability to clinical ischemia-reperfusion injury outcomes in humans has yet to be definitively established