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The high stability of the structural disulphide bonds found in the IMS (redox potentials in the range of 320 mV) and the low redox potential of the active site cysteine pair of the oxidoreductase Mia40 (290 mV

In summary, we found that KG was required for histone acetylation via TMHLE-catalyzed carnitine synthesis to facilitate HR-mediated DNA repair in CCNE1-driven models

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protocols are based on clinical practice and empirical use [5]