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Furthermore, p-JNK leads to the activation of Bax and translocation to mitochondria to trigger the mitochondrial permeability transition (MPT) pore formation, along with collapsed ATP depletion and membrane potential, eventually causing DNA fragmentation and necrosis (Kim et al., 2006)

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SO(4)(=) uptake and catalase role in preconditioning after H(2)O(2)-induced oxidative stress in human erythrocytes

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