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doi:10.2217/whe-2016-0018 T

We demonstrate that the carboxy-terminal domain is crucial for the catalytic activity and ferroptosis inhibition of FSP1 by mediating the functional dimerization of FSP1, and the formation of two active sites located on two sides of FAD, which are responsible for ubiquinone reduction and a unique FAD hydroxylation respectively

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Alternatively, miRNAs can repress translation by inducing premature ribosome detachment (Silvestro et al., 2019)

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