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Therefore, we hypothesized and validated the mechanism by which GDIL not only interacted with XRN2, but also promoted its re-localization from the nucleus to the cytoplasm, where XRN2 could meet CHAC1 mRNA and further degrade it (Fig

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The peaks for S 2p appeared at 161.8, 163.7, 164.8, and 168.1 eV, corresponding to S 2- , S n 2- , S 0 , and SO 4 2- , respectively 38