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Arginine (R) mutations were introduced at lysine (K)242 (K242R), K384 (K384R), and K626 (K626R) sites of TFR1

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Tumor-promoting effects of myeloid-derived suppressor cells are potentiated by hypoxia-induced expression of miR-210

The test was performed on each mouse once a day over 5 d, and the results were averaged

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