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These findings highlighted ASCT2 as a promising therapeutic target for DSMTs
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250 The potential of FMD in clinical settings has been supported by the DIRECT study involving HER2-negative stage II/III breast cancer patients
In addition, BODIPY- C1-27A also strongly labelled a 57 kDa band corresponding to protein disulfide isomerase (PDI), a chaperone protein with cysteine at its active site (Fig
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