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doi: 10.1016/j.apsb.2023.02.018 59 PalmqvistPLundbergPPerssonEJohanssonALundgrenILieAet al
This inhibitor targets a stereo-specific pocket in the substrate binding site of ASCT2 and demonstrates submicromolar potency and stereo-selectivity
Anticancer properties of low molecular weight oat beta-glucan - an in vitro study
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