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This review aims to fill these gaps by offering a comprehensive assessment of GSHs dual role in cancer biology, systematically examining nanotechnology-enabled approaches (such as disulfide and diselenide linkages, transition metal systems, and prodrugs), and critically evaluating their strengths, limitations, and potential for clinical translation

Previous studies have described developmental, phenotypic, functional and transcriptomic differences between MZB and FoB 7,8,9,10,11,12,13,14

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