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glutathione thioether bonds The role of glutathione-S-transferase in anti-cancer drug resistance Cysteine
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glutathione thioether bonds The role of glutathione-S-transferase in anti-cancer drug resistance Cysteine
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glutathione thioether bonds The role of glutathione-S-transferase in anti-cancer drug resistance Cysteine
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glutathione thioether bonds The role of glutathione-S-transferase in anti-cancer drug resistance Cysteine
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Interestingly, focusing on progression in gap closure between 6 h and 12 h from monolayer disruption, both hAAT OX 0.5mM and hAAT OX 5mM allowed gap closure advancement, most notable in the hAAT OX 5mM setting (from 62.12 ± 5.05% gap area at 6 h to 23.39 ± 4.28% at 12 h, p = 0.0011)
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Ginsenoside Rh4 facilitates the sensitivity of renal cell carcinoma to ferroptosis via the NRF2 pathway
glutathione thioether bonds The role of glutathione-S-transferase in anti-cancer drug resistance Cysteine
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