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glutathione parasites PfK13-associated artemisinin resistance slows drug activation and enhances antioxidant defence, which can be overcome with sulforaphane
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glutathione parasites PfK13-associated artemisinin resistance slows drug activation and enhances antioxidant defence, which can be overcome with sulforaphane
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X ray structure of glutathione S transferase from the malarial parasite Plasmodium falciparum PNAS Role of glutathione metabolism genes in malaria parasite development: implications for YouTube Parasites: the future of biotherapy One Health Advances Springer Nature Link The essential host genome for Cryptosporidium survival exposes metabolic dependencies that can be leveraged for treatment: Cell
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glutathione parasites PfK13-associated artemisinin resistance slows drug activation and enhances antioxidant defence, which can be overcome with sulforaphane
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