The essential host genome for Cryptosporidium survival exposes metabolic dependencies that can be leveraged for treatment: Cell An Optimized Dihydrodibenzothiazepine Lead Compound (SBI 0797750) as a Potent and Selective Inhibitor of Plasmodium falciparum and P. vivax Glucose 6 Phosphate Dehydrogenase 6 Phosphogluconolactonase Antimicrobial Agents and Chemotherapy The Thioredoxin System of the Malaria Parasite Plasmodium falciparum: GLUTATHIONE REDUCTION REVISITED ScienceDirect Determination of glutathione redox potential and pH value in subcellular compartments of malaria parasites ScienceDirect Natural Perylenequinone Compounds as Potent Inhibitors of Schistosoma mansoni Glutathione S Transferase
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glutathione parasites Thiol-based redox metabolism of protozoan parasites