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X ray structure of glutathione S transferase from the malarial parasite Plasmodium falciparum PNAS PfK13 associated artemisinin resistance slows drug activation and enhances antioxidant defence, which can be overcome with sulforaphane bioRxiv Thioredoxin Glutathione Reductase from Schistosoma mansoni: An Essential Parasite Enzyme and a Key Drug Target PLOS Medicine The Beneficial Use of Artemisia annua, Artemisinin, and Other Compounds in Animal Health 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 University of Glasgow Postgraduate study Centres for Doctoral Training Wellcome Trust Integrative Infection Biology PhD Partners and collaborations Projects Parasite
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X-ray structure of glutathione S-transferase from the malarial parasite  Plasmodium falciparum | PNAS
PfK13-associated artemisinin resistance slows drug activation and enhances  antioxidant defence, which can be overcome with sulforaphane | bioRxiv
Thioredoxin Glutathione Reductase from Schistosoma mansoni: An Essential  Parasite Enzyme and a Key Drug Target | PLOS Medicine
The Beneficial Use of Artemisia annua, Artemisinin, and Other Compounds in  Animal Health
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

glutathione parasites The Architecture of Thiol Antioxidant Systems among Invertebrate Parasites

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