about
Targeting the cell stress response of Plasmodium falciparum to overcome artemisinin resistanceAltered temporal response of malaria parasites determines differential sensitivity to artemisininHaemoglobin degradation underpins the sensitivity of early ring stage Plasmodium falciparum to artemisininsStructure- and function-based design of Plasmodium-selective proteasome inhibitorsOptimal assay design for determining the in vitro sensitivity of ring stage Plasmodium falciparum to artemisinins.Comparison of the Exposure Time Dependence of the Activities of Synthetic Ozonide Antimalarials and Dihydroartemisinin against K13 Wild-Type and Mutant Plasmodium falciparum Strains.A Dynamic Stress Model Explains the Delayed Drug Effect in Artemisinin Treatment of Plasmodium falciparum.Target Validation and Identification of Novel Boronate Inhibitors of the Plasmodium falciparum ProteasomeArtemisinin kills malaria parasites by damaging proteins and inhibiting the proteasomeThe proteasome as a target for protozoan parasitesDecreased K13 Abundance Reduces Hemoglobin Catabolism and Proteotoxic Stress, Underpinning Artemisinin ResistanceThe structure of the PA28-20S proteasome complex from Plasmodium falciparum and implications for proteostasis
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description
researcher
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wetenschapper
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հետազոտող
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name
Stanley C. Xie
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Stanley C. Xie
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Stanley C. Xie
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Stanley C. Xie
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Stanley C. Xie
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Stanley C. Xie
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Stanley C. Xie
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Stanley C. Xie
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Stanley C. Xie
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Stanley C. Xie
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Stanley C Xie
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Stanley C. Xie
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Stanley C. Xie
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Stanley C. Xie
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Stanley C. Xie
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Stanley C. Xie
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P106
P1153
55908189400
P31
P4012
P496
0000-0001-7003-4677