about
The malaria parasite cation ATPase PfATP4 and its role in the mechanism of action of a new arsenal of antimalarial drugsExported Epoxide Hydrolases Modulate Erythrocyte Vasoactive Lipids during Plasmodium falciparum InfectionNa(+) regulation in the malaria parasite Plasmodium falciparum involves the cation ATPase PfATP4 and is a target of the spiroindolone antimalarialsPyrazoleamide compounds are potent antimalarials that target Na+ homeostasis in intraerythrocytic Plasmodium falciparum.The chaperonin TRiC forms an oligomeric complex in the malaria parasite cytosol(+)-SJ733, a clinical candidate for malaria that acts through ATP4 to induce rapid host-mediated clearance of Plasmodium.Protein export into malaria parasite-infected erythrocytes: mechanisms and functional consequences.Na+ extrusion imposes an acid load on the intraerythrocytic malaria parasite.Acid extrusion from the intraerythrocytic malaria parasite is not via a Na(+)/H(+) exchanger.Artemisinin kills malaria parasites by damaging proteins and inhibiting the proteasomeNa+-dependent acid efflux from P. falciparum: PfNHE or residual nigericin?Delayed death in the malaria parasite Plasmodium falciparum is caused by disruption of prenylation-dependent intracellular traffickingThe structure of the PA28-20S proteasome complex from Plasmodium falciparum and implications for proteostasis
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description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Natalie J Spillman
@ast
Natalie J Spillman
@en
Natalie J Spillman
@es
Natalie J Spillman
@nl
Natalie J Spillman
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type
label
Natalie J Spillman
@ast
Natalie J Spillman
@en
Natalie J Spillman
@es
Natalie J Spillman
@nl
Natalie J Spillman
@sl
prefLabel
Natalie J Spillman
@ast
Natalie J Spillman
@en
Natalie J Spillman
@es
Natalie J Spillman
@nl
Natalie J Spillman
@sl
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P21
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P4012
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0000-0002-3454-1636