Malaria parasite-infected erythrocytes inhibit glucose utilization in uninfected red cells.
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1H NMR metabonomics indicates continued metabolic changes and sexual dimorphism post-parasite clearance in self-limiting murine malaria modelClinicopathological Analysis and Multipronged Quantitative Proteomics Reveal Oxidative Stress and Cytoskeletal Proteins as Possible Markers for Severe Vivax Malaria.Plasmodium falciparum enolase: stage-specific expression and sub-cellular localizationA lactate and formate transporter in the intraerythrocytic malaria parasite, Plasmodium falciparumThe Malaria Parasite's Lactate Transporter PfFNT Is the Target of Antiplasmodial Compounds Identified in Whole Cell Phenotypic ScreensAlterations in urine, serum and brain metabolomic profiles exhibit sexual dimorphism during malaria disease progression.Metabolomics and malaria biology1H-NMR metabolite profiles of different strains of Plasmodium falciparum.Liver Metabolic Alterations and Changes in Host Intercompartmental Metabolic Correlation during Progression of MalariaRegulation of extracellular ATP in human erythrocytes infected with Plasmodium falciparumSub-cellular localization and post-translational modifications of the Plasmodium yoelii enolase suggest moonlighting functionsGlobal host metabolic response to Plasmodium vivax infection: a 1H NMR based urinary metabonomic study.Functional genomics of Plasmodium falciparum using metabolic modelling and analysisDeciphering the Duality of Clock and Growth Metabolism in a Cell Autonomous System Using NMR Profiling of the Secretome.Global transformation of erythrocyte properties via engagement of an SH2-like sequence in band 3.The evolution of metabolic profiling in parasitology.Central carbon metabolism of Plasmodium parasites.Nuclear magnetic resonance-based analysis of urine for the rapid etiological diagnosis of pneumonia.Membrane transport in the malaria parasite and its host erythrocyte.Brucella abortus Induces a Warburg Shift in Host Metabolism That Is Linked to Enhanced Intracellular Survival of the Pathogen.Time is ripe: maturation of metabolomics in chronobiology.Replacement of Ser108 in Plasmodium falciparum enolase results in weak Mg(II) binding: role of a parasite-specific pentapeptide insert in stabilizing the active conformation of the enzyme.Clonal diversity within infections and the virulence of a malaria parasite, Plasmodium mexicanum.Differential susceptibility of Plasmodium falciparum versus yeast and mammalian enolases to dissociation into active monomers.
P2860
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P2860
Malaria parasite-infected erythrocytes inhibit glucose utilization in uninfected red cells.
description
2005 nî lūn-bûn
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2005年の論文
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2005年学术文章
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2005年学术文章
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2005年学术文章
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name
Malaria parasite-infected eryt ...... ation in uninfected red cells.
@en
Malaria parasite-infected eryt ...... ation in uninfected red cells.
@nl
type
label
Malaria parasite-infected eryt ...... ation in uninfected red cells.
@en
Malaria parasite-infected eryt ...... ation in uninfected red cells.
@nl
prefLabel
Malaria parasite-infected eryt ...... ation in uninfected red cells.
@en
Malaria parasite-infected eryt ...... ation in uninfected red cells.
@nl
P2860
P1433
P1476
Malaria parasite-infected eryt ...... ation in uninfected red cells.
@en
P2093
Haripalsingh M Sonawat
Monika Mehta
P2860
P304
P356
10.1016/J.FEBSLET.2005.09.088
P407
P577
2005-10-11T00:00:00Z