Mitochondrial metabolism of sexual and asexual blood stages of the malaria parasite Plasmodium falciparum. - Wikidata - wikimedia - TriplyDB

Mitochondrial metabolism of sexual and asexual blood stages of the malaria parasite Plasmodium falciparum.

Mitochondrial metabolism of sexual and asexual blood stages of the malaria parasite Plasmodium falciparum.

http://www.wikidata.org/entity/Q34771510

about

The metabolic roles of the endosymbiotic organelles of Toxoplasma and Plasmodium spp Ensuring transmission through dynamic host environments: host-pathogen interactions in Plasmodium sexual development A small mitochondrial protein present in myzozoans is essential for malaria transmission.Genetic investigation of tricarboxylic acid metabolism during the Plasmodium falciparum life cycle Deconvoluting heme biosynthesis to target blood-stage malaria parasites Characterization of Precursor PfHsp60 in Plasmodium falciparum Cytosol during Its Asexual Development in Human Erythrocytes Plasmodium falciparum glucose-6-phosphate dehydrogenase 6-phosphogluconolactonase is a potential drug target Stage-Specific Changes in Plasmodium Metabolism Required for Differentiation and Adaptation to Different Host and Vector Environments A flow cytometry-based quantitative drug sensitivity assay for all Plasmodium falciparum gametocyte stages Phosphoenolpyruvate carboxylase identified as a key enzyme in erythrocytic Plasmodium falciparum carbon metabolism BCKDH: the missing link in apicomplexan mitochondrial metabolism is required for full virulence of Toxoplasma gondii and Plasmodium berghei Host reticulocytes provide metabolic reservoirs that can be exploited by malaria parasites Biological characterization of chemically diverse compounds targeting the Plasmodium falciparum coenzyme A synthesis pathway Plasmodium falciparum is dependent on de novo myo-inositol biosynthesis for assembly of GPI glycolipids and infectivity The heme biosynthesis pathway is essential for Plasmodium falciparum development in mosquito stage but not in blood stages A lactate and formate transporter in the intraerythrocytic malaria parasite, Plasmodium falciparum The Malaria Parasite's Lactate Transporter PfFNT Is the Target of Antiplasmodial Compounds Identified in Whole Cell Phenotypic Screens Suppression of experimental cerebral malaria by disruption of malate:quinone oxidoreductase.Parasites resistant to the antimalarial atovaquone fail to transmit by mosquitoes Mitochondrial ATP synthase is dispensable in blood-stage Plasmodium berghei rodent malaria but essential in the mosquito phase Proteomics analysis of antimalarial targets of Garcinia mangostana Linn.Lysine acetylation in sexual stage malaria parasites is a target for antimalarial small molecules.A Novel Methodology for Bioenergetic Analysis of Plasmodium falciparum Reveals a Glucose-Regulated Metabolic Shift and Enables Mode of Action Analyses of Mitochondrial Inhibitors.Toxoplasma gondii is dependent on glutamine and alters migratory profile of infected host bone marrow derived immune cells through SNAT2 and CXCR4 pathways.1H-NMR metabolite profiles of different strains of Plasmodium falciparum.Changes in metabolic phenotypes of Plasmodium falciparum in vitro cultures during gametocyte development Identification of MMV malaria box inhibitors of plasmodium falciparum early-stage gametocytes using a luciferase-based high-throughput assay.Isoprenoid precursor biosynthesis is the essential metabolic role of the apicoplast during gametocytogenesis in Plasmodium falciparum.Antiapicoplast and gametocytocidal screening to identify the mechanisms of action of compounds within the malaria box.Antimalarial iron chelator FBS0701 blocks transmission by Plasmodium falciparum gametocyte activation inhibition.The newest "omics"--metagenomics and metabolomics--enter the battle against the neglected tropical diseases Probing the metabolic network in bloodstream-form Trypanosoma brucei using untargeted metabolomics with stable isotope labelled glucose Nowhere to hide: interrogating different metabolic parameters of Plasmodium falciparum gametocytes in a transmission blocking drug discovery pipeline towards malaria elimination.From METS to malaria: RRx-001, a multi-faceted anticancer agent with activity in cerebral malaria.Metabolic Signature Profiling as a Diagnostic and Prognostic Tool in Pediatric Plasmodium falciparum Malaria A novel targeted/untargeted GC-Orbitrap metabolomics methodology applied to Candida albicans and Staphylococcus aureus biofilms.Plasmodium berghei bio-burden correlates with parasite lactate dehydrogenase: application to murine Plasmodium diagnostics.The Effect of Aqueous Extract of Cinnamon on the Metabolome of Plasmodium falciparum Using (1)HNMR Spectroscopy.Metabolomic Profiling of the Malaria Box Reveals Antimalarial Target Pathways.Kinetic flux profiling elucidates two independent acetyl-CoA biosynthetic pathways in Plasmodium falciparum.

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Mitochondrial metabolism of sexual and asexual blood stages of the malaria parasite Plasmodium falciparum.

http://www.wikidata.org/entity/Q34771510

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2013 nî lūn-bûn

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P2860

Gametocytogenesis: the puberty of Plasmodium falciparum

Artemisinin and a Series of Novel Endoperoxide Antimalarials Exert Early Effects on Digestive Vacuole Morphology

Purification and characterization of branched chain alpha-keto acid dehydrogenase complex of bovine kidney

The signal sequence of exported protein-1 directs the green fluorescent protein to the parasitophorous vacuole of transfected malaria parasites

The malaria parasite Plasmodium falciparum has only one pyruvate dehydrogenase complex, which is located in the apicoplast

Origin, composition, organization and function of the inner membrane complex of Plasmodium falciparum gametocytes

Plasmodium falciparum glutamate dehydrogenase a is dispensable and not a drug target during erythrocytic development

Toward understanding the role of mitochondrial complex II in the intraerythrocytic stages of Plasmodium falciparum: gene targeting of the Fp subunit

Plasmodium falciparum biology: analysis of in vitro versus in vivo growth conditions

Global mass spectrometry based metabolomics profiling of erythrocytes infected with Plasmodium falciparum

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