Choline uptake into the malaria parasite is energized by the membrane potential.
about
Polymorphism of the PEMT gene and susceptibility to nonalcoholic fatty liver disease (NAFLD)Inhibition of Plasmodium falciparum choline kinase by hexadecyltrimethylammonium bromide: a possible antimalarial mechanismMalaria parasite mutants with altered erythrocyte permeability: a new drug resistance mechanism and important molecular tool.Antimalarial drug targets in Plasmodium falciparum predicted by stage-specific metabolic network analysisTargeting the Lipid Metabolic Pathways for the Treatment of Malaria.A class of pantothenic acid analogs inhibits Plasmodium falciparum pantothenate kinase and represses the proliferation of malaria parasites1H-NMR metabolite profiles of different strains of Plasmodium falciparum.Potent antihematozoan activity of novel bisthiazolium drug T16: evidence for inhibition of phosphatidylcholine metabolism in erythrocytes infected with Babesia and Plasmodium spp.Metabolic host responses to malarial infection during the intraerythrocytic developmental cycleGenetic evidence for the essential role of PfNT1 in the transport and utilization of xanthine, guanine, guanosine and adenine by Plasmodium falciparumLipid metabolism in Trypanosoma bruceiCytometric measurement of in vitro inhibition of Plasmodium falciparum field isolates by drugs: a new approach for re-invasion inhibition study.Quaternary ammonium salts and their antimicrobial potential: targets or nonspecific interactions?Membrane transport in the malaria parasite and its host erythrocyte.Transport proteins of parasitic protists and their role in nutrient salvage.Rapid kill of malaria parasites by artemisinin and semi-synthetic endoperoxides involves ROS-dependent depolarization of the membrane potentialSequestration and metabolism of host cell arginine by the intraerythrocytic malaria parasite Plasmodium falciparum.Plasmodium falciparum Na+/H+ exchanger activity and quinine resistance.Characterisation of exogenous folate transport in Plasmodium falciparum.In vivo evidence for the specificity of Plasmodium falciparum phosphoethanolamine methyltransferase and its coupling to the Kennedy pathway.Modeling metabolism and stage-specific growth of Plasmodium falciparum HB3 during the intraerythrocytic developmental cycle.Feedback inhibition of pantothenate kinase regulates pantothenol uptake by the malaria parasite.
P2860
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P2860
Choline uptake into the malaria parasite is energized by the membrane potential.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh
2004年學術文章
@zh-hant
name
Choline uptake into the malaria parasite is energized by the membrane potential.
@en
Choline uptake into the malaria parasite is energized by the membrane potential.
@nl
type
label
Choline uptake into the malaria parasite is energized by the membrane potential.
@en
Choline uptake into the malaria parasite is energized by the membrane potential.
@nl
prefLabel
Choline uptake into the malaria parasite is energized by the membrane potential.
@en
Choline uptake into the malaria parasite is energized by the membrane potential.
@nl
P50
P1476
Choline uptake into the malaria parasite is energized by the membrane potential.
@en
P2093
Richard J W Allen
P304
P356
10.1016/J.BBRC.2004.05.164
P407
P577
2004-07-01T00:00:00Z