Probing the multifactorial basis of Plasmodium falciparum quinine resistance: Evidence for a strain-specific contribution of the sodium-proton exchanger PfNHE
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Antimalarial Drug Resistance: Literature Review and Activities and Findings of the ICEMR NetworkPlasmodium falciparum susceptibility to antimalarial drugs: global data issued from the Pasteur Institutes international networkThe interplay between drug resistance and fitness in malaria parasitesApplication of genomics to field investigations of malaria by the international centers of excellence for malaria researchGlobal analysis of Plasmodium falciparum Na(+)/H(+) exchanger (pfnhe-1) allele polymorphism and its usefulness as a marker of in vitro resistance to quinineA HECT ubiquitin-protein ligase as a novel candidate gene for altered quinine and quinidine responses in Plasmodium falciparumIn vitro selection of Plasmodium falciparum drug-resistant parasite lines.In vitro sensitivities of Plasmodium falciparum to different antimalarial drugs in Uganda.Identification of inhibitors for putative malaria drug targets among novel antimalarial compounds.Analysis of malaria parasite phenotypes using experimental genetic crosses of Plasmodium falciparum.Polymorphisms in Pfmdr1, Pfcrt, and Pfnhe1 genes are associated with reduced in vitro activities of quinine in Plasmodium falciparum isolates from western KenyaAssociation of microsatellite variations of Plasmodium falciparum Na+/H+ exchanger (Pfnhe-1) gene with reduced in vitro susceptibility to quinine: lack of confirmation in clinical isolates from AfricaArtemisone effective against murine cerebral malariaIn vitro sensitivity of Plasmodium falciparum clinical isolates from the China-Myanmar border area to quinine and association with polymorphism in the Na+/H+ exchanger.Limited ability of Plasmodium falciparum pfcrt, pfmdr1, and pfnhe1 polymorphisms to predict quinine in vitro sensitivity or clinical effectiveness in UgandaPolymorphism of Plasmodium falciparum Na(+)/H(+) exchanger is indicative of a low in vitro quinine susceptibility in isolates from Viet Nam.Differential association of Plasmodium falciparum Na+/H+ exchanger polymorphism and quinine responses in field- and culture-adapted isolates of Plasmodium falciparum.Polymorphisms of the pfmdr1 but not the pfnhe-1 gene is associated with in vitro quinine sensitivity in Thai isolates of Plasmodium falciparumMalaria drug resistance: new observations and developments.Quinine treatment selects the pfnhe-1 ms4760-1 polymorphism in Malian patients with Falciparum malariaIn vitro susceptibility to quinine and microsatellite variations of the Plasmodium falciparum Na+/H+ exchanger transporter (Pfnhe-1) gene in 393 isolates from Dakar, SenegalMolecular and physiologic basis of quinoline drug resistance in Plasmodium falciparum malariaGancidin W, a potential low-toxicity antimalarial agent isolated from an endophytic Streptomyces SUK10Antimalarial drugs: modes of action and mechanisms of parasite resistance.How can we identify parasite genes that underlie antimalarial drug resistance?Drug-resistant malaria: molecular mechanisms and implications for public health.Know your enemy: understanding the role of PfCRT in drug resistance could lead to new antimalarial tactics.Harnessing genomics and genome biology to understand malaria biology.Membrane transport in the malaria parasite and its host erythrocyte.Recent advances in novel heterocyclic scaffolds for the treatment of drug-resistant malaria.Antimalarial Drug Resistance: A Threat to Malaria Elimination.Atorvastatin as a potential anti-malarial drug: in vitro synergy in combinational therapy with quinine against Plasmodium falciparum.In vitro susceptibility to quinine and microsatellite variations of the Plasmodium falciparum Na+/H+ exchanger (Pfnhe-1) gene: the absence of association in clinical isolates from the Republic of CongoInvestigating the activity of quinine analogues versus chloroquine resistant Plasmodium falciparum.Genetic linkage analyses redefine the roles of PfCRT and PfMDR1 in drug accumulation and susceptibility in Plasmodium falciparum.Quinine localizes to a non-acidic compartment within the food vacuole of the malaria parasite Plasmodium falciparum.Amodiaquine resistance in Plasmodium berghei is associated with PbCRT His95Pro mutation, loss of chloroquine, artemisinin and primaquine sensitivity, and high transcript levels of key transporters.
P2860
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P2860
Probing the multifactorial basis of Plasmodium falciparum quinine resistance: Evidence for a strain-specific contribution of the sodium-proton exchanger PfNHE
description
2009 nî lūn-bûn
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2009 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2009年の論文
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2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Probing the multifactorial bas ...... sodium-proton exchanger PfNHE
@ast
Probing the multifactorial bas ...... sodium-proton exchanger PfNHE
@en
Probing the multifactorial bas ...... sodium-proton exchanger PfNHE
@nl
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label
Probing the multifactorial bas ...... sodium-proton exchanger PfNHE
@ast
Probing the multifactorial bas ...... sodium-proton exchanger PfNHE
@en
Probing the multifactorial bas ...... sodium-proton exchanger PfNHE
@nl
prefLabel
Probing the multifactorial bas ...... sodium-proton exchanger PfNHE
@ast
Probing the multifactorial bas ...... sodium-proton exchanger PfNHE
@en
Probing the multifactorial bas ...... sodium-proton exchanger PfNHE
@nl
P2093
P2860
P1476
Probing the multifactorial bas ...... sodium-proton exchanger PfNHE
@en
P2093
David J Johnson
Jigar Patel
Karen Hayton
Louis J Nkrumah
Michael T Ferdig
Paul M Riegelhaupt
Pedro Moura
Thomas E Wellems
P2860
P304
P356
10.1016/J.MOLBIOPARA.2009.01.011
P577
2009-06-01T00:00:00Z