Plasmodium falciparum Na+/H+ exchanger activity and quinine resistance.
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sodium/hydrogen exchangersodium/hydrogen exchanger, putativesodium/hydrogen exchanger, putativesodium/hydrogen exchanger, putativesodium/hydrogen exchanger, putativesodium/hydrogen exchanger, putativesodium/hydrogen exchanger, putativesodium/hydrogen exchanger, putativesodium/hydrogen exchanger, putativesodium/hydrogen exchanger, putativesodium/hydrogen exchanger, putative
P1343
Genome scanning of Amazonian Plasmodium falciparum shows subtelomeric instability and clindamycin-resistant parasitesAntimalarial drug resistance: An overviewApplication 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 falciparumProbing the multifactorial basis of Plasmodium falciparum quinine resistance: Evidence for a strain-specific contribution of the sodium-proton exchanger PfNHEAdvances in understanding the genetic basis of antimalarial drug resistanceMalaria parasites tolerate a broad range of ionic environments and do not require host cation remodellingThe hydroxyl functionality and a rigid proximal N are required for forming a novel non-covalent quinine-heme complex.In vitro sensitivity of Plasmodium falciparum clinical isolates from the China-Myanmar border area to quinine and association with polymorphism in the Na+/H+ exchanger.Polymorphism of Plasmodium falciparum Na(+)/H(+) exchanger is indicative of a low in vitro quinine susceptibility in isolates from Viet Nam.Analysis of chloroquine resistance transporter (CRT) isoforms and orthologues in S. cerevisiae yeastDifferential association of Plasmodium falciparum Na+/H+ exchanger polymorphism and quinine responses in field- and culture-adapted isolates of Plasmodium falciparum.Mutation in the Plasmodium falciparum CRT protein determines the stereospecific activity of antimalarial cinchona alkaloids.Extensive genetic diversity in the Plasmodium falciparum Na+/H+ exchanger 1 transporter protein implicated in quinine resistanceQuinine treatment selects the pfnhe-1 ms4760-1 polymorphism in Malian patients with Falciparum malariaA Novel Polyclonal Antiserum against Toxoplasma gondii Sodium Hydrogen Exchanger 1.Plasmodium falciparum Na+/H+ exchanger 1 transporter is involved in reduced susceptibility to quinine.Molecular and physiologic basis of quinoline drug resistance in Plasmodium falciparum malariaWhy do malaria parasites increase host erythrocyte permeability?Antimalarial drugs: modes of action and mechanisms of parasite 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.Membrane transport in the malaria parasite and its host erythrocyte.Unexpected selections of Plasmodium falciparum polymorphisms in previously treatment-naïve areas after monthly presumptive administration of three different anti-malarial drugs in Liberia 1976-78.In vitro activity of ferroquine is independent of polymorphisms in transport protein genes implicated in quinoline resistance in Plasmodium falciparum.4-N-, 4-S-, and 4-O-chloroquine analogues: influence of side chain length and quinolyl nitrogen pKa on activity vs chloroquine resistant malaria.Investigating 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.Atorvastatin is a promising partner for antimalarial drugs in treatment of Plasmodium falciparum malariaP. falciparum Na(+)/H(+) exchanger (PfNHE) function and quinine resistance (QNR) [Reply to: Spillman et al. "Acid extrusion from the intraerythrocytic malaria parasite is not via a Na(+)/H(+) exchanger" Mol. Biochem. Parasitol. 2008 162 (1) 96-99].Dissecting the components of quinine accumulation in Plasmodium falciparum.Characterization of cerebral malaria in the outbred Swiss Webster mouse infected by Plasmodium berghei ANKA.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.Longitudinal surveillance of drug resistance in Plasmodium falciparum isolates from the China-Myanmar border reveals persistent circulation of multidrug resistant parasites
P2860
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P1343
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P2860
Plasmodium falciparum Na+/H+ exchanger activity and quinine resistance.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Plasmodium falciparum Na+/H+ exchanger activity and quinine resistance.
@en
type
label
Plasmodium falciparum Na+/H+ exchanger activity and quinine resistance.
@en
prefLabel
Plasmodium falciparum Na+/H+ exchanger activity and quinine resistance.
@en
P2093
P2860
P921
P1476
Plasmodium falciparum Na+/H+ exchanger activity and quinine resistance.
@en
P2093
Jigar Patel
Michael T Ferdig
Paul D Roepe
Tyler N Bennett
P2860
P356
10.1016/J.MOLBIOPARA.2007.01.018
P577
2007-02-08T00:00:00Z