Dissecting the loci of low-level quinine resistance in malaria parasites.
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Challenges of drug-resistant malariaGenome scanning of Amazonian Plasmodium falciparum shows subtelomeric instability and clindamycin-resistant parasitesPlasmodium falciparum genome-wide scans for positive selection, recombination hot spots and resistance to antimalarial drugsComposite genome map and recombination parameters derived from three archetypal lineages of Toxoplasma gondii.The genetic map and comparative analysis with the physical map of Trypanosoma bruceiAssessment of Plasmodium falciparum resistance to ferroquine (SSR97193) in field isolates and in W2 strain under pressure.Antimalarial drug resistance: An overviewAntimalarial 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 quinineDisruption of a Plasmodium falciparum Multidrug Resistance-associated Protein (PfMRP) Alters Its Fitness and Transport of Antimalarial Drugs and GlutathioneA HECT ubiquitin-protein ligase as a novel candidate gene for altered quinine and quinidine responses in Plasmodium falciparumPfCRT and its role in antimalarial drug resistanceProbing the multifactorial basis of Plasmodium falciparum quinine resistance: Evidence for a strain-specific contribution of the sodium-proton exchanger PfNHEPlasmodium falciparum Na+/H+ Exchanger (pfnhe-1) Genetic Polymorphism in Indian Ocean Malaria-Endemic AreasModulation of PF10_0355 (MSPDBL2) alters Plasmodium falciparum response to antimalarial drugsA genome wide association study of Plasmodium falciparum susceptibility to 22 antimalarial drugs in KenyaCharacterization of drug resistance associated genetic polymorphisms among Plasmodium falciparum field isolates in Ujjain, Madhya Pradesh, IndiaAdvances in understanding the genetic basis of antimalarial drug resistanceRegulatory hotspots in the malaria parasite genome dictate transcriptional variationIdentification of a mutant PfCRT-mediated chloroquine tolerance phenotype in Plasmodium falciparumFunctional characterization of the Plasmodium falciparum chloroquine-resistance transporter (PfCRT) in transformed Dictyostelium discoideum vesiclesIn vitro sensitivity of Plasmodium falciparum from China-Myanmar border area to major ACT drugs and polymorphisms in potential target genesA process similar to autophagy is associated with cytocidal chloroquine resistance in Plasmodium falciparumPfCRT and PfMDR1 modulate interactions of artemisinin derivatives and ion channel blockersGeographic patterns of Plasmodium falciparum drug resistance distinguished by differential responses to amodiaquine and chloroquineDrug resistance in eukaryotic microorganisms.A database of antimalarial drug resistance.World Antimalarial Resistance Network (WARN) III: molecular markers for drug resistant malaria.A major genetic locus in Trypanosoma brucei is a determinant of host pathology.High-throughput Plasmodium falciparum growth assay for malaria drug discovery.Eating at the table of another: metabolomics of host-parasite interactions.Diverse mutational pathways converge on saturable chloroquine transport via the malaria parasite's chloroquine resistance transporterIn vitro sensitivities of Plasmodium falciparum to different antimalarial drugs in Uganda.Analysis of malaria parasite phenotypes using experimental genetic crosses of Plasmodium falciparum.Experimental evolution, genetic analysis and genome re-sequencing reveal the mutation conferring artemisinin resistance in an isogenic lineage of malaria parasites.Quantitative trait loci mapping reveals candidate pathways regulating cell cycle duration in Plasmodium falciparum.Quinine dimers are potent inhibitors of the Plasmodium falciparum chloroquine resistance transporter and are active against quinoline-resistant P. falciparum
P2860
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P2860
Dissecting the loci of low-level quinine resistance in malaria parasites.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Dissecting the loci of low-level quinine resistance in malaria parasites.
@en
type
label
Dissecting the loci of low-level quinine resistance in malaria parasites.
@en
prefLabel
Dissecting the loci of low-level quinine resistance in malaria parasites.
@en
P2093
P2860
P1476
Dissecting the loci of low-level quinine resistance in malaria parasites.
@en
P2093
Bingbing Deng
Deirdre A Joy
Jianbing Mu
Michael T Ferdig
Roland A Cooper
Thomas E Wellems
P2860
P304
P356
10.1111/J.1365-2958.2004.04035.X
P407
P50
P577
2004-05-01T00:00:00Z