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P50 | author | Daouda Ndiaye | Q28870686 |
Philip J Rosenthal | Q60060211 | ||
Liwang Cui | Q60429811 | ||
Pradipsinh K. Rathod | Q88838215 | ||
P2093 | author name string | Sungano Mharakurwa | |
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Selection of parasites with diminished drug susceptibility by amodiaquine-containing antimalarial regimens in Uganda | Q37436582 | ||
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Prevalence of polymorphisms in antifolate drug resistance molecular marker genes pvdhfr and pvdhps in clinical isolates of Plasmodium vivax from Kolkata, India | Q37544364 | ||
Selection for mefloquine resistance in Plasmodium falciparum is linked to amplification of the pfmdr1 gene and cross-resistance to halofantrine and quinine | Q37559063 | ||
Changes in drug sensitivity and anti-malarial drug resistance mutations over time among Plasmodium falciparum parasites in Senegal | Q37583332 | ||
Validation of the ligase detection reaction fluorescent microsphere assay for the detection of Plasmodium falciparum resistance mediating polymorphisms in Uganda | Q37731834 | ||
Transporters as mediators of drug resistance in Plasmodium falciparum | Q37732867 | ||
The ABCs of multidrug resistance in malaria | Q37764523 | ||
The role of antimalarial treatment in the elimination of malaria | Q37939421 | ||
The P-glycoprotein multidrug transporter. | Q37941756 | ||
Mapping 'partially resistant', 'fully resistant', and 'super resistant' malaria | Q38136762 | ||
Combination therapy for uncomplicated falciparum malaria in Ugandan children: a randomized trial | Q38397102 | ||
Artemether-lumefantrine versus amodiaquine plus sulfadoxine-pyrimethamine for uncomplicated falciparum malaria in Burkina Faso: a randomised non-inferiority trial | Q38399521 | ||
Evidence that a point mutation in dihydrofolate reductase-thymidylate synthase confers resistance to pyrimethamine in falciparum malaria | Q27861937 | ||
PfCRT and its role in antimalarial drug resistance | Q27861957 | ||
Probing the multifactorial basis of Plasmodium falciparum quinine resistance: Evidence for a strain-specific contribution of the sodium-proton exchanger PfNHE | Q27861959 | ||
Polymorphisms in K13 and Falcipain-2 Associated with Artemisinin Resistance Are Not Prevalent in Plasmodium falciparum Isolated from Ugandan Children | Q27861962 | ||
Na(+) regulation in the malaria parasite Plasmodium falciparum involves the cation ATPase PfATP4 and is a target of the spiroindolone antimalarials | Q27976482 | ||
Temporal changes in prevalence of molecular markers mediating antimalarial drug resistance in a high malaria transmission setting in Uganda | Q28125904 | ||
Intermittent preventive treatment of malaria provides substantial protection against malaria in children already protected by an insecticide-treated bednet in Burkina Faso: a randomised, double-blind, placebo-controlled trial | Q28477053 | ||
A head-to-head comparison of four artemisinin-based combinations for treating uncomplicated malaria in African children: a randomized trial | Q28477853 | ||
Effect of transmission reduction by insecticide-treated bednets (ITNs) on antimalarial drug resistance in western Kenya | Q28477925 | ||
Novel polymorphisms in Plasmodium falciparum ABC transporter genes are associated with major ACT antimalarial drug resistance | Q28478286 | ||
In vitro sensitivity of Plasmodium falciparum from China-Myanmar border area to major ACT drugs and polymorphisms in potential target genes | Q28484068 | ||
Pyrazoleamide compounds are potent antimalarials that target Na+ homeostasis in intraerythrocytic Plasmodium falciparum | Q28649962 | ||
Mutations in the P. falciparum digestive vacuole transmembrane protein PfCRT and evidence for their role in chloroquine resistance | Q29615118 | ||
Mefloquine resistance in Plasmodium falciparum and increased pfmdr1 gene copy number | Q29615128 | ||
A P-glycoprotein homologue of Plasmodium falciparum is localized on the digestive vacuole | Q30039339 | ||
The malaria parasite's chloroquine resistance transporter is a member of the drug/metabolite transporter superfamily | Q30041677 | ||
Absence of putative artemisinin resistance mutations among Plasmodium falciparum in Sub-Saharan Africa: a molecular epidemiologic study | Q30389796 | ||
A better resolution for integrating methods for monitoring Plasmodium falciparum resistance to antimalarial drugs | Q30486953 | ||
Diverse chemotypes disrupt ion homeostasis in the Malaria parasite | Q30487225 | ||
(+)-SJ733, a clinical candidate for malaria that acts through ATP4 to induce rapid host-mediated clearance of Plasmodium. | Q30610467 | ||
Artesunate versus quinine for treatment of severe falciparum malaria: a randomised trial | Q33222370 | ||
Artemisinin combination therapies for treatment of uncomplicated malaria in Uganda | Q33251914 | ||
Effect of sulfadoxine-pyrimethamine resistance on the efficacy of intermittent preventive therapy for malaria control during pregnancy: a systematic review | Q33288230 | ||
Multidrug-resistant Plasmodium vivax associated with severe and fatal malaria: a prospective study in Papua, Indonesia | Q33344900 | ||
No seasonal accumulation of resistant P. falciparum when high-dose chloroquine is used | Q33498521 | ||
Seasonal distribution of anti-malarial drug resistance alleles on the island of Sumba, Indonesia | Q33507449 | ||
A non-radioactive DAPI-based high-throughput in vitro assay to assess Plasmodium falciparum responsiveness to antimalarials--increased sensitivity of P. falciparum to chloroquine in Senegal | Q33617554 | ||
In vitro sensitivities of Plasmodium falciparum to different antimalarial drugs in Uganda | Q33676088 | ||
Amino acid changes linked to pyrimethamine resistance in the dihydrofolate reductase-thymidylate synthase gene of Plasmodium falciparum | Q33680054 | ||
Efficacy of amodiaquine, sulphadoxine-pyrimethamine and their combination for the treatment of uncomplicated Plasmodium falciparum malaria in children in Cameroon at the time of policy change to artemisinin-based combination therapy | Q33702580 | ||
Association 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 Africa | Q33817484 | ||
Malaria antifolate resistance with contrasting Plasmodium falciparum dihydrofolate reductase (DHFR) polymorphisms in humans and Anopheles mosquitoes | Q35558706 | ||
Impact of antimalarial treatment and chemoprevention on the drug sensitivity of malaria parasites isolated from ugandan children | Q35607844 | ||
Amodiaquine and artemether-lumefantrine select distinct alleles of the Plasmodium falciparum mdr1 gene in Tanzanian children treated for uncomplicated malaria. | Q35647706 | ||
Common origin and fixation of Plasmodium falciparum dhfr and dhps mutations associated with sulfadoxine-pyrimethamine resistance in a low-transmission area in South America | Q35840784 | ||
Resistance-mediating Plasmodium falciparum pfcrt and pfmdr1 alleles after treatment with artesunate-amodiaquine in Uganda | Q35912645 | ||
A major genome region underlying artemisinin resistance in malaria | Q35969854 | ||
Plasmodium falciparum transmission rate and selection for drug resistance: a vexed association or a key to successful control? | Q35975158 | ||
The impact of antimalarial drug resistance mutations on parasite fitness, and its implications for the evolution of resistance. | Q36153724 | ||
Mechanisms of in vitro resistance to dihydroartemisinin in Plasmodium falciparum | Q36269058 | ||
Assessment of the molecular marker of Plasmodium falciparum chloroquine resistance (Pfcrt) in Senegal after several years of chloroquine withdrawal | Q36450797 | ||
Clinical Efficacy of Dihydroartemisinin-Piperaquine for the Treatment of Uncomplicated Plasmodium falciparum Malaria at the China-Myanmar Border | Q36485224 | ||
Genetic loci associated with delayed clearance of Plasmodium falciparum following artemisinin treatment in Southeast Asia | Q36512312 | ||
Reduced artemisinin susceptibility of Plasmodium falciparum ring stages in western Cambodia | Q36558472 | ||
Selection of known Plasmodium falciparum resistance-mediating polymorphisms by artemether-lumefantrine and amodiaquine-sulfadoxine-pyrimethamine but not dihydroartemisinin-piperaquine in Burkina Faso | Q33826359 | ||
Resistance to chloroquine unhinges vivax malaria therapeutics | Q33839067 | ||
Plasmodium falciparum multidrug resistance protein 1 (pfmrp1) gene and its association with in vitro drug susceptibility of parasite isolates from north-east Myanmar | Q33910002 | ||
Comparative impacts over 5 years of artemisinin-based combination therapies on Plasmodium falciparum polymorphisms that modulate drug sensitivity in Ugandan children | Q33947834 | ||
Independent origin of plasmodium falciparum antifolate super-resistance, Uganda, Tanzania, and Ethiopia | Q33950981 | ||
Spiroindolone KAE609 for falciparum and vivax malaria | Q34085717 | ||
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 | Q34151002 | ||
Transporters involved in resistance to antimalarial drugs. | Q34151405 | ||
Differential prevalence of transporter polymorphisms in symptomatic and asymptomatic falciparum malaria infections in Uganda | Q34169765 | ||
Chloroquine resistance in Plasmodium falciparum malaria parasites conferred by pfcrt mutations | Q34198094 | ||
Compensatory mutations restore fitness during the evolution of dihydrofolate reductase | Q34310777 | ||
Different allele prevalence in the dihydrofolate reductase and dihydropteroate synthase genes in Plasmodium vivax populations from China | Q34341770 | ||
Plasmodium prevalence and artemisinin-resistant falciparum malaria in Preah Vihear Province, Cambodia: a cross-sectional population-based study | Q34354821 | ||
Piperaquine: a resurgent antimalarial drug. | Q34378146 | ||
Anti-malarial drugs and the prevention of malaria in the population of malaria endemic areas | Q34407217 | ||
Drug resistance. Population transcriptomics of human malaria parasites reveals the mechanism of artemisinin resistance | Q34453540 | ||
Limited ability of Plasmodium falciparum pfcrt, pfmdr1, and pfnhe1 polymorphisms to predict quinine in vitro sensitivity or clinical effectiveness in Uganda | Q34529355 | ||
Artemisinin-based combination treatment of falciparum malaria. | Q34731529 | ||
Burden of complicated malaria in a densely forested Bastar region of Chhattisgarh State (Central India). | Q34757045 | ||
Molecular epidemiology of Plasmodium vivax anti-folate resistance in India | Q34995136 | ||
Multiple origins of Plasmodium falciparum dihydropteroate synthetase mutant alleles associated with sulfadoxine resistance in India | Q35005151 | ||
Discovery, mechanisms of action and combination therapy of artemisinin | Q35006418 | ||
Polymorphism of Plasmodium falciparum Na(+)/H(+) exchanger is indicative of a low in vitro quinine susceptibility in isolates from Viet Nam. | Q35069374 | ||
High frequency of Plasmodium falciparum chloroquine resistance marker (pfcrt T76 mutation) in Yemen: an urgent need to re-examine malaria drug policy | Q35074416 | ||
Harnessing evolutionary fitness in Plasmodium falciparum for drug discovery and suppressing resistance | Q35079297 | ||
Malaria drug-sensitivity testing: new assays, new perspectives | Q35104740 | ||
Therapeutic responses of Plasmodium vivax malaria to chloroquine and primaquine treatment in northeastern Myanmar | Q35105826 | ||
Drug resistance. K13-propeller mutations confer artemisinin resistance in Plasmodium falciparum clinical isolates | Q35146682 | ||
Combining indoor residual spraying and insecticide-treated nets for malaria control in Africa: a review of possible outcomes and an outline of suggestions for the future | Q35163863 | ||
Prolonged selection of pfmdr1 polymorphisms after treatment of falciparum malaria with artemether-lumefantrine in Uganda | Q35188480 | ||
Multidrug-resistant genotypes of Plasmodium falciparum, Myanmar | Q35193462 | ||
Spread of artemisinin-resistant Plasmodium falciparum in Myanmar: a cross-sectional survey of the K13 molecular marker | Q35217991 | ||
Structure and function of efflux pumps that confer resistance to drugs | Q35294152 | ||
A thirteen-year analysis of Plasmodium falciparum populations reveals high conservation of the mutant pfcrt haplotype despite the withdrawal of chloroquine from national treatment guidelines in Gabon | Q35549781 | ||
Fansidar-resistant falciparum malaria in Papua New Guinea. | Q54539949 | ||
Experiment to determine if a proguanil-resistant strain of P. falciparum would respond to large doses of pyrimethamine. | Q55502424 | ||
Evolution of drug-resistance genes in Plasmodium falciparum in an area of seasonal malaria transmission in Eastern Sudan | Q38855059 | ||
Large differences in prevalence of Pfcrt and Pfmdr1 mutations between Mwanza, Tanzania and Iganga, Uganda-a reflection of differences in policies regarding withdrawal of chloroquine? | Q38868907 | ||
Increased sensitivity to the antimalarials mefloquine and artemisinin is conferred by mutations in the pfmdr1 gene of Plasmodium falciparum | Q38980049 | ||
The tyrosine-86 allele of the pfmdr1 gene of Plasmodium falciparum is associated with increased sensitivity to the anti-malarials mefloquine and artemisinin | Q38980054 | ||
Fitness costs of resistance to antimalarial drugs | Q39001694 | ||
High prevalence of markers for sulfadoxine and pyrimethamine resistance in Plasmodium falciparum in the absence of drug pressure in the Ashanti region of Ghana | Q39215959 | ||
Recovery of chloroquine sensitivity and low prevalence of the Plasmodium falciparum chloroquine resistance transporter gene mutation K76T following the discontinuance of chloroquine use in Malawi | Q39254734 | ||
Seasonal carriage of pfcrt and pfmdr1 alleles in Gambian Plasmodium falciparum imply reduced fitness of chloroquine-resistant parasites | Q39326401 | ||
Prevalence of sulfadoxine-pyrimethamine resistance-associated mutations in dhfr and dhps genes of Plasmodium falciparum three years after SP withdrawal in Bahir Dar, Northwest Ethiopia | Q39346727 | ||
Plasmodium falciparum pfmdr1 amplification, mefloquine resistance, and parasite fitness | Q39367622 | ||
Quinine in severe falciparum malaria: evidence of declining efficacy in Thailand | Q39370966 | ||
Intercontinental spread of pyrimethamine-resistant malaria | Q39408056 | ||
Mutations in Plasmodium falciparum cytochrome b that are associated with atovaquone resistance are located at a putative drug-binding site | Q39474607 | ||
Monitoring chloroquine resistance using Plasmodium falciparum parasites isolated from wild mosquitoes in Tanzania. | Q39516937 | ||
Screening for mutations related to atovaquone/proguanil resistance in treatment failures and other imported isolates of Plasmodium falciparum in Europe | Q39591275 | ||
Resistance to antimalarials in Southeast Asia and genetic polymorphisms in pfmdr1. | Q39792488 | ||
Response of Kampuchean strains of Plasmodium falciparum to antimalarials: in-vivo assessment of quinine and quinine plus tetracycline; multiple drug resistance in vitro | Q40784576 | ||
Drug-resistant falciparum malaria among the Mayongong Indians in the Brazilian Amazon | Q41103268 | ||
Decreased prevalence of Plasmodium falciparum resistance markers to amodiaquine despite its wide scale use as ACT partner drug in Zanzibar | Q41827965 | ||
Deamplification of pfmdr1-containing amplicon on chromosome 5 in Plasmodium falciparum is associated with reduced resistance to artelinic acid in vitro | Q41846791 | ||
pfmdr1 mutations contribute to quinine resistance and enhance mefloquine and artemisinin sensitivity in Plasmodium falciparum | Q41911870 | ||
A critical role for PfCRT K76T in Plasmodium falciparum verapamil-reversible chloroquine resistance. | Q41912137 | ||
Evidence of increased chloroquine sensitivity in Thai isolates of Plasmodium falciparum | Q41912797 | ||
Dissecting the loci of low-level quinine resistance in malaria parasites | Q41914069 | ||
The principal chloroquine resistance protein of Plasmodium falciparum is a member of the drug/metabolite transporter superfamily | Q41914784 | ||
Multiple transporters associated with malaria parasite responses to chloroquine and quinine | Q41915501 | ||
Reemergence of chloroquine-sensitive Plasmodium falciparum malaria after cessation of chloroquine use in Malawi | Q41915777 | ||
Resistance of Plasmodium falciparum malaria to sulfadoxine-pyrimethamine ('Fansidar') in a refugee camp in Thailand | Q41925042 | ||
Atovaquone, a broad spectrum antiparasitic drug, collapses mitochondrial membrane potential in a malarial parasite | Q41929069 | ||
Changes in genotypes of Plasmodium falciparum human malaria parasite following withdrawal of chloroquine in Tiwi, Kenya | Q41929428 | ||
In vitro activities of quinine and other antimalarials and pfnhe polymorphisms in Plasmodium isolates from Kenya | Q41935745 | ||
Sensitivity of Plasmodium vivax to chloroquine in Laza City, Myanmar | Q41937411 | ||
In vitro activities of piperaquine, lumefantrine, and dihydroartemisinin in Kenyan Plasmodium falciparum isolates and polymorphisms in pfcrt and pfmdr1. | Q41937598 | ||
Innate resistance to new antimalarial drugs in Plasmodium falciparum from Nigeria | Q41940520 | ||
Selection of Plasmodium falciparum multidrug resistance gene 1 alleles in asexual stages and gametocytes by artemether-lumefantrine in Nigerian children with uncomplicated falciparum malaria | Q41940547 | ||
Pyrimethamine-resistant dihydrofolate reductase enzymes of Plasmodium falciparum are not enzymatically compromised in vitro | Q41943140 | ||
Several alleles of the multidrug-resistance gene are closely linked to chloroquine resistance in Plasmodium falciparum | Q41943905 | ||
Amino acid mutations in Plasmodium vivax DHFR and DHPS from several geographical regions and susceptibility to antifolate drugs | Q41944385 | ||
Decreasing pfmdr1 copy number in plasmodium falciparum malaria heightens susceptibility to mefloquine, lumefantrine, halofantrine, quinine, and artemisinin | Q41944932 | ||
Association between the pfmdr1 gene and in vitro artemether and lumefantrine sensitivity in Thai isolates of Plasmodium falciparum. | Q42072395 | ||
Border malaria associated with multidrug resistance on Thailand-Myanmar and Thailand-Cambodia borders: transmission dynamic, vulnerability, and surveillance | Q42181962 | ||
Structural features of Plasmodium cytochrome b that may underlie susceptibility to 8-aminoquinolines and hydroxynaphthoquinones | Q42620844 | ||
Plasmodium falciparum multidrug resistance protein 1 and artemisinin-based combination therapy in Africa | Q42635798 | ||
Intermittent preventive therapy for malaria in pregnancy: is sulfadoxine-pyrimethamine the right drug? | Q43182467 | ||
Increasing prevalence of wildtypes in the dihydrofolate reductase gene of Plasmodium falciparum in an area with high levels of sulfadoxine/pyrimethamine resistance after introduction of treated bed nets | Q43949108 | ||
In vivo selection of Plasmodium falciparum pfmdr1 86N coding alleles by artemether-lumefantrine (Coartem). | Q45270651 | ||
Fansidar resistant falciparum malaria in Indonesia | Q47824731 | ||
Dihydroartemisinin-piperaquine failure in Cambodia | Q47877123 | ||
Seasonal fluctuation of drug-resistant malaria parasites: a sign of fitness cost | Q47909648 | ||
Studies in human malaria. XXXIV. Acquired resistance to pyrimethamine (daraprim) by the Chesson strain of plasmodium vivax | Q47940624 | ||
Clinical atovaquone-proguanil resistance of Plasmodium falciparum associated with cytochrome b codon 268 mutations | Q48035243 | ||
P275 | copyright license | Creative Commons Attribution | Q6905323 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 3 Suppl | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | antimalarial | Q521616 |
malaria | Q12156 | ||
drug resistance | Q12147416 | ||
P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
P304 | page(s) | 57-68 | |
P577 | publication date | 2015-09-01 | |
P1433 | published in | American Journal of Tropical Medicine and Hygiene | Q15766943 |
P1476 | title | Antimalarial Drug Resistance: Literature Review and Activities and Findings of the ICEMR Network | |
P478 | volume | 93 |
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