Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique
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Pfmdr1 copy number and arteminisin derivatives combination therapy failure in falciparum malaria in CambodiaMalarone treatment failure and in vitro confirmation of resistance of Plasmodium falciparum isolate from Lagos, NigeriaExpression in Yeast Links Field Polymorphisms in PfATP6 to in Vitro Artemisinin Resistance and Identifies New Inhibitor ClassesIdentification of an antimalarial synthetic trioxolane drug development candidateAntimalarial activities of peptide antibiotics isolated from fungiAlternative oxidase inhibitors potentiate the activity of atovaquone against Plasmodium falciparumThe traditional medicine Spilanthes acmella, and the alkylamides spilanthol and undeca-2E-ene-8,10-diynoic acid isobutylamide, demonstrate in vitro and in vivo antimalarial activityRecent advances in malaria parasite cultivation and their application to studies on host-parasite relationships: a reviewTetracyclines specifically target the apicoplast of the malaria parasite Plasmodium falciparumInhibition of Plasmodium falciparum choline kinase by hexadecyltrimethylammonium bromide: a possible antimalarial mechanismSynthesis and evaluation of febrifugine analogues as potential antimalarial agentsAnti-Plasmodium activity of ceramide analogsIn vitro antimalarial drug susceptibility in Thai border areas from 1998-2003.Assessment of Plasmodium falciparum resistance to ferroquine (SSR97193) in field isolates and in W2 strain under pressure.Therapeutic efficacy test in malaria falciparum in Antioquia, Colombia.Structural elucidation of the specificity of the antibacterial agent triclosan for malarial enoyl acyl carrier protein reductaseResistance mutations at the lipid substrate binding site of Plasmodium falciparum protein farnesyltransferaseX-ray structural analysis of Plasmodium falciparum enoyl acyl carrier protein reductase as a pathway toward the optimization of triclosan antimalarial efficacyExploiting Structural Analysis, in Silico Screening, and Serendipity To Identify Novel Inhibitors of Drug-Resistant Falciparum MalariaStructural and Metabolic Specificity of Methylthiocoformycin for Malarial Adenosine DeaminasesStructure-Guided Lead Optimization of Triazolopyrimidine-Ring Substituents Identifies Potent Plasmodium falciparum Dihydroorotate Dehydrogenase Inhibitors with Clinical Candidate PotentialThe bacterial redox signaller pyocyanin as an antiplasmodial agent: comparisons with its thioanalog methylene blueDesign and Synthesis of High Affinity Inhibitors of Plasmodium falciparum and Plasmodium vivax N -Myristoyltransferases Directed by Ligand Efficiency Dependent Lipophilicity (LELP)Synthesis and Evaluation of Novel Acyclic Nucleoside Phosphonates as Inhibitors of Plasmodium falciparum and Human 6-Oxopurine PhosphoribosyltransferasesA genomic and evolutionary approach reveals non-genetic drug resistance in malariaEvidence for a Central Role for PfCRT in Conferring Plasmodium falciparum Resistance to Diverse Antimalarial AgentsFunctional characterization and target validation of alternative complex I of Plasmodium falciparum mitochondriaBiochemical and structural characterization of the apicoplast dihydrolipoamide dehydrogenase of Plasmodium falciparumCharacterization of a Plasmodium falciparum Orthologue of the Yeast Ubiquinone-Binding Protein, Coq10pPlasmodium falciparum glutamate dehydrogenase a is dispensable and not a drug target during erythrocytic developmentModulation of PF10_0355 (MSPDBL2) alters Plasmodium falciparum response to antimalarial drugsCharacterization of Plasmodium falciparum adenylyl cyclase-β and its role in erythrocytic stage parasitesNa(+) regulation in the malaria parasite Plasmodium falciparum involves the cation ATPase PfATP4 and is a target of the spiroindolone antimalarialsApplication of multi-target phytotherapeutic concept in malaria drug discovery: a systems biology approach in biomarker identificationNovel biologically active bibenzyls from Bauhinia saccocalyx PierreHigh-throughput screening for small-molecule inhibitors of plasmodium falciparum glucose-6-phosphate dehydrogenase 6-phosphogluconolactonaseDiscovery of a Plasmodium falciparum glucose-6-phosphate dehydrogenase 6-phosphogluconolactonase inhibitor (R,Z)-N-((1-ethylpyrrolidin-2-yl)methyl)-2-(2-fluorobenzylidene)-3-oxo-3,4-dihydro-2H-benzo[b][1,4]thiazine-6-carboxamide (ML276) that reducesStructure-activity relationships of analogs of pentamidine against Plasmodium falciparum and Leishmania mexicana amazonensis8-Aminoquinolines active against blood stage Plasmodium falciparum in vitro inhibit hematin polymerizationA plant-derived morphinan as a novel lead compound active against malaria liver stages
P2860
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P2860
Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique
description
1979 nî lūn-bûn
@nan
1979 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1979 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
name
Quantitative assessment of ant ...... omated microdilution technique
@ast
Quantitative assessment of ant ...... omated microdilution technique
@en
type
label
Quantitative assessment of ant ...... omated microdilution technique
@ast
Quantitative assessment of ant ...... omated microdilution technique
@en
prefLabel
Quantitative assessment of ant ...... omated microdilution technique
@ast
Quantitative assessment of ant ...... omated microdilution technique
@en
P2093
P2860
P3181
P356
P1476
Quantitative assessment of ant ...... omated microdilution technique
@en
P2093
Canfield CJ
Desjardins RE
P2860
P3181
P356
10.1128/AAC.16.6.710
P407
P577
1979-12-01T00:00:00Z