Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique - Wikidata - awgldk - TriplyDB

Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique

Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique

http://www.wikidata.org/entity/Q29616826

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Pfmdr1 copy number and arteminisin derivatives combination therapy failure in falciparum malaria in Cambodia Malarone treatment failure and in vitro confirmation of resistance of Plasmodium falciparum isolate from Lagos, Nigeria Expression in Yeast Links Field Polymorphisms in PfATP6 to in Vitro Artemisinin Resistance and Identifies New Inhibitor Classes Identification of an antimalarial synthetic trioxolane drug development candidate Antimalarial activities of peptide antibiotics isolated from fungi Alternative oxidase inhibitors potentiate the activity of atovaquone against Plasmodium falciparum The traditional medicine Spilanthes acmella, and the alkylamides spilanthol and undeca-2E-ene-8,10-diynoic acid isobutylamide, demonstrate in vitro and in vivo antimalarial activity Recent advances in malaria parasite cultivation and their application to studies on host-parasite relationships: a review Tetracyclines specifically target the apicoplast of the malaria parasite Plasmodium falciparum Inhibition of Plasmodium falciparum choline kinase by hexadecyltrimethylammonium bromide: a possible antimalarial mechanism Synthesis and evaluation of febrifugine analogues as potential antimalarial agents Anti-Plasmodium activity of ceramide analogs In 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 reductase Resistance mutations at the lipid substrate binding site of Plasmodium falciparum protein farnesyltransferase X-ray structural analysis of Plasmodium falciparum enoyl acyl carrier protein reductase as a pathway toward the optimization of triclosan antimalarial efficacy Exploiting Structural Analysis, in Silico Screening, and Serendipity To Identify Novel Inhibitors of Drug-Resistant Falciparum Malaria Structural and Metabolic Specificity of Methylthiocoformycin for Malarial Adenosine Deaminases Structure-Guided Lead Optimization of Triazolopyrimidine-Ring Substituents Identifies Potent Plasmodium falciparum Dihydroorotate Dehydrogenase Inhibitors with Clinical Candidate Potential The bacterial redox signaller pyocyanin as an antiplasmodial agent: comparisons with its thioanalog methylene blue Design 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 Phosphoribosyltransferases A genomic and evolutionary approach reveals non-genetic drug resistance in malaria Evidence for a Central Role for PfCRT in Conferring Plasmodium falciparum Resistance to Diverse Antimalarial Agents Functional characterization and target validation of alternative complex I of Plasmodium falciparum mitochondria Biochemical and structural characterization of the apicoplast dihydrolipoamide dehydrogenase of Plasmodium falciparum Characterization of a Plasmodium falciparum Orthologue of the Yeast Ubiquinone-Binding Protein, Coq10p Plasmodium falciparum glutamate dehydrogenase a is dispensable and not a drug target during erythrocytic development Modulation of PF10_0355 (MSPDBL2) alters Plasmodium falciparum response to antimalarial drugs Characterization of Plasmodium falciparum adenylyl cyclase-β and its role in erythrocytic stage parasites Na(+) regulation in the malaria parasite Plasmodium falciparum involves the cation ATPase PfATP4 and is a target of the spiroindolone antimalarials Application of multi-target phytotherapeutic concept in malaria drug discovery: a systems biology approach in biomarker identification Novel biologically active bibenzyls from Bauhinia saccocalyx Pierre High-throughput screening for small-molecule inhibitors of plasmodium falciparum glucose-6-phosphate dehydrogenase 6-phosphogluconolactonase Discovery 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 reduces Structure-activity relationships of analogs of pentamidine against Plasmodium falciparum and Leishmania mexicana amazonensis 8-Aminoquinolines active against blood stage Plasmodium falciparum in vitro inhibit hematin polymerization A 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

http://www.wikidata.org/entity/Q29616826

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1979 nî lūn-bûn

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1979 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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1979 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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1979年の論文

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1979年論文

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1979年論文

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1979年論文

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1979年論文

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1979年論文

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1979年论文

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Quantitative assessment of ant ...... omated microdilution technique

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Quantitative assessment of ant ...... omated microdilution technique

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Antimicrobial Agents and Chemotherapy

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Quantitative assessment of ant ...... omated microdilution technique

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Canfield CJ

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Chulay JD

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Desjardins RE

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Haynes JD

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P2860

Human malaria parasites in continuous culture

Antimalarial activities of various 4-quinolonemethanols with special attention to WR-142,490 (mefloquine)

Activities of various 4-aminoquinolines against infections with chloroquine-resistant strains of Plasmodium falciparum.

A quinoline methanol (WR 30090) for treatment of acute malaria

Drug sensitivity of plasmodium falciparum. An in-vitro microtechnique.

Plasmodium falciparum and Plasmodium vivax infections in the owl monkey (Aotus trivirgatus). III. Methods employed in the search for new blood schizonticidal drugs.

Evaluation of two phenanthrenemethanols for antimalarial activity in man: WR 122,455 and WR 171,669.

Mefloquine (WR 142,490) in the treatment of human malaria.

Chloroquine-resistant falciparum malaria from Africa.

The chemotherapy of rodent malaria, XXII. The value of drug-resistant strains of P. berghei in screening for blood schizontocidal activity.

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710-8

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scholarly article

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17482

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10.1128/AAC.16.6.710

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6

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16

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394674

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352941

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