Susceptibility of Plasmodium falciparum to five drugs: an in vitro study of isolates mainly from Thailand.
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Molecular characterisation of drug-resistant Plasmodium falciparum from ThailandIdentification of compounds with anti-proliferative activity against Trypanosoma brucei brucei strain 427 by a whole cell viability based HTS campaignMolecular characterization of Plasmodium falciparum uracil-DNA glycosylase and its potential as a new anti-malarial drug targetA comparative study of a flow-cytometry-based assessment of in vitro Plasmodium falciparum drug sensitivityA new nonpolar N-hydroxy imidazoline lead compound with improved activity in a murine model of late-stage Trypanosoma brucei brucei infection is not cross-resistant with diamidines.Plants as sources of antimalarial drugs: in vitro antimalarial activities of some quassinoidsArtemisinin effectiveness in erythrocytes is reduced by heme and heme-containing proteins.Biochemical and functional characterization of Plasmodium falciparum DNA polymerase δSimple, fast, and accurate fluorometric method to determine drug susceptibility of Plasmodium falciparum in 24-well suspension cultures.Synthesis of a potent antimalarial agent through natural products conjugation.Antiprotozoal activity of 1-phenethyl-4-aminopiperidine derivatives.Characterization of Plasmodium falciparum ATP-dependent DNA helicase RuvB3.Discovery and optimisation studies of antimalarial phenotypic hits.Quinine pharmacokinetics: ototoxic and cardiotoxic effects in healthy Caucasian subjects and in patients with falciparum malaria.5HT1A serotonin receptor agonists inhibit Plasmodium falciparum by blocking a membrane channel.Purification and characterization of a novel 3'-5' DNA helicase from Plasmodium falciparum and its sensitivity to anthracycline antibiotics.In vitro study of anticancer acridines as potential antitrypanosomal and antimalarial agents.Chloroquine susceptibility and reversibility in a Plasmodium falciparum genetic crossClones of different sensitivities in drug-resistant isolates of Plasmodium falciparum.[In vitro studies of the levels of resistance of Plasmodium falciparum to drugs from 1983 to 1986]The PfCRT (K76T) point mutation favours clone multiplicity and disease severity in Plasmodium falciparum infection.In vivo and in vitro Plasmodium falciparum resistance to chloroquine, amodiaquine and quinine in the Brazilian Amazon.
P2860
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P2860
Susceptibility of Plasmodium falciparum to five drugs: an in vitro study of isolates mainly from Thailand.
description
1983 nî lūn-bûn
@nan
1983年の論文
@ja
1983年論文
@yue
1983年論文
@zh-hant
1983年論文
@zh-hk
1983年論文
@zh-mo
1983年論文
@zh-tw
1983年论文
@wuu
1983年论文
@zh
1983年论文
@zh-cn
name
Susceptibility of Plasmodium f ...... isolates mainly from Thailand.
@ast
Susceptibility of Plasmodium f ...... isolates mainly from Thailand.
@en
type
label
Susceptibility of Plasmodium f ...... isolates mainly from Thailand.
@ast
Susceptibility of Plasmodium f ...... isolates mainly from Thailand.
@en
prefLabel
Susceptibility of Plasmodium f ...... isolates mainly from Thailand.
@ast
Susceptibility of Plasmodium f ...... isolates mainly from Thailand.
@en
P2093
P1476
Susceptibility of Plasmodium f ...... isolates mainly from Thailand.
@en
P2093
Chutmongkonkul M
Thaithong S
P304
P356
10.1016/0035-9203(83)90080-9
P577
1983-01-01T00:00:00Z