The chemotherapy of rodent malaira. XV. Fine-structural studies on the sporogonic stages of Plasmodium berghei following exposure to primaquine.
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Biomedical subjects
W Peters
Publications and source records attributed to W Peters.
The action of sulphonamide-folic reductase inhibitor combinations against normal and drug-resistant strains of rodent malaria.
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Theory for the mechanism of chloroquine resistance in rodent malaria.
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A new type of antimalarial drug potentiation.
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The antimalarial activity of some quinolone esters.
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Gametocytogenesis and cyclical transmission of drug-resistant Plasmodium berghei lines derived from Keyberg 173 strain.
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Drug sensitivity of exoerythrocytic stages of rodent malaria parasites.
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Action of chloroquine on infectivity of gametocytes of rodent malarias.
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The chemotherapy of rodent malaria. IX. Causal prophylaxis. I. A method for demonstrating drug action on exo-erythrocytic stages.
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The chemotherapy of rodent malaria. X. Dynamics of drug resistance. II. Acquisition and loss of chloroquine resistance in Plasmodium berghei observed by continuous bioassay.
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The chemotherapy of rodent malaria. XI. Cyclically transmitted, chloroquine-resistant variants of the Keyberg 173 strain of Plasmodium berghei.
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The chemotherapy of rodent malaria. XII. Substituted tetrahydrofurans, a new chemical family of antimalarials. The action of 2-(p-chlorophenyl)-2-(4-piperidyl)-tetrahydrofuran against Plasmodium berghei and Plasmodium chabaudi.
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Aminobenzoates↗
Partial inhibition by mepacrine of the development of sulphonamide resistance in Plasmodium berghei.
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Infectivity of chloroquine resistant Plasmodium berghei to Anopheles stephensi enhanced by chloroquine.
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The ultrastructural distribution of cytochrome oxidase activity in Plasmodium Berghei and P. Gallinaceum.
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Cytochemical observations on Plasmodium berghei and P. gallinaceum.
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Cytochrome oxidase activity in a normal and some drug-resistant strains of Plasmodium berghei--a cytochemical study. I. Asexual erythrocytic stages.
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