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Karl H. Rieckmann

Researcher at University of New Mexico

Publications -  6
Citations -  290

Karl H. Rieckmann is an academic researcher from University of New Mexico. The author has contributed to research in topics: Plasmodium falciparum & Pyrimethamine. The author has an hindex of 5, co-authored 6 publications receiving 284 citations.

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Enzymes of purine and pyrimidine metabolism from the human malaria parasite, Plasmodium falciparum.

TL;DR: Two enzymes involved in the de novo synthesis of pyrimidines, orotic acid PRTase, and orotidine 5'-phosphate decarboxylase, were present in parasite extracts as were the enzymes for pyrimidine nucleotide phosphorylation.
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Plasmodium falciparum: isolation and purification of spontaneously released merozoites by nylon membrane sieves.

TL;DR: A new procedure for isolating spontaneously released merozoites from in vitro cultures of Plasmodium falciparum (FVO and FCB strains) is described and it is shown that purifiedmerozoite preparations will be invaluable for malaria immunization studies, for identification of protective antigens of P. falcIParum, and for other immunological and biochemical studies.
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In vitro microtechnique for determining the drug susceptibility of cultured parasites of Plasmodium falciparum

TL;DR: Studies were initiated with pyri- methamine and sulphadiazine in order to develop a system for monitoring the susceptibility of parasites to sulphonamide-pyrimethamine combinations, such as Fansidar, which are widely used in the treatment of chloroquine-resistant infections.
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The activity of pyrimethamine and sulphadoxine against Plasmodium falciparum determined by the in vitro microtechnique

TL;DR: Further studies are indicated to determine to what extent findings obtained with the in vitro microtechnique can be correlated with the response of falciparum infection to treatment with pyrimethamine-sulphadoxine combinations.
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A rabbit-in vitro system to evaluate drug action against Plasmodium falciparum

TL;DR: The results indicate that this rabbit-in vitro model system may be a useful system for identifying potential agents against drug-resistant falciparum malaria, particularly compounds which are converted in vitro to their active metabolites or which exert a prolonged suppressive activity after drug administration.