Structure-based drug discovery against a novel antimalarial drug target, S-adenosylmethionine decarboxylase/ornithine decarboxylase
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- Type
- dissertation
- Published
- 2013-04-25
- Cited by
- 2
- References
- 132
- Access
- Open access
- OpenAlex
- https://openalex.org/W177743095
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:82311532
Keywords
Ornithine decarboxylase, Drug, Pharmacology, Eflornithine, Drug discovery
References
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- Effect of drugs inhibiting spermidine biosynthesis and metabolism on the in vitro development of Plasmodium falciparum
- Plasmodium biology: genomic gleanings.
- Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase
- Molecular modeling elucidates parasite-specific features of polyamine pathway enzymes of Plasmodium falciparus
- Principles of early drug discovery
- The dihydrofolate reductase domain of Plasmodium falciparum thymidylate synthase-dihydrofolate reductase. Gene synthesis, expression, and anti-folate-resistant mutants.
- Molecular mechanisms of Plasmodium falciparum placental adhesion
- Cytoadhesion of Plasmodium falciparum ring-stage-infected erythrocytes
- Aquatic insect predators and mosquito control.
- Mutants of Escherichia coli that do not contain 1,4-diaminobutane (putrescine) or spermidine.
- Insecticide resistance issues in vector-borne disease control.
- Swedish traveller with Plasmodium knowlesi malaria after visiting Malaysian Borneo
- Over-production of lactate dehydrogenase from Plasmodium falciparum opens a route to new antimalarials
- Molecular genetics of polyamine synthesis in eukaryotic cells.
- A putrescine–anthracene conjugate: a paradigm for selective drug delivery
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