Similar Items: Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum
- Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum
- Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism
- Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum
- Functional genomics analysis of the effects of co-inhibition of the malarial S-adenosylmethionine decarboxylase/ornithine decarboxylase
- Inhibition of the histone deacetylase family as a drug target in the human malaria parasite, plasmodium falciparum
- Target indicators and mechanistic function of epidrugs with activity against multiple stages of Plasmodium falciparum parasites
Author: Birkholtz, Lyn-Marie
- Target indicators and mechanistic function of epidrugs with activity against multiple stages of Plasmodium falciparum parasites
- Targeted inhibition of the Plasmodium falciparum Vitamin B6 producing enzyme Pdx1 and the biochemical and functional consequences thereof
- Proteolysis-targeting chimeras as a novel strategy for targeting epigenetic mechanisms in Plasmodium falciparum parasites
- Novel acid-labile and targeted nanoparticles as possible antimalarial drug delivery systems
- Integrative transcriptome and phenome analysis reveal unique regulatory cascades controlling the intraerythrocytic asexual and sexual development of human malaria parasites
- Machine learning and network-based approaches unveil key aspects of gene regulation that drive Plasmodium falciparum pathogenesis