Similar Items: Target indicators and mechanistic function of epidrugs with activity against multiple stages of Plasmodium falciparum parasites
- Inhibition of the histone deacetylase family as a drug target in the human malaria parasite, plasmodium falciparum
- Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum
- Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum
- In silico prediction of host-pathogen protein - protein interactions in the malaria parasite, Plasmodium falciparum
- Dynamic bioinformatics and isotopic evaluation of the permeome of intraerythrocytic Plasmodium falciparum parasites
- High-content and super-resolution microscopy reveals the dynamic nuclear architecture and mobile epigenetic marks in Plasmodium falciparum
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