All Stories

  1. Artemisone and Artemiside Are Potent Panreactive Antimalarial Agents That Also Synergize Redox Imbalance in Plasmodium falciparum Transmissible Gametocyte Stages
  2. Interrogating alkyl and arylalkylpolyamino (bis)urea and (bis)thiourea isosteres as potent antimalarial chemotypes against multiple lifecycle forms of Plasmodium falciparum parasites
  3. Synthesis and in vitro biological evaluation of dihydroartemisinyl-chalcone esters
  4. A novel inhibitor of Plasmodium falciparum spermidine synthase: a twist in the tail
  5. Differential activity of novel gametocytocidal compounds: drug mode-of-action and ex vivo efficacy
  6. Novel S-adenosyl-L-methionine decarboxylase inhibitors as potent antiproliferative agents against intraerythrocytic Plasmodium falciparum parasites
  7. Discovery of Compounds Blocking the Proliferation of Toxoplasma gondii and Plasmodium falciparum in a Chemical Space Based on Piperidinyl-Benzimidazolone Analogs
  8. 17-beta-estradiol analog inhibits cell proliferation by induction of apoptosis in breast cell lines
  9. Anthracene-Polyamine Conjugates InhibitIn VitroProliferation of Intraerythrocytic Plasmodium falciparum Parasites
  10. Polyamine Metabolism
  11. Exploring inhibition of Pdx1, a component of the PLP synthase complex of the human malaria parasite Plasmodium falciparum
  12. Sustainable malaria control: transdisciplinary approaches for translational applications
  13. Polyamine uptake by the intraerythrocytic malaria parasite, Plasmodium falciparum
  14. Inhibition of p-Aminobenzoate and Folate Syntheses in Plants and Apicomplexan Parasites by Natural Product Rubreserine
  15. The structure of Plasmodium falciparum spermidine synthase in complex with 5'-methylthioadenosine and N-(3-aminopropyl)-trans-cyclohexane-1,4-diamine
  16. Thermo‐responsive non‐woven scaffolds for “smart” 3D cell culture
  17. Biochemical characterisation and novel classification of monofunctional S-adenosylmethionine decarboxylase of Plasmodium falciparum
  18. Discovery of Novel Alkylated (bis)Urea and (bis)Thiourea Polyamine Analogues with Potent Antimalarial Activities
  19. Polyamine homoeostasis as a drug target in pathogenic protozoa: peculiarities and possibilities
  20. Polyamine uptake in the malaria parasite, Plasmodium falciparum, is dependent on the parasite's membrane potential
  21. Polyamine uptake in the malaria parasite, Plasmodium falciparum, is dependent on the parasite's membrane potential
  22. Proteomic Profiling of Plasmodium falciparum through Improved, Semiquantitative Two-Dimensional Gel Electrophoresis
  23. Plasmodium falciparum spermidine synthase inhibition results in unique perturbation-specific effects observed on transcript, protein and metabolite levels
  24. Functional consequences of perturbing polyamine metabolism in the malaria parasite, Plasmodium falciparum
  25. In silico Discovery of Chemotherapeutic Agents
  26. Antimalarial Drug Discovery: In Silico Structural Biology and Rational Drug Design
  27. Co-inhibition of Plasmodium falciparum S-Adenosylmethionine Decarboxylase/Ornithine Decarboxylase Reveals Perturbation-specific Compensatory Mechanisms by Transcriptome, Proteome, and Metabolome Analyses
  28. Transcriptional responses of Plasmodium falciparum to α-difluoromethylornithine-induced polyamine depletion
  29. Exploring functional genomics for drug target and therapeutics discovery in Plasmodia
  30. Heterologous expression of plasmodial proteins for structural studies and functional annotation
  31. Structural and mechanistic insights into the action of Plasmodium falciparum spermidine synthase
  32. Deletion mutagenesis of large areas in Plasmodium falciparum genes: a comparative study
  33. Novel properties of malarial S-adenosylmethionine decarboxylase as revealed by structural modelling
  34. Parasite-specific inserts in the bifunctional S-adenosylmethionine decarboxylase/ornithine decarboxylase of Plasmodium falciparum modulate catalytic activities and domain interactions
  35. Comparative properties of a three-dimensional model of Plasmodium falciparum ornithine decarboxylase