-
Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum
-
The interaction of verapamil with the human malaria parasite : Plasmodium falciparum
-
The effect of herbicides as novel antimalarial drugs on the transcriptome and proteome of Plasmodium falciparum
-
Inhibition of the histone deacetylase family as a drug target in the human malaria parasite, plasmodium falciparum
-
Biochemical and immunochemical investigation of some South African strains of the human malaria parasite, Plasmodium falciparum
-
Gene expression profiling of polyamine-depleted Plasmodium falciparum
-
High-throughput prioritization of putative drug targets in the malaria parasite, Plasmodium falciparum
-
Transcriptional and post-transcriptional gene regulatory mechanisms in the malaria parasite, Plasmodium falciparum
-
Probing the chemical biology involved in the haem detoxification pathway of the human malaria parasite, plasmodium falciparum
-
In silico prediction of host-pathogen protein - protein interactions in the malaria parasite, Plasmodium falciparum
-
Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum
-
Epigenetic repression of gene expression controls the initial phases of gametocytogenesis in the malaria parasite, Plasmodium falciparum
-
Characterising the role of actin and PI (3) kinases in endocytosis in the malaria parasite Plasmodium falciparum
-
Development of analytical techniques for probing the effects of -haematin inhibiting compounds on the malaria parasite Plasmodium falciparum
-
Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum
-
Radiolabelled antibodies as a detection tool for malaria parasite (Plasmodium falciparum 3D7)- infected human erythrocytes
-
DETERMINANTS OF RESPONSES TO ANTIMALARIAL DRUGS IN CHILDREN WITH UNCOMPLICATED PLASMODIUM FALCIPARUM MALARIA
-
Mechanisms of potential novel antimalarials and proteomics of Plasmodium falciparum resistance
-
Design, synthesis and evaluation of potential dual drugs targeting the haemoglobin degradation pathway in the malaria parasite Plasmodium falciparum
-
iTRAQ-mediated proteome analysis of the response of Plasmodium falciparum to a novel antimalarial compound
-
Molecular characterisation of the ornithine decarboxylase gene of the human malaria parasite, plasmidium falciparum
-
Dynamic bioinformatics and isotopic evaluation of the permeome of intraerythrocytic Plasmodium falciparum parasites
-
Development of transgenic Plasmodium falciparum parasites for K+ channel functional investigation
-
Whole-body modelling of glucose and lactate dynamics in plasmodium falciparum malaria