Select Publications
Preprints
2023, A novel computational pipeline forvargene expression augments the discovery of changes in thePlasmodium falciparumtranscriptome during transition fromin vivoto short-termin vitroculture, http://dx.doi.org/10.1101/2023.03.21.533599
,2022, A fast-killing tyrosine amide ((S)-SW228703) with blood and liver-stage antimalarial activity associated with the Cyclic Amine Resistance Locus (PfCARL), http://dx.doi.org/10.1101/2022.10.16.512381
,2022, Mechanism of small molecule inhibition of Plasmodium falciparum myosin A informs antimalarial drug design, http://dx.doi.org/10.1101/2022.09.09.507123
,2022, Electricity-free nucleic acid extraction method from dried blood spots on filter paper for point-of-care diagnostics, http://dx.doi.org/10.1101/2022.07.28.501845
,2021, 4D live-cell imaging of microgametogenesis in the human malaria parasite Plasmodium falciparum, http://dx.doi.org/10.1101/2021.07.28.454129
,2021, Plasmodium falciparumprotein Pfs16 is a target for transmission-blocking antimalarial drug development, http://dx.doi.org/10.1101/2021.06.14.448287
,2021, Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183, http://dx.doi.org/10.1101/2021.05.12.443866
,2021, Automated detection and staging of malaria parasites from cytological smears using convolutional neural networks, http://dx.doi.org/10.1101/2021.01.26.21250284
,2021, Prioritization of antimicrobial targets by CRISPR-based oligo recombineering, http://dx.doi.org/10.1101/2021.02.04.429737
,2020, A single-cell atlas of Plasmodium falciparum transmission through the mosquito, http://dx.doi.org/10.1101/2020.10.11.333179
,2020, Dissection-independent production of a protective whole-sporozoite malaria vaccine, http://dx.doi.org/10.1101/2020.06.22.164756
,2020, Actomyosin forces and the energetics of red blood cell invasion by the malaria parasitePlasmodium falciparum, http://dx.doi.org/10.1101/2020.06.25.171900
,2020, Artemisinin-resistant malaria parasites show enhanced transmission to mosquitoes under drug pressure, http://dx.doi.org/10.1101/2020.02.04.933572
,2020, Identification and characterisation of a phospholipid scramblase in the malaria parasite Plasmodium falciparum, http://dx.doi.org/10.1101/2020.06.22.165258
,2020, Structure of Full Length Plasmodium Myosin A and its light chain PfELC, dual targets against malaria parasite pathogenesis, http://dx.doi.org/10.1101/2020.06.30.179788
,2019, Apicomplexan F-actin is required for efficient nuclear entry during host cell invasion, http://dx.doi.org/10.1101/646463
,2019, Quantitative and rapid Plasmodium falciparum malaria diagnosis and artemisinin-resistance detection using a CMOS Lab-on-Chip platform, http://dx.doi.org/10.1101/638221
,2019, The effects of dyslipidaemia and cholesterol modulation on erythrocyte susceptibility to malaria parasite infection, http://dx.doi.org/10.1101/630251
,2019, A biosynthetic platform for antimalarial drug discovery, http://dx.doi.org/10.1101/814715
,2019, A machine learning approach to define antimalarial drug action from heterogeneous cell-based screens, http://dx.doi.org/10.1101/2019.12.19.882480
,2019, Single-molecule nanopore sensing of actin dynamics and drug binding, http://dx.doi.org/10.1101/829150
,2018, Stable knockout and complementation of receptor expression using in vitro cell line derived reticulocytes for dissection of host malaria invasion requirements, http://dx.doi.org/10.1101/495853
,2018, A high-throughput in vitro translation screen towards discovery of novel antimalarial protein translation inhibitors, http://dx.doi.org/10.1101/248740
,2017, Binding of a Newly Identified Essential Light Chain to ExpressedPlasmodium falciparumClass XIV Myosin Enhances Actin Motility, http://dx.doi.org/10.1101/127118
,2017, Failure of in vitro differentiation of Plasmodium falciparum gametocytes into ookinetes arises because of poor gamete fertilisation, http://dx.doi.org/10.1101/216721
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