Mohammed Al-Helal

HDQ, a Potent Inhibitor of Plasmodium falciparum Proliferation, Binds to the Quinone Reduction Site of the Cytochrome bc1 Complex

P. Stocks, G. Biagini, N. Berry, 2012, Antimicrobial Agents and Chemotherapy.

Cytochrome b Mutation Y268S Conferring Atovaquone Resistance Phenotype in Malaria Parasite Results in Reduced Parasite bc1 Catalytic Turnover and Protein Expression

H. Ranson, G. Biagini, S. Ward, 2012, The Journal of Biological Chemistry.

Glycerol: An unexpected major metabolite of energy metabolism by the human malaria parasite

Nicholas Fisher, Lu-Yun Lian, L. Lian, 2009, Malaria Journal.

Evidence for a common non-heme chelatable-iron-dependent activation mechanism for semisynthetic and synthetic endoperoxide antimalarial drugs.

Ruth H. Hughes, Peter D Gibbons, V. Barton, 2007, Angewandte Chemie.

The development of quinolone esters as novel antimalarial agents targeting the Plasmodium falciparum bc1 protein complex

G. Biagini, Raman Sharma, N. Berry, 2012 .

Evidence for a common non-heme chelatable-iron-dependent activation mechanism for semisynthetic and synthetic endoperoxide antimalarial drugs.

Ruth H. Hughes, R. Amewu, G. Biagini, 2007, Angewandte Chemie.