L
Lindsay B. Stewart
Researcher at University of London
Publications - 49
Citations - 1659
Lindsay B. Stewart is an academic researcher from University of London. The author has contributed to research in topics: Plasmodium falciparum & Gene. The author has an hindex of 19, co-authored 43 publications receiving 1360 citations.
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Journal ArticleDOI
Artemisone—A Highly Active Antimalarial Drug of the Artemisinin Class†
Richard K. Haynes,Burkhard Fugmann,Jörg Dr. Stetter,Karl H. Rieckmann,Hans-Dietrich Heilmann,Ho-Wai Chan,Man-Ki Cheung,Wai-Lun Lam,Ho-Ning Wong,Simon L. Croft,Livia Vivas,Lauren Rattray,Lindsay B. Stewart,Wallace Peters,Brian L. Robinson,Michael D. Edstein,Barbara M. Kotecka,Dennis E. Kyle,Bernhard Beckermann,Michael Gerisch,Martin Radtke,Gabriele Schmuck,Wolfram Steinke,Ute Wollborn,Karl Schmeer,Axel Römer +25 more
TL;DR: Efficacies of artemisone against the malaria parasite are substantially greater than those of the current artemisinin "gold standard", artesunate and it displays low lipophilicity and negligible neuro- and cytotoxicity in in vitro and in vivo assays.
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Population genomic scan for candidate signatures of balancing selection to guide antigen characterization in malaria parasites.
Alfred Amambua-Ngwa,Kevin K. A. Tetteh,Magnus Manske,Natalia Gomez-Escobar,Lindsay B. Stewart,M. Elizabeth Deerhake,Ian H. Cheeseman,Ian H. Cheeseman,Chris I. Newbold,Anthony A. Holder,Ellen Knuepfer,Omar Janha,Muminatou Jallow,Susana Campino,Bronwyn MacInnis,Dominic P. Kwiatkowski,Dominic P. Kwiatkowski,David J. Conway,David J. Conway +18 more
TL;DR: Against an overall background of negatively skewed frequencies, as expected from historical population expansion combined with purifying selection, the outlying minority of genes with signatures indicating exceptionally intermediate frequencies were identified; such signatures were most common in those with peak expression at the merozoite stage that invades erythrocytes.
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A barcode of organellar genome polymorphisms identifies the geographic origin of Plasmodium falciparum strains.
Mark D. Preston,Susana Campino,Samuel Assefa,Diego F. Echeverry,Harold Ocholla,Alfred Amambua-Ngwa,Lindsay B. Stewart,David J. Conway,Steffen Borrmann,Pascal Michon,Issaka Zongo,Jean-Bosco Ouédraogo,Abdoulaye A. Djimde,Ogobara K. Doumbo,François Nosten,Arnab Pain,Teun Bousema,Chris Drakeley,Rick M. Fairhurst,Colin J. Sutherland,Cally Roper,Taane G. Clark +21 more
TL;DR: The mitochondrion and apicoplast genomes of 711 Plasmodium falciparum isolates from 14 countries are analysed and it is found that they are non-recombining and co-inherited.
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Long read assemblies of geographically dispersed Plasmodium falciparum isolates reveal highly structured subtelomeres.
Thomas D. Otto,Thomas D. Otto,Ulrike Böhme,Mandy Sanders,Adam J. Reid,Ellen Bruske,Craig W. Duffy,Peter C. Bull,Richard D. Pearson,Richard D. Pearson,Abdirahman I. Abdi,Sandra Dimonte,Lindsay B. Stewart,Susana Campino,Susana Campino,Mihir Kekre,William L Hamilton,Antoine Claessens,Sarah K. Volkman,Sarah K. Volkman,Sarah K. Volkman,Daouda Ndiaye,Alfred Amambua-Ngwa,Mahamadou Diakite,Rick M. Fairhurst,David J. Conway,Matthias Franck,Chris I. Newbold,Chris I. Newbold,Matthew Berriman +29 more
TL;DR: 15 manually curated new reference genome sequences with their nearly complete subtelomeric regions and fully assembled genes are an important new resource for the malaria research community and report the overall conserved structure and pattern of important gene families and the more clearly defined subtelomersic regions.
Journal ArticleDOI
A potent series targeting the malarial cGMP-dependent protein kinase clears infection and blocks transmission.
David A. Baker,Lindsay B. Stewart,Jonathan M. Large,Paul W. Bowyer,Keith H. Ansell,María Belén Jiménez-Díaz,Majida El Bakkouri,Majida El Bakkouri,Kristian Birchall,Koen J. Dechering,Nathalie Bouloc,P.J. Coombs,David Whalley,Denise J. Harding,Ela Smiljanic-Hurley,Mary C. Wheldon,Eloise M. Walker,Johannes T. Dessens,Maria Lafuente,Laura Sanz,Francisco-Javier Gamo,Santiago Ferrer,Raymond Hui,Raymond Hui,Teun Bousema,Iñigo Angulo-Barturen,Andy Merritt,Simon L. Croft,Winston E. Gutteridge,Catherine A. Kettleborough,Simon A. Osborne +30 more
TL;DR: An imidazopyridine series is generated that selectively targets Plasmodium falciparum PKG, inhibits blood stage parasite growth in vitro and in mice and blocks transmission to mosquitoes and warrants consideration for further development to produce an antimalarial drug.