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Janet Cox-Singh

Researcher at University of St Andrews

Publications -  48
Citations -  5208

Janet Cox-Singh is an academic researcher from University of St Andrews. The author has contributed to research in topics: Plasmodium knowlesi & Malaria. The author has an hindex of 28, co-authored 46 publications receiving 4802 citations. Previous affiliations of Janet Cox-Singh include Universiti Sains Malaysia & Universiti Malaysia Sarawak.

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HLA degenerate T-cell epitopes from Plasmodium falciparum liver stage-specific antigen 1 (LSA-1) are highly conserved in isolates from geographically distinct areas

TL;DR: The extent of polymorphism within the N‐terminal non‐repetitive region of the LSA‐1 gene from Malaysian P. falciparum field isolates was sequenced and compared with data of isolates from Brazil, Kenya and Papua New Guinea, and three of the T‐cell epitopes were completely conserved while the remaining two were highly conserved.
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Adaptation of in vitro cytoadherence assay to Plasmodium knowlesi field isolates

TL;DR: A static protein assay is used to determine if naturally occurring human P. knowlesi infections can cause erythrocytes to bind to ICAM-1, VCAM-2, and CD36, and to identify the receptors associated with PfEMP1.
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Plasmodium knowlesi - Clinical Isolate Genome Sequencing to Inform Translational Same-Species Model System for Severe Malaria

TL;DR: A method to generate long-read third-generation Plasmodium genome sequence data from archived clinical samples using the MinION platform and it is proposed that by widely adopting this methodology important information on clinically relevant parasite diversity, including multiple gene family members, from geographically distinct study sites will emerge.
Journal Article

Stage specific differences in steady state levels of mRNA encoding the major surface glycoprotein of Brugia pahangi.

TL;DR: It is reported that the gp30 transcript is present in each of the life cycle stages, including mosquito derived L3's, and that there is a 50 fold increase in the transcription of gp30 in young adults (28 days post infection) compared to mature adults.
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De Novo Assembly of Plasmodium knowlesi Genomes From Clinical Samples Explains the Counterintuitive Intrachromosomal Organization of Variant SICAvar and kir Multiple Gene Family Members

TL;DR: It is demonstrated that, in contrast to conserved core genes, SICAvar and kir genes occupy otherwise gene-sparse chromosomal locations that accommodate rapid evolution and change, and offers new insight into the complexity of clinically important real-world parasites.