scispace - formally typeset
S

Susan Wyllie

Researcher at University of Dundee

Publications -  84
Citations -  3771

Susan Wyllie is an academic researcher from University of Dundee. The author has contributed to research in topics: Trypanosoma brucei & Trypanothione. The author has an hindex of 32, co-authored 72 publications receiving 3061 citations. Previous affiliations of Susan Wyllie include East Tennessee State University James H. Quillen College of Medicine & University of Edinburgh.

Papers
More filters
Journal ArticleDOI

Anti-trypanosomatid drug discovery: an ongoing challenge and a continuing need

TL;DR: The combination of new drugs, new technologies and public health initiatives is essential for the management, and hopefully eventual elimination, of trypanosomatid diseases from the human population.
Journal ArticleDOI

Dual action of antimonial drugs on thiol redox metabolism in the human pathogen leishmania donovani

TL;DR: It is shown that trivalent antimony (SbIII) interferes with trypanothione metabolism in drug-sensitive Leishmania parasites by two inherently distinct mechanisms, which combine to profoundly compromise the thiol redox potential in both amastigote and promastigotes stages of the life cycle.
Journal ArticleDOI

Nitro drugs for the treatment of trypanosomatid diseases: past, present, and future prospects

TL;DR: Two nitro drugs are currently used in the treatment of trypanosomatid diseases and several new nitroaromatics are being developed against the trypano-somatica diseases.
Journal ArticleDOI

The Anti-Trypanosome Drug Fexinidazole Shows Potential for Treating Visceral Leishmaniasis

TL;DR: Fexinidazole, a drug currently in phase 1 clinical trials for treating African trypanosomiasis, shows promise for treating visceral leishmaniasis, and is comparable to that of drugs currently in clinical use against this deadly tropical disease.
Journal ArticleDOI

Comparison of a high-throughput high-content intracellular Leishmania donovani assay with an axenic amastigote assay.

TL;DR: It is concluded that the intramacrophage assay is more suited as a primary hit-discovery platform than the current form of axenic assay, and how modifications to theAxenic assay may render it more suitable for hit-Discovery is discussed.