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Michael P. Barrett

Researcher at University of Glasgow

Publications -  332
Citations -  15731

Michael P. Barrett is an academic researcher from University of Glasgow. The author has contributed to research in topics: Trypanosoma brucei & Metabolomics. The author has an hindex of 65, co-authored 318 publications receiving 13859 citations. Previous affiliations of Michael P. Barrett include University of Bordeaux & Wellcome Trust.

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Drug resistance and treatment failure in leishmaniasis: A 21st century challenge

TL;DR: The meaning of “resistance” related to leishmaniasis and its molecular epidemiology are discussed, particularly for Leishmania donovani that causes visceral leish maniasis, and how resistance can affect drug combination therapies are discussed.
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Chemotherapy of trypanosomiases and leishmaniasis

TL;DR: Financial constraints continue to represent a major hurdle to drug development, however, the appearance of not-for-profit product-development partnerships offers a new paradigm for bringing new drugs to patients.
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Human African trypanosomiasis: pharmacological re-engagement with a neglected disease

TL;DR: The challenges of chemotherapy for human African trypanosomiasis (HAT) are discussed, and the few drugs registered for use against the disease are unsatisfactory for a number of reasons.
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Toward global metabolomics analysis with hydrophilic interaction liquid chromatography-mass spectrometry: improved metabolite identification by retention time prediction.

TL;DR: It is demonstrated that a retention time prediction model can improve metabolite identification on a hydrophilic interaction chromatography-high-resolution mass spectrometry metabolomics platform, allowing identified metabolites to be mapped onto an organism-wide metabolic network, providing opportunities for future studies of cellular metabolism from a global systems biology perspective.
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IDEOM : an Excel interface for analysis of LC-MS-based metabolomics data

TL;DR: IDEOM provides a user-friendly data processing application that automates filtering and identification of metabolite peaks, paying particular attention to common sources of noise and false identifications generated by liquid chromatography-mass spectrometry platforms.