Author

G. D. Campagnaro

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Approach:mechanistic / dynamical model· 1

Frequent Co-Authors

J. C. Munday· 2 shared A. A. Eze· 1 shared A. Alghamdi· 1 shared A. Dimitriou· 1 shared A. Kumar· 1 shared A.-M. Donachie· 1 shared C. Dardonville· 1 shared C. E. Okpara· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersMicrobiology

J. C. Munday

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2 papers

Recent·Most cited

MicrobiologybioRxivJul 28, 2020

Diminazene resistance in Trypanosoma congolense is linked to reduced mitochondrial membrane potential and not to reduced transport capacity

H. De Koning, L. V. Carruthers, J. C. Munday…·M. P. Barrett

This study investigates diminazene resistance in Trypanosoma congolense and finds that resistance is due to reduced mitochondrial membrane potential rather than reduced drug transport capacity.

DOI 10.1111/mmi.14733

humanexperimental assay

𝕏 PostBluesky

BiochemistrybioRxivMar 8, 2020

Positively selected modifications in the pore of TbAQP2 allow pentamidine to enter Trypanosoma brucei

A. Alghamdi, J. C. Munday, G. D. Campagnaro…·H. P. De Koning

The paper identifies mutations in TbAQP2 that enable pentamidine permeation, showing how specific structural changes in the aquaporin pore allow drug entry in Trypanosoma brucei.

DOI 10.7554/elife.56416

humanmechanistic / dynamical model

𝕏 PostBluesky