Jane C. Munday - Concepedia

Author

Jane C. Munday

University of Glasgow ORCID

Also Known As

J. C. Munday, J. Munday, Jane C Munday, Jane C. Munday, Jane Munday

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

University of Glasgow Wellcome Centre for Molecular Parasitology Wellcome Trust University of Edinburgh Swiss Tropical and Public Health Institute

About

Jane C. Munday is an author at University of Glasgow specializing in medicine, molecular biology, and drug resistance.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	125
2	Natural Sciences	2	2	119
3	Biochemistry	2	2	83
4	Health Sciences	1	1	14
5	Biomolecular Engineering	1	1	69

Jane C. Munday

Publications

Citations

H-Index

Page 1

	Year	Citations
Aquaglyceroporin 2 controls susceptibility to melarsoprol and pentamidine in African trypanosomes Nicola Baker, Lucy Glover, Jane C. Munday, Proceedings of the National Academy of Sciences	2012	159
Trypanosoma brucei aquaglyceroporin 2 is a high-affinity transporter for pentamidine and melaminophenyl arsenic drugs and the main genetic determinant of resistance to these drugs Jane C. Munday, Anthonius A. Eze, Nicola Baker, Journal of Antimicrobial Chemotherapy	2013	127
Cyclic AMP Effectors in African Trypanosomes Revealed by Genome-Scale RNA Interference Library Screening for Resistance to the Phosphodiesterase Inhibitor CpdA Matthew K. Gould, Sabine Bachmaier, Juma A. M. Ali, Antimicrobial Agents and Chemotherapy GeneticsAfrican TrypanosomesMolecular BiologyMolecular GeneticsParasite Genomics	2013	69
Functional expression of TcoAT1 reveals it to be a P1-type nucleoside transporter with no capacity for diminazene uptake Jane C. Munday, Karla E. Rojas López, Anthonius A. Eze, International Journal for Parasitology Drugs and Drug Resistance	2013	63
Chimerization at the AQP2–AQP3 locus is the genetic basis of melarsoprol–pentamidine cross-resistance in clinical Trypanosoma brucei gambiense isolates Fabrice E. Graf, Nicola Baker, Jane C. Munday, International Journal for Parasitology Drugs and Drug Resistance	2015	60
Functional analysis of drug resistance‐associated mutations in the <scp><i>T</i></scp><i>rypanosoma brucei</i> adenosine transporter 1 (<scp>TbAT</scp>1) and the proposal of a structural model for the protein Jane C. Munday, Daniel N. A. Tagoe, Anthonius A. Eze, Molecular Microbiology	2015	56
The Diamidine Diminazene Aceturate Is a Substrate for the High-Affinity Pentamidine Transporter: Implications for the Development of High Resistance Levels in Trypanosomes Ibrahim A. Teka, Anne Kazibwe, Nasser El-Sabbagh, Molecular Pharmacology	2011	54
Oligopeptidase B deficient mutants of Leishmania major Jane C. Munday, Karen McLuskey, Elaine Brown, Molecular and Biochemical Parasitology Parasitic ProtozoaNatural SciencesMolecular BiologyMolecular GeneticsProteomics	2010	50
Positively selected modifications in the pore of TbAQP2 allow pentamidine to enter Trypanosoma brucei Ali H. Alghamdi, Jane C. Munday, Gustavo D. Campagnaro, eLife	2020	44
Reduced Mitochondrial Membrane Potential Is a Late Adaptation of Trypanosoma brucei brucei to Isometamidium Preceded by Mutations in the γ Subunit of the F1Fo-ATPase Anthonius A. Eze, Matthew K. Gould, Jane C. Munday, PLoS neglected tropical diseases	2016	43

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