Dr Jane Munday

  • Research Associate (Parasitology)

telephone: 01413306069
email: Jane.Munday@glasgow.ac.uk

Room B6/28 Level 6, III - Sir Graeme Davies Building, 120 University Place, Glasgow G12 8TA

ORCID iDhttps://orcid.org/0000-0001-7792-2749

Publications

List by: Type | Date

Jump to: 2021 | 2020 | 2019 | 2018 | 2016 | 2015 | 2014 | 2013 | 2012 | 2011
Number of items: 22.

2021

Carruthers, L. V. et al. (2021) Diminazene resistance in Trypanosoma congolense is not caused by reduced transport capacity but associated with reduced mitochondrial membrane potential. Molecular Microbiology, 116(2), pp. 564-588. (doi: 10.1111/mmi.14733) (PMID:33932053)

2020

Munday, J. C. et al. (2020) Cloning and functional complementation of ten Schistosoma mansoni phosphodiesterases expressed in the mammalian host stages. PLoS Neglected Tropical Diseases, 14(7), e0008447. (doi: 10.1371/journal.pntd.0008447) (PMID:32730343) (PMCID:PMC7430754)

Alghamdi, A. et al. (2020) Positively selected modifications in the pore of TbAQP2 allow pentamidine to enter Trypanosoma brucei. eLife, 9, e56416. (doi: 10.7554/eLife.56416) (PMID:32762841) (PMCID:PMC7473772)

2019

Sebastián-Pérez, V. et al. (2019) Discovery of novel Schistosoma mansoni PDE4A inhibitors as potential agents against schistosomiasis. Future Medicinal Chemistry, 11(14), pp. 1703-1720. (doi: 10.4155/fmc-2018-0592) (PMID:31370708)

Botros, S. S. et al. (2019) Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity. International Journal for Parasitology: Drugs and Drug Resistance, 9, pp. 35-43. (doi: 10.1016/j.ijpddr.2019.01.001)

Giordani, F. , Khalaf, A. I., Gillingwater, K., Munday, J. C. , de Koning, H. P. , Suckling, C. J., Barrett, M. P. and Scott, F. J. (2019) Novel minor groove binders cure animal African trypanosomiasis in an in vivo mouse model. Journal of Medicinal Chemistry, 62(6), pp. 3021-3035. (doi: 10.1021/acs.jmedchem.8b01847) (PMID:30763102)

2018

Sebastián-Pérez, V., Hendrickx, S., Munday, J. C. , Kalejaiye, T., Martínez, A., Campillo, N. E., de Koning, H. , Caljon, G., Maes, L. and Gil, C. (2018) Cyclic nucleotide specific phosphodiesterases as potential drug targets for anti-Leishmania therapy. Antimicrobial Agents and Chemotherapy, 62(10), e00603-18. (doi: 10.1128/AAC.00603-18) (PMID:30104270)

Blaazer, A. R. et al. (2018) Targeting a subpocket in Trypanosoma brucei phosphodiesterase B1 (TbrPDEB1) enables the structure-based discovery of selective Inhibitors with trypanocidal activity. Journal of Medicinal Chemistry, 61(9), pp. 3870-3888. (doi: 10.1021/acs.jmedchem.7b01670) (PMID:29672041) (PMCID:PMC5949723)

Campagnaro, G. D., Alzahrani, K. J., Munday, J. C. and De Koning, H. P. (2018) Trypanosoma brucei bloodstream forms express highly specific and separate transporters for adenine and hypoxanthine; evidence for a new protozoan purine transporter family? Molecular and Biochemical Parasitology, 220, pp. 46-56. (doi: 10.1016/j.molbiopara.2018.01.005) (PMID:29371154)

2016

Eze, A. A., Gould, M. K., Munday, J. C. , Tagoe, D. N.A., Stelmanis, V., Schnaufer, A. and De Koning, H. P. (2016) 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. PLoS Neglected Tropical Diseases, 10(8), e0004791. (doi: 10.1371/journal.pntd.0004791) (PMID:27518185) (PMCID:PMC4982688)

Graf, F. E. et al. (2016) Comparative genomics of drug resistance in Trypanosoma brucei rhodesiense. Cellular and Molecular Life Sciences, 73(17), pp. 3387-3400. (doi: 10.1007/s00018-016-2173-6) (PMID:26973180) (PMCID:PMC4967103)

2015

Graf, F. E., Baker, N., Munday, J. C. , De Koning, H. P. , Horn, D. and Mäser, P. (2015) Chimerization at the AQP2–AQP3 locus is the genetic basis of melarsoprol–pentamidine cross-resistance in clinical Trypanosoma brucei gambiense isolates. International Journal for Parasitology: Drugs and Drug Resistance, 5(2), pp. 65-68. (doi: 10.1016/j.ijpddr.2015.04.002) (PMID:26042196) (PMCID:PMC4443405)

Munday, J. C. et al. (2015) Functional analysis of drug resistance-associated mutations in the Trypanosoma brucei Adenosine Transporter 1 (TbAT1) and the proposal of a structural model for the protein. Molecular Microbiology, 96(4), pp. 887-900. (doi: 10.1111/mmi.12979) (PMID:25708978) (PMCID:PMC4755147)

Munday, J. C. , Settimo, L. and De Koning, H. P. (2015) Transport proteins determine drug sensitivity and resistance in a protozoan parasite, Trypanosoma brucei. Frontiers in Pharmacology, 6, 32. (doi: 10.3389/fphar.2015.00032) (PMID:24235095) (PMCID:PMC3922157)

2014

Munday, J. C. et al. (2014) 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. Journal of Antimicrobial Chemotherapy, 69(3), pp. 651-663. (doi: 10.1093/jac/dkt442) (PMID:24235095) (PMCID:PMC3922157)

Garcia-Salcedo, J. A., Munday, J. C. , Unciti-Broceta, J. D. and De Koning, H. P. (2014) Progress towards new treatments for human African trypanosomiasis. In: Magez, S. and Radwanska, M. (eds.) Trypanosomes and Trypanosomiasis. Springer, pp. 217-238. ISBN 9783709115558 (doi:10.1007/978-3-7091-1556-5_9)

2013

Munday, J.C. , Rojas López, K.E., Eze, A.A., Delespaux, V., Van Den Abbeele, J., Rowan, T., Barrett, M.P. , Morrison, L.J. and De Koning, H.P. (2013) Functional expression of TcoAT1 reveals it to be a P1-type nucleoside transporter with no capacity for diminazene uptake. International Journal for Parasitology: Drugs and Drug Resistance, 3, pp. 69-76. (doi: 10.1016/j.ijpddr.2013.01.004)

Gould, M.K., Bachmaier, S., Ali, J.A.M., Alsford, S., Tagoe, D.N.A., Munday, J.C. , Schnaufer, A.C., Horn, D., Boshart, M. and De Koning, H. (2013) Cyclic AMP effectors in African trypanosomes revealed by genome-scale RNA interference library screening for resistance to the phosphodiesterase inhibitor CpdA. Antimicrobial Agents and Chemotherapy, 57(10), pp. 4882-4893. (doi: 10.1128/AAC.00508-13)

Ali, J. A.., Tagoe, D. N.A., Munday, J. C. , Donachie, A., Morrison, L. J. and De Koning, H. P. (2013) Pyrimidine biosynthesis is not an essential function for trypanosoma brucei bloodstream forms. PLoS ONE, 8(3), e58034. (doi: 10.1371/journal.pone.0058034) (PMID:23505454) (PMCID:PMC3591441)

2012

Baker, N., Glover, L., Munday, J. C. , Aguinaga Andres, D., Barrett, M. P. , De Koning, H. P. and Horn, D. (2012) Aquaglyceroporin 2 controls susceptibility to melarsoprol and pentamidine in African trypanosomes. Proceedings of the National Academy of Sciences of the United States of America, 109(27), pp. 10996-11001. (doi: 10.1073/pnas.1202885109)

2011

Teka, I. A. et al. (2011) The diamidine diminazene aceturate is a substrate for the high-affinity pentamidine transporter: implications for the development of high resistance levels in trypanosomes. Molecular Pharmacology, 80(1), pp. 110-116. (doi: 10.1124/mol.111.071555)

Munday, J. C. , McLuskey, K., Brown, E., Coombs, G. H. and Mottram, J. C. (2011) Oligopeptidase B deficient mutants of Leishmania major. Molecular and Biochemical Parasitology, 175(1), pp. 49-57. (doi: 10.1016/j.molbiopara.2010.09.003)

This list was generated on Mon Oct 25 05:14:26 2021 BST.
Number of items: 22.

Articles

Carruthers, L. V. et al. (2021) Diminazene resistance in Trypanosoma congolense is not caused by reduced transport capacity but associated with reduced mitochondrial membrane potential. Molecular Microbiology, 116(2), pp. 564-588. (doi: 10.1111/mmi.14733) (PMID:33932053)

Munday, J. C. et al. (2020) Cloning and functional complementation of ten Schistosoma mansoni phosphodiesterases expressed in the mammalian host stages. PLoS Neglected Tropical Diseases, 14(7), e0008447. (doi: 10.1371/journal.pntd.0008447) (PMID:32730343) (PMCID:PMC7430754)

Alghamdi, A. et al. (2020) Positively selected modifications in the pore of TbAQP2 allow pentamidine to enter Trypanosoma brucei. eLife, 9, e56416. (doi: 10.7554/eLife.56416) (PMID:32762841) (PMCID:PMC7473772)

Sebastián-Pérez, V. et al. (2019) Discovery of novel Schistosoma mansoni PDE4A inhibitors as potential agents against schistosomiasis. Future Medicinal Chemistry, 11(14), pp. 1703-1720. (doi: 10.4155/fmc-2018-0592) (PMID:31370708)

Botros, S. S. et al. (2019) Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity. International Journal for Parasitology: Drugs and Drug Resistance, 9, pp. 35-43. (doi: 10.1016/j.ijpddr.2019.01.001)

Giordani, F. , Khalaf, A. I., Gillingwater, K., Munday, J. C. , de Koning, H. P. , Suckling, C. J., Barrett, M. P. and Scott, F. J. (2019) Novel minor groove binders cure animal African trypanosomiasis in an in vivo mouse model. Journal of Medicinal Chemistry, 62(6), pp. 3021-3035. (doi: 10.1021/acs.jmedchem.8b01847) (PMID:30763102)

Sebastián-Pérez, V., Hendrickx, S., Munday, J. C. , Kalejaiye, T., Martínez, A., Campillo, N. E., de Koning, H. , Caljon, G., Maes, L. and Gil, C. (2018) Cyclic nucleotide specific phosphodiesterases as potential drug targets for anti-Leishmania therapy. Antimicrobial Agents and Chemotherapy, 62(10), e00603-18. (doi: 10.1128/AAC.00603-18) (PMID:30104270)

Blaazer, A. R. et al. (2018) Targeting a subpocket in Trypanosoma brucei phosphodiesterase B1 (TbrPDEB1) enables the structure-based discovery of selective Inhibitors with trypanocidal activity. Journal of Medicinal Chemistry, 61(9), pp. 3870-3888. (doi: 10.1021/acs.jmedchem.7b01670) (PMID:29672041) (PMCID:PMC5949723)

Campagnaro, G. D., Alzahrani, K. J., Munday, J. C. and De Koning, H. P. (2018) Trypanosoma brucei bloodstream forms express highly specific and separate transporters for adenine and hypoxanthine; evidence for a new protozoan purine transporter family? Molecular and Biochemical Parasitology, 220, pp. 46-56. (doi: 10.1016/j.molbiopara.2018.01.005) (PMID:29371154)

Eze, A. A., Gould, M. K., Munday, J. C. , Tagoe, D. N.A., Stelmanis, V., Schnaufer, A. and De Koning, H. P. (2016) 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. PLoS Neglected Tropical Diseases, 10(8), e0004791. (doi: 10.1371/journal.pntd.0004791) (PMID:27518185) (PMCID:PMC4982688)

Graf, F. E. et al. (2016) Comparative genomics of drug resistance in Trypanosoma brucei rhodesiense. Cellular and Molecular Life Sciences, 73(17), pp. 3387-3400. (doi: 10.1007/s00018-016-2173-6) (PMID:26973180) (PMCID:PMC4967103)

Graf, F. E., Baker, N., Munday, J. C. , De Koning, H. P. , Horn, D. and Mäser, P. (2015) Chimerization at the AQP2–AQP3 locus is the genetic basis of melarsoprol–pentamidine cross-resistance in clinical Trypanosoma brucei gambiense isolates. International Journal for Parasitology: Drugs and Drug Resistance, 5(2), pp. 65-68. (doi: 10.1016/j.ijpddr.2015.04.002) (PMID:26042196) (PMCID:PMC4443405)

Munday, J. C. et al. (2015) Functional analysis of drug resistance-associated mutations in the Trypanosoma brucei Adenosine Transporter 1 (TbAT1) and the proposal of a structural model for the protein. Molecular Microbiology, 96(4), pp. 887-900. (doi: 10.1111/mmi.12979) (PMID:25708978) (PMCID:PMC4755147)

Munday, J. C. , Settimo, L. and De Koning, H. P. (2015) Transport proteins determine drug sensitivity and resistance in a protozoan parasite, Trypanosoma brucei. Frontiers in Pharmacology, 6, 32. (doi: 10.3389/fphar.2015.00032) (PMID:24235095) (PMCID:PMC3922157)

Munday, J. C. et al. (2014) 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. Journal of Antimicrobial Chemotherapy, 69(3), pp. 651-663. (doi: 10.1093/jac/dkt442) (PMID:24235095) (PMCID:PMC3922157)

Munday, J.C. , Rojas López, K.E., Eze, A.A., Delespaux, V., Van Den Abbeele, J., Rowan, T., Barrett, M.P. , Morrison, L.J. and De Koning, H.P. (2013) Functional expression of TcoAT1 reveals it to be a P1-type nucleoside transporter with no capacity for diminazene uptake. International Journal for Parasitology: Drugs and Drug Resistance, 3, pp. 69-76. (doi: 10.1016/j.ijpddr.2013.01.004)

Gould, M.K., Bachmaier, S., Ali, J.A.M., Alsford, S., Tagoe, D.N.A., Munday, J.C. , Schnaufer, A.C., Horn, D., Boshart, M. and De Koning, H. (2013) Cyclic AMP effectors in African trypanosomes revealed by genome-scale RNA interference library screening for resistance to the phosphodiesterase inhibitor CpdA. Antimicrobial Agents and Chemotherapy, 57(10), pp. 4882-4893. (doi: 10.1128/AAC.00508-13)

Ali, J. A.., Tagoe, D. N.A., Munday, J. C. , Donachie, A., Morrison, L. J. and De Koning, H. P. (2013) Pyrimidine biosynthesis is not an essential function for trypanosoma brucei bloodstream forms. PLoS ONE, 8(3), e58034. (doi: 10.1371/journal.pone.0058034) (PMID:23505454) (PMCID:PMC3591441)

Baker, N., Glover, L., Munday, J. C. , Aguinaga Andres, D., Barrett, M. P. , De Koning, H. P. and Horn, D. (2012) Aquaglyceroporin 2 controls susceptibility to melarsoprol and pentamidine in African trypanosomes. Proceedings of the National Academy of Sciences of the United States of America, 109(27), pp. 10996-11001. (doi: 10.1073/pnas.1202885109)

Teka, I. A. et al. (2011) The diamidine diminazene aceturate is a substrate for the high-affinity pentamidine transporter: implications for the development of high resistance levels in trypanosomes. Molecular Pharmacology, 80(1), pp. 110-116. (doi: 10.1124/mol.111.071555)

Munday, J. C. , McLuskey, K., Brown, E., Coombs, G. H. and Mottram, J. C. (2011) Oligopeptidase B deficient mutants of Leishmania major. Molecular and Biochemical Parasitology, 175(1), pp. 49-57. (doi: 10.1016/j.molbiopara.2010.09.003)

Book Sections

Garcia-Salcedo, J. A., Munday, J. C. , Unciti-Broceta, J. D. and De Koning, H. P. (2014) Progress towards new treatments for human African trypanosomiasis. In: Magez, S. and Radwanska, M. (eds.) Trypanosomes and Trypanosomiasis. Springer, pp. 217-238. ISBN 9783709115558 (doi:10.1007/978-3-7091-1556-5_9)

This list was generated on Mon Oct 25 05:14:26 2021 BST.