Suchergebnisse - (Person:"Munday, Jane C")

PubPharm (40)

21

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

enthalten in: PLoS neglected tropical diseases | 2016

von Eze, A. | Gould, M. | Munday, J. | +4

22

Comparative genomics of drug resistance in Trypanosoma brucei rhodesiense

enthalten in: Cellular and molecular life sciences | 2016

von Graf, F. | Ludin, P. | Arquint, C. | +11

23

Comparative genomics of drug resistance in Trypanosoma brucei rhodesiense

enthalten in: Cellular and molecular life sciences | 2016

von Graf, F. | Ludin, P. | Arquint, C. | +11

24

Chimerization at the AQP2-AQP3 locus is the genetic basis of melarsoprol-pentamidine cross-resistance in clinical Trypanosoma brucei gambiense isolates

enthalten in: International journal for parasitology. Drugs and drug resistance | 2015

von Graf, F. | Baker, N. | Munday, J. | +3

25

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

enthalten in: Molecular microbiology | 2015

von Munday, J. | Tagoe, D. | Eze, A. | +8

26

Transport proteins determine drug sensitivity and resistance in a protozoan parasite, Trypanosoma brucei

enthalten in: Frontiers in pharmacology | 2015

von Munday, J. | Settimo, L. | de Koning, H.

27

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

enthalten in: Molecular microbiology | 2015

von Munday, J. | Tagoe, D. | Eze, A. | +8

28

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

enthalten in: The Journal of antimicrobial chemotherapy | 2014

von Munday, J. | Eze, A. | Baker, N. | +17

29

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

enthalten in: The journal of antimicrobial chemotherapy | 2014

von Munday, J. | Eze, A. | Baker, N. | +17

30

Functional expression of TcoAT1 reveals it to be a P1-type nucleoside transporter with no capacity for diminazene uptake

enthalten in: International journal for parasitology. Drugs and drug resistance | 2013

von Munday, J. | Rojas López, K. | Eze, A. | +6