Lista de obras - Jane Munday - Dominio Público Uruguay

Aquaglyceroporin 2 controls susceptibility to melarsoprol and pentamidine in African trypanosomes

artículo científico publicado en 2012

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

artículo científico publicado en 2015

Comparative genomics of drug resistance in Trypanosoma brucei rhodesiense

artículo científico publicado en 2016

Cyclic AMP effectors in African trypanosomes revealed by genome-scale RNA interference library screening for resistance to the phosphodiesterase inhibitor CpdA

artículo científico publicado en 2013

Cyclic Nucleotide-Specific Phosphodiesterases as Potential Drug Targets for Anti-Leishmania Therapy

artículo científico publicado en 2018

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

artículo científico

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

artículo científico publicado en 2013

In vitro interactions between sitamaquine and amphotericin B, sodium stibogluconate, miltefosine, paromomycin and pentamidine against Leishmania donovani

artículo científico publicado en 2011

Oligopeptidase B deficient mutants of Leishmania major

artículo científico publicado en 2010

Pyrimidine biosynthesis is not an essential function for Trypanosoma brucei bloodstream forms

artículo científico publicado en 2013

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

artículo científico publicado en 2016

Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity

artículo científico publicado en 2019

Targeting a Subpocket in Trypanosoma brucei Phosphodiesterase B1 (TbrPDEB1) Enables the Structure-Based Discovery of Selective Inhibitors with Trypanocidal Activity.

artículo científico publicado en 2018

The diamidine diminazene aceturate is a substrate for the high-affinity pentamidine transporter: implications for the development of high resistance levels in trypanosomes

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Trypanosoma brucei bloodstream forms express highly specific and separate transporters for adenine and hypoxanthine; evidence for a new protozoan purine transporter family?

artículo científico publicado en 2018

Lista de obras de Jane Munday

Aquaglyceroporin 2 controls susceptibility to melarsoprol and pentamidine in African trypanosomes

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

Comparative genomics of drug resistance in Trypanosoma brucei rhodesiense

Cyclic AMP effectors in African trypanosomes revealed by genome-scale RNA interference library screening for resistance to the phosphodiesterase inhibitor CpdA

Cyclic Nucleotide-Specific Phosphodiesterases as Potential Drug Targets for Anti-Leishmania Therapy

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

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

In vitro interactions between sitamaquine and amphotericin B, sodium stibogluconate, miltefosine, paromomycin and pentamidine against Leishmania donovani

Oligopeptidase B deficient mutants of Leishmania major

Pyrimidine biosynthesis is not an essential function for Trypanosoma brucei bloodstream forms

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

Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity

Targeting a Subpocket in Trypanosoma brucei Phosphodiesterase B1 (TbrPDEB1) Enables the Structure-Based Discovery of Selective Inhibitors with Trypanocidal Activity.

The diamidine diminazene aceturate is a substrate for the high-affinity pentamidine transporter: implications for the development of high resistance levels in trypanosomes

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

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

Trypanosoma brucei bloodstream forms express highly specific and separate transporters for adenine and hypoxanthine; evidence for a new protozoan purine transporter family?