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ATPaseTb2, a unique membrane-bound FoF1-ATPase component, is essential in bloodstream and dyskinetoplastic trypanosomes

PLoS pathogens, 2015-02, Vol.11 (2), p.e1004660-e1004660

2015

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Trypanosoma brucei TbIF1 inhibits the essential F1-ATPase in the infectious form of the parasite

PLoS neglected tropical diseases, 2017-04, Vol.11 (4), p.e0005552-e0005552

2017

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An ancestral interaction module promotes oligomerization in divergent mitochondrial ATP synthases

Nature communications, 2022-10, Vol.13 (1), p.5989-5989, Article 5989

2022

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Mitochondrion of the Trypanosoma brucei long slender bloodstream form is capable of ATP production by substrate-level phosphorylation

PLoS pathogens, 2023-10, Vol.19 (10), p.e1011699-e1011699

2023

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Cell-based and multi-omics profiling reveals dynamic metabolic repurposing of mitochondria to drive developmental progression of Trypanosoma brucei

PLoS biology, 2020-06, Vol.18 (6), p.e3000741-e3000741

2020

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Enigmatic Presence of Mitochondrial Complex I in Trypanosoma brucei Bloodstream Forms

Eukaryotic Cell, 2012-02, Vol.11 (2), p.183-193

2012

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Erratum for Cadena et al., “Mitochondrial Contact Site and Cristae Organization System and F1FO-ATP Synthase Crosstalk Is a Fundamental Property of Mitochondrial Cristae”

mSphere, 2022-05, Vol.7 (3), p.e0018922-e0018922

2022

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Mitochondrial Contact Site and Cristae Organization System and F 1 F O -ATP Synthase Crosstalk Is a Fundamental Property of Mitochondrial Cristae

mSphere, 2021-06, Vol.6 (3), p.e0032721

2021

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KREX2 is not essential for either procyclic or bloodstream form Trypanosoma brucei

PloS one, 2012-03, Vol.7 (3), p.e33405

2012

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Method for Isolation of Myxozoan Proliferative Stages from Fish at High Yield and Purity: An Essential Prerequisite for In Vitro, In Vivo and Genomics-Based Research Developments

Cells (Basel, Switzerland), 2022-01, Vol.11 (3), p.377

2022

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Differential functions of two editosome exoUases in Trypanosoma brucei

RNA (Cambridge), 2009-05, Vol.15 (5), p.947-957

2009

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Trypanocidal action of bisphosphonium salts through a mitochondrial target in bloodstream form Trypanosoma brucei

International journal for parasitology -- drugs and drug resistance, 2016-04, Vol.6 (1), p.23-34

2016

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TbMP57 Is a 3′ Terminal Uridylyl Transferase (TUTase) of the Trypanosoma brucei Editosome

Molecular cell, 2003-06, Vol.11 (6), p.1525-1536

2003

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Bioenergetic consequences of FoF1–ATP synthase/ATPase deficiency in two life cycle stages of Trypanosoma brucei

The Journal of biological chemistry, 2021-01, Vol.296, p.100357-100357, Article 100357

2021

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Mitochondrial ATP synthase of trypanosomes reveals the mechanism of oligomerization and its evolution

BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2022-09, Vol.1863, p.148628, Article 148628

2022

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Cultured bloodstream Trypanosoma brucei adapt to life without mitochondrial translation release factor 1

Scientific reports, 2018-03, Vol.8 (1), p.5135-15, Article 5135

2018

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Inhibition of F 1 -ATPase from Trypanosoma brucei by its regulatory protein inhibitor TbIF 1

The FEBS journal, 2018-12, Vol.285 (23), p.4413

2018

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Inhibition of F1‐ATPase from Trypanosoma brucei by its regulatory protein inhibitor TbIF1

The FEBS journal, 2018-12, Vol.285 (23), p.4413-4423

2018

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Inhibition of F 1 ‐ ATP ase from Trypanosoma brucei by its regulatory protein inhibitor Tb IF 1

The FEBS journal, 2018-12, Vol.285 (23), p.4413-4423

2018

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Trypanosoma brucei TbIF1 inhibits the essential F.sub.1-ATPase in the infectious form of the parasite

PLoS neglected tropical diseases, 2017-04, Vol.11 (4)

2017

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The F1‐ATPase from Trypanosoma brucei is elaborated by three copies of an additional p18‐subunit

The FEBS journal, 2018-02, Vol.285 (3), p.614-628

2018

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ATPaseTb2, a Unique Membrane-bound FoF1-ATPase Component, Is Essential in Bloodstream and Dyskinetoplastic Trypanosomes: e1004660

PLoS pathogens, 2015-02, Vol.11 (2)

2015

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The F 1 ‐ ATP ase from Trypanosoma brucei is elaborated by three copies of an additional p18‐subunit

The FEBS journal, 2018-02, Vol.285 (3), p.614-628

2018

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Erratum for Cadena et al., "Mitochondrial Contact Site and Cristae Organization System and F 1 F O -ATP Synthase Crosstalk Is a Fundamental Property of Mitochondrial Cristae"

mSphere, 2022-06, Vol.7 (3), p.e0018922

2022

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Mitochondrial Contact Site and Cristae Organization System and F1FO-ATP Synthase Crosstalk Is a Fundamental Property of Mitochondrial Cristae

mSphere, 2021-06, Vol.6 (3), p.e0032721-e0032721

2021

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ATPaseTb2, a unique membrane-bound FoF1-ATPase component, is essential in bloodstream and dyskinetoplastic trypanosomes

Trypanosoma brucei TbIF1 inhibits the essential F1-ATPase in the infectious form of the parasite

An ancestral interaction module promotes oligomerization in divergent mitochondrial ATP synthases

Mitochondrion of the Trypanosoma brucei long slender bloodstream form is capable of ATP production by substrate-level phosphorylation

Cell-based and multi-omics profiling reveals dynamic metabolic repurposing of mitochondria to drive developmental progression of Trypanosoma brucei

Enigmatic Presence of Mitochondrial Complex I in Trypanosoma brucei Bloodstream Forms

Erratum for Cadena et al., “Mitochondrial Contact Site and Cristae Organization System and F1FO-ATP Synthase Crosstalk Is a Fundamental Property of Mitochondrial Cristae”

Mitochondrial Contact Site and Cristae Organization System and F 1 F O -ATP Synthase Crosstalk Is a Fundamental Property of Mitochondrial Cristae

KREX2 is not essential for either procyclic or bloodstream form Trypanosoma brucei

Method for Isolation of Myxozoan Proliferative Stages from Fish at High Yield and Purity: An Essential Prerequisite for In Vitro, In Vivo and Genomics-Based Research Developments

Differential functions of two editosome exoUases in Trypanosoma brucei

Trypanocidal action of bisphosphonium salts through a mitochondrial target in bloodstream form Trypanosoma brucei

TbMP57 Is a 3′ Terminal Uridylyl Transferase (TUTase) of the Trypanosoma brucei Editosome

Bioenergetic consequences of FoF1–ATP synthase/ATPase deficiency in two life cycle stages of Trypanosoma brucei

Mitochondrial ATP synthase of trypanosomes reveals the mechanism of oligomerization and its evolution

Cultured bloodstream Trypanosoma brucei adapt to life without mitochondrial translation release factor 1

Inhibition of F 1 -ATPase from Trypanosoma brucei by its regulatory protein inhibitor TbIF 1

Inhibition of F1‐ATPase from Trypanosoma brucei by its regulatory protein inhibitor TbIF1

Inhibition of F 1 ‐ ATP ase from Trypanosoma brucei by its regulatory protein inhibitor Tb IF 1

Trypanosoma brucei TbIF1 inhibits the essential F.sub.1-ATPase in the infectious form of the parasite

The F1‐ATPase from Trypanosoma brucei is elaborated by three copies of an additional p18‐subunit

ATPaseTb2, a Unique Membrane-bound FoF1-ATPase Component, Is Essential in Bloodstream and Dyskinetoplastic Trypanosomes: e1004660

The F 1 ‐ ATP ase from Trypanosoma brucei is elaborated by three copies of an additional p18‐subunit

Erratum for Cadena et al., "Mitochondrial Contact Site and Cristae Organization System and F 1 F O -ATP Synthase Crosstalk Is a Fundamental Property of Mitochondrial Cristae"

Mitochondrial Contact Site and Cristae Organization System and F1FO-ATP Synthase Crosstalk Is a Fundamental Property of Mitochondrial Cristae

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