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Why are many mRNAs translated to the vicinity of mitochondria: A role in protein complex assembly?

Gene, 2005-07, Vol.354, p.64-71

2005

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Energetic requirements and bioenergetic modulation of mitochondrial morphology and dynamics

Seminars in cell & developmental biology, 2010-08, Vol.21 (6), p.558-565

2010

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Mitochondrial ATP synthase disorders: Molecular mechanisms and the quest for curative therapeutic approaches

Biochimica et biophysica acta, 2009, Vol.1793 (1), p.186-199

2009

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yeast-based assay identifies drugs active against human mitochondrial disorders

Proceedings of the National Academy of Sciences - PNAS, 2011-07, Vol.108 (29), p.11989-11994

2011

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Consequences of the pathogenic T9176C mutation of human mitochondrial DNA on yeast mitochondrial ATP synthase

Biochimica et biophysica acta, 2010-06, Vol.1797 (6-7), p.1105-1112

2010

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A Yeast Model of the Neurogenic Ataxia Retinitis Pigmentosa (NARP) T8993G Mutation in the Mitochondrial ATP Synthase-6 Gene

The Journal of biological chemistry, 2007-11, Vol.282 (47), p.34039-34047

2007

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A genetic screen targeted on the F0 component of mitochodnrial ATP synthase in Saccharomyces cerevisiae

The Journal of biological chemistry, 2011, Vol.286 (20), p.18181-9

2011

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Introducing the human Leigh syndrom mutation T9176G into Saccharomyces cerevisiae mitochondrial DNA leads to severe defects in the incorporation of Atp6p into the ATP synthase and in the mitochondrial morphology

Human molecular genetics, 2009, Vol.18 (15), p.2889-98

2009

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The Leader Peptide of Yeast Atp6p Is Required for Efficient Interaction with the Atp9p Ring of the Mitochondrial ATPase

The Journal of biological chemistry, 2007-12, Vol.282 (50), p.36167-36176

2007

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Leigh syndrome leads to severe defects in the incorporation of Atp6p within the ATP synthase and mitochondrial morphology in Saccharomyces cerevisiae

New biotechnology, 2010-04, Vol.27, p.S59-S59

2010

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Defining the Pathogenesis of the Human Atp12p W94R Mutation Using a Saccharomyces cerevisiae Yeast Model

The Journal of biological chemistry, 2010-02, Vol.285 (6), p.4099-4109

2010

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Increasing Mitochondrial Substrate-level Phosphorylation Can Rescue Respiratory Growth of an ATP Synthase-deficient Yeast

The Journal of biological chemistry, 2005-09, Vol.280 (35), p.30751-30759

2005

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Yeast Cells Depleted in Atp14p Fail to Assemble Atp6p within the ATP Synthase and Exhibit Altered Mitochondrial Cristae Morphology

The Journal of biological chemistry, 2008-04, Vol.283 (15), p.9749-9758

2008

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PPA2 gene is involved in neonatal fatal acute dilated cardiomyopathy

Archives of Cardiovascular Diseases Supplements, 2019-01, Vol.11 (1), p.134-134

2019

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Cytochrome b-deficient mutants of the ubiquinol-cytochrome c oxidoreductase in Saccharomyces cerevisiae. Consequence for the functional and structural characteristics of the complex

The Journal of biological chemistry, 1993-07, Vol.268 (21), p.15626-15632

1993

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Investigating the on-site of the cytochrome bc1 complex in S. Cerevisiae with mutants resistant to Ilicicolin H, a novel on site inhibitor

The Journal of biological chemistry, 2006, Vol.281 (47), p.36036-43

2006

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Combining Inhibitor Resistance-conferring Mutations in Cytochrome b Creates Conditional Synthetic Lethality in Saccharomyces cerevisiae

The Journal of biological chemistry, 2009-03, Vol.284 (13), p.8478-8485

2009

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Yeast models of human mitochondrial diseases: from molecular mechanisms to drug screening

Biotechnology journal, 2006-03, Vol.1 (3), p.270-281

2006

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Introduction of cytochrome b mutations in Saccharomyces cerevisiae by a method that allows selection for both functional and non-functional cytochrome b proteins

Biochimica et biophysica acta, 2008-09, Vol.1777 (9), p.1147-1156

2008

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Yeast cells lacking the mitochondrial gene encoding the ATP synthase subunit 6 exhibit a selective loss of complex IV and unsual mitochondrial morphology

The Journal of biological chemistry, 2007, Vol.282 (15), p.10853-64.

2007

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A 'petite obligate' mutant of Saccharomyces cerevisiae : functional mDNA is lethal in cells lacking the delta subunit of mitochondrial F1-ATPase

The Journal of biological chemistry, 2006, Vol.281 (24), p.16305-13.

2006

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Molecular basis for resistance to antimycin and diuron, Q-cycle inhibitors acting at the Qi site in the mitochondrial ubiquinol-cytochrome c reductase in Saccharomyces cerevisiae

The Journal of biological chemistry, 1988-09, Vol.263 (25), p.12564-12570

1988

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Role of the Evolutionarily Conserved Cytochrome b Tryptophan 142 in the Ubiquinol Oxidation Catalyzed by the bc1 Complex in the Yeast Saccharomyces cerevisiae(∗)

The Journal of biological chemistry, 1995-09, Vol.270 (38), p.22321-22328

1995

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A point mutation in the mitochondrial cytochrome b gene obviates the requirement for the nuclear encoded core protein 2 subunit in the cytochrome bc1 complex in Saccharomyces cerevisiae

The Journal of biological chemistry, 1997-02, Vol.272 (8), p.4699-4704

1997

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Intragenic suppressors reveal long distance interactions between inactivating and reactivating amino acid replacements generating three-dimensional constraints in the structure of mitochondrial cytochrome b

The Journal of biological chemistry, 1990-09, Vol.265 (26), p.15750-15757

1990

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Why are many mRNAs translated to the vicinity of mitochondria: A role in protein complex assembly?

Energetic requirements and bioenergetic modulation of mitochondrial morphology and dynamics

Mitochondrial ATP synthase disorders: Molecular mechanisms and the quest for curative therapeutic approaches

yeast-based assay identifies drugs active against human mitochondrial disorders

Consequences of the pathogenic T9176C mutation of human mitochondrial DNA on yeast mitochondrial ATP synthase

A Yeast Model of the Neurogenic Ataxia Retinitis Pigmentosa (NARP) T8993G Mutation in the Mitochondrial ATP Synthase-6 Gene

A genetic screen targeted on the F0 component of mitochodnrial ATP synthase in Saccharomyces cerevisiae

Introducing the human Leigh syndrom mutation T9176G into Saccharomyces cerevisiae mitochondrial DNA leads to severe defects in the incorporation of Atp6p into the ATP synthase and in the mitochondrial morphology

The Leader Peptide of Yeast Atp6p Is Required for Efficient Interaction with the Atp9p Ring of the Mitochondrial ATPase

Leigh syndrome leads to severe defects in the incorporation of Atp6p within the ATP synthase and mitochondrial morphology in Saccharomyces cerevisiae

Defining the Pathogenesis of the Human Atp12p W94R Mutation Using a Saccharomyces cerevisiae Yeast Model

Increasing Mitochondrial Substrate-level Phosphorylation Can Rescue Respiratory Growth of an ATP Synthase-deficient Yeast

Yeast Cells Depleted in Atp14p Fail to Assemble Atp6p within the ATP Synthase and Exhibit Altered Mitochondrial Cristae Morphology

PPA2 gene is involved in neonatal fatal acute dilated cardiomyopathy

Cytochrome b-deficient mutants of the ubiquinol-cytochrome c oxidoreductase in Saccharomyces cerevisiae. Consequence for the functional and structural characteristics of the complex

Investigating the on-site of the cytochrome bc1 complex in S. Cerevisiae with mutants resistant to Ilicicolin H, a novel on site inhibitor

Combining Inhibitor Resistance-conferring Mutations in Cytochrome b Creates Conditional Synthetic Lethality in Saccharomyces cerevisiae

Yeast models of human mitochondrial diseases: from molecular mechanisms to drug screening

Introduction of cytochrome b mutations in Saccharomyces cerevisiae by a method that allows selection for both functional and non-functional cytochrome b proteins

Yeast cells lacking the mitochondrial gene encoding the ATP synthase subunit 6 exhibit a selective loss of complex IV and unsual mitochondrial morphology

A 'petite obligate' mutant of Saccharomyces cerevisiae : functional mDNA is lethal in cells lacking the delta subunit of mitochondrial F1-ATPase

Molecular basis for resistance to antimycin and diuron, Q-cycle inhibitors acting at the Qi site in the mitochondrial ubiquinol-cytochrome c reductase in Saccharomyces cerevisiae

Role of the Evolutionarily Conserved Cytochrome b Tryptophan 142 in the Ubiquinol Oxidation Catalyzed by the bc1 Complex in the Yeast Saccharomyces cerevisiae(∗)

A point mutation in the mitochondrial cytochrome b gene obviates the requirement for the nuclear encoded core protein 2 subunit in the cytochrome bc1 complex in Saccharomyces cerevisiae

Intragenic suppressors reveal long distance interactions between inactivating and reactivating amino acid replacements generating three-dimensional constraints in the structure of mitochondrial cytochrome b

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