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Mitochondrial DNA damage and reactive oxygen species in neurodegenerative disease

FEBS letters, 2018-03, Vol.592 (5), p.728-742

2018

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Mechanisms of Mitochondrial DNA Deletion Formation

Trends in genetics, 2019-03, Vol.35 (3), p.235-244

2019

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Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs

Nature medicine, 2013-09, Vol.19 (9), p.1111-1113

2013

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Lack of Parkin Anticipates the Phenotype and Affects Mitochondrial Morphology and mtDNA Levels in a Mouse Model of Parkinson's Disease

The Journal of neuroscience, 2018-01, Vol.38 (4), p.1042-1053

2018

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The mitochondrial DNA polymerase gamma degrades linear DNA fragments precluding the formation of deletions

Nature communications, 2018-06, Vol.9 (1), p.2491-9, Article 2491

2018

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MitoTALEN reduces mutant mtDNA load and restores tRNAAla levels in a mouse model of heteroplasmic mtDNA mutation

Nature medicine, 2018-11, Vol.24 (11), p.1696-1700

2018

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Increased muscle PGC-1α expression protects from sarcopenia and metabolic disease during aging

Proceedings of the National Academy of Sciences - PNAS, 2009-12, Vol.106 (48), p.20405-20410

2009

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The CoQH2/CoQ Ratio Serves as a Sensor of Respiratory Chain Efficiency

Cell reports (Cambridge), 2016-04, Vol.15 (1), p.197-209

2016

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Mechanisms of formation and accumulation of mitochondrial DNA deletions in aging neurons

Human molecular genetics, 2009-03, Vol.18 (6), p.1028-1036

2009

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Nuclear-Mitochondrial Interactions

Biomolecules (Basel, Switzerland), 2022-03, Vol.12 (3), p.427

2022

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Mitochondrial targeted meganuclease as a platform to eliminate mutant mtDNA in vivo

Nature communications, 2021-05, Vol.12 (1), p.3210-3210, Article 3210

2021

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MitoTALEN: A General Approach to Reduce Mutant mtDNA Loads and Restore Oxidative Phosphorylation Function in Mitochondrial Diseases

Molecular therapy, 2015-10, Vol.23 (10), p.1592-1599

2015

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ATAD3 controls mitochondrial cristae structure in mouse muscle, influencing mtDNA replication and cholesterol levels

Journal of cell science, 2018-07, Vol.131 (13), p.jcs217075-jcs217075

2018

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The mitochondrial impairment, oxidative stress and neurodegeneration connection: reality or just an attractive hypothesis?

Trends in neurosciences (Regular ed.), 2008-05, Vol.31 (5), p.251-256

2008

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Current strategies towards therapeutic manipulation of mtDNA heteroplasmy

Frontiers in bioscience, 2017-01, Vol.22 (6), p.991-1010, Article 4529

2017

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Somatic mtDNA mutation spectra in the aging human putamen

PLoS genetics, 2013-12, Vol.9 (12), p.e1003990-e1003990

2013

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ATAD3A has a scaffolding role regulating mitochondria inner membrane structure and protein assembly

Cell reports (Cambridge), 2021-12, Vol.37 (12), p.110139-110139, Article 110139

2021

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Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency

Nature communications, 2020-02, Vol.11 (1), p.970-970, Article 970

2020

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Linear DNA-driven recombination in mammalian mitochondria

Nucleic acids research, 2024-04, Vol.52 (6), p.3088-3105

2024

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mitoTev‐TALE: a monomeric DNA editing enzyme to reduce mutant mitochondrial DNA levels

EMBO molecular medicine, 2018-09, Vol.10 (9), p.n/a

2018

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Qo site of the mitochondrial complex III is required for the transduction of hypoxic signaling via reactive oxygen species production

The Journal of cell biology, 2007-06, Vol.177 (6), p.1029-1036

2007

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Myopathy reversion in mice after restauration of mitochondrial complex I

EMBO molecular medicine, 2020-02, Vol.12 (2), p.e10674-n/a

2020

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Enhanced Transcriptional Activity and Mitochondrial Localization of STAT3 Co-induce Axon Regrowth in the Adult Central Nervous System

Cell reports (Cambridge), 2016-04, Vol.15 (2), p.398-410

2016

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The role of PGC‐1 coactivators in aging skeletal muscle and heart

IUBMB life, 2012-03, Vol.64 (3), p.231-241

2012

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Mitochondrial DNA damage and reactive oxygen species in neurodegenerative disease

Mechanisms of Mitochondrial DNA Deletion Formation

Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs

Selective elimination of mitochondrial mutations in the germline by genome editing

Lack of Parkin Anticipates the Phenotype and Affects Mitochondrial Morphology and mtDNA Levels in a Mouse Model of Parkinson's Disease

The mitochondrial DNA polymerase gamma degrades linear DNA fragments precluding the formation of deletions

MitoTALEN reduces mutant mtDNA load and restores tRNAAla levels in a mouse model of heteroplasmic mtDNA mutation

Increased muscle PGC-1α expression protects from sarcopenia and metabolic disease during aging

The CoQH2/CoQ Ratio Serves as a Sensor of Respiratory Chain Efficiency

Mechanisms of formation and accumulation of mitochondrial DNA deletions in aging neurons

Nuclear-Mitochondrial Interactions

Mitochondrial targeted meganuclease as a platform to eliminate mutant mtDNA in vivo

MitoTALEN: A General Approach to Reduce Mutant mtDNA Loads and Restore Oxidative Phosphorylation Function in Mitochondrial Diseases

ATAD3 controls mitochondrial cristae structure in mouse muscle, influencing mtDNA replication and cholesterol levels

The mitochondrial impairment, oxidative stress and neurodegeneration connection: reality or just an attractive hypothesis?

Current strategies towards therapeutic manipulation of mtDNA heteroplasmy

Somatic mtDNA mutation spectra in the aging human putamen

ATAD3A has a scaffolding role regulating mitochondria inner membrane structure and protein assembly

Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency

Linear DNA-driven recombination in mammalian mitochondria

mitoTev‐TALE: a monomeric DNA editing enzyme to reduce mutant mitochondrial DNA levels

Qo site of the mitochondrial complex III is required for the transduction of hypoxic signaling via reactive oxygen species production

Myopathy reversion in mice after restauration of mitochondrial complex I

Enhanced Transcriptional Activity and Mitochondrial Localization of STAT3 Co-induce Axon Regrowth in the Adult Central Nervous System

The role of PGC‐1 coactivators in aging skeletal muscle and heart

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