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Mitochondrial transplantation-a possible therapeutic for mitochondrial dysfunction?: Mitochondrial transfer is a potential cure for many diseases but proof of efficacy and safety is still lacking

EMBO reports, 2020-09, Vol.21 (9), p.e50964-e50964

2020

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OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

EMBO molecular medicine, 2018-11, Vol.10 (11), p.n/a

2018

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Salvaging hope: Is increasing NAD+ a key to treating mitochondrial myopathy?

EMBO molecular medicine, 2014-06, Vol.6 (6), p.705-707

2014

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How much does a disrupted mitochondrial network influence neuronal dysfunction?

EMBO molecular medicine, 2019-01, Vol.11 (1), p.n/a

2019

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The process of mammalian mitochondrial protein synthesis

Cell and tissue research, 2017-01, Vol.367 (1), p.5-20

2017

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A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency

European journal of human genetics : EJHG, 2015-07, Vol.23 (7), p.935-939

2015

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The human mitochondrial ribosome recycling factor is essential for cell viability

Nucleic acids research, 2008-10, Vol.36 (18), p.5787

2008

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Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency

Biochimica et biophysica acta, 2014-01, Vol.1842 (1), p.56-64

2014

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Defective Mitochondrial mRNA Maturation Is Associated with Spastic Ataxia

American journal of human genetics, 2010-11, Vol.87 (5), p.655-660

2010

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Human pentatricopeptide proteins: Only a few and what do they do?

RNA biology, 2013, Vol.10 (9), p.1433-1438

2013

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Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency

Brain (London, England : 1878), 2011-01, Vol.134 (Pt 1), p.183-195

2011

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The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families

Brain (London, England : 1878), 2010-10, Vol.133 (10), p.2952-2963

2010

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The role of the mitochondrial ribosome in human disease: searching for mutations in 12S mitochondrial rRNA with high disruptive potential

Human molecular genetics, 2014-02, Vol.23 (4), p.949-967

2014

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Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy

Brain (London, England : 1878), 2009-11, Vol.132 (11), p.3165-3174

2009

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Clinical, biochemical, and genetic features associated with VARS2‐related mitochondrial disease

Human mutation, 2018-04, Vol.39 (4), p.563-578

2018

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Mitochondrial transplantation—a possible therapeutic for mitochondrial dysfunction?

EMBO reports, 2020-09, Vol.21 (9), p.n/a

2020

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Structure based hypothesis of a mitochondrial ribosome rescue mechanism

Biology direct, 2012-05, Vol.7 (1), p.14-14

2012

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An mtDNA Mutation in the Initiation Codon of the Cytochrome C Oxidase Subunit II Gene Results in Lower Levels of the Protein and a Mitochondrial Encephalomyopathy

American journal of human genetics, 1999-05, Vol.64 (5), p.1330-1339

1999

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A novel point mutation in the mitochondrial tRNA gene produces a neurogastrointestinal syndrome

European journal of human genetics : EJHG, 2004-06, Vol.12 (6), p.509-512

2004

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Mitochondrial transplantation-a possible therapeutic for mitochondrial dysfunction?: Mitochondrial transfer is a potential cure for many diseases but proof of efficacy and safety is still lacking

OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

Salvaging hope: Is increasing NAD+ a key to treating mitochondrial myopathy?

How much does a disrupted mitochondrial network influence neuronal dysfunction?

The process of mammalian mitochondrial protein synthesis

A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency

OXA 1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

The human mitochondrial ribosome recycling factor is essential for cell viability

Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency

Defective Mitochondrial mRNA Maturation Is Associated with Spastic Ataxia

Human pentatricopeptide proteins: Only a few and what do they do?

Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency

The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families

The role of the mitochondrial ribosome in human disease: searching for mutations in 12S mitochondrial rRNA with high disruptive potential

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy

Clinical, biochemical, and genetic features associated with VARS2‐related mitochondrial disease

Mitochondrial transplantation—a possible therapeutic for mitochondrial dysfunction?

Structure based hypothesis of a mitochondrial ribosome rescue mechanism

An mtDNA Mutation in the Initiation Codon of the Cytochrome C Oxidase Subunit II Gene Results in Lower Levels of the Protein and a Mitochondrial Encephalomyopathy

A novel point mutation in the mitochondrial tRNA gene produces a neurogastrointestinal syndrome

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