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miR-379 links glucocorticoid treatment with mitochondrial response in Duchenne muscular dystrophy

Scientific reports, 2020-06, Vol.10 (1), p.9139, Article 9139

2020

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BH3 mimetics activate multiple pro-autophagic pathways

Oncogene, 2011-09, Vol.30 (37), p.3918-3929

2011

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Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations

Human molecular genetics, 2005-08, Vol.14 (15), p.2231-2239

2005

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The R22X Mutation of the SDHD Gene in Hereditary Paraganglioma Abolishes the Enzymatic Activity of Complex II in the Mitochondrial Respiratory Chain and Activates the Hypoxia Pathway

American journal of human genetics, 2001-12, Vol.69 (6), p.1186-1197

2001

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Pro-oxidant/antioxidant balance controls pancreatic β-cell differentiation through the ERK1/2 pathway

Cell death & disease, 2014-10, Vol.5 (10), p.e1487-e1487

2014

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Effect of idebenone on cardiomyopathy in Friedreich's ataxia: a preliminary study

The Lancet (British edition), 1999-08, Vol.354 (9177), p.477-479

1999

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HIV-1 Tat protein directly induces mitochondrial membrane permeabilization and inactivates cytochrome c oxidase

Cell death & disease, 2012-03, Vol.3 (3), p.e282-e282

2012

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A brain-specific isoform of mitochondrial apoptosis-inducing factor: AIF2

Cell death and differentiation, 2010-07, Vol.17 (7), p.1155-1166

2010

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Idebenone and reduced cardiac hypertrophy in Friedreich's ataxia

Heart (British Cardiac Society), 2002-04, Vol.87 (4), p.346-349

2002

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Idebenone delays the onset of cardiac functional alteration without correction of Fe-S enzymes deficit in a mouse model for Friedreich ataxia

Human molecular genetics, 2004-05, Vol.13 (10), p.1017-1024

2004

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Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

Journal of medical genetics, 2004-01, Vol.41 (1), p.14-17

2004

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PO23 Contrôle de la différenciation des cellules bêta pancréatiques par les espèces réactives de l’oxygène

Diabetes & metabolism, 2015-03, Vol.41, p.A28-A29

2015

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Biochemical and molecular investigations in respiratory chain deficiencies

Clinica chimica acta, 1994-07, Vol.228 (1), p.35-51

1994

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Succinate dehydrogenase deficiency in human

Cellular and molecular life sciences : CMLS, 2005-10, Vol.62 (19-20), p.2317-2324

2005

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Long-term follow-up of neonatal mitochondrial cytopathies: a study of 57 patients

Pediatrics (Evanston), 2005-11, Vol.116 (5), p.1170

2005

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Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency

Journal of medical genetics, 2003-12, Vol.40 (12), p.896-899

2003

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The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency

Journal of medical genetics, 2003-03, Vol.40 (3), p.188-191

2003

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Invasive Haemaphysalis longicornis (Acari: Ixodidae) investigation in South Carolina: new records of establishment, pathogen prevalence, and blood meal analyses

Journal of medical entomology, 2023-11, Vol.60 (6), p.1398-1405

2023

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Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits

Molecular genetics and metabolism, 2002-09, Vol.77 (1-2), p.21-30

2002

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Mitochondria and diabetes mellitus: untangling a conflictive relationship

Journal of inherited metabolic disease, 2009-12, Vol.32 (6), p.684-698

2009

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Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome

Human genetics, 2000-02, Vol.106 (2), p.236-243

2000

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The molecular archaeology of a mitochondrial death effector: AIF in Drosophila

Cell death and differentiation, 2008-06, Vol.15 (6), p.1009-1018

2008

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Quinone analogues regulate mitochondrial substrate competitive oxidation

Biochemical and biophysical research communications, 2004-04, Vol.316 (4), p.1138-1142

2004

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Targeting neonatal ischemic brain injury with a pentapeptide-based irreversible caspase inhibitor

Cell death & disease, 2011-09, Vol.2 (9), p.e203-e203

2011

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Heart Hypertrophy and Function Are Improved by Idebenone in Friedreich's Ataxia

Free radical research, 2002-04, Vol.36 (4), p.467-469

2002

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miR-379 links glucocorticoid treatment with mitochondrial response in Duchenne muscular dystrophy

BH3 mimetics activate multiple pro-autophagic pathways

Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations

The R22X Mutation of the SDHD Gene in Hereditary Paraganglioma Abolishes the Enzymatic Activity of Complex II in the Mitochondrial Respiratory Chain and Activates the Hypoxia Pathway

Pro-oxidant/antioxidant balance controls pancreatic β-cell differentiation through the ERK1/2 pathway

Effect of idebenone on cardiomyopathy in Friedreich's ataxia: a preliminary study

HIV-1 Tat protein directly induces mitochondrial membrane permeabilization and inactivates cytochrome c oxidase

A brain-specific isoform of mitochondrial apoptosis-inducing factor: AIF2

Idebenone and reduced cardiac hypertrophy in Friedreich's ataxia

Idebenone delays the onset of cardiac functional alteration without correction of Fe-S enzymes deficit in a mouse model for Friedreich ataxia

Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

PO23 Contrôle de la différenciation des cellules bêta pancréatiques par les espèces réactives de l’oxygène

Biochemical and molecular investigations in respiratory chain deficiencies

Succinate dehydrogenase deficiency in human

Long-term follow-up of neonatal mitochondrial cytopathies: a study of 57 patients

Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency

The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency

Invasive Haemaphysalis longicornis (Acari: Ixodidae) investigation in South Carolina: new records of establishment, pathogen prevalence, and blood meal analyses

Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits

Mitochondria and diabetes mellitus: untangling a conflictive relationship

Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome

The molecular archaeology of a mitochondrial death effector: AIF in Drosophila

Quinone analogues regulate mitochondrial substrate competitive oxidation

Targeting neonatal ischemic brain injury with a pentapeptide-based irreversible caspase inhibitor

Heart Hypertrophy and Function Are Improved by Idebenone in Friedreich's Ataxia

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