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Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis

Mitochondrion, 2009-09, Vol.9 (5), p.331-339

2009

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Modulation of mitochondrial morphology by bioenergetics defects in primary human fibroblasts

Neuromuscular disorders : NMD, 2008-04, Vol.18 (4), p.319-330

2008

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Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins

Molecular biology of the cell, 2002-12, Vol.13 (12), p.4343-4354

2002

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Organization and dynamics of human mitochondrial DNA

Journal of cell science, 2004-06, Vol.117 (Pt 13), p.2653-2662

2004

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Impact on oxidative phosphorylation of immortalization with the telomerase gene

Neuromuscular disorders : NMD, 2007-05, Vol.17 (5), p.368-375

2007

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Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation

Annals of neurology, 2001-05, Vol.49 (5), p.607-617

2001

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Respiratory mutations lead to different pleiotropic effects on OXPHOS complexes in yeast and in human cells

FEBS letters, 2008-10, Vol.582 (23-24), p.3489-3493

2008

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In vivo functional investigations of lactic acid in patients with respiratory chain disorders

Archives of disease in childhood, 1997-01, Vol.76 (1), p.16-21

1997

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Chronic progressive external ophthalmoplegia with ragged-red fibers: Clinical, morphological and genetic investigations in 43 patients

Neuromuscular disorders : NMD, 1995-09, Vol.5 (5), p.399-413

1995

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The first pathogenic mitochondrial methionine tRNA point mutation is discovered in splenic lymphoma

Human mutation, 1998, Vol.11 (S1), p.S175-S183

1998

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Mutation « MELAS » (a3243g) de l'ADN mitochondrial : étude chez 19 patients des relations entre le phénotype clinique, les données morphologiques et moléculaires

Revue neurologique, 2000, Vol.156 (12), p.1136-1147

2000

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Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newborn

Journal of inherited metabolic disease, 1996-01, Vol.19 (3), p.286-295

1996

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Functional characterization of novel mutations in the human cytochrome b gene

European journal of human genetics : EJHG, 2001-07, Vol.9 (7), p.510-518

2001

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Morphological studies of skeletal muscle in lactic acidosis

Journal of inherited metabolic disease, 1996-01, Vol.19 (4), p.528-534

1996

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Ophtalmoplégies externes progressives d'origine mitochondriale : Apport des investigations morphologiques et moléculaires

Revue neurologique, 1997-02, Vol.153 (1), p.51-58

1997

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Functional mitochondrial heterogeneity in heteroplasmic cells carrying the mitochondrial DNA mutation associated with the MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes)

Pediatric research, 2000-08, Vol.48 (2), p.143-150

2000

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"MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data

Revue neurologique, 2000-12, Vol.156 (12), p.1136-1147

2000

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The first pathogenic mitochondrial methionine tRNA point mutation is discovered in splenic lymphoma

Human mutation, 1998, Vol.Suppl 1, p.S175-S183

1998

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ATP-Dependent calcium uptake by cholinergic synaptic vesicles isolated fromtorpedo electric organ

The Journal of membrane biology, 1980-05, Vol.54 (2), p.115-126

1980

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Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies

Revue neurologique, 1997-02, Vol.153 (1), p.51-58

1997

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Clinical and molecular heterogeneity of cytochromec oxidase deficiency in the newborn

Journal of inherited metabolic disease, 1996-05, Vol.19 (3), p.286-295

1996

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Evidence that the anti-coagulant and lethal properties of a basic phospholipase A sub(2) from snake venom are unrelated

FEBS letters, 1989-01, Vol.248 (1-2), p.1-4

1989

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Labelling of presynaptic membranes with the triplet probe, eosin, and its application in the study of protein rotational mobility

Biochemical Society transactions, 1986-12, Vol.14 (6), p.1253-1254

1986

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Uncovering genes involved in pollinator‐driven mating system shifts and selfing syndrome evolution in Brassica rapa

The New phytologist, 2024-08, Vol.243 (3), p.1220-1230

2024

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Combining biotechnology and evolution for understanding the mechanisms of pollinator attraction

Current opinion in biotechnology, 2021-08, Vol.70, p.213-219

2021

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Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis

Modulation of mitochondrial morphology by bioenergetics defects in primary human fibroblasts

Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins

Organization and dynamics of human mitochondrial DNA

Impact on oxidative phosphorylation of immortalization with the telomerase gene

Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation

Respiratory mutations lead to different pleiotropic effects on OXPHOS complexes in yeast and in human cells

In vivo functional investigations of lactic acid in patients with respiratory chain disorders

Chronic progressive external ophthalmoplegia with ragged-red fibers: Clinical, morphological and genetic investigations in 43 patients

The first pathogenic mitochondrial methionine tRNA point mutation is discovered in splenic lymphoma

Mutation « MELAS » (a3243g) de l'ADN mitochondrial : étude chez 19 patients des relations entre le phénotype clinique, les données morphologiques et moléculaires

Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newborn

Functional characterization of novel mutations in the human cytochrome b gene

Morphological studies of skeletal muscle in lactic acidosis

Ophtalmoplégies externes progressives d'origine mitochondriale : Apport des investigations morphologiques et moléculaires

Functional mitochondrial heterogeneity in heteroplasmic cells carrying the mitochondrial DNA mutation associated with the MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes)

"MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data

The first pathogenic mitochondrial methionine tRNA point mutation is discovered in splenic lymphoma

ATP-Dependent calcium uptake by cholinergic synaptic vesicles isolated fromtorpedo electric organ

Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies

Clinical and molecular heterogeneity of cytochromec oxidase deficiency in the newborn

Evidence that the anti-coagulant and lethal properties of a basic phospholipase A sub(2) from snake venom are unrelated

Labelling of presynaptic membranes with the triplet probe, eosin, and its application in the study of protein rotational mobility

Uncovering genes involved in pollinator‐driven mating system shifts and selfing syndrome evolution in Brassica rapa

Combining biotechnology and evolution for understanding the mechanisms of pollinator attraction

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