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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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Immunological properties of notexin, a potent presynaptic and myotoxic component from venom of the Australian tiger snake Notechis scutatus scutatus

FEBS letters, 1989-07, Vol.250 (2), p.479-482

1989

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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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Isolation of Pure Cholinergic Nerve Endings from Torpedo Electric Organ: Evaluation of Their Metabolic Properties

The Journal of cell biology, 1977-10, Vol.75 (1), p.43-55

1977

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Evidence that the anti-coagulant and lethal properties of a basic phospholipase A2 from snake venom are unrelated

FEBS letters, 1989-05, Vol.248 (1-2), p.1-4

1989

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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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Isolation of pure cholinergic nerve endings from the electric organ of Torpedo marmorata

Biochemical journal, 1976-10, Vol.160 (1), p.113-115

1976

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Retrograde Inhibition of Transmitter Release by ATP

Journal of neurochemistry, 1980-04, Vol.34 (4), p.923-932

1980

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ATP-dependent calcium uptake by cholinergic synaptic vesicles isolated from Torpedo electric organ

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

1980

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RELATED CHANGES IN AMOUNTS OF ACh AND ATP IN RESTING AND ACTIVE TORPEDO NERVE ELECTROPLAQUE SYNAPSES

Journal of neurochemistry, 1977-06, Vol.28 (6), p.1259-1267

1977

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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

Volltextzugriff (PDF)

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

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

1998

Volltextzugriff (PDF)

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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

Immunological properties of notexin, a potent presynaptic and myotoxic component from venom of the Australian tiger snake Notechis scutatus scutatus

Functional characterization of novel mutations in the human cytochrome b gene

Morphological studies of skeletal muscle in lactic acidosis

Isolation of Pure Cholinergic Nerve Endings from Torpedo Electric Organ: Evaluation of Their Metabolic Properties

Evidence that the anti-coagulant and lethal properties of a basic phospholipase A2 from snake venom are unrelated

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)

Isolation of pure cholinergic nerve endings from the electric organ of Torpedo marmorata

Retrograde Inhibition of Transmitter Release by ATP

ATP-dependent calcium uptake by cholinergic synaptic vesicles isolated from Torpedo electric organ

RELATED CHANGES IN AMOUNTS OF ACh AND ATP IN RESTING AND ACTIVE TORPEDO NERVE ELECTROPLAQUE SYNAPSES

"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

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