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P Rustin

Showing results (81-90 of 157) with videos related to

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The Journal of Biological Chemistry|June 21, 1996
Fluxes of nicotinamide adenine dinucleotides through mitochondrial membranes in human cultured cellsP Rustin, B Parfait, D Chretien, et al.
Journal of Inherited Metabolic Disease|November 20, 1998
Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiencyJ P Harpey, D Heron, M Prudent, et al.
The Journal of Pediatrics|February 1, 1994
Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathiesP Rustin, J Lebidois, D Chretien, et al.
Nature Genetics|November 5, 1997
Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxiaA Rötig, P de Lonlay, D Chretien, et al.
Biochemical and Biophysical Research Communications|March 7, 1996
Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chainM A Birch-Machin, C Marsac, G Ponsot, et al.
Biochemical and Biophysical Research Communications|July 30, 1997
The consequences of a mild respiratory chain deficiency on substrate competitive oxidation in human mitochondriaV Geromel, B Parfait, J C von Kleist-Retzow, et al.
Cellular and Molecular Life Sciences : CMLS|September 7, 2005
Succinate dehydrogenase deficiency in humanJ-J Brière, J Favier, V El Ghouzzi, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2000
Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathyH Li, J Wang, H Wilhelmsson, et al.
Heart (British Cardiac Society)|October 17, 2001
Heart transplantation in children with mitochondrial cardiomyopathyD Bonnet, P Rustin, A Rötig, et al.
Human Molecular Genetics|May 24, 2001
Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNAV Geromel, N Kadhom, I Cebalos-Picot, et al.
Pageof 16

Showing results (81-90 of 157) with videos related to

Sort By:
Pageof 16
The Journal of Biological Chemistry|June 21, 1996
Fluxes of nicotinamide adenine dinucleotides through mitochondrial membranes in human cultured cellsP Rustin, B Parfait, D Chretien, et al.
Journal of Inherited Metabolic Disease|November 20, 1998
Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiencyJ P Harpey, D Heron, M Prudent, et al.
The Journal of Pediatrics|February 1, 1994
Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathiesP Rustin, J Lebidois, D Chretien, et al.
Nature Genetics|November 5, 1997
Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxiaA Rötig, P de Lonlay, D Chretien, et al.
Biochemical and Biophysical Research Communications|March 7, 1996
Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chainM A Birch-Machin, C Marsac, G Ponsot, et al.
Biochemical and Biophysical Research Communications|July 30, 1997
The consequences of a mild respiratory chain deficiency on substrate competitive oxidation in human mitochondriaV Geromel, B Parfait, J C von Kleist-Retzow, et al.
Cellular and Molecular Life Sciences : CMLS|September 7, 2005
Succinate dehydrogenase deficiency in humanJ-J Brière, J Favier, V El Ghouzzi, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2000
Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathyH Li, J Wang, H Wilhelmsson, et al.
Heart (British Cardiac Society)|October 17, 2001
Heart transplantation in children with mitochondrial cardiomyopathyD Bonnet, P Rustin, A Rötig, et al.
Human Molecular Genetics|May 24, 2001
Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNAV Geromel, N Kadhom, I Cebalos-Picot, et al.
Pageof 16