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D Chretien

Showing results (31-40 of 49) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1995
Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndromeJ Poulton, C Sewry, C G Potter, et al.
The Journal of Pediatrics|May 1, 1997
Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylationV Cormier-Daire, D Chretien, P Rustin, et al.
The Journal of Pediatrics|April 1, 1995
Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritisA Rötig, F Goutières, P Niaudet, et al.
Human Genetics|August 24, 1999
A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiencyI Valnot, J Kassis, D Chretien, et al.
Journal of Medical Genetics|January 20, 2004
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndromeP Bénit, A Slama, F Cartault, et al.
Neuromuscular Disorders : NMD|July 1, 1995
Cytochrome c oxidase deficiency presenting as recurrent neonatal myoglobinuriaP Saunier, D Chretien, C Wood, et al.
Cell Death and Differentiation|August 5, 2006
Cardiolipin deficiency releases cytochrome c from the inner mitochondrial membrane and accelerates stimuli-elicited apoptosisS-Y Choi, F Gonzalvez, G M Jenkins, et al.
European Journal of Pediatrics|March 1, 1994
Liver cytochrome c oxidase deficiency in a case of neonatal-onset hepatic failureP Edery, B Gérard, D Chretien, et al.
The Journal of Clinical Investigation|June 1, 1994
Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiencyT Bourgeron, D Chretien, J Poggi-Bach, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Clinical aspects of mitochondrial disordersA Munnich, P Rustin, A Rötig, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Journal of Inherited Metabolic Disease|January 1, 1995
Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndromeJ Poulton, C Sewry, C G Potter, et al.
The Journal of Pediatrics|May 1, 1997
Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylationV Cormier-Daire, D Chretien, P Rustin, et al.
The Journal of Pediatrics|April 1, 1995
Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritisA Rötig, F Goutières, P Niaudet, et al.
Human Genetics|August 24, 1999
A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiencyI Valnot, J Kassis, D Chretien, et al.
Journal of Medical Genetics|January 20, 2004
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndromeP Bénit, A Slama, F Cartault, et al.
Neuromuscular Disorders : NMD|July 1, 1995
Cytochrome c oxidase deficiency presenting as recurrent neonatal myoglobinuriaP Saunier, D Chretien, C Wood, et al.
Cell Death and Differentiation|August 5, 2006
Cardiolipin deficiency releases cytochrome c from the inner mitochondrial membrane and accelerates stimuli-elicited apoptosisS-Y Choi, F Gonzalvez, G M Jenkins, et al.
European Journal of Pediatrics|March 1, 1994
Liver cytochrome c oxidase deficiency in a case of neonatal-onset hepatic failureP Edery, B Gérard, D Chretien, et al.
The Journal of Clinical Investigation|June 1, 1994
Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiencyT Bourgeron, D Chretien, J Poggi-Bach, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Clinical aspects of mitochondrial disordersA Munnich, P Rustin, A Rötig, et al.
Pageof 5