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C Marsac

Showing results (11-20 of 91) with videos related to

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The Journal of Sports Medicine and Physical Fitness|June 1, 1991
Blood mononuclear cells energy metabolism response to muscular exerciseA Ferry, C Marsac, A Duvallet, et al.
Annales De Biologie Clinique|January 1, 1976
[Enzymopathic congenital hyperlactacidemia]J P Leroux, C Marsac, J M Saudubray
European Journal of Biochemistry|November 1, 1993
Expression of human cytochrome c oxidase subunits during fetal developmentG Bonne, P Seibel, S Possekel, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 1, 1993
Sequence analysis of a deleted mitochondrial DNA molecule in heteroplasmic miceI Nelson, S Gerasimov, C Marsac, et al.
Biochemical and Biophysical Research Communications|December 14, 1990
Identification of point mutations by mispairing PCR as exemplified in MERRF diseaseP Seibel, F Degoul, N Romero, et al.
Lyon Medical|January 1, 1971
[Brucella hepatitis with caseous necrosis]R Bastin, J L Vilde, C Lapresle, et al.
Journal of the Neurological Sciences|September 1, 1994
Expression of cytochrome c oxidase subunits encoded by mitochondrial or nuclear DNA in the muscle of patients with zidovudine myopathyP Chariot, G Bonne, F J Authier, et al.
Medecine & Chirurgie Digestives|January 1, 1973
[Brucellian hepatitis with caseiform necrosis]R Bastin, J L Vilde, C Lapresle, et al.
Annals of Neurology|March 1, 1994
Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutationF Degoul, M Diry, A Pou-Serradell, et al.
Human Genetics|April 4, 2000
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndromeB Parfait, D Chretien, A Rötig, et al.
Pageof 10

Showing results (11-20 of 91) with videos related to

Sort By:
Pageof 10
The Journal of Sports Medicine and Physical Fitness|June 1, 1991
Blood mononuclear cells energy metabolism response to muscular exerciseA Ferry, C Marsac, A Duvallet, et al.
Annales De Biologie Clinique|January 1, 1976
[Enzymopathic congenital hyperlactacidemia]J P Leroux, C Marsac, J M Saudubray
European Journal of Biochemistry|November 1, 1993
Expression of human cytochrome c oxidase subunits during fetal developmentG Bonne, P Seibel, S Possekel, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 1, 1993
Sequence analysis of a deleted mitochondrial DNA molecule in heteroplasmic miceI Nelson, S Gerasimov, C Marsac, et al.
Biochemical and Biophysical Research Communications|December 14, 1990
Identification of point mutations by mispairing PCR as exemplified in MERRF diseaseP Seibel, F Degoul, N Romero, et al.
Lyon Medical|January 1, 1971
[Brucella hepatitis with caseous necrosis]R Bastin, J L Vilde, C Lapresle, et al.
Journal of the Neurological Sciences|September 1, 1994
Expression of cytochrome c oxidase subunits encoded by mitochondrial or nuclear DNA in the muscle of patients with zidovudine myopathyP Chariot, G Bonne, F J Authier, et al.
Medecine & Chirurgie Digestives|January 1, 1973
[Brucellian hepatitis with caseiform necrosis]R Bastin, J L Vilde, C Lapresle, et al.
Annals of Neurology|March 1, 1994
Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutationF Degoul, M Diry, A Pou-Serradell, et al.
Human Genetics|April 4, 2000
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndromeB Parfait, D Chretien, A Rötig, et al.
Pageof 10