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C Marsac

Showing results (61-70 of 91) with videos related to

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Digestive Diseases and Sciences|March 1, 1992
Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorderV Li, J Hostein, N B Romero, et al.
American Journal of Human Genetics|December 18, 1997
Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosisB Aral, C Benelli, G Ait-Ghezala, et al.
Experimental Neurology|July 23, 1999
Overproduction of Cu/Zn-superoxide dismutase or Bcl-2 prevents the brain mitochondrial respiratory dysfunction induced by glutathione depletionM Mérad-Saïdoune, E Boitier, A Nicole, 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.
Journal of Leukocyte Biology|March 25, 2000
Regulation of ICAM-1/CD54 expression on human endothelial cells by hydrogen peroxide involves inducible NO synthaseM S Zadeh, J P Kolb, D Geromin, et al.
Human Molecular Genetics|February 1, 1995
Pyruvate dehydrogenase deficiency in a female due to a 4 base pair deletion in exon 10 of the E1 alpha geneW Lissens, I Desguerre, C Benelli, et al.
Revue Neurologique|January 1, 1991
[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]C Marsac, F Degoul, G Bonne, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 1, 1991
[Demonstration of abnormalities of myocardial mitochondrial oxygenation in cardiac graft rejection]P Abastado, D Duboc, C Marsac, et al.
Journal of the Neurological Sciences|October 1, 1991
Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF)P Seibel, F Degoul, G Bonne, et al.
European Journal of Neurology|November 29, 2013
Intrafamilial heterogeneous clinical presentation of the mitochondrial 3243 MELAS mutation; molecular investigations among four generationsF Degoul, M Diry, F Viader, et al.
Pageof 10

Showing results (61-70 of 91) with videos related to

Sort By:
Pageof 10
Digestive Diseases and Sciences|March 1, 1992
Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorderV Li, J Hostein, N B Romero, et al.
American Journal of Human Genetics|December 18, 1997
Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosisB Aral, C Benelli, G Ait-Ghezala, et al.
Experimental Neurology|July 23, 1999
Overproduction of Cu/Zn-superoxide dismutase or Bcl-2 prevents the brain mitochondrial respiratory dysfunction induced by glutathione depletionM Mérad-Saïdoune, E Boitier, A Nicole, 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.
Journal of Leukocyte Biology|March 25, 2000
Regulation of ICAM-1/CD54 expression on human endothelial cells by hydrogen peroxide involves inducible NO synthaseM S Zadeh, J P Kolb, D Geromin, et al.
Human Molecular Genetics|February 1, 1995
Pyruvate dehydrogenase deficiency in a female due to a 4 base pair deletion in exon 10 of the E1 alpha geneW Lissens, I Desguerre, C Benelli, et al.
Revue Neurologique|January 1, 1991
[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]C Marsac, F Degoul, G Bonne, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 1, 1991
[Demonstration of abnormalities of myocardial mitochondrial oxygenation in cardiac graft rejection]P Abastado, D Duboc, C Marsac, et al.
Journal of the Neurological Sciences|October 1, 1991
Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF)P Seibel, F Degoul, G Bonne, et al.
European Journal of Neurology|November 29, 2013
Intrafamilial heterogeneous clinical presentation of the mitochondrial 3243 MELAS mutation; molecular investigations among four generationsF Degoul, M Diry, F Viader, et al.
Pageof 10