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M Zeviani

Showing results (31-40 of 184) with videos related to

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Human Molecular Genetics|January 1, 1996
Complex I deficiency is associated with 3243G:C mitochondrial DNA in osteosarcoma cell cybridsD R Dunbar, P A Moonie, M Zeviani, et al.
Nucleic Acids Research|August 11, 1991
A full-length cDNA encoding a mitochondrial DNA-specific single-stranded DNA binding protein from Xenopus laevisV Tiranti, B Barat-Gueride, J Bijl, et al.
Annals of Neurology|June 1, 1985
Mitochondrial myopathiesS DiMauro, E Bonilla, M Zeviani, et al.
Gene|September 30, 1988
Subunit Va of human and bovine cytochrome c oxidase is highly conservedR Rizzuto, H Nakase, M Zeviani, et al.
Gene Therapy|July 29, 2017
AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndromeI Di Meo, S Marchet, C Lamperti, et al.
Cell Death & Disease|July 10, 2015
Loss of apoptosis-inducing factor critically affects MIA40 functionK Meyer, S Buettner, D Ghezzi, et al.
Genomics|June 10, 1995
The gene (NFE2L1) for human NRF-1, an activator involved in nuclear-mitochondrial interactions, maps to 7q32V Tiranti, E Rossi, M Rocchi, et al.
Archives of Neurology|September 1, 1986
Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentrationH Reichmann, R Rohkamm, M Zeviani, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Neuromuscular syndrome associated with the 3291T-->C mutation of mitochondrial DNA: a second caseG Uziel, F Carrara, T Granata, et al.
European Journal of Biochemistry|April 1, 1994
Single-stranded-DNA-binding proteins from human mitochondria and Escherichia coli have analogous physicochemical propertiesU Curth, C Urbanke, J Greipel, et al.
Pageof 19

Showing results (31-40 of 184) with videos related to

Sort By:
Pageof 19
Human Molecular Genetics|January 1, 1996
Complex I deficiency is associated with 3243G:C mitochondrial DNA in osteosarcoma cell cybridsD R Dunbar, P A Moonie, M Zeviani, et al.
Nucleic Acids Research|August 11, 1991
A full-length cDNA encoding a mitochondrial DNA-specific single-stranded DNA binding protein from Xenopus laevisV Tiranti, B Barat-Gueride, J Bijl, et al.
Annals of Neurology|June 1, 1985
Mitochondrial myopathiesS DiMauro, E Bonilla, M Zeviani, et al.
Gene|September 30, 1988
Subunit Va of human and bovine cytochrome c oxidase is highly conservedR Rizzuto, H Nakase, M Zeviani, et al.
Gene Therapy|July 29, 2017
AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndromeI Di Meo, S Marchet, C Lamperti, et al.
Cell Death & Disease|July 10, 2015
Loss of apoptosis-inducing factor critically affects MIA40 functionK Meyer, S Buettner, D Ghezzi, et al.
Genomics|June 10, 1995
The gene (NFE2L1) for human NRF-1, an activator involved in nuclear-mitochondrial interactions, maps to 7q32V Tiranti, E Rossi, M Rocchi, et al.
Archives of Neurology|September 1, 1986
Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentrationH Reichmann, R Rohkamm, M Zeviani, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Neuromuscular syndrome associated with the 3291T-->C mutation of mitochondrial DNA: a second caseG Uziel, F Carrara, T Granata, et al.
European Journal of Biochemistry|April 1, 1994
Single-stranded-DNA-binding proteins from human mitochondria and Escherichia coli have analogous physicochemical propertiesU Curth, C Urbanke, J Greipel, et al.
Pageof 19