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DiMauro

Showing results (371-380 of 942) with videos related to

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Acta Neuropathologica|May 20, 2004
Hepato-cerebral syndrome: genetic and pathological studies in an infant with a dGK mutationMassimiliano Filosto, Michelangelo Mancuso, Giuliano Tomelleri, et al.
Journal of Medicinal Chemistry|January 16, 2013
Discovery of a class of novel tankyrase inhibitors that bind to both the nicotinamide pocket and the induced pocketHoward Bregman, Hakan Gunaydin, Yan Gu, et al.
Journal of Medical Genetics|July 1, 1997
The mitochondrial A3243G mutation presenting as severe cardiomyopathyL Vilarinho, F M Santorelli, M J Rosas, et al.
Journal of Lipid Research|September 14, 1999
Microanalysis of cardiolipin in small biopsies including skeletal muscle from patients with mitochondrial diseaseM Schlame, S Shanske, S Doty, et al.
BMC Genomics|November 17, 2017
Physical activity in the prevention of human diseases: role of epigenetic modificationsElisa Grazioli, Ivan Dimauro, Neri Mercatelli, et al.
Human Molecular Genetics|March 1, 1994
Extremely high levels of mutant mtDNAs co-localize with cytochrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243V Petruzzella, C T Moraes, M C Sano, et al.
Neuromuscular Disorders : NMD|January 1, 1996
Cloning of bovine muscle glycogen phosphorylase cDNA and identification of a mutation in cattle with myophosphorylase deficiency, an animal model for McArdle's diseaseS Tsujino, S Shanske, S J Valberg, et al.
Physical Review Letters|February 7, 2003
Observation of a transition in the dynamics of strong-field double ionizationJ L Chaloupka, J Rudati, R Lafon, et al.
Physical Review Letters|February 4, 2017
Precise Access to the Molecular-Frame Complex Recombination Dipole through High-Harmonic SpectroscopyS B Schoun, A Camper, P Salières, et al.
Journal of the Neurological Sciences|April 11, 2003
Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b geneMichelangelo Mancuso, Massimiliano Filosto, J Clarke Stevens, et al.
Pageof 95

Showing results (371-380 of 942) with videos related to

Sort By:
Pageof 95
Acta Neuropathologica|May 20, 2004
Hepato-cerebral syndrome: genetic and pathological studies in an infant with a dGK mutationMassimiliano Filosto, Michelangelo Mancuso, Giuliano Tomelleri, et al.
Journal of Medicinal Chemistry|January 16, 2013
Discovery of a class of novel tankyrase inhibitors that bind to both the nicotinamide pocket and the induced pocketHoward Bregman, Hakan Gunaydin, Yan Gu, et al.
Journal of Medical Genetics|July 1, 1997
The mitochondrial A3243G mutation presenting as severe cardiomyopathyL Vilarinho, F M Santorelli, M J Rosas, et al.
Journal of Lipid Research|September 14, 1999
Microanalysis of cardiolipin in small biopsies including skeletal muscle from patients with mitochondrial diseaseM Schlame, S Shanske, S Doty, et al.
BMC Genomics|November 17, 2017
Physical activity in the prevention of human diseases: role of epigenetic modificationsElisa Grazioli, Ivan Dimauro, Neri Mercatelli, et al.
Human Molecular Genetics|March 1, 1994
Extremely high levels of mutant mtDNAs co-localize with cytochrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243V Petruzzella, C T Moraes, M C Sano, et al.
Neuromuscular Disorders : NMD|January 1, 1996
Cloning of bovine muscle glycogen phosphorylase cDNA and identification of a mutation in cattle with myophosphorylase deficiency, an animal model for McArdle's diseaseS Tsujino, S Shanske, S J Valberg, et al.
Physical Review Letters|February 7, 2003
Observation of a transition in the dynamics of strong-field double ionizationJ L Chaloupka, J Rudati, R Lafon, et al.
Physical Review Letters|February 4, 2017
Precise Access to the Molecular-Frame Complex Recombination Dipole through High-Harmonic SpectroscopyS B Schoun, A Camper, P Salières, et al.
Journal of the Neurological Sciences|April 11, 2003
Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b geneMichelangelo Mancuso, Massimiliano Filosto, J Clarke Stevens, et al.
Pageof 95