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DiMauro

Showing results (531-540 of 942) with videos related to

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The Biochemical Journal|April 5, 2002
Copper supplementation restores cytochrome c oxidase activity in cultured cells from patients with SCO2 mutationsLeonardo Salviati, Evelyn Hernandez-Rosa, Winsome F Walker, et al.
Human Mutation|January 1, 1994
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathyG Silvestri, F M Santorelli, S Shanske, et al.
Neurology|August 17, 2018
Level of residual enzyme activity modulates the phenotype in phosphoglycerate kinase deficiencyJohn Vissing, H Orhan Akman, Jan Aasly, et al.
Scientific Reports|June 25, 2017
Regular exercise participation improves genomic stability in diabetic patients: an exploratory study to analyse telomere length and DNA damageIvan Dimauro, Antonella Sgura, Monica Pittaluga, et al.
Journal of the Neurological Sciences|December 22, 2009
Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNA(Leu(CUN)) geneJorida Coku, Sara Shanske, Mahsa Mehrazin, et al.
Neurology|June 1, 1985
Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscleN Bresolin, M Zeviani, E Bonilla, et al.
Cell Reports|December 4, 2025
Cadherin-1-mediated communication at the leader-follower boundary controls mouse breast tumor organoid collective migrationVasilios A Morikis, Diego Barra Avila, Alessandra DiMauro, et al.
International Journal of Molecular Sciences|June 24, 2022
Hydrogen Peroxide Stimulates Dihydrotestosterone Release in C2C12 Myotubes: A New Perspective for Exercise-Related Muscle Steroidogenesis?Cristina Antinozzi, Guglielmo Duranti, Roberta Ceci, et al.
Annals of Neurology|October 2, 2003
Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathiesMassimiliano Filosto, Michelangelo Mancuso, Cristofol Vives-Bauza, et al.
Animal : an International Journal of Animal Bioscience|July 18, 2018
Genetic parameters of milk fatty acid profile in sheep: comparison between gas chromatographic measurements and Fourier-transform IR spectroscopy predictionsF Correddu, M Cellesi, J Serdino, et al.
Pageof 95

Showing results (531-540 of 942) with videos related to

Sort By:
Pageof 95
The Biochemical Journal|April 5, 2002
Copper supplementation restores cytochrome c oxidase activity in cultured cells from patients with SCO2 mutationsLeonardo Salviati, Evelyn Hernandez-Rosa, Winsome F Walker, et al.
Human Mutation|January 1, 1994
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathyG Silvestri, F M Santorelli, S Shanske, et al.
Neurology|August 17, 2018
Level of residual enzyme activity modulates the phenotype in phosphoglycerate kinase deficiencyJohn Vissing, H Orhan Akman, Jan Aasly, et al.
Scientific Reports|June 25, 2017
Regular exercise participation improves genomic stability in diabetic patients: an exploratory study to analyse telomere length and DNA damageIvan Dimauro, Antonella Sgura, Monica Pittaluga, et al.
Journal of the Neurological Sciences|December 22, 2009
Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNA(Leu(CUN)) geneJorida Coku, Sara Shanske, Mahsa Mehrazin, et al.
Neurology|June 1, 1985
Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscleN Bresolin, M Zeviani, E Bonilla, et al.
Cell Reports|December 4, 2025
Cadherin-1-mediated communication at the leader-follower boundary controls mouse breast tumor organoid collective migrationVasilios A Morikis, Diego Barra Avila, Alessandra DiMauro, et al.
International Journal of Molecular Sciences|June 24, 2022
Hydrogen Peroxide Stimulates Dihydrotestosterone Release in C2C12 Myotubes: A New Perspective for Exercise-Related Muscle Steroidogenesis?Cristina Antinozzi, Guglielmo Duranti, Roberta Ceci, et al.
Annals of Neurology|October 2, 2003
Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathiesMassimiliano Filosto, Michelangelo Mancuso, Cristofol Vives-Bauza, et al.
Animal : an International Journal of Animal Bioscience|July 18, 2018
Genetic parameters of milk fatty acid profile in sheep: comparison between gas chromatographic measurements and Fourier-transform IR spectroscopy predictionsF Correddu, M Cellesi, J Serdino, et al.
Pageof 95