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Massimo Zeviani

Showing results (171-180 of 289) with videos related to

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EMBO Reports|June 14, 2022
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7BMichele Brischigliaro, Alfredo Cabrera-Orefice, Mattia Sturlese, et al.
Annals of Neurology|October 2, 2003
Genotypes from patients indicate no paternal mitochondrial DNA contributionRobert W Taylor, Martina T McDonnell, Emma L Blakely, et al.
Journal of Hepatology|November 18, 2008
Glucose metabolism and diet-based prevention of liver dysfunction in MPV17 mutant patientsRossella Parini, Francesca Furlan, Luigi Notarangelo, et al.
Biochimica Et Biophysica Acta|November 4, 2008
Identification of novel mutations in five patients with mitochondrial encephalomyopathyLucia Valente, Daniela Piga, Eleonora Lamantea, et al.
Cell Metabolism|May 13, 2014
NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial diseaseRaffaele Cerutti, Eija Pirinen, Costanza Lamperti, et al.
The Biochemical Journal|June 10, 2014
Complex IV-deficient Surf1(-/-) mice initiate mitochondrial stress responsesDaniel A Pulliam, Sathyaseelan S Deepa, Yuhong Liu, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 18, 2012
Improved insulin sensitivity associated with reduced mitochondrial complex IV assembly and activitySathyaseelan S Deepa, Daniel Pulliam, Shauna Hill, et al.
Mitochondrion|November 6, 2007
Liver mtDNA content increases during development: a comparison of methods and the importance of age- and tissue-specific controls for the diagnosis of mtDNA depletionKarl J Morten, Neil Ashley, Frits Wijburg, et al.
Cell Reports|February 16, 2017
MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human Cytochrome c OxidaseSara Vidoni, Michael E Harbour, Sergio Guerrero-Castillo, et al.
Nature Genetics|February 1, 2011
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and fliesDaniele Ghezzi, Paola Arzuffi, Mauro Zordan, et al.
Pageof 29

Showing results (171-180 of 289) with videos related to

Sort By:
Pageof 29
EMBO Reports|June 14, 2022
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7BMichele Brischigliaro, Alfredo Cabrera-Orefice, Mattia Sturlese, et al.
Annals of Neurology|October 2, 2003
Genotypes from patients indicate no paternal mitochondrial DNA contributionRobert W Taylor, Martina T McDonnell, Emma L Blakely, et al.
Journal of Hepatology|November 18, 2008
Glucose metabolism and diet-based prevention of liver dysfunction in MPV17 mutant patientsRossella Parini, Francesca Furlan, Luigi Notarangelo, et al.
Biochimica Et Biophysica Acta|November 4, 2008
Identification of novel mutations in five patients with mitochondrial encephalomyopathyLucia Valente, Daniela Piga, Eleonora Lamantea, et al.
Cell Metabolism|May 13, 2014
NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial diseaseRaffaele Cerutti, Eija Pirinen, Costanza Lamperti, et al.
The Biochemical Journal|June 10, 2014
Complex IV-deficient Surf1(-/-) mice initiate mitochondrial stress responsesDaniel A Pulliam, Sathyaseelan S Deepa, Yuhong Liu, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 18, 2012
Improved insulin sensitivity associated with reduced mitochondrial complex IV assembly and activitySathyaseelan S Deepa, Daniel Pulliam, Shauna Hill, et al.
Mitochondrion|November 6, 2007
Liver mtDNA content increases during development: a comparison of methods and the importance of age- and tissue-specific controls for the diagnosis of mtDNA depletionKarl J Morten, Neil Ashley, Frits Wijburg, et al.
Cell Reports|February 16, 2017
MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human Cytochrome c OxidaseSara Vidoni, Michael E Harbour, Sergio Guerrero-Castillo, et al.
Nature Genetics|February 1, 2011
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and fliesDaniele Ghezzi, Paola Arzuffi, Mauro Zordan, et al.
Pageof 29