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Vittoria Petruzzella

Showing results (1-10 of 51) with videos related to

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Autophagy Reports|May 21, 2025
Autophagy and proliferation are dysregulated in Charcot-Marie-Tooth disease type 2A cells harboring MFN2 (mitofusin 2) mutationPaola Zanfardino, Vittoria Petruzzella
Gene|April 12, 2002
Mutations in human nuclear genes encoding for subunits of mitochondrial respiratory complex I: the NDUFS4 geneVittoria Petruzzella, Sergio Papa
FEBS Letters|September 11, 2003
Differential expression of ATPAF1 and ATPAF2 genes encoding F(1)-ATPase assembly proteins in mouse tissuesAndrea Picková, Jan Paul, Vittoria Petruzzella, et al.
Biomolecules|March 28, 2025
The Balance of MFN2 and OPA1 in Mitochondrial Dynamics, Cellular Homeostasis, and DiseasePaola Zanfardino, Alessandro Amati, Mirko Perrone, et al.
International Journal of Molecular Sciences|August 7, 2021
Tackling Dysfunction of Mitochondrial Bioenergetics in the BrainPaola Zanfardino, Stefano Doccini, Filippo M Santorelli, et al.
Plos Genetics|August 1, 2020
RCC1L (WBSCR16) isoforms coordinate mitochondrial ribosome assembly through their interaction with GTPasesAurelio Reyes, Paola Favia, Sara Vidoni, et al.
FEBS Letters|June 25, 2005
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variantsVittoria Petruzzella, Damiano Panelli, Alessandra Torraco, et al.
Clinical Neurology and Neurosurgery|February 8, 2024
A novel mutation in the LRSAM1 gene in a family with early onset autosomal dominant Charcot-Marie-Tooth type 2PGiammarco Milella, Alessandro Amati, Patrizia Lastella, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 16, 2023
Torin1 restores proliferation rate in Charcot-Marie-Tooth disease type 2A cells harbouring MFN2 (mitofusin 2) mutationPaola Zanfardino, Alessandro Amati, Easter Anna Petracca, et al.
Middle East African Journal of Ophthalmology|May 17, 2011
Bilateral progressive visual loss in an epileptic, mentally retarded boySilvana Guerriero, Michele Vetrugno, Lorenza Ciracì, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
Autophagy Reports|May 21, 2025
Autophagy and proliferation are dysregulated in Charcot-Marie-Tooth disease type 2A cells harboring MFN2 (mitofusin 2) mutationPaola Zanfardino, Vittoria Petruzzella
Gene|April 12, 2002
Mutations in human nuclear genes encoding for subunits of mitochondrial respiratory complex I: the NDUFS4 geneVittoria Petruzzella, Sergio Papa
FEBS Letters|September 11, 2003
Differential expression of ATPAF1 and ATPAF2 genes encoding F(1)-ATPase assembly proteins in mouse tissuesAndrea Picková, Jan Paul, Vittoria Petruzzella, et al.
Biomolecules|March 28, 2025
The Balance of MFN2 and OPA1 in Mitochondrial Dynamics, Cellular Homeostasis, and DiseasePaola Zanfardino, Alessandro Amati, Mirko Perrone, et al.
International Journal of Molecular Sciences|August 7, 2021
Tackling Dysfunction of Mitochondrial Bioenergetics in the BrainPaola Zanfardino, Stefano Doccini, Filippo M Santorelli, et al.
Plos Genetics|August 1, 2020
RCC1L (WBSCR16) isoforms coordinate mitochondrial ribosome assembly through their interaction with GTPasesAurelio Reyes, Paola Favia, Sara Vidoni, et al.
FEBS Letters|June 25, 2005
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variantsVittoria Petruzzella, Damiano Panelli, Alessandra Torraco, et al.
Clinical Neurology and Neurosurgery|February 8, 2024
A novel mutation in the LRSAM1 gene in a family with early onset autosomal dominant Charcot-Marie-Tooth type 2PGiammarco Milella, Alessandro Amati, Patrizia Lastella, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 16, 2023
Torin1 restores proliferation rate in Charcot-Marie-Tooth disease type 2A cells harbouring MFN2 (mitofusin 2) mutationPaola Zanfardino, Alessandro Amati, Easter Anna Petracca, et al.
Middle East African Journal of Ophthalmology|May 17, 2011
Bilateral progressive visual loss in an epileptic, mentally retarded boySilvana Guerriero, Michele Vetrugno, Lorenza Ciracì, et al.
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