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Alessandra Torraco

Showing results (1-10 of 48) with videos related to

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Mitochondrion|February 3, 2015
Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial functionLuisa Iommarini, Susana Peralta, Alessandra Torraco, et al.
Mitochondrion|February 2, 2015
Mitochondrial Diseases Part III: Therapeutic interventions in mouse models of OXPHOS deficienciesSusana Peralta, Alessandra Torraco, Luisa Iommarini, et al.
Methods (San Diego, Calif.)|October 14, 2008
Mouse models of oxidative phosphorylation dysfunction and diseaseUma D Vempati, Alessandra Torraco, Carlos T Moraes
Mitochondrion|February 10, 2015
Mitochondrial Diseases Part I: mouse models of OXPHOS deficiencies caused by defects in respiratory complex subunits or assembly factorsAlessandra Torraco, Susana Peralta, Luisa Iommarini, et al.
Cell Metabolism|June 4, 2009
mTERF2 regulates oxidative phosphorylation by modulating mtDNA transcriptionTina Wenz, Corneliu Luca, Alessandra Torraco, et al.
Biochimica Et Biophysica Acta|July 8, 2008
Mouse models of oxidative phosphorylation defects: powerful tools to study the pathobiology of mitochondrial diseasesAlessandra Torraco, Francisca Diaz, Uma D Vempati, 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.
Human Molecular Genetics|October 25, 2013
Partial complex I deficiency due to the CNS conditional ablation of Ndufa5 results in a mild chronic encephalopathy but no increase in oxidative damageSusana Peralta, Alessandra Torraco, Tina Wenz, et al.
Genes|February 13, 2021
Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic ApproachesMichela Di Nottia, Daniela Verrigni, Alessandra Torraco, et al.
Functional Neurology|June 1, 2006
Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNAStefano Zoccolella, Alessandra Torraco, Angela Amati, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Mitochondrion|February 3, 2015
Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial functionLuisa Iommarini, Susana Peralta, Alessandra Torraco, et al.
Mitochondrion|February 2, 2015
Mitochondrial Diseases Part III: Therapeutic interventions in mouse models of OXPHOS deficienciesSusana Peralta, Alessandra Torraco, Luisa Iommarini, et al.
Methods (San Diego, Calif.)|October 14, 2008
Mouse models of oxidative phosphorylation dysfunction and diseaseUma D Vempati, Alessandra Torraco, Carlos T Moraes
Mitochondrion|February 10, 2015
Mitochondrial Diseases Part I: mouse models of OXPHOS deficiencies caused by defects in respiratory complex subunits or assembly factorsAlessandra Torraco, Susana Peralta, Luisa Iommarini, et al.
Cell Metabolism|June 4, 2009
mTERF2 regulates oxidative phosphorylation by modulating mtDNA transcriptionTina Wenz, Corneliu Luca, Alessandra Torraco, et al.
Biochimica Et Biophysica Acta|July 8, 2008
Mouse models of oxidative phosphorylation defects: powerful tools to study the pathobiology of mitochondrial diseasesAlessandra Torraco, Francisca Diaz, Uma D Vempati, 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.
Human Molecular Genetics|October 25, 2013
Partial complex I deficiency due to the CNS conditional ablation of Ndufa5 results in a mild chronic encephalopathy but no increase in oxidative damageSusana Peralta, Alessandra Torraco, Tina Wenz, et al.
Genes|February 13, 2021
Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic ApproachesMichela Di Nottia, Daniela Verrigni, Alessandra Torraco, et al.
Functional Neurology|June 1, 2006
Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNAStefano Zoccolella, Alessandra Torraco, Angela Amati, et al.
Pageof 5