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Alessandra Torraco

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Biochimica Et Biophysica Acta. General Subjects|October 20, 2022
Silencing of the mitochondrial ribosomal protein L-24 gene activates the oxidative stress response in Caenorhabditis elegansGraziella Ficociello, Emily Schifano, Michela Di Nottia, et al.
Life (Basel, Switzerland)|January 21, 2022
Spinal Cord Involvement in Adult Mitochondrial Diseases: A Cohort StudyGuido Primiano, Paolo Mariotti, Ida Turrini, et al.
Neurology. Genetics|July 11, 2022
Novel <i>TOP3A</i> Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha-Related DiseasesGuido Primiano, Alessandra Torraco, Daniela Verrigni, et al.
The Italian Journal of Biochemistry|February 6, 2007
Mutations in structural genes of complex I associated with neurological diseasesSalvatore Scacco, Vittoria Petruzzella, Enrico Bertini, et al.
Annals of Clinical and Translational Neurology|February 8, 2024
Biallelic variants in GTPBP3: New patients, phenotypic spectrum, and outcomeFrancesca Nardecchia, Rosalba Carrozzo, Alice Innocenti, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 18, 2008
Ischemic preconditioning targets the respiration of synaptic mitochondria via protein kinase C epsilonKunjan R Dave, R Anthony DeFazio, Ami P Raval, et al.
International Journal of Molecular Sciences|April 10, 2014
Frataxin silencing inactivates mitochondrial Complex I in NSC34 motoneuronal cells and alters glutathione homeostasisBarbara Carletti, Emanuela Piermarini, Giulia Tozzi, et al.
Cerebellum (London, England)|November 29, 2022
AFG3L2 Biallelic Mutation: Clinical Heterogeneity in Two Italian PatientsFabiana Colucci, Marcella Neri, Fernanda Fortunato, et al.
Biochemical and Biophysical Research Communications|February 13, 2007
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathyVittoria Petruzzella, Alessandra Tessa, Alessandra Torraco, et al.
Clinical Genetics|March 5, 2022
A novel homozygous variant in COX5A causes an attenuated phenotype with failure to thrive, lactic acidosis, hypoglycemia, and short statureAlessandra Torraco, Silvia Morlino, Teresa Rizza, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Biochimica Et Biophysica Acta. General Subjects|October 20, 2022
Silencing of the mitochondrial ribosomal protein L-24 gene activates the oxidative stress response in Caenorhabditis elegansGraziella Ficociello, Emily Schifano, Michela Di Nottia, et al.
Life (Basel, Switzerland)|January 21, 2022
Spinal Cord Involvement in Adult Mitochondrial Diseases: A Cohort StudyGuido Primiano, Paolo Mariotti, Ida Turrini, et al.
Neurology. Genetics|July 11, 2022
Novel <i>TOP3A</i> Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha-Related DiseasesGuido Primiano, Alessandra Torraco, Daniela Verrigni, et al.
The Italian Journal of Biochemistry|February 6, 2007
Mutations in structural genes of complex I associated with neurological diseasesSalvatore Scacco, Vittoria Petruzzella, Enrico Bertini, et al.
Annals of Clinical and Translational Neurology|February 8, 2024
Biallelic variants in GTPBP3: New patients, phenotypic spectrum, and outcomeFrancesca Nardecchia, Rosalba Carrozzo, Alice Innocenti, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 18, 2008
Ischemic preconditioning targets the respiration of synaptic mitochondria via protein kinase C epsilonKunjan R Dave, R Anthony DeFazio, Ami P Raval, et al.
International Journal of Molecular Sciences|April 10, 2014
Frataxin silencing inactivates mitochondrial Complex I in NSC34 motoneuronal cells and alters glutathione homeostasisBarbara Carletti, Emanuela Piermarini, Giulia Tozzi, et al.
Cerebellum (London, England)|November 29, 2022
AFG3L2 Biallelic Mutation: Clinical Heterogeneity in Two Italian PatientsFabiana Colucci, Marcella Neri, Fernanda Fortunato, et al.
Biochemical and Biophysical Research Communications|February 13, 2007
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathyVittoria Petruzzella, Alessandra Tessa, Alessandra Torraco, et al.
Clinical Genetics|March 5, 2022
A novel homozygous variant in COX5A causes an attenuated phenotype with failure to thrive, lactic acidosis, hypoglycemia, and short statureAlessandra Torraco, Silvia Morlino, Teresa Rizza, et al.
Pageof 5