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Gaia Tioli

Showing results (1-10 of 7) with videos related to

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Biochimica Et Biophysica Acta|January 29, 2016
Complex I function in mitochondrial supercomplexesGiorgio Lenaz, Gaia Tioli, Anna Ida Falasca, et al.
Life (Basel, Switzerland)|April 3, 2021
Molecular and Supramolecular Structure of the Mitochondrial Oxidative Phosphorylation System: Implications for PathologySalvatore Nesci, Fabiana Trombetti, Alessandra Pagliarani, et al.
Heliyon|January 27, 2025
The landscape of rare mitochondrial DNA variants in sudden cardiac death: A potential role for ATP synthaseElena Luppi, Monica De Luise, Carla Bini, et al.
International Journal of Molecular Sciences|February 13, 2025
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome <i>b</i> (<i>MT-CYB</i>) GeneConcetta Valentina Tropeano, Chiara La Morgia, Alessandro Achilli, et al.
Nature|February 26, 2025
Macrophages recycle phagocytosed bacteria to fuel immunometabolic responsesJuliette Lesbats, Aurélia Brillac, Julie A Reisz, et al.
Brain : a Journal of Neurology|November 14, 2025
Recessive variants in mitochondrial Complex I nuclear subunits are an underrated cause of optic atrophyClaudio Fiorini, Neringa Jurkute, Alessandra Torraco, et al.
Cell Reports. Medicine|January 25, 2024
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathySerena Jasmine Aleo, Valentina Del Dotto, Martina Romagnoli, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Biochimica Et Biophysica Acta|January 29, 2016
Complex I function in mitochondrial supercomplexesGiorgio Lenaz, Gaia Tioli, Anna Ida Falasca, et al.
Life (Basel, Switzerland)|April 3, 2021
Molecular and Supramolecular Structure of the Mitochondrial Oxidative Phosphorylation System: Implications for PathologySalvatore Nesci, Fabiana Trombetti, Alessandra Pagliarani, et al.
Heliyon|January 27, 2025
The landscape of rare mitochondrial DNA variants in sudden cardiac death: A potential role for ATP synthaseElena Luppi, Monica De Luise, Carla Bini, et al.
International Journal of Molecular Sciences|February 13, 2025
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome <i>b</i> (<i>MT-CYB</i>) GeneConcetta Valentina Tropeano, Chiara La Morgia, Alessandro Achilli, et al.
Nature|February 26, 2025
Macrophages recycle phagocytosed bacteria to fuel immunometabolic responsesJuliette Lesbats, Aurélia Brillac, Julie A Reisz, et al.
Brain : a Journal of Neurology|November 14, 2025
Recessive variants in mitochondrial Complex I nuclear subunits are an underrated cause of optic atrophyClaudio Fiorini, Neringa Jurkute, Alessandra Torraco, et al.
Cell Reports. Medicine|January 25, 2024
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathySerena Jasmine Aleo, Valentina Del Dotto, Martina Romagnoli, et al.
Pageof 1