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STAR Protocols|July 16, 2024
Protocol for evaluating mitochondrial respiration in iPSC-derived neurons by the Seahorse XF analyzerChiara Fasano, Andrea Cavaliere, Valeria Tiranti, et al.Journal of Visualized Experiments : Jove|March 28, 2022
An In Vitro Approach to Study Mitochondrial Dysfunction: A Cybrid ModelAndrea Cavaliere, Silvia Marchet, Ivano Di Meo, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 24, 2023
VCP-related myopathy: a case series and a review of literatureEliana Iannibelli, Sara Gibertini, Marta Cheli, et al.Frontiers in Neurology|June 25, 2021
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future PerspectivesCamille Peron, Alessandra Maresca, Andrea Cavaliere, et al.Stem Cell Research|January 12, 2021
Generation of two human iPSC lines, FINCBi002-A and FINCBi003-A, carrying heteroplasmic macrodeletion of mitochondrial DNA causing Pearson's syndromeCamille Peron, Roberta Mauceri, Angelo Iannielli, et al.Stem Cell Research|March 29, 2024
Generation of iPSCs from identical twin, one affected by LHON and one unaffected, both carrying a combination of two mitochondrial variants: m.14484 T>C and m.10680G>ACamille Peron, Andrea Cavaliere, Chiara Fasano, et al.Cell Reports|July 20, 2022
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathyAlberto Danese, Simone Patergnani, Alessandra Maresca, 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