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Valerio Carelli

Showing results (201-210 of 332) with videos related to

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Cell Reports|February 22, 2018
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease ModelsAngelo Iannielli, Simone Bido, Lucrezia Folladori, et al.
American Journal of Ophthalmology|May 5, 2022
Capturing the Pattern of Transition From Carrier to Affected in Leber Hereditary Optic NeuropathyMichele Carbonelli, Chiara La Morgia, Martina Romagnoli, et al.
Human Molecular Genetics|October 29, 2013
Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairmentLuisa Iommarini, Ivana Kurelac, Mariantonietta Capristo, et al.
Stem Cell Reports|July 30, 2021
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCsFlavia Palombo, Camille Peron, Leonardo Caporali, et al.
Research Square|November 14, 2023
Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum DisorderElena Bacchelli, Marta Viggiano, Fabiola Ceroni, et al.
Archives of Neurology|September 15, 2010
Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutationsRaffaele Lodi, Caterina Tonon, Maria Lucia Valentino, et al.
Frontiers in Neurology|June 28, 2021
Leber's Hereditary Optic Neuropathy: A Report on Novel mtDNA Pathogenic VariantsLorenzo Peverelli, Alessia Catania, Silvia Marchet, et al.
EMBO Molecular Medicine|May 24, 2023
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathyNneka Southwell, Guido Primiano, Viraj Nadkarni, et al.
Plos One|December 5, 2012
Secondary post-geniculate involvement in Leber's hereditary optic neuropathyGiovanni Rizzo, Kevin R Tozer, Caterina Tonon, et al.
Neurogenetics|November 12, 2015
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutationsMichelangelo Cao, Marta Donà, M Lucia Valentino, et al.
Pageof 34

Showing results (201-210 of 332) with videos related to

Sort By:
Pageof 34
Cell Reports|February 22, 2018
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease ModelsAngelo Iannielli, Simone Bido, Lucrezia Folladori, et al.
American Journal of Ophthalmology|May 5, 2022
Capturing the Pattern of Transition From Carrier to Affected in Leber Hereditary Optic NeuropathyMichele Carbonelli, Chiara La Morgia, Martina Romagnoli, et al.
Human Molecular Genetics|October 29, 2013
Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairmentLuisa Iommarini, Ivana Kurelac, Mariantonietta Capristo, et al.
Stem Cell Reports|July 30, 2021
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCsFlavia Palombo, Camille Peron, Leonardo Caporali, et al.
Research Square|November 14, 2023
Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum DisorderElena Bacchelli, Marta Viggiano, Fabiola Ceroni, et al.
Archives of Neurology|September 15, 2010
Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutationsRaffaele Lodi, Caterina Tonon, Maria Lucia Valentino, et al.
Frontiers in Neurology|June 28, 2021
Leber's Hereditary Optic Neuropathy: A Report on Novel mtDNA Pathogenic VariantsLorenzo Peverelli, Alessia Catania, Silvia Marchet, et al.
EMBO Molecular Medicine|May 24, 2023
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathyNneka Southwell, Guido Primiano, Viraj Nadkarni, et al.
Plos One|December 5, 2012
Secondary post-geniculate involvement in Leber's hereditary optic neuropathyGiovanni Rizzo, Kevin R Tozer, Caterina Tonon, et al.
Neurogenetics|November 12, 2015
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutationsMichelangelo Cao, Marta Donà, M Lucia Valentino, et al.
Pageof 34