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Massimo Zeviani

Showing results (81-90 of 289) with videos related to

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Frontiers in Genetics|December 6, 2014
Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutationsFederica Invernizzi, Anna Ardissone, Eleonora Lamantea, et al.
Mitochondrion|December 26, 2009
Isolation of mitochondria for biogenetical studies: An updateErika Fernández-Vizarra, Gustavo Ferrín, Acisclo Pérez-Martos, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2002
Frequency of DYT1 mutation in early onset primary dystonia in Italian patientsGiovanna Zorzi, Barbara Garavaglia, Federica Invernizzi, et al.
Data in Brief|July 14, 2016
Data on cytochrome c oxidase assembly in mice and human fibroblasts or tissues induced by SURF1 defectNikola Kovářová, Petr Pecina, Hana Nůsková, et al.
Neuromuscular Disorders : NMD|May 28, 2008
Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathyGiuliana Galassi, Eleonora Lamantea, Federica Invernizzi, et al.
Biochimica Et Biophysica Acta. Bioenergetics|February 18, 2021
Duplexing complexome profiling with SILAC to study human respiratory chain assembly defectsPetra Páleníková, Michael E Harbour, Federica Prodi, et al.
Journal of Virology|February 29, 2008
Epstein-Barr virus immediate-early protein Zta co-opts mitochondrial single-stranded DNA binding protein to promote viral and inhibit mitochondrial DNA replicationAndreas Wiedmer, Pu Wang, Jing Zhou, et al.
Biochimica Et Biophysica Acta|January 26, 2016
Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defectsNikola Kovářová, Petr Pecina, Hana Nůsková, et al.
Neuromuscular Disorders : NMD|July 27, 2012
MELAS-like encephalomyopathy caused by a new pathogenic mutation in the mitochondrial DNA encoded cytochrome c oxidase subunit ICostanza Lamperti, Daria Diodato, Eleonora Lamantea, et al.
Journal of Child Neurology|March 27, 2018
Cavitating Leukoencephalopathy With Posterior Predominance Caused by a Deletion in the APOPT1 Gene in an Indian BoySuvasini Sharma, Preeti Singh, Erika Fernandez-Vizarra, et al.
Pageof 29

Showing results (81-90 of 289) with videos related to

Sort By:
Pageof 29
Frontiers in Genetics|December 6, 2014
Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutationsFederica Invernizzi, Anna Ardissone, Eleonora Lamantea, et al.
Mitochondrion|December 26, 2009
Isolation of mitochondria for biogenetical studies: An updateErika Fernández-Vizarra, Gustavo Ferrín, Acisclo Pérez-Martos, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2002
Frequency of DYT1 mutation in early onset primary dystonia in Italian patientsGiovanna Zorzi, Barbara Garavaglia, Federica Invernizzi, et al.
Data in Brief|July 14, 2016
Data on cytochrome c oxidase assembly in mice and human fibroblasts or tissues induced by SURF1 defectNikola Kovářová, Petr Pecina, Hana Nůsková, et al.
Neuromuscular Disorders : NMD|May 28, 2008
Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathyGiuliana Galassi, Eleonora Lamantea, Federica Invernizzi, et al.
Biochimica Et Biophysica Acta. Bioenergetics|February 18, 2021
Duplexing complexome profiling with SILAC to study human respiratory chain assembly defectsPetra Páleníková, Michael E Harbour, Federica Prodi, et al.
Journal of Virology|February 29, 2008
Epstein-Barr virus immediate-early protein Zta co-opts mitochondrial single-stranded DNA binding protein to promote viral and inhibit mitochondrial DNA replicationAndreas Wiedmer, Pu Wang, Jing Zhou, et al.
Biochimica Et Biophysica Acta|January 26, 2016
Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defectsNikola Kovářová, Petr Pecina, Hana Nůsková, et al.
Neuromuscular Disorders : NMD|July 27, 2012
MELAS-like encephalomyopathy caused by a new pathogenic mutation in the mitochondrial DNA encoded cytochrome c oxidase subunit ICostanza Lamperti, Daria Diodato, Eleonora Lamantea, et al.
Journal of Child Neurology|March 27, 2018
Cavitating Leukoencephalopathy With Posterior Predominance Caused by a Deletion in the APOPT1 Gene in an Indian BoySuvasini Sharma, Preeti Singh, Erika Fernandez-Vizarra, et al.
Pageof 29