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Massimo Zeviani

Showing results (71-80 of 289) with videos related to

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Molecular Vision|January 18, 2008
X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathyGavin Hudson, Valerio Carelli, Rita Horvath, et al.
Elife|October 12, 2023
Structural rather than catalytic role for mitochondrial respiratory chain supercomplexesMichele Brischigliaro, Alfredo Cabrera-Orefice, Susanne Arnold, et al.
Human Molecular Genetics|January 7, 2009
Paroxysmal non-kinesigenic dyskinesia is caused by mutations of the MR-1 mitochondrial targeting sequenceDaniele Ghezzi, Carlo Viscomi, Alessandra Ferlini, et al.
Brain & Development|June 2, 2006
Effects of riboflavin in children with complex II deficiencyMarianna Bugiani, Eleonora Lamantea, Federica Invernizzi, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 18, 2021
Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogasterMichele Brischigliaro, Elena Frigo, Samantha Corrà, et al.
Frontiers in Cell and Developmental Biology|June 6, 2022
Mitochondrial Cytochrome <i>c</i> Oxidase Defects Alter Cellular Homeostasis of Transition MetalsMichele Brischigliaro, Denis Badocco, Rodolfo Costa, et al.
Brain : a Journal of Neurology|April 18, 2007
The A467T and W748S POLG substitutions are a rare cause of adult-onset ataxia in EuropeKate Craig, Gianfrancesco Ferrari, Watcharee Tiangyou, et al.
Biochimica Et Biophysica Acta|November 22, 2012
LYRM7/MZM1L is a UQCRFS1 chaperone involved in the last steps of mitochondrial Complex III assembly in human cellsEster Sánchez, Teresa Lobo, Jennifer L Fox, et al.
Biomedicines|August 6, 2021
Role of PITRM1 in Mitochondrial Dysfunction and NeurodegenerationDario Brunetti, Alessia Catania, Carlo Viscomi, et al.
Frontiers in Physiology|September 27, 2019
Knockdown of <i>APOPT1/COA8</i> Causes Cytochrome <i>c</i> Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in <i>Drosophila melanogaster</i>Michele Brischigliaro, Samantha Corrà, Claudia Tregnago, et al.
Pageof 29

Showing results (71-80 of 289) with videos related to

Sort By:
Pageof 29
Molecular Vision|January 18, 2008
X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathyGavin Hudson, Valerio Carelli, Rita Horvath, et al.
Elife|October 12, 2023
Structural rather than catalytic role for mitochondrial respiratory chain supercomplexesMichele Brischigliaro, Alfredo Cabrera-Orefice, Susanne Arnold, et al.
Human Molecular Genetics|January 7, 2009
Paroxysmal non-kinesigenic dyskinesia is caused by mutations of the MR-1 mitochondrial targeting sequenceDaniele Ghezzi, Carlo Viscomi, Alessandra Ferlini, et al.
Brain & Development|June 2, 2006
Effects of riboflavin in children with complex II deficiencyMarianna Bugiani, Eleonora Lamantea, Federica Invernizzi, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 18, 2021
Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogasterMichele Brischigliaro, Elena Frigo, Samantha Corrà, et al.
Frontiers in Cell and Developmental Biology|June 6, 2022
Mitochondrial Cytochrome <i>c</i> Oxidase Defects Alter Cellular Homeostasis of Transition MetalsMichele Brischigliaro, Denis Badocco, Rodolfo Costa, et al.
Brain : a Journal of Neurology|April 18, 2007
The A467T and W748S POLG substitutions are a rare cause of adult-onset ataxia in EuropeKate Craig, Gianfrancesco Ferrari, Watcharee Tiangyou, et al.
Biochimica Et Biophysica Acta|November 22, 2012
LYRM7/MZM1L is a UQCRFS1 chaperone involved in the last steps of mitochondrial Complex III assembly in human cellsEster Sánchez, Teresa Lobo, Jennifer L Fox, et al.
Biomedicines|August 6, 2021
Role of PITRM1 in Mitochondrial Dysfunction and NeurodegenerationDario Brunetti, Alessia Catania, Carlo Viscomi, et al.
Frontiers in Physiology|September 27, 2019
Knockdown of <i>APOPT1/COA8</i> Causes Cytochrome <i>c</i> Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in <i>Drosophila melanogaster</i>Michele Brischigliaro, Samantha Corrà, Claudia Tregnago, et al.
Pageof 29