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Massimo Zeviani

Showing results (101-110 of 289) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|June 21, 2020
Opa1 Overexpression Protects from Early-Onset Mpv17<sup>-/-</sup>-Related Mouse Kidney DiseaseMarta Luna-Sanchez, Cristiane Benincá, Raffaele Cerutti, et al.
Scientific Reports|March 11, 2022
The relevance of migraine in the clinical spectrum of mitochondrial disordersAlberto Terrin, Luca Bello, Maria Lucia Valentino, et al.
Human Molecular Genetics|May 20, 2008
Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutationsNeil Ashley, Anthony O'Rourke, Conrad Smith, et al.
EMBO Molecular Medicine|October 13, 2018
Rapamycin rescues mitochondrial myopathy via coordinated activation of autophagy and lysosomal biogenesisGabriele Civiletto, Sukru Anil Dogan, Raffaele Cerutti, et al.
Human Molecular Genetics|September 27, 2008
Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout miceCarlo Viscomi, Antonella Spinazzola, Marco Maggioni, et al.
American Journal of Human Genetics|March 17, 2015
Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndromeVanessa A van Rahden, Erika Fernandez-Vizarra, Malik Alawi, et al.
Human Gene Therapy|December 30, 2017
Long-Term Sustained Effect of Liver-Targeted Adeno-Associated Virus Gene Therapy for Mitochondrial Neurogastrointestinal EncephalomyopathyJavier Torres-Torronteras, Raquel Cabrera-Pérez, Ferran Vila-Julià, et al.
Cell Metabolism|July 5, 2011
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axisCarlo Viscomi, Emanuela Bottani, Gabriele Civiletto, et al.
Brain : a Journal of Neurology|February 2, 2008
POLG1 mutations cause a syndromic epilepsy with occipital lobe predilectionBernt A Engelsen, Charalampos Tzoulis, Bjørn Karlsen, et al.
EMBO Reports|March 19, 2014
UCP4C mediates uncoupled respiration in larvae of Drosophila melanogasterCaterina Da-Ré, Cristiano De Pittà, Mauro A Zordan, et al.
Pageof 29

Showing results (101-110 of 289) with videos related to

Sort By:
Pageof 29
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 21, 2020
Opa1 Overexpression Protects from Early-Onset Mpv17<sup>-/-</sup>-Related Mouse Kidney DiseaseMarta Luna-Sanchez, Cristiane Benincá, Raffaele Cerutti, et al.
Scientific Reports|March 11, 2022
The relevance of migraine in the clinical spectrum of mitochondrial disordersAlberto Terrin, Luca Bello, Maria Lucia Valentino, et al.
Human Molecular Genetics|May 20, 2008
Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutationsNeil Ashley, Anthony O'Rourke, Conrad Smith, et al.
EMBO Molecular Medicine|October 13, 2018
Rapamycin rescues mitochondrial myopathy via coordinated activation of autophagy and lysosomal biogenesisGabriele Civiletto, Sukru Anil Dogan, Raffaele Cerutti, et al.
Human Molecular Genetics|September 27, 2008
Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout miceCarlo Viscomi, Antonella Spinazzola, Marco Maggioni, et al.
American Journal of Human Genetics|March 17, 2015
Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndromeVanessa A van Rahden, Erika Fernandez-Vizarra, Malik Alawi, et al.
Human Gene Therapy|December 30, 2017
Long-Term Sustained Effect of Liver-Targeted Adeno-Associated Virus Gene Therapy for Mitochondrial Neurogastrointestinal EncephalomyopathyJavier Torres-Torronteras, Raquel Cabrera-Pérez, Ferran Vila-Julià, et al.
Cell Metabolism|July 5, 2011
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axisCarlo Viscomi, Emanuela Bottani, Gabriele Civiletto, et al.
Brain : a Journal of Neurology|February 2, 2008
POLG1 mutations cause a syndromic epilepsy with occipital lobe predilectionBernt A Engelsen, Charalampos Tzoulis, Bjørn Karlsen, et al.
EMBO Reports|March 19, 2014
UCP4C mediates uncoupled respiration in larvae of Drosophila melanogasterCaterina Da-Ré, Cristiano De Pittà, Mauro A Zordan, et al.
Pageof 29