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Journal of Medical Genetics|October 29, 2017
A novel de novo dominant mutation in ISCU associated with mitochondrial myopathyAndrea Legati, Aurelio Reyes, Camilla Ceccatelli Berti, et al.Biomolecules|February 25, 2023
Mitochondrial Neurodegeneration: Lessons from Drosophila melanogaster ModelsMichele Brischigliaro, Erika Fernandez-Vizarra, Carlo ViscomiPsychiatry and Clinical Neurosciences|September 12, 2014
First Japanese family with primary familial brain calcification due to a mutation in the PDGFB gene: an exome analysis studyTeruo Hayashi, Andrea Legati, Tadashi Nishikawa, et al.Bioinformatics (Oxford, England)|April 19, 2018
GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGSViola Ravasio, Marco Ritelli, Andrea Legati, et al.Nature Communications|April 9, 2021
Exploiting pyocyanin to treat mitochondrial disease due to respiratory complex III dysfunctionRoberta Peruzzo, Samantha Corrà, Roberto Costa, et al.Journal of Inherited Metabolic Disease|January 3, 2024
Gene therapy for mitochondrial disordersNandaki Keshavan, Michal Minczuk, Carlo Viscomi, et al.EMBO Molecular Medicine|December 16, 2018
APOPT1/COA8 assists COX assembly and is oppositely regulated by UPS and ROSAlba Signes, Raffaele Cerutti, Anna S Dickson, et al.Seminars in Fetal & Neonatal Medicine|May 31, 2011
Infantile mitochondrial encephalopathyGraziella Uziel, Daniele Ghezzi, Massimo ZevianiInternational Journal of Cell Biology|March 19, 2014
The Mitochondrial Aminoacyl tRNA Synthetases: Genes and SyndromesDaria Diodato, Daniele Ghezzi, Valeria TirantiInternational Journal of Molecular Sciences|January 25, 2025
De Novo DNM1L Pathogenic Variant Associated with Lethal Encephalocardiomyopathy-Case Report and Literature ReviewMartina Magistrati, Luisa Zupin, Eleonora Lamantea, et al.Pageof 26