Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Flavio Dal Canto"'
Autor:
Michela Di Nottia, Teresa Rizza, Enrico Baruffini, Claudia Nesti, Alessandra Torraco, Daria Diodato, Diego Martinelli, Flavio Dal Canto, Alexandru Ionut Gilea, Martina Zoccola, Barbara Siri, Carlo Dionisi-Vici, Enrico Bertini, Filippo Maria Santorelli, Paola Goffrini, Rosalba Carrozzo
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
BackgroundMitochondria adjust their shape in response to the different energetic and metabolic requirements of the cell, through extremely dynamic fusion and fission events. Several highly conserved dynamin-like GTPases are involved in these processe
Externí odkaz:
https://doaj.org/article/d224f79529b348b7af84168ca8604f37
Autor:
Daniele Galatolo, Silvia Rocchiccioli, Nicoletta Di Giorgi, Flavio Dal Canto, Giovanni Signore, Federica Morani, Elisa Ceccherini, Stefano Doccini, Filippo Maria Santorelli
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
IntroductionAutosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a rare incurable neurodegenerative disease caused by mutations in the SACS gene, which codes for sacsin, a large protein involved in protein homeostasis, mitochondrial
Externí odkaz:
https://doaj.org/article/b3f9d6025b1443dbb0af7a0a70363fb0
Autor:
Chenelle A. Caron-Godon, Stefania Della Vecchia, Alessandro Romano, Stefano Doccini, Flavio Dal Canto, Rosa Pasquariello, Anna Rubegni, Roberta Battini, Filippo Maria Santorelli, D. Moira Glerum, Claudia Nesti
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 23, p 16636 (2023)
Genetic defects in the nuclear encoded subunits and assembly factors of cytochrome c oxidase (mitochondrial complex IV) are very rare and are associated with a wide variety of phenotypes. Biallelic pathogenic variants in the COX11 protein were previo
Externí odkaz:
https://doaj.org/article/b9810c181f33489dbe67343dcd693641
Autor:
Domenico Giannese, Vincenzo Montano, Piervito Lopriore, Claudia Nesti, Annalisa LoGerfo, Maria Adelaide Caligo, Flavio Dal Canto, Gianandrea Pasquinelli, Angelo Giovanni Bonadio, Diego Moriconi, Gabriele Siciliano, Michelangelo Mancuso
Publikováno v:
Journal of neuromuscular diseases. 10(1)
Background: Mitochondrial tRNA (MTT) genes are hotspot for mitochondrial DNA mutation and are responsible of half mitochondrial disease. MTT mutations are associated with a broad spectrum of phenotype often with complex multisystem involvement and co