BRISCHIGLIARO, MICHELE
BRISCHIGLIARO, MICHELE
Dipartimento di Biologia - DiBio
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7B
2022 Brischigliaro, Michele; Cabrera-Orefice, Alfredo; Sturlese, Mattia; Elurbe, Dei M; Frigo, Elena; Fernandez-Vizarra, Erika; Moro, Stefano; Huynen, Martijn A; Arnold, Susanne; Viscomi, Carlo; Zeviani, Massimo
Cytochrome c oxidase deficiency
2020 Brischigliaro, M.; Zeviani, M.
Exploiting pyocyanin to treat mitochondrial disease due to respiratory complex III dysfunction
2021 Peruzzo, Roberta; Corrà, Samantha; Costa, Roberto; Brischigliaro, Michele; Varanita, Tatiana; Biasutto, Lucia; Rampazzo, Chiara; Ghezzi, Daniele; Leanza, Luigi; Zoratti, Mario; Zeviani, Massimo; De Pittà, Cristiano; Viscomi, Carlo; Costa, Rodolfo; Szabò, Ildikò
Knockdown of APOPT1/COA8 Causes Cytochrome c Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in Drosophila melanogaster
2019 Brischigliaro, Michele; Corrà, Samantha; Tregnago, Claudia; Fernandez-Vizarra, Erika; Zeviani, Massimo; Costa, Rodolfo; De Pittà, Cristiano
Knockdown of APOPT1/COA8 Causes Cytochrome c Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in Drosophila melanogaster
2019 Brischigliaro, Michele; Corra', Samantha; Tregnago, Claudia; Fernandez-Vizarra, Erika; Zeviani, Massimo; Costa, Rodolfo; DE PITTA', Cristiano
Measurement of mitochondrial respiratory chain enzymatic activities in Drosophila melanogaster samples
2022 Brischigliaro, Michele; Frigo, Elena; Fernandez-Vizarra, Erika; Bernardi, Paolo; Viscomi, Carlo
Mitochondrial Cytochrome c Oxidase Defects Alter Cellular Homeostasis of Transition Metals
2022 Brischigliaro, Michele; Badocco, Denis; Costa, Rodolfo; Viscomi, Carlo; Zeviani, Massimo; Pastore, Paolo; Fernández-Vizarra, Erika
Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogaster
2021 Brischigliaro, M.; Frigo, E.; Corra, S.; De Pitta, C.; Szabo, I.; Zeviani, M.; Costa, R.
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features
2020 Beninca, C.; Zanette, V.; Brischigliaro, M.; Johnson, M.; Reyes, A.; Valle, D. A. D.; J. Robinson, A.; Degiorgi, A.; Yeates, A.; Telles, B. A.; Prudent, J.; Baruffini, E.; S. F. Santos M., L.; R. De Souza R., L.; Fernandez-Vizarra, E.; J. Whitworth, A.; Zeviani, M.
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features
2021 Benincá, Cristiane; Zanette, Vanessa; Brischigliaro, Michele; Johnson, Mark; Reyes, Aurelio; Valle, Daniel Almeida do; J Robinson, Alan; Degiorgi, Andrea; Yeates, Anna; Telles, Bruno Augusto; Prudent, Julien; Baruffini, Enrico; S F Santos, Mara Lucia; R de Souza, Ricardo Lehtonen; Fernandez-Vizarra, Erika; Whitworth, Alexander J; Zeviani, Massimo
Two independent respiratory chains adapt OXPHOS performance to glycolytic switch
2022 Fernández-Vizarra, Erika; López-Calcerrada, Sandra; Sierra Magro, Ana; Pérez-Pérez, Rafael; Formosa Luke, E; Illescas, María; Peñas, Ana; Brischigliaro, Michele; Ding, Shujing; Fearnley Ian, M; Tzoulis, Charalampos; Pitceathly Robert, Ds; Martín Miguel, Angel; Stroud David, A; Zeviani, Massimo; Ryan Michael, T; Ugalde, Cristina