Cytochrome c oxidase deficiency M Brischigliaro, M Zeviani Biochimica et Biophysica Acta (BBA)-Bioenergetics 1862 (1), 148335, 2021 | 105 | 2021 |
Two independent respiratory chains adapt OXPHOS performance to glycolytic switch E Fernandez-Vizarra, S Lopez-Calcerrada, A Sierra-Magro, ... Cell Metabolism 34 (11), 1792-1808. e6, 2022 | 47 | 2022 |
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features C Benincá, V Zanette, M Brischigliaro, M Johnson, A Reyes, DA do Valle, ... Journal of medical genetics 58 (3), 155-167, 2021 | 47 | 2021 |
Exploiting pyocyanin to treat mitochondrial disease due to respiratory complex III dysfunction R Peruzzo, S Corrà, R Costa, M Brischigliaro, T Varanita, L Biasutto, ... Nature Communications 12 (1), 2103, 2021 | 24 | 2021 |
Knockdown of APOPT1/COA8 causes cytochrome c oxidase deficiency, neuromuscular impairment, and reduced resistance to oxidative stress in Drosophila melanogaster M Brischigliaro, S Corrà, C Tregnago, E Fernandez-Vizarra, M Zeviani, ... Frontiers in Physiology 10, 1143, 2019 | 19 | 2019 |
Structural rather than catalytic role for mitochondrial respiratory chain supercomplexes M Brischigliaro, A Cabrera-Orefice, S Arnold, C Viscomi, M Zeviani, ... elife 12, RP88084, 2023 | 16 | 2023 |
Measurement of mitochondrial respiratory chain enzymatic activities in Drosophila melanogaster samples M Brischigliaro, E Frigo, E Fernandez-Vizarra, P Bernardi, C Viscomi STAR protocols 3 (2), 101322, 2022 | 13 | 2022 |
Mitochondrial Cytochrome c Oxidase Defects Alter Cellular Homeostasis of Transition Metals M Brischigliaro, D Badocco, R Costa, C Viscomi, M Zeviani, P Pastore, ... Frontiers in Cell and Developmental Biology 10, 892069, 2022 | 12 | 2022 |
Mitochondrial Neurodegeneration: Lessons from Drosophila melanogaster Models M Brischigliaro, E Fernandez-Vizarra, C Viscomi Biomolecules 13 (2), 378, 2023 | 10 | 2023 |
The human mitochondrial mRNA structurome reveals mechanisms of gene expression JC Moran, A Brivanlou, M Brischigliaro, F Fontanesi, S Rouskin, ... Science 385 (6706), eadm9238, 2024 | 9 | 2024 |
Mitochondrial ribosome biogenesis and redox sensing M Brischigliaro, A Sierra‐Magro, A Ahn, A Barrientos FEBS Open Bio, 2024 | 6 | 2024 |
Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogaster M Brischigliaro, E Frigo, S Corrà, C De Pittà, I Szabò, M Zeviani, R Costa Journal of Molecular Medicine 99 (10), 1471-1485, 2021 | 6 | 2021 |
The human mitochondrial translation factor TACO1 alleviates mitoribosome stalling at polyproline stretches M Brischigliaro, A Krüger, JC Moran, H Antonicka, A Ahn, EA Shoubridge, ... Nucleic acids research 52 (16), 9710-9726, 2024 | 5 | 2024 |
Emerging mechanisms in the redox regulation of mitochondrial cytochrome c oxidase assembly and function S Povea-Cabello, M Brischigliaro, E Fernández-Vizarra Biochemical Society Transactions 52 (2), 873-885, 2024 | 5 | 2024 |
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7B M Brischigliaro, A Cabrera‐Orefice, M Sturlese, DM Elurbe, E Frigo, ... EMBO reports 23 (8), e54825, 2022 | 5 | 2022 |
Drosophila Mpv17 forms an ion channel and regulates energy metabolism S Corrà, V Checchetto, M Brischigliaro, C Rampazzo, E Bottani, ... Iscience 26 (10), 2023 | 2 | 2023 |
Investigating the functions of ATP synthase subunits e and g in Drosophila melanogaster E Frigo, M Carraro, M Brischigliaro, P Bernardi Biochimica et Biophysica Acta (BBA)-Bioenergetics 1865, 149303, 2024 | | 2024 |
COA8 is a COX10-binding protein involved in the early biogenesis of cytochrome c oxidase M Brischigliaro, K Čunátová, A Cabrera-Orefice, J Pei, C Franchin, ... bioRxiv, 2024.04. 02.587738, 2024 | | 2024 |
Sprint interval exercise disrupts mitochondrial ultrastructure driving a unique mitochondrial stress response and remodelling in humans J Botella, E Perri, NJ Caruana, S Lopez-Calcerrada, M Brischigliaro, ... bioRxiv, 2024.12. 19.629456, 2024 | | 2024 |
Mitochondrial complex I deficiency occurs in skeletal muscle of a subgroup of individuals with Parkinson's disease SU Kverneng, KE Stige, H Berven, S Mostafavi, K Lundervold, ... bioRxiv, 2024.09. 09.611610, 2024 | | 2024 |