Paola Costantini
6PUBLICATIONS
32CO-AUTHORS
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Publications (6)
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|Dec 10, 2025
A novel mutation in FDX2 provides insights into the pathogenesis of MEOAL mitochondrial neuromuscular disease.Davide Doni, Deborah Grifagni, Federica Cavion
|Oct 28, 2024
Unraveling the molecular determinants of a rare human mitochondrial disorder caused by the P144L mutation of FDX2.Deborah Grifagni, Davide Doni, Bianca Susini
|Sep 04, 2024
BioID-based intact cell interactome of the Kv1.3 potassium channel identifies a Kv1.3-STAT3-p53 cellular signaling pathway.Elena Prosdocimi, Veronica Carpanese, Luca Matteo Todesca
|Jan 29, 2024
Correction: Human frataxin, the Friedreich ataxia deficient protein, interacts with mitochondrial respiratory chain.Davide Doni, Federica Cavion, Marco Bortolus
|Dec 07, 2023
Human frataxin, the Friedreich ataxia deficient protein, interacts with mitochondrial respiratory chain.Davide Doni, Federica Cavion, Marco Bortolus
|Feb 25, 2021
The displacement of frataxin from the mitochondrial cristae correlates with abnormal respiratory supercomplexes formation and bioenergetic defects in cells of Friedreich ataxia patients.Davide Doni, Giovanni Rigoni, Elisa Palumbo
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Frequent Collaborators
3 joint publications
Antonella Russo
3 joint publications
Luigi Leanza
2 joint publications
Elisa Greggio
2 joint publications
Elena Ziviani
2 joint publications
Davide Doni
1 joint publications
Elena Prosdocimi
1 joint publications
Veronica Carpanese
1 joint publications
Luca Matteo Todesca
1 joint publications
Tatiana Varanita
1 joint publications
Magdalena Bachmann
