Priscila Pereira Sena
7PUBLICATIONS
77CO-AUTHORS
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Publications (7)
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|Feb 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.Benita Menden, Rana D Incebacak Eltemur, German Demidov
|Aug 01, 2024
The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy.Jonasz J Weber, Leah Czisch, Priscila Pereira Sena
|Jul 06, 2022
KPNB1 modulates the Machado-Joseph disease protein ataxin-3 through activation of the mitochondrial protease CLPP.Mahkameh Abeditashi, Jonasz Jeremiasz Weber, Priscila Pereira Sena
|Apr 28, 2022
Calpains as novel players in the molecular pathogenesis of spinocerebellar ataxia type 17.Jonasz Jeremiasz Weber, Stefanie Cari Anger, Priscila Pereira Sena
|Nov 17, 2021
Pathophysiological interplay between O-GlcNAc transferase and the Machado-Joseph disease protein ataxin-3.Priscila Pereira Sena, Jonasz J Weber, Maxinne Watchon
|Mar 20, 2021
Neurodegenerative phosphoprotein signaling landscape in models of SCA3.Anna S Sowa, Taissia G Popova, Tina Harmuth
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Frequent Collaborators
7 joint publications
Jonasz Jeremiasz Weber
5 joint publications
Olaf Riess
4 joint publications
Rana Dilara Incebacak Eltemur
3 joint publications
Jeannette Hübener-Schmid
3 joint publications
Thorsten Schmidt
3 joint publications
Chrisovalantou Huridou
2 joint publications
Caspar Gross
2 joint publications
Jana Schmidt
2 joint publications
Florian Fath
2 joint publications
Stefan Hauser
