Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Giulia Fagnocchi"'
Autor:
Federica Banfi, Alicia Rubio, Mattia Zaghi, Luca Massimino, Giulia Fagnocchi, Edoardo Bellini, Mirko Luoni, Cinzia Cancellieri, Anna Bagliani, Chiara Di Resta, Camilla Maffezzini, Angelo Ianielli, Maurizio Ferrari, Rocco Piazza, Luca Mologni, Vania Broccoli, Alessandro Sessa
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-21 (2021)
Schinzel-Giedion syndrome (SGS) is a fatal developmental syndrome characterized by severe intellectual and physical deficits due, at least in part, to early neurodegeneration. Here the authors introduce a human SGS model that displays disease-relevan
Externí odkaz:
https://doaj.org/article/9f82d3e4675e4ed291494e6ac2e0dfe7
Autor:
Giuseppina Mastrototaro, Mattia Zaghi, Luca Massimino, Matteo Moneta, Neda Mohammadi, Federica Banfi, Edoardo Bellini, Marzia Indrigo, Giulia Fagnocchi, Anna Bagliani, Stefano Taverna, Maria Rohm, Stephan Herzig, Alessandro Sessa
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
TBL1XR1 gene is associated with multiple developmental disorders presenting several neurological aspects. The relative protein is involved in the modulation of important cellular pathways and master regulators of transcriptional output, including nuc
Externí odkaz:
https://doaj.org/article/076eed598f6b43d8bc228831b23603d0
Autor:
Angelo Ianielli, Mattia Zaghi, Chiara Di Resta, Federica Banfi, Edoardo Bellini, Mirko Luoni, Luca Massimino, Rocco Piazza, Alicia Rubio, Alessandro Sessa, Anna Bagliani, Vania Broccoli, Giulia Fagnocchi, Cinzia Cancellieri, Maurizio Ferrari, Luca Mologni, Camilla Maffezzini
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-21 (2021)
Nature Communications
Nature Communications
The investigation of genetic forms of juvenile neurodegeneration could shed light on the causative mechanisms of neuronal loss. Schinzel-Giedion syndrome (SGS) is a fatal developmental syndrome caused by mutations in the SETBP1 gene, inducing the acc