Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Maria E. Cicardi"'
Autor:
Chiara Scopa, Samantha M. Barnada, Maria E. Cicardi, Mo Singer, Davide Trotti, Marco Trizzino
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-16 (2023)
Abstract Adult neurogenic decline, inflammation, and neurodegeneration are phenotypic hallmarks of Alzheimer’s disease (AD). Mobilization of transposable elements (TEs) in heterochromatic regions was recently reported in AD, but the underlying mech
Externí odkaz:
https://doaj.org/article/4512ae3de9b742d5a9a921bd03292325
Autor:
Francesco Antoniani, Marco Cimino, Laura Mediani, Jonathan Vinet, Enza M. Verde, Valentina Secco, Alfred Yamoah, Priyanka Tripathi, Eleonora Aronica, Maria E. Cicardi, Davide Trotti, Jared Sterneckert, Anand Goswami, Serena Carra
Publikováno v:
Cell Death Discovery, Vol 9, Iss 1, Pp 1-16 (2023)
Abstract Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD) are two neurodegenerative disorders that share genetic causes and pathogenic mechanisms. The critical genetic players of ALS and FTD are the TARDBP, FUS and C9orf72 genes,
Externí odkaz:
https://doaj.org/article/6a9ffd2c23cc47febd11d60c19088ee9
Autor:
Paola Rusmini, Riccardo Cristofani, Mariarita Galbiati, Maria E. Cicardi, Marco Meroni, Veronica Ferrari, Giulia Vezzoli, Barbara Tedesco, Elio Messi, Margherita Piccolella, Serena Carra, Valeria Crippa, Angelo Poletti
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 10 (2017)
Amyotrophic lateral sclerosis (ALS) and spinal and bulbar muscular atrophy (SBMA) are two motoneuron diseases (MNDs) characterized by aberrant protein behavior in affected cells. In familial ALS (fALS) and in SBMA specific gene mutations lead to the
Externí odkaz:
https://doaj.org/article/ddf144e4575b4063a17376f3d85f1f5d
Autor:
Veronica Ferrari, Riccardo Cristofani, Maria E. Cicardi, Barbara Tedesco, Valeria Crippa, Marta Chierichetti, Elena Casarotto, Marta Cozzi, Francesco Mina, Mariarita Galbiati, Margherita Piccolella, Serena Carra, Thomas Vaccari, Angele Nalbandian, Virginia Kimonis, Tyler R. Fortuna, Udai B. Pandey, Maria C. Gagliani, Katia Cortese, Paola Rusmini, Angelo Poletti
Mutations in the valosin-containing protein (VCP) gene cause various lethal proteinopathies that mainly include inclusion body myopathy with Paget's disease of bone and frontotemporal dementia (IBMPFD) and amyotrophic lateral sclerosis (ALS). Differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44c1ced20d9cbccee8e3fbbbd646df8d
https://hdl.handle.net/11380/1287009
https://hdl.handle.net/11380/1287009