Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Cristina Rivellini"'
Autor:
Cristina Rivellini, Emanuela Porrello, Giorgia Dina, Simona Mrakic-Sposta, Alessandra Vezzoli, Marco Bacigaluppi, Giorgia Serena Gullotta, Linda Chaabane, Letizia Leocani, Silvia Marenna, Emanuela Colombo, Cinthia Farina, Jia Newcombe, Klaus-Armin Nave, Ruggero Pardi, Angelo Quattrini, Stefano C. Previtali
Publikováno v:
The Journal of Clinical Investigation, Vol 132, Iss 3 (2022)
Oligodendrocytes are the primary target of demyelinating disorders, and progressive neurodegenerative changes may evolve in the CNS. DNA damage and oxidative stress are considered key pathogenic events, but the underlying molecular mechanisms remain
Externí odkaz:
https://doaj.org/article/a2d1294778d64ffa80a0437adb09bfc7
Autor:
Alessandra Bolino, Françoise Piguet, Valeria Alberizzi, Marta Pellegatta, Cristina Rivellini, Marta Guerrero‐Valero, Roberta Noseda, Chiara Brombin, Alessandro Nonis, Patrizia D'Adamo, Carla Taveggia, Stefano Carlo Previtali
Publikováno v:
EMBO Molecular Medicine, Vol 8, Iss 12, Pp 1438-1454 (2016)
Abstract Charcot–Marie–Tooth (CMT) neuropathies are highly heterogeneous disorders caused by mutations in more than 70 genes, with no available treatment. Thus, it is difficult to envisage a single suitable treatment for all pathogenetic mechanis
Externí odkaz:
https://doaj.org/article/c9084326117846fcb36a849fe5607d3a
Autor:
Giulio Cossu, Stefano C Previtali, Sara Napolitano, Maria Pia Cicalese, Francesco Saverio Tedesco, Francesca Nicastro, Maddalena Noviello, Urmas Roostalu, Maria Grazia Natali Sora, Marina Scarlato, Maurizio De Pellegrin, Claudia Godi, Serena Giuliani, Francesca Ciotti, Rossana Tonlorenzi, Isabella Lorenzetti, Cristina Rivellini, Sara Benedetti, Roberto Gatti, Sarah Marktel, Benedetta Mazzi, Andrea Tettamanti, Martina Ragazzi, Maria Adele Imro, Giuseppina Marano, Alessandro Ambrosi, Rossana Fiori, Maria Pia Sormani, Chiara Bonini, Massimo Venturini, Letterio S Politi, Yvan Torrente, Fabio Ciceri
Publikováno v:
EMBO Molecular Medicine, Vol 8, Iss 12, Pp 1470-1471 (2016)
Externí odkaz:
https://doaj.org/article/ae9385598910469daa5f09e553a2f3b3
Autor:
Cristina Rivellini, Giorgia Dina, Emanuela Porrello, Federica Cerri, Marina Scarlato, Teuta Domi, Daniela Ungaro, Ubaldo Del Carro, Alessandra Bolino, Angelo Quattrini, Giancarlo Comi, Stefano C Previtali
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e32059 (2012)
Remodeling of extracellular matrix (ECM) is a critical step in peripheral nerve regeneration. In fact, in human neuropathies, endoneurial ECM enriched in fibrin and vitronectin associates with poor regeneration and worse clinical prognosis. According
Externí odkaz:
https://doaj.org/article/0c9589ee107d4f678178467b3e89d746
Autor:
Silvia Cipriani, Marta Guerrero‐Valero, Stefano Tozza, Edward Zhao, Veith Vollmer, Danique Beijer, Matt Danzi, Cristina Rivellini, Dejan Lazarevic, Giovanni Battista Pipitone, Bianca Rose Grosz, Costanza Lamperti, Stefania Bianchi Marzoli, Paola Carrera, Marcella Devoto, Chiara Pisciotta, Davide Pareyson, Marina Kennerson, Stefano C. Previtali, Stephan Zuchner, Steven S. Scherer, Fiore Manganelli, Martin Bähler, Alessandra Bolino
Publikováno v:
European journal of neurologyREFERENCES. 30(2)
Charcot-Marie-Tooth disease (CMT) is a heterogeneous group of disorders caused by mutations in at least 100 genes. However, approximately 60% of cases with axonal neuropathies (CMT2) still remain without a genetic diagnosis. We aimed at identifying n
Autor:
Cristina Rivellini, Giorgia Serena Gullotta, Marco Bacigaluppi, Carla Taveggia, Maria Grazia Forese, Angelo Quattrini, Marta Pellegatta, Paola Podini, Paolo Canevazzi, Stefano C. Previtali
Publikováno v:
Glia. 68:95-110
We have previously reported that prostaglandin D2 Synthase (L-PGDS) participates in peripheral nervous system (PNS) myelination during development. We now describe the role of L-PGDS in the resolution of PNS injury, similarly to other members of the
Autor:
Roberta Romano, Eeva-Liisa Eskelinen, Cristina Rivellini, Raffaella Beli, Fiore Manganelli, Stefano C. Previtali, Rossana Tonlorenzi, Maria De Luca, Maria Nolano, Cecilia Bucci, Lucio Santoro
Publikováno v:
Cellular and Molecular Life Sciences
The small GTPase RAB7A regulates late stages of the endocytic pathway and plays specific roles in neurons, controlling neurotrophins trafficking and signaling, neurite outgrowth and neuronal migration. Mutations in the RAB7A gene cause the autosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47a6cf8b56c146a39a01e391f5dc0518
http://hdl.handle.net/11588/803117
http://hdl.handle.net/11588/803117
Autor:
Cristina Rivellini, Emanuela Porrello, Giorgia Dina, Simona Mrakic-Sposta, 211 Alessandra Vezzoli, Marco Bacigaluppi, Giorgia Serena Gullotta, Linda 1, 3 1, 4 1 1 Chaabane, Letizia Leocani, Silvia Marenna, Emanuela Colombo, Cinthia 2567 Farina, Jia Newcombe, Klaus-Armin Nave, Ruggero Pardi, Angelo 11 Quattrini, Stefano Carlo Previtali
Oligodendrocytes are the primary target of demyelinating disorders and progressive neurodegenerative changes may evolve in the CNS. DNA damage and oxidative stress are considered key pathogenic events, but the underlying molecular mechanisms remain u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10495::11c301ba38750c8e285d82ebf3081f95
Autor:
Roberta Noseda, Stefano C. Previtali, Chiara Brombin, Marta Pellegatta, Françoise Piguet, Valeria Alberizzi, Cristina Rivellini, Marta Guerrero-Valero, Alessandra Bolino, Carla Taveggia, Alessandro Nonis, Patrizia D'Adamo
Publikováno v:
EMBO Molecular Medicine
Charcot–Marie–Tooth (CMT) neuropathies are highly heterogeneous disorders caused by mutations in more than 70 genes, with no available treatment. Thus, it is difficult to envisage a single suitable treatment for all pathogenetic mechanisms. Axona
Autor:
Antonietta Carbone, Yevgeniya A. Mironova, Guy M. Lenk, Miriam H. Meisler, Alessandra Bolino, Roman J. Giger, Stefano C. Previtali, Ilaria Vaccari, Maurizio D'Antonio, Cristina Rivellini, Lawrence Wrabetz, Ubaldo Del Carro, Valeria Alberizzi, Francesca Bianchi, Roberta Noseda
Publikováno v:
Human Molecular Genetics
Mutations of FIG4 are responsible for Yunis-Varón syndrome, familial epilepsy with polymicrogyria, and Charcot-Marie-Tooth type 4J neuropathy (CMT4J). Although loss of the FIG4 phospholipid phosphatase consistently causes decreased PtdIns(3,5)P₂ l