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BACHETTI, TIZIANA

BACHETTI, TIZIANA  

100022 - Dipartimento di Scienze della terra, dell'ambiente e della vita  

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A Common 3'UTR Variant of the PHOX2B Gene Is Associated With Infant Life-Threatening and Sudden Death Events in the Italian Population 1-gen-2021 Bachetti, Tiziana; Bagnasco, Simona; Piumelli, Raffaele; Palmieri, Antonella; Ceccherini, Isabella
A COMMON HAPLOTYPE AT THE 5' END OF THE RET PROTO-ONCOGENE, OVERREPRESENTED IN HIRSCHSPRUNG PATIENTS, IS ASSOCIATED WITH REDUCED GENE EXPRESSION 1-gen-2005 Griseri, P; Bachetti, T; Puppo, F; Lantieri, Francesca; Ravazzolo, Roberto; Devoto, M; Ceccherini, I.
A common variant located in the 3'UTR of the RET gene is associated with protection from Hirschsprung disease 1-gen-2007 Griseri, P; Lantieri, Francesca; Puppo, F; Bachetti, T; DI DUCA, M; Ravazzolo, Roberto; Ceccherini, I.
A focus on regulatory networks linking micrornas, transcription factors and target genes in neuroblastoma 1-gen-2021 Perri, P.; Ponzoni, M.; Corrias, M. V.; Ceccherini, I.; Candiani, S.; Bachetti, T.
A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activities 1-gen-2010 Bachetti, T; DI ZANNI, E; Lantieri, Francesca; Caroli, F; Regis, S; Filocamo, M; Rainero, I; Gallone, S; Cilia, R; Romano, S; Savoiardo, M; Pareyson, D; Biancheri, R; Ravazzolo, Roberto; Ceccherini, I.
A Proteomics Approach Identifies RREB1 as a Crucial Molecular Target of Imidazo–Pyrazole Treatment in SKMEL-28 Melanoma Cells 1-gen-2024 Iervasi, Erika; Coronel Vargas, Gabriela; Bachetti, Tiziana; Tkachenko, Kateryna; Spallarossa, Andrea; Brullo, Chiara; Rosano, Camillo; Carta, Sonia; Barboro, Paola; Profumo, Aldo; Ponassi, Marco
Alexander Disease Modeling in Zebrafish: An In Vivo System Suitable to Perform Drug Screening 1-gen-2020 Candiani, Simona; Carestiato, Silvia; F Mack, Andreas; Bani, Daniele; Bozzo, Matteo; Obino, Valentina; Ori, Michela; Rosamilia, Francesca; De Sarlo, Miriam; Pestarino, Mario; Ceccherini, Isabella; Bachetti, Tiziana
AMPHIOXUS NEUROGLIA: MOLECULAR CHARACTERIZATION AND EVIDENCE FOR EARLY COMPARTMENTALIZATION OF THE DEVELOPING NERVE CORD 1-gen-2021 Bozzo, Matteo; Lacalli, Thurston C.; Obino, Valentina; Marcenaro, Emanuela; Bachetti, Tiziana; Manni, Lucia; Pestarino, Mario; Schubert, Michael; Candiani, Simona
Amphioxus neuroglia: Molecular characterization and evidence for early compartmentalization of the developing nerve cord 1-gen-2021 Bozzo, M.; Lacalli, T. C.; Obino, V.; Caicci, F.; Marcenaro, E.; Bachetti, T.; Manni, L.; Pestarino, M.; Schubert, M.; Candiani, S.
An in vitro approach to test the possible role of candidate factors in the transcriptional regulation of the RET proto-oncogene 1-gen-2005 Bachetti, T; Borghini, S; Ravazzolo, Roberto; Ceccherini, I.
Autophagy contributes to inflammation in patients with TNFR-associated periodic syndrome (TRAPS) 1-gen-2013 Bachetti, T; Chiesa, Sabrina; Castagnola, P; Bani, D; Di Zanni, E; Omenetti, A; D'Osualdo, A; Fraldi, A; Ballabio, A; Ravazzolo, Roberto; Martini, Alberto; Gattorno, M; Ceccherini, I.
Beneficial Effect of Phenytoin and Carbamazepine on GFAP Gene Expression and Mutant GFAP Folding in a Cellular Model of Alexander’s Disease 1-gen-2021 Bachetti, T.; Zanni, E. D.; Adamo, A.; Rosamilia, F.; Sechi, M. M.; Solla, P.; Bozzo, M.; Ceccherini, I.; Sechi, G.
Beneficial effects of curcumin on GFAP filament organization and down-regulation of GFAP expression in an in vitro model of Alexander disease 1-gen-2012 Bachetti, T; Di Zanni, E; Balbi, P; Ravazzolo, Roberto; Sechi, G; Ceccherini, I.
Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome 1-gen-2006 Bachetti, T; Robbiano, A; Parodi, S; Matera, I; Merello, E; Capra, V; Baglietto, Mp; Rossi, A; Ceccherini, I; Ottonello, G.
Causative and common PHOX2B variants define a broad phenotypic spectrum 1-gen-2019 Bachetti, T; Ceccherini, Isabella
Ceftriaxone for Alexander's Disease: A Four-Year Follow-Up 1-gen-2013 Sechi, G; Ceccherini, I; Bachetti, T; Deiana, Ga; Sechi, E; Balbi, P
Ceftriaxone has a therapeutic role in Alexander disease 1-gen-2010 Sechi, G.; Balbi, P.; Bachetti, T.; Matta, M.; Serra, A.; Deiana, G. A.; Di Zanni, E.; Ceccherini, I.
Common PHOX2B poly-alanine contractions impair RET gene transcription, predisposing to Hirschsprung disease 1-gen-2017 Di Zanni, Eleonora; Adamo, Annalisa; Belligni, Elga; Lerone, Margherita; Martucciello, Giuseppe; Mattioli, Girolamo; Pini Prato, Alessio; Ravazzolo, Roberto; Silengo, Margherita; Bachetti, Tiziana; Ceccherini, Isabella
Comparative genomic sequence analysis coupled to Chromatin Immunoprecipitation: a screening procedure applied to search for regulatory elements at the RET locus 1-gen-2005 Puppo, F; Musso, M; Pirulli, D; Griseri, P; Bachetti, T; Crovella, S; Patrone, G; Ceccherini, I; Ravazzolo, Roberto
Correspondence regarding: Alexander disease mutant glial fibrillary acidic protein compromises glutamate transport in astrocytes J Neuropathol Exp Neurol 2010;69:335-45 1-gen-2010 Sechi, G.; Balbi, P.; Bachetti, T.; Ceccherini, I.