CRISPINO, GIULIA
CRISPINO, GIULIA
Dipartimento di Fisica e Astronomia "Galileo Galilei" - DFA
BAAV Mediated GJB2 Gene Transfer Restores Gap Junction Coupling in Cochlear Organotypic Cultures from Deaf Cx26Sox10Cre Mice
2011 Crispino, Giulia; DI PASQUALE, G; Scimemi, Pietro; Rodriguez, L; Ramirez, Fg; DE SIATI, Rd; Santarelli, Rosamaria; Arslan, Edoardo; Bortolozzi, Mario; Chiorini, Ja; Mammano, Fabio
Connexin-mediated signaling in nonsensory cells is crucial for the development of sensory inner hair cells in the mouse cochlea
2017 Johnson, Stuart L.; Ceriani, Federico; Houston, Oliver; Polishchuk, Roman; Polishchuk, Elena; Crispino, Giulia; Zorzi, Veronica; Mammano, Fabio; Marcotti, Walter
Cues to opening mechanisms from in silico electric field excitation of cx26 hemichannel and in vitro mutagenesis studies in HeLa transfectans
2018 Zonta, Francesco; Buratto, Damiano; Crispino, Giulia; Carrer, Andrea; Bruno, Francesca; Yang, Guang; Mammano, Fabio; Pantano, Sergio
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway
2018 Fetoni, Anna Rita; Zorzi, Veronica; Paciello, Fabiola; Ziraldo, Gaia; Peres, Chiara; Raspa, Marcello; Scavizzi, Ferdinando; Salvatore, Anna Maria; Crispino, Giulia; Tognola, Gabriella; Gentile, Giulia; Spampinato, Antonio Gianmaria; Cuccaro, Denis; Guarnaccia, Maria; Morello, Giovanna; Van Camp, Guy; Fransen, Erik; Brumat, Marco; Girotto, Giorgia; Paludetti, Gaetano; Gasparini, Paolo; Cavallaro, Sebastiano; Mammano, Fabio
Cx32 hemichannel opening by cytosolic Ca2+ is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease
2017 Carrer, Andrea; Leparulo, Alessandro; Crispino, Giulia; Ciubotaru, Catalin Dacian; Marin, Oriano; Zonta, Francesco; Bortolozzi, Mario
Cx32 hemichannel opening by cytosolic Ca2+is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease
2018 Carrer, Andrea; Leparulo, Alessandro; Crispino, Giulia; Ciubotaru, Catalin Dacian; Marin, Oriano; Zonta, Francesco; Bortolozzi, Mario
Design and Characterization of a Human Monoclonal Antibody that Modulates Mutant Connexin 26 Hemichannels Implicated in Deafness and Skin Disorders
2017 Xu, Liang; Carrer, Andrea; Zonta, Francesco; Qu, Zhihu; Ma, Peixiang; Li, Sheng; Ceriani, Federico; Buratto, Damiano; Crispino, Giulia; Zorzi, Veronica; Ziraldo, Gaia; Bruno, Francesca; Nardin, Chiara; Peres, Chiara; Mazzarda, Flavia; Salvatore, Anna M; Raspa, Marcello; Scavizzi, Ferdinando; Chu, Youjun; Xie, Sichun; Yang, Xuemei; Liao, Jun; Liu, Xiao; Wang, Wei; Wang, Shanshan; Yang, Guang; Lerner, Richard A; Mammano, Fabio
In vivo genetic manipulation of inner ear connexin expression by bovine adeno-Associated viral vectors
2017 Crispino, Giulia; Galindo Ramirez, Fabian; Campioni, Matteo; Zorzi, Veronica; Praetorius, Mark; Di Pasquale, Giovanni; Chiorini, John A.; Mammano, Fabio
miRNA and mRNA Profiling Links Connexin Deficiency to Deafness via Early Oxidative Damage in the Mouse Stria Vascularis
2021 Gentile, G.; Paciello, F.; Zorzi, V.; Spampinato, A. G.; Guarnaccia, M.; Crispino, G.; Tettey-Matey, A.; Scavizzi, F.; Raspa, M.; Fetoni, A. R.; Cavallaro, S.; Mammano, F.
MOuse models of hereditary hearing loss: connexin expression and functional analyses
2011 Crispino, Giulia
Mouse Panx1 Is Dispensable for Hearing Acquisition and Auditory Function
2017 Zorzi, Veronica; Paciello, Fabiola; Ziraldo, Gaia; Peres, Chiara; Mazzarda, Flavia; Nardin, Chiara; Pasquini, Miriam; Chiani, Francesco; Raspa, Marcello; Scavizzi, Ferdinando; Carrer, Andrea; Crispino, Giulia; Ciubotaru, Catalin D.; Monyer, Hannah; Fetoni, Anna R.; M. Salvatore, Anna; Mammano, Fabio
PNS Abstracts 2024
2024 Imran, S.; Bayraktar, E.; Caballé, R. B.; Crispino, G.; Pellizzon, A.; Marino, S.; Rakovic, A.; Andrews, P.; Bortolozzi, M.
The Novel PMCA2 Pump Mutation Tommy Impairs Cytosolic Calcium Clearance in Hair Cells and Links to Deafness in Mice
2010 Bortolozzi, Mario; Brini, Marisa; Parkinson, N; Crispino, Giulia; Scimemi, Pietro; DE SIATI, ROMOLO DANIELE; DI LEVA, F; Parker, A; Ortolano, S; Arslan, Edoardo; Brown, Sd; Carafoli, E; Mammano, Fabio
The p.Cys169Tyr variant of connexin 26 is not a polymorphism
2015 Zonta, Francesco; G., Girotto; Buratto, Damiano; Crispino, Giulia; A., Morgan; K., Abdulhadi; M., Alkowari; R., Badii; P., Gasparini; Mammano, Fabio