CRISPINO, GIULIA

CRISPINO, GIULIA  

Dipartimento di Fisica e Astronomia "Galileo Galilei" - DFA  

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Risultati 1 - 13 di 13 (tempo di esecuzione: 0.127 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
The Novel PMCA2 Pump Mutation Tommy Impairs Cytosolic Calcium Clearance in Hair Cells and Links to Deafness in Mice 2010 BORTOLOZZI, MARIOBRINI, MARISACRISPINO, GIULIASCIMEMI, PIETRODE SIATI, ROMOLO DANIELEARSLAN, EDOARDOMAMMANO, FABIO + THE JOURNAL OF BIOLOGICAL CHEMISTRY - -
BAAV Mediated GJB2 Gene Transfer Restores Gap Junction Coupling in Cochlear Organotypic Cultures from Deaf Cx26Sox10Cre Mice 2011 CRISPINO, GIULIASCIMEMI, PIETROSANTARELLI, ROSAMARIAARSLAN, EDOARDOBORTOLOZZI, MARIOMAMMANO, FABIO + PLOS ONE - -
MOuse models of hereditary hearing loss: connexin expression and functional analyses 2011 Crispino, Giulia - - -
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 2015 ZONTA, FRANCESCOBURATTO, DAMIANOCRISPINO, GIULIAMAMMANO, FABIO + HUMAN MOLECULAR GENETICS - -
Cx32 hemichannel opening by cytosolic Ca2+ is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease 2017 Carrer, AndreaLeparulo, AlessandroCrispino, GiuliaCiubotaru, Catalin DacianMarin, OrianoZonta, Francesco + HUMAN MOLECULAR GENETICS ONLINE - -
Mouse Panx1 Is Dispensable for Hearing Acquisition and Auditory Function 2017 Zorzi, VeronicaZiraldo, GaiaCarrer, AndreaCrispino, GiuliaCiubotaru, Catalin D.Mammano, Fabio + FRONTIERS IN MOLECULAR NEUROSCIENCE - -
Design and Characterization of a Human Monoclonal Antibody that Modulates Mutant Connexin 26 Hemichannels Implicated in Deafness and Skin Disorders 2017 CARRER, ANDREAZONTA, FRANCESCOCERIANI, FEDERICOBURATTO, DAMIANOCRISPINO, GIULIAZORZI, VERONICAZIRALDO, GAIABRUNO, FRANCESCAMAMMANO, FABIO + FRONTIERS IN MOLECULAR NEUROSCIENCE - -
In vivo genetic manipulation of inner ear connexin expression by bovine adeno-Associated viral vectors 2017 CRISPINO, GIULIACampioni, MatteoZORZI, VERONICAMAMMANO, FABIO + SCIENTIFIC REPORTS - -
Connexin-mediated signaling in nonsensory cells is crucial for the development of sensory inner hair cells in the mouse cochlea 2017 CERIANI, FEDERICOCRISPINO, GIULIAZORZI, VERONICAMAMMANO, FABIO + THE JOURNAL OF NEUROSCIENCE - -
Cx32 hemichannel opening by cytosolic Ca2+is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease 2018 CARRER, ANDREALEPARULO, ALESSANDROCrispino, GiuliaCiubotaru, Catalin DacianMarin, OrianoZonta, FrancescoBortolozzi, Mario HUMAN MOLECULAR GENETICS - -
Cues to opening mechanisms from in silico electric field excitation of cx26 hemichannel and in vitro mutagenesis studies in HeLa transfectans 2018 Damiano BurattoGiulia CrispinoAndrea CarrerFrancesca BrunoFabio Mammano + FRONTIERS IN MOLECULAR NEUROSCIENCE - -
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 2018 Zorzi, VeronicaZiraldo, GaiaCrispino, GiuliaMammano, Fabio + REDOX BIOLOGY - -
miRNA and mRNA Profiling Links Connexin Deficiency to Deafness via Early Oxidative Damage in the Mouse Stria Vascularis 2021 Crispino G.Mammano F. + FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY - -