CRISPINO, GIULIA

CRISPINO, GIULIA  

Dipartimento di Fisica e Astronomia "Galileo Galilei" - DFA  

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Risultati 1 - 14 di 14 (tempo di esecuzione: 0.044 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
PNS Abstracts 2024 2024 Imran S.Bayraktar E.Crispino G.Bortolozzi M. + JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM - -
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 - -
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 - -
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 - -
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 2017 Carrer, AndreaLeparulo, AlessandroCrispino, GiuliaCiubotaru, Catalin DacianMarin, OrianoZonta, Francesco + HUMAN MOLECULAR GENETICS ONLINE - -
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 - -
Mouse Panx1 Is Dispensable for Hearing Acquisition and Auditory Function 2017 Zorzi, VeronicaZiraldo, GaiaCarrer, AndreaCrispino, GiuliaCiubotaru, Catalin D.Mammano, Fabio + FRONTIERS IN MOLECULAR NEUROSCIENCE - -
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 2015 ZONTA, FRANCESCOBURATTO, DAMIANOCRISPINO, GIULIAMAMMANO, FABIO + HUMAN MOLECULAR GENETICS - -
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 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 - -