BORTOLOZZI, MARIO
BORTOLOZZI, MARIO
Dipartimento di Fisica e Astronomia "Galileo Galilei" - DFA
Ca2+ dynamics in auditory and vestibular hair cells: Monte Carlo simulations and experimental results.
2006 Bortolozzi, Mario; Lelli, A; Mammano, Fabio
PMCA2 mutations and deafness
2007 DI LEVA, F.; Domi, T.; Bortolozzi, Mario; Gasparini, P.; Mammano, Fabio; Brini, Marisa; Carafoli, E.
Ca2+ signaling in the inner ear
2007 Mammano, Fabio; Bortolozzi, Mario; Ortolano, S.; Anselmi, F.
Unitary permeability of gap junction channels tosecond messengers measured by FRET microscopy
2007 Hernandez, V.; Bortolozzi, Mario; Pertegato, V; Beltramello, M; Giarin, M; Zaccolo, M; Pantano, S; Mammano, Fabio
A functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafness
2007 Ficarella, R; DI LEVA, F; Bortolozzi, Mario; Ortolano, S; Donaudy, F; Petrillo, M; Melchionda, S; Lelli, A; Domi, T; Fedrizzi, L; Lim, D; Shull, Ge; Gasparini, P; Brini, Marisa; Mammano, Fabio; Carafoli, E.
Calcium microdomains at presynaptic active zones of vertebrate hair cells unmasked by stochastic deconvolution
2008 Bortolozzi, Mario; Lelli, A; Mammano, Fabio
A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function.
2008 Spinazzi, Marco; Cazzola, S; Bortolozzi, Mario; Baracca, A; Loro, Emanuele; Casarin, Alberto; Solaini, G; Sgarbi, G; Casalena, G; Cenacchi, G; Malena, Adriana; Frezza, C; Carrara, F; Angelini, Corrado; Scorrano, Luca; Salviati, Leonardo; Vergani, L.
The Novel Mouse Mutation Oblivion Inactivates the PMCA2 Pump and Causes Progressive Hearing Loss
2008 Spiden, Sl; Bortolozzi, Mario; DI LEVA, F; DE ANGELIS, Mh; Fuchs, H; Lim, D; Ortolano, S; Ingham, Nj; Brini, Marisa; Carafoli, E; Mammano, Fabio; Steel, Kp
Dominant optic atrophy caused by a novel OPA1 mutation: Disruption of the mitochondrial network with preserved bioenergetics.
2008 Spinazzi, Marco; Cazzola, S; Bortolozzi, Mario; Baracca, A; Loro, Emanuele; Solaini, G; Sgarbi, G; Cenacchi, G; Malena, Adriana; Scorrano, Luca; Frezza, C; Angelini, Corrado; Vergani, Lodovica
Calcium dynamics in inner ear health and disease
2008 Bortolozzi, Mario
Calcium Dynamics in Inner Ear Health and Disease
2009 Bortolozzi, Mario
CA2+ IMAGING PRINCIPLES OF ANALYSIS AND ENHANCEMENT
2009 Bortolozzi, Mario; Mammano, Fabio
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock in mice
2010 Schütz, M; Scimemi, Pietro; Majumder, P; DE SIATI R., D; Crispino, G; Rodriguez, L; Bortolozzi, Mario; Santarelli, Rosamaria; Seydel, A; Sonntag, S; Ingham, N; STEEL K., P; Willecke, K; Mammano, Fabio
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
ATP-mediated cell-cell signaling in the organ of Corti: the role of connexin channels.
2010 Majumder, P; Crispino, G; Rodriguez, L; Ciubotaru, Cd; Anselmi, F; Piazza, V; Bortolozzi, Mario; Mammano, Fabio
Ca2+ Hot Spots on the Mitochondrial Surface Are Generated by Ca2+ Mobilization from Stores, but Not by Activation of Store-Operated Ca2+ Channels
2010 Giacomello, M; Drago, I; Bortolozzi, Mario; Scorzeto, M; Gianelle, A; Pizzo, Paola; Pozzan, Tullio
Defects in the ATP2B2 gene causing hereditary hearing and balance loss in mice and humans: a biophysical study of normal and mutated PMCA2 pump function.
2010 Bortolozzi, Mario
La mutazione T5M della connessina 30 associata a sordità nell’uomo causa ipoacusia di entità media e riduce l’accoppiamento biochimico tra cellule non sensoriali nei topi knock in
2011 Schutz, M; Scimemi, Pietro; Majumder, P; De Siati, Rd; Crispino, G; Rodriguez, L; Bortolozzi, Mario; Santarelli, Rosamaria; Seydel, A; Sonntag, S; Ingham, N; Steel, Kp; Willecke, K; Mammano, Fabio
Presenilin 2 modulates endoplasmic reticulum (ER)-mitochondria interactions and Ca2+ cross-talk.
2011 Zampese, Enrico; Fasolato, Cristina; Kipanyula, Mj; Bortolozzi, Mario; Pozzan, Tullio; Pizzo, Paola
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