Sfoglia per Autore
Molecular dynamics simulations highlight structural and functional alterations in deafness-related M34T mutation of connexin 26
2014 Zonta, Francesco; Buratto, Damiano; Cassini, Chiara; Bortolozzi, Mario; Mammano, Fabio
Molecular dynamics simulations highlight structural and functional alterations in deafness-related M34T mutation of connexin 26
2014 Zonta, F; Buratto, D; Cassini, C; Bortolozzi, Mario; Mammano, Fabio
Global and Local Effects of Intracellular pH on Ca2+ Waves in Rat Ventricular Myocytes
2013 Ford, K. L.; Moorhouse, E. L.; Bortolozzi, Mario; Vaughan, Jones; R., D.
The 3.5 ångström X−ray structure of the human connexin26 gap junction channel is unlikely that of a fully open channel
2013 Zonta, Francesco; Guido, Polles; Maria, Sanasi; Bortolozzi, Mario; Mammano, Fabio
Heterogeneity of Ca2+ handling among and within Golgi compartments
2013 Wong, ANDREA KUAN CIE; Capitanio, Paola; Valentina, Lissandron; Bortolozzi, Mario; Pozzan, Tullio; Pizzo, Paola
A biophysical approach to the study of the structure and function of connexin channel nanopores.
2012 Bortolozzi, Mario; Mammano, Fabio
A biophysical approach to the study of the structure and function of connexin channel nanopores
2012 Bortolozzi, Mario; Mammano, Fabio
Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisition.
2012 Rodriguez, L; Simeonato, E; Scimemi, Pietro; Anselmi, F; Cali', Bianca; Crispino, G; Ciubotaru, Cd; Bortolozzi, Mario; Ramirez, Fg; Majumder, P; Arslan, Edoardo; DE CAMILLI, P; Pozzan, Tullio; 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
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
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
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
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
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
Calcium Dynamics in Inner Ear Health and Disease
2009 Bortolozzi, Mario
CA2+ IMAGING PRINCIPLES OF ANALYSIS AND ENHANCEMENT
2009 Bortolozzi, Mario; Mammano, Fabio
Calcium dynamics in inner ear health and disease
2008 Bortolozzi, Mario
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.
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