BORTOLOZZI, MARIO
BORTOLOZZI, MARIO
Ca signaling, apoptosis and autophagy in the developing cochlea: Milestones to hearing acquisition.
2018 Mammano, Fabio; 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
PMCA2 pump mutations and hereditary deafness
2018 Bortolozzi, Mario; Mammano, Fabio
Design and Construction of a Cost-Effective Spinning Disk System for Live Imaging of Inner Ear Tissue
2016 Mammano, Fabio; Ceriani, Federico; D Ciubotaru, Catalin; Bortolozzi, Mario
PMCA2w/a Splice Variant: A Key Regulator of Hair Cell Mechano-transduction Machinery
2016 Bortolozzi Mario; Mammano Fabio
Critical role of gap junction communication, calcium and nitric oxide signaling in bystander responses to focal photodynamic injury
2015 Cali, Bianca; Ceolin, Stefano; Ceriani, Federico; Bortolozzi, Mario; Agnellini Andrielly, H R; Zorzi, Veronica; Predonzani, Andrea; Bronte, Vincenzo; Molon, Barbara; Mammano, Fabio
A biophysical approach to the study of the structure and function of connexin channel nanopores
2012 Bortolozzi, Mario; Mammano, Fabio
Ca2+ Imaging: Principles of Analysis and Enhancement
2010 Mammano, Fabio; 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, Nick; Crispino, Giulia; Scimemi, Pietro; De Siati, Romolo Daniele; Di Leva, Francesca; Parker, Andrew; Ortolano, Saida; Arslan, Edoardo; Brown, Steve D.; Carafoli, Ernesto; Mammano, Fabio.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Ca signaling, apoptosis and autophagy in the developing cochlea: Milestones to hearing acquisition. | 1-gen-2018 | Mammano, Fabio; Bortolozzi, Mario | |
Cx32 hemichannel opening by cytosolic Ca2+ is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease | 1-gen-2018 | Carrer, Andrea; Leparulo, Alessandro; Crispino, Giulia; Ciubotaru, CATALIN DACIAN; Marin, Oriano; Zonta, Francesco; Bortolozzi, Mario | |
PMCA2 pump mutations and hereditary deafness | 1-gen-2018 | Bortolozzi, Mario; Mammano, Fabio | |
Design and Construction of a Cost-Effective Spinning Disk System for Live Imaging of Inner Ear Tissue | 1-gen-2016 | Mammano, Fabio; Ceriani, Federico; D Ciubotaru, Catalin; Bortolozzi, Mario | |
PMCA2w/a Splice Variant: A Key Regulator of Hair Cell Mechano-transduction Machinery | 1-gen-2016 | Bortolozzi Mario; Mammano Fabio | |
Critical role of gap junction communication, calcium and nitric oxide signaling in bystander responses to focal photodynamic injury | 1-gen-2015 | Cali, Bianca; Ceolin, Stefano; Ceriani, Federico; Bortolozzi, Mario; Agnellini Andrielly, H R; Zorzi, Veronica; Predonzani, Andrea; Bronte, Vincenzo; Molon, Barbara; Mammano, Fabio | |
A biophysical approach to the study of the structure and function of connexin channel nanopores | 1-gen-2012 | Bortolozzi, Mario; Mammano, Fabio | |
Ca2+ Imaging: Principles of Analysis and Enhancement | 1-gen-2010 | Mammano, Fabio; Bortolozzi, Mario | |
The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in mice | 1-gen-2010 | Bortolozzi, Mario; Brini, Marisa; Parkinson, Nick; Crispino, Giulia; Scimemi, Pietro; De Siati, Romolo Daniele; Di Leva, Francesca; Parker, Andrew; Ortolano, Saida; Arslan, Edoardo; Brown, Steve D.; Carafoli, Ernesto; Mammano, Fabio. |