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Mario Bortolozzi

Showing results (31-40 of 39) with videos related to

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Elife|August 3, 2023
Structure of the connexin-43 gap junction channel in a putative closed stateChao Qi, Silvia Acosta Gutierrez, Pia Lavriha, et al.
The Journal of Biological Chemistry|September 10, 2010
The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in miceMario Bortolozzi, Marisa Brini, Nick Parkinson, et al.
Plos Genetics|November 1, 2008
The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing lossSarah L Spiden, Mario Bortolozzi, Francesca Di Leva, et al.
Human Molecular Genetics|September 23, 2010
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in miceMelanie Schütz, Pietro Scimemi, Paromita Majumder, et al.
Elife|May 3, 2017
PDE2A2 regulates mitochondria morphology and apoptotic cell death via local modulation of cAMP/PKA signallingStefania Monterisi, Miguel J Lobo, Craig Livie, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2012
Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisitionLaura Rodriguez, Elena Simeonato, Pietro Scimemi, et al.
Human Molecular Genetics|August 6, 2008
A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in functionMarco Spinazzi, Silvia Cazzola, Mario Bortolozzi, et al.
Communications Biology|November 23, 2024
Modeling early phenotypes of Parkinson's disease by age-induced midbrain-striatum assembloidsKyriaki Barmpa, Claudia Saraiva, Diego Lopez-Pigozzi, et al.
Brain : a Journal of Neurology|November 21, 2024
Lewy pathology formation in patient-derived GBA1 Parkinson's disease midbrain organoidsEmanuele Frattini, Gaia Faustini, Gianluca Lopez, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Elife|August 3, 2023
Structure of the connexin-43 gap junction channel in a putative closed stateChao Qi, Silvia Acosta Gutierrez, Pia Lavriha, et al.
The Journal of Biological Chemistry|September 10, 2010
The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in miceMario Bortolozzi, Marisa Brini, Nick Parkinson, et al.
Plos Genetics|November 1, 2008
The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing lossSarah L Spiden, Mario Bortolozzi, Francesca Di Leva, et al.
Human Molecular Genetics|September 23, 2010
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in miceMelanie Schütz, Pietro Scimemi, Paromita Majumder, et al.
Elife|May 3, 2017
PDE2A2 regulates mitochondria morphology and apoptotic cell death via local modulation of cAMP/PKA signallingStefania Monterisi, Miguel J Lobo, Craig Livie, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2012
Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisitionLaura Rodriguez, Elena Simeonato, Pietro Scimemi, et al.
Human Molecular Genetics|August 6, 2008
A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in functionMarco Spinazzi, Silvia Cazzola, Mario Bortolozzi, et al.
Communications Biology|November 23, 2024
Modeling early phenotypes of Parkinson's disease by age-induced midbrain-striatum assembloidsKyriaki Barmpa, Claudia Saraiva, Diego Lopez-Pigozzi, et al.
Brain : a Journal of Neurology|November 21, 2024
Lewy pathology formation in patient-derived GBA1 Parkinson's disease midbrain organoidsEmanuele Frattini, Gaia Faustini, Gianluca Lopez, et al.
Pageof 4