Lista de obras - Mario Bortolozzi - Dominio Público Uruguay

A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function

artículo científico publicado en 2008

BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice

artículo científico publicado en 2011

Ca(2+) signaling, apoptosis and autophagy in the developing cochlea: Milestones to hearing acquisition.

artículo científico publicado en 2017

Ca2+ hot spots on the mitochondrial surface are generated by Ca2+ mobilization from stores, but not by activation of store-operated Ca2+ channels.

artículo científico publicado en 2010

Ca2+ signaling in the inner ear.

artículo científico publicado en 2007

Calcium Signaling in the Photodamaged Skin: In Vivo Experiments and Mathematical Modeling

artículo científico publicado en 2021

Critical role of gap junction communication, calcium and nitric oxide signaling in bystander responses to focal photodynamic injury.

artículo científico publicado en 2015

Cx32 hemichannel opening by cytosolic Ca2+ is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease.

artículo científico publicado en 2017

Design and Construction of a Cost-Effective Spinning Disk System for Live Imaging of Inner Ear Tissue

artículo científico publicado en 2016

Heterogeneity of Ca2+ handling among and within Golgi compartments.

artículo científico publicado en 2013

Mitochondrial Calcium Uptake Is Instrumental to Alternative Macrophage Polarization and Phagocytic Activity

scientific article published on 08 October 2019

Molecular dynamics simulations highlight structural and functional alterations in deafness-related M34T mutation of connexin 26.

artículo científico publicado en 2014

PDE2A2 regulates mitochondria morphology and apoptotic cell death via local modulation of cAMP/PKA signalling

artículo científico publicado en 2017

PMCA2 pump mutations and hereditary deafness

artículo científico publicado en 2018

Phosphatases control PKA-dependent functional microdomains at the outer mitochondrial membrane

artículo científico publicado en 2018

Presenilin 2 modulates endoplasmic reticulum (ER)-mitochondria interactions and Ca2+ cross-talk.

artículo científico publicado en 2011

Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisition

artículo científico publicado en 2012

Regional acidosis locally inhibits but remotely stimulates Ca2+ waves in ventricular myocytes

artículo científico publicado en 2017

The 3.5 ångström X-ray structure of the human connexin26 gap junction channel is unlikely that of a fully open channel.

artículo científico publicado en 2013

The antidiabetic drug metformin blunts NETosis in vitro and reduces circulating NETosis biomarkers in vivo

artículo científico publicado en 2018

The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in mice.

artículo científico publicado en 2010

The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss

artículo científico publicado en 2008

Unitary permeability of gap junction channels to second messengers measured by FRET microscopy

artículo científico publicado en 2007

What's the Function of Connexin 32 in the Peripheral Nervous System?

scholarly article by Mario Bortolozzi published in January 2018

Lista de obras de Mario Bortolozzi

A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function

BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice

Ca(2+) signaling, apoptosis and autophagy in the developing cochlea: Milestones to hearing acquisition.

Ca2+ hot spots on the mitochondrial surface are generated by Ca2+ mobilization from stores, but not by activation of store-operated Ca2+ channels.

Ca2+ signaling in the inner ear.

Calcium Signaling in the Photodamaged Skin: In Vivo Experiments and Mathematical Modeling

Critical role of gap junction communication, calcium and nitric oxide signaling in bystander responses to focal photodynamic injury.

Cx32 hemichannel opening by cytosolic Ca2+ is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease.

Design and Construction of a Cost-Effective Spinning Disk System for Live Imaging of Inner Ear Tissue

Heterogeneity of Ca2+ handling among and within Golgi compartments.

Mitochondrial Calcium Uptake Is Instrumental to Alternative Macrophage Polarization and Phagocytic Activity

Molecular dynamics simulations highlight structural and functional alterations in deafness-related M34T mutation of connexin 26.

PDE2A2 regulates mitochondria morphology and apoptotic cell death via local modulation of cAMP/PKA signalling

PMCA2 pump mutations and hereditary deafness

Phosphatases control PKA-dependent functional microdomains at the outer mitochondrial membrane

Presenilin 2 modulates endoplasmic reticulum (ER)-mitochondria interactions and Ca2+ cross-talk.

Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisition

Regional acidosis locally inhibits but remotely stimulates Ca2+ waves in ventricular myocytes

The 3.5 ångström X-ray structure of the human connexin26 gap junction channel is unlikely that of a fully open channel.

The antidiabetic drug metformin blunts NETosis in vitro and reduces circulating NETosis biomarkers in vivo

The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in mice.

The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss

Unitary permeability of gap junction channels to second messengers measured by FRET microscopy

What's the Function of Connexin 32 in the Peripheral Nervous System?