Lista de obras - Chiara Mozzetta - Dominio Público Uruguay

Acetylcholine-induced neuronal differentiation: muscarinic receptor activation regulates EGR-1 and REST expression in neuroblastoma cells

artículo científico publicado en 2009

Autocrine activation of nicotinic acetylcholine receptors contributes to Ca2+ spikes in mouse myotubes during myogenesis.

artículo científico publicado en 2005

Challenging the "chromatin hypothesis" of cardiac laminopathies with LMNA mutant iPS cells

scientific article published on 19 August 2019

Chromatin regulated interchange between polycomb repressive complex 2 (PRC2)-Ezh2 and PRC2-Ezh1 complexes controls myogenin activation in skeletal muscle cells

artículo científico publicado en 2011

Dysfunctional polycomb transcriptional repression contributes to lamin A/C-dependent muscular dystrophy

scientific article published on 06 April 2020

Fibroadipogenic progenitors mediate the ability of HDAC inhibitors to promote regeneration in dystrophic muscles of young, but not old Mdx mice ⬇️

artículo científico publicado el 18 de marzo de 2013

Functional and morphological recovery of dystrophic muscles in mice treated with deacetylase inhibitors.

artículo científico publicado en 2006

Functional interdependence at the chromatin level between the MKK6/p38 and IGF1/PI3K/AKT pathways during muscle differentiation.

artículo científico publicado en 2007

HDAC-regulated myomiRs control BAF60 variant exchange and direct the functional phenotype of fibro-adipogenic progenitors in dystrophic muscles.

scientific article published on 28 March 2014

HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment

scholarly article

Histone deacetylase inhibitors in the treatment of muscular dystrophies: epigenetic drugs for genetic diseases.

artículo científico publicado en 2011

Histone deacetylase inhibitors: a potential epigenetic treatment for Duchenne muscular dystrophy.

artículo científico publicado en 2014

Isolation and Culture of Muscle Stem Cells

artículo científico publicado en 2016

Lamin A/C sustains PcG protein architecture, maintaining transcriptional repression at target genes.

artículo científico publicado en 2015

Nitric oxide deficiency determines global chromatin changes in Duchenne muscular dystrophy.

artículo científico publicado en 2009

Preclinical studies in the mdx mouse model of duchenne muscular dystrophy with the histone deacetylase inhibitor givinostat

artículo científico publicado en 2013

Regenerative pharmacology in the treatment of genetic diseases: the paradigm of muscular dystrophy

artículo científico publicado en 2008

Selective control of Pax7 expression by TNF-activated p38α/polycomb repressive complex 2 (PRC2) signaling during muscle satellite cell differentiation

artículo científico publicado en 2011

Sound of silence: the properties and functions of repressive Lys methyltransferases.

artículo científico

TNF/p38α/polycomb signaling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration.

artículo científico publicado en 2010

The mechanisms and possible sites of acetylcholine release during chick primary sensory neuron differentiation.

artículo científico publicado en 2012

Lista de obras de Chiara Mozzetta

Acetylcholine-induced neuronal differentiation: muscarinic receptor activation regulates EGR-1 and REST expression in neuroblastoma cells

Autocrine activation of nicotinic acetylcholine receptors contributes to Ca2+ spikes in mouse myotubes during myogenesis.

Challenging the "chromatin hypothesis" of cardiac laminopathies with LMNA mutant iPS cells

Chromatin regulated interchange between polycomb repressive complex 2 (PRC2)-Ezh2 and PRC2-Ezh1 complexes controls myogenin activation in skeletal muscle cells

Dysfunctional polycomb transcriptional repression contributes to lamin A/C-dependent muscular dystrophy

Fibroadipogenic progenitors mediate the ability of HDAC inhibitors to promote regeneration in dystrophic muscles of young, but not old Mdx mice ⬇️

Functional and morphological recovery of dystrophic muscles in mice treated with deacetylase inhibitors.

Functional interdependence at the chromatin level between the MKK6/p38 and IGF1/PI3K/AKT pathways during muscle differentiation.

HDAC-regulated myomiRs control BAF60 variant exchange and direct the functional phenotype of fibro-adipogenic progenitors in dystrophic muscles.

HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment

Histone deacetylase inhibitors in the treatment of muscular dystrophies: epigenetic drugs for genetic diseases.

Histone deacetylase inhibitors: a potential epigenetic treatment for Duchenne muscular dystrophy.

Isolation and Culture of Muscle Stem Cells

Lamin A/C sustains PcG protein architecture, maintaining transcriptional repression at target genes.

Nitric oxide deficiency determines global chromatin changes in Duchenne muscular dystrophy.

Preclinical studies in the mdx mouse model of duchenne muscular dystrophy with the histone deacetylase inhibitor givinostat

Regenerative pharmacology in the treatment of genetic diseases: the paradigm of muscular dystrophy

Selective control of Pax7 expression by TNF-activated p38α/polycomb repressive complex 2 (PRC2) signaling during muscle satellite cell differentiation

Sound of silence: the properties and functions of repressive Lys methyltransferases.

TNF/p38α/polycomb signaling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration.

The mechanisms and possible sites of acetylcholine release during chick primary sensory neuron differentiation.