Lista de obras - Paola Rusmini - Dominio Público Uruguay

17-AAG increases autophagic removal of mutant androgen receptor in spinal and bulbar muscular atrophy.

artículo científico publicado en 2010

A presynaptically toxic secreted phospholipase A2 is internalized into motoneuron-like cells where it is rapidly translocated into the cytosol.

artículo científico publicado en 2008

A role of small heat shock protein B8 (HspB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases

artículo científico publicado en 2010

ALS-related misfolded protein management in motor neurons and muscle cells

artículo científico publicado en 2014

Aberrant Autophagic Response in The Muscle of A Knock-in Mouse Model of Spinal and Bulbar Muscular Atrophy.

artículo científico publicado en 2015

Aggregation and proteasome: the case of elongated polyglutamine aggregation in spinal and bulbar muscular atrophy.

artículo científico publicado en 2006

Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins.

artículo científico publicado en 2011

Androgen-induced neurite outgrowth is mediated by neuritin in motor neurones.

artículo científico publicado en 2005

Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy.

artículo científico publicado en 2013

Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders.

artículo científico

Differential autophagy power in the spinal cord and muscle of transgenic ALS mice.

artículo científico publicado en 2013

Dysregulation of axonal transport and motorneuron diseases.

artículo científico publicado en 2011

Enhanced Clearance of Neurotoxic Misfolded Proteins by the Natural Compound Berberine and Its Derivatives ⬇️

artículo científico publicado en 2020

Estrogen receptor beta and the progression of prostate cancer: role of 5alpha-androstane-3beta,17beta-diol.

artículo científico publicado en 2010

Functional interaction between FUS and SMN underlies SMA-like splicing changes in wild-type hFUS mice.

artículo científico publicado en 2017

Human adipose-derived mesenchymal stem cells as a new model of spinal and bulbar muscular atrophy.

artículo científico publicado en 2014

Inhibition of retrograde transport modulates misfolded protein accumulation and clearance in motoneuron diseases.

artículo científico publicado en 2017

Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling

artículo científico publicado en 2016

Motoneuronal and muscle-selective removal of ALS-related misfolded proteins.

artículo científico

Multiple Roles of Transforming Growth Factor Beta in Amyotrophic Lateral Sclerosis

scientific article published on 16 June 2020

Muscle cells and motoneurons differentially remove mutant SOD1 causing familial amyotrophic lateral sclerosis

artículo científico publicado en 2011

Mutation of SOD1 in ALS: a gain of a loss of function

artículo científico publicado en 2007

Proteasomal and autophagic degradative activities in spinal and bulbar muscular atrophy.

artículo científico publicado en 2010

Quantitative assessment of the degradation of aggregated TDP-43 mediated by the ubiquitin proteasome system and macroautophagy

artículo científico publicado en 2017

Synergic prodegradative activity of Bicalutamide and trehalose on the mutant androgen receptor responsible for spinal and bulbar muscular atrophy

artículo científico publicado en 2014

Tetracycline-regulated gene expression in the NSC-34-tTA cell line for investigation of motor neuron diseases.

artículo científico publicado en 2005

The Role of the Heat Shock Protein B8 (HSPB8) in Motoneuron Diseases.

artículo científico publicado en 2017

The Role of the Protein Quality Control System in SBMA.

artículo científico publicado en 2015

The anabolic/androgenic steroid nandrolone exacerbates gene expression modifications induced by mutant SOD1 in muscles of mice models of amyotrophic lateral sclerosis

artículo científico publicado en 2011

The role of the polyglutamine tract in androgen receptor.

artículo científico publicado en 2007

The small heat shock protein B8 (HSPB8) efficiently removes aggregating species of dipeptides produced in C9ORF72-related neurodegenerative diseases.

artículo científico publicado en 2017

The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cells

artículo científico publicado en 2017

The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).

artículo científico publicado en 2010

Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases

artículo científico publicado en 2016

Trehalose induces autophagy via lysosomal-mediated TFEB activation in models of motoneuron degeneration

scientific article published on 05 November 2018

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

artículo científico publicado en 2016

Lista de obras de Paola Rusmini

17-AAG increases autophagic removal of mutant androgen receptor in spinal and bulbar muscular atrophy.

A presynaptically toxic secreted phospholipase A2 is internalized into motoneuron-like cells where it is rapidly translocated into the cytosol.

A role of small heat shock protein B8 (HspB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases

ALS-related misfolded protein management in motor neurons and muscle cells

Aberrant Autophagic Response in The Muscle of A Knock-in Mouse Model of Spinal and Bulbar Muscular Atrophy.

Aggregation and proteasome: the case of elongated polyglutamine aggregation in spinal and bulbar muscular atrophy.

Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins.

Androgen-induced neurite outgrowth is mediated by neuritin in motor neurones.

Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy.

Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders.

Differential autophagy power in the spinal cord and muscle of transgenic ALS mice.

Dysregulation of axonal transport and motorneuron diseases.

Enhanced Clearance of Neurotoxic Misfolded Proteins by the Natural Compound Berberine and Its Derivatives ⬇️

Estrogen receptor beta and the progression of prostate cancer: role of 5alpha-androstane-3beta,17beta-diol.

Functional interaction between FUS and SMN underlies SMA-like splicing changes in wild-type hFUS mice.

Human adipose-derived mesenchymal stem cells as a new model of spinal and bulbar muscular atrophy.

Inhibition of retrograde transport modulates misfolded protein accumulation and clearance in motoneuron diseases.

Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling

Motoneuronal and muscle-selective removal of ALS-related misfolded proteins.

Multiple Roles of Transforming Growth Factor Beta in Amyotrophic Lateral Sclerosis

Muscle cells and motoneurons differentially remove mutant SOD1 causing familial amyotrophic lateral sclerosis

Mutation of SOD1 in ALS: a gain of a loss of function

Proteasomal and autophagic degradative activities in spinal and bulbar muscular atrophy.

Quantitative assessment of the degradation of aggregated TDP-43 mediated by the ubiquitin proteasome system and macroautophagy

Synergic prodegradative activity of Bicalutamide and trehalose on the mutant androgen receptor responsible for spinal and bulbar muscular atrophy

Tetracycline-regulated gene expression in the NSC-34-tTA cell line for investigation of motor neuron diseases.

The Role of the Heat Shock Protein B8 (HSPB8) in Motoneuron Diseases.

The Role of the Protein Quality Control System in SBMA.

The anabolic/androgenic steroid nandrolone exacerbates gene expression modifications induced by mutant SOD1 in muscles of mice models of amyotrophic lateral sclerosis

The role of the polyglutamine tract in androgen receptor.

The small heat shock protein B8 (HSPB8) efficiently removes aggregating species of dipeptides produced in C9ORF72-related neurodegenerative diseases.

The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cells

The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).

Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases

Trehalose induces autophagy via lysosomal-mediated TFEB activation in models of motoneuron degeneration

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)