Lista de obras - Monica Nizzardo - Dominio Público Uruguay

Antisense oligonucleotide therapy for the treatment of C9ORF72 ALS/FTD diseases.

artículo científico

Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanisms

artículo científico publicado en 2011

Cellular therapy to target neuroinflammation in amyotrophic lateral sclerosis ⬇️

artículo científico

Direct reprogramming of adult somatic cells into other lineages: past evidence and future perspectives

artículo científico publicado en 2012

Direct reprogramming of human astrocytes into neural stem cells and neurons.

artículo científico publicado en 2012

Downregulation of glutamic acid decarboxylase in Drosophila TDP-43-null brains provokes paralysis by affecting the organization of the neuromuscular synapses

artículo científico publicado en 2018

Effect of Combined Systemic and Local Morpholino Treatment on the Spinal Muscular Atrophy Δ7 Mouse Model Phenotype

artículo científico publicado en 2014

Embryonic stem cell-derived neural stem cells improve spinal muscular atrophy phenotype in mice.

artículo científico publicado en 2009

Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis mice

artículo científico publicado en 2007

Glycogen storage disease type III: A novel Agl knockout mouse model.

artículo científico publicado en 2014

In vitro neurogenesis: development and functional implications of iPSC technology

artículo científico publicado en 2013

Investigation of New Morpholino Oligomers to Increase Survival Motor Neuron Protein Levels in Spinal Muscular Atrophy

artículo científico publicado en 2018

Isolation and characterization of murine neural stem/progenitor cells based on Prominin-1 expression

artículo científico publicado en 2007

MFN2-related neuropathies: Clinical features, molecular pathogenesis and therapeutic perspectives.

artículo científico

MicroRNA expression analysis identifies a subset of downregulated miRNAs in ALS motor neuron progenitors.

artículo científico publicado en 2018

Minimally invasive transplantation of iPSC-derived ALDHhiSSCloVLA4+ neural stem cells effectively improves the phenotype of an amyotrophic lateral sclerosis model.

artículo científico publicado en 2013

Molecular therapeutic strategies for spinal muscular atrophies: current and future clinical trials.

artículo científico publicado en 2013

Molecular, genetic and stem cell-mediated therapeutic strategies for spinal muscular atrophy (SMA)

artículo científico publicado en 2014

Motoneuron Transplantation Rescues the Phenotype of SMARD1 (Spinal Muscular Atrophy with Respiratory Distress Type 1)

artículo científico publicado en 2009

Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectives

artículo científico publicado en 2014

Motor neurons with differential vulnerability to degeneration show distinct protein signatures in health and ALS.

artículo científico publicado en 2015

Neural Stem Cell Transplantation for Neurodegenerative Diseases

scientific article published on 28 April 2020

Neural stem cells LewisX+ CXCR4+ modify disease progression in an amyotrophic lateral sclerosis model.

artículo científico publicado en 2007

Pluripotent stem cell-based models of spinal muscular atrophy

artículo científico publicado en 2014

Research advances in gene therapy approaches for the treatment of amyotrophic lateral sclerosis

artículo científico publicado en 2011

Resveratrol-induced apoptosis in human T-cell acute lymphoblastic leukaemia MOLT-4 cells

artículo científico publicado en 2007

Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutations

artículo científico publicado en 2012

Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches

artículo científico publicado en 2015

Spinal muscular atrophy--recent therapeutic advances for an old challenge.

artículo científico

Stem cell transplantation for amyotrophic lateral sclerosis: therapeutic potential and perspectives on clinical translation.

artículo científico publicado en 2014

Systematic elucidation of neuron-astrocyte interaction in models of amyotrophic lateral sclerosis using multi-modal integrated bioinformatics workflow

scientific article published on 04 November 2020

Systemic transplantation of c-kit+ cells exerts a therapeutic effect in a model of amyotrophic lateral sclerosis

artículo científico publicado en 2010

The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency

artículo científico publicado en 2009

The wide spectrum of clinical phenotypes of spinal muscular atrophy with respiratory distress type 1: a systematic review

artículo científico publicado en 2014

Therapeutic applications of the cell-penetrating HIV-1 Tat peptide

artículo científico

Therapeutic development in amyotrophic lateral sclerosis.

artículo científico

iPSC-Derived neural stem cells act via kinase inhibition to exert neuroprotective effects in spinal muscular atrophy with respiratory distress type 1

artículo científico publicado en 2014

Lista de obras de Monica Nizzardo

Antisense oligonucleotide therapy for the treatment of C9ORF72 ALS/FTD diseases.

Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanisms

Cellular therapy to target neuroinflammation in amyotrophic lateral sclerosis ⬇️

Direct reprogramming of adult somatic cells into other lineages: past evidence and future perspectives

Direct reprogramming of human astrocytes into neural stem cells and neurons.

Downregulation of glutamic acid decarboxylase in Drosophila TDP-43-null brains provokes paralysis by affecting the organization of the neuromuscular synapses

Effect of Combined Systemic and Local Morpholino Treatment on the Spinal Muscular Atrophy Δ7 Mouse Model Phenotype

Embryonic stem cell-derived neural stem cells improve spinal muscular atrophy phenotype in mice.

Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis mice

Glycogen storage disease type III: A novel Agl knockout mouse model.

In vitro neurogenesis: development and functional implications of iPSC technology

Investigation of New Morpholino Oligomers to Increase Survival Motor Neuron Protein Levels in Spinal Muscular Atrophy

Isolation and characterization of murine neural stem/progenitor cells based on Prominin-1 expression

MFN2-related neuropathies: Clinical features, molecular pathogenesis and therapeutic perspectives.

MicroRNA expression analysis identifies a subset of downregulated miRNAs in ALS motor neuron progenitors.

Minimally invasive transplantation of iPSC-derived ALDHhiSSCloVLA4+ neural stem cells effectively improves the phenotype of an amyotrophic lateral sclerosis model.

Molecular therapeutic strategies for spinal muscular atrophies: current and future clinical trials.

Molecular, genetic and stem cell-mediated therapeutic strategies for spinal muscular atrophy (SMA)

Motoneuron Transplantation Rescues the Phenotype of SMARD1 (Spinal Muscular Atrophy with Respiratory Distress Type 1)

Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectives

Motor neurons with differential vulnerability to degeneration show distinct protein signatures in health and ALS.

Neural Stem Cell Transplantation for Neurodegenerative Diseases

Neural stem cells LewisX+ CXCR4+ modify disease progression in an amyotrophic lateral sclerosis model.

Pluripotent stem cell-based models of spinal muscular atrophy

Research advances in gene therapy approaches for the treatment of amyotrophic lateral sclerosis

Resveratrol-induced apoptosis in human T-cell acute lymphoblastic leukaemia MOLT-4 cells

Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutations

Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches

Spinal muscular atrophy--recent therapeutic advances for an old challenge.

Stem cell transplantation for amyotrophic lateral sclerosis: therapeutic potential and perspectives on clinical translation.

Systematic elucidation of neuron-astrocyte interaction in models of amyotrophic lateral sclerosis using multi-modal integrated bioinformatics workflow

Systemic transplantation of c-kit+ cells exerts a therapeutic effect in a model of amyotrophic lateral sclerosis

The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency

The wide spectrum of clinical phenotypes of spinal muscular atrophy with respiratory distress type 1: a systematic review

Therapeutic applications of the cell-penetrating HIV-1 Tat peptide

Therapeutic development in amyotrophic lateral sclerosis.

iPSC-Derived neural stem cells act via kinase inhibition to exert neuroprotective effects in spinal muscular atrophy with respiratory distress type 1