Lista de obras - Livio Pellizzoni - Dominio Público Uruguay

A Stem Cell Model of the Motor Circuit Uncouples Motor Neuron Death from Hyperexcitability Induced by SMN Deficiency.

artículo científico publicado en 2016

A cell system for phenotypic screening of modifiers of SMN2 gene expression and function

artículo científico publicado en 2013

A functional interaction between the survival motor neuron complex and RNA polymerase II

artículo científico publicado en 2001

A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing

artículo científico publicado en 1998

A role for SMN exon 7 splicing in the selective vulnerability of motor neurons in spinal muscular atrophy

scientific journal article

A systems view of spliceosomal assembly and branchpoints with iCLIP

scientific article published on 30 September 2019

AXenopus laevisHomologue of the La Autoantigen Binds the Pyrimidine Tract of the 5′ UTR of Ribosomal Protein mRNAsin Vitro: Implication of a Protein Factor in Complex Formation

scientific article published on 01 June 1996

Advances in modeling and treating spinal muscular atrophy

artículo científico publicado en 2016

An SMN-dependent U12 splicing event essential for motor circuit function

artículo científico publicado en 2012

Author Correction: A systems view of spliceosomal assembly and branchpoints with iCLIP

artículo científico publicado en 2020

Cellular nucleic acid binding protein binds a conserved region of the 5' UTR of Xenopus laevis ribosomal protein mRNAs

scientific article published on 01 March 1997

Chaperoning ribonucleoprotein biogenesis in health and disease

artículo científico publicado en 2007

Converging Mechanisms of p53 Activation Drive Motor Neuron Degeneration in Spinal Muscular Atrophy.

artículo científico publicado en 2017

Different forms of U15 snoRNA are encoded in the introns of the ribosomal protein S1 gene of Xenopus laevis

artículo científico publicado en 1994

Disease mechanisms and therapeutic approaches in spinal muscular atrophy

artículo científico publicado en 2015

Dysregulation of Mdm2 and Mdm4 alternative splicing underlies motor neuron death in spinal muscular atrophy.

artículo científico publicado en 2018

Effects of 2,4-diaminoquinazoline derivatives on SMN expression and phenotype in a mouse model for spinal muscular atrophy

artículo científico publicado en 2009

Essential role for the SMN complex in the specificity of snRNP assembly

artículo científico publicado en 2002

Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems

artículo científico publicado en 1999

Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli

artículo científico publicado en 2000

Gemin8 is a novel component of the survival motor neuron complex and functions in small nuclear ribonucleoprotein assembly

artículo científico publicado en 2006

Gemin8 is required for the architecture and function of the survival motor neuron complex

artículo científico publicado en 2006

Identification and characterization of Gemin7, a novel component of the survival of motor neuron complex

artículo científico publicado en 2002

Involvement of the Xenopus laevis Ro60 autoantigen in the alternative interaction of La and CNBP proteins with the 5'UTR of L4 ribosomal protein mRNA

artículo científico publicado en 1998

Pharmacokinetics, pharmacodynamics, and efficacy of a small-molecule SMN2 splicing modifier in mouse models of spinal muscular atrophy

artículo científico publicado en 2016

Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy.

artículo científico publicado en 2011

Protective effects of butyrate-based compounds on a mouse model for spinal muscular atrophy.

artículo científico publicado en 2016

Purification of native survival of motor neurons complexes and identification of Gemin6 as a novel component

artículo científico publicado en 2002

Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs

artículo científico publicado en 2007

SMN control of RNP assembly: from post-transcriptional gene regulation to motor neuron disease.

artículo científico

SMN is essential for the biogenesis of U7 small nuclear ribonucleoprotein and 3'-end formation of histone mRNAs.

scientific article published on December 2013

SMN is required for sensory-motor circuit function in Drosophila

artículo científico publicado en 2012

SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins.

artículo científico publicado en 1999

Sequence of the cDNA and gene coding for ribosomal protein S1 of Xenopus laevis

artículo científico publicado en 1995

Sequence-specific interaction of U1 snRNA with the SMN complex

artículo científico publicado en 2002

Stasimon/Tmem41b localizes to mitochondria-associated ER membranes and is essential for mouse embryonic development

article

The DcpS inhibitor RG3039 improves motor function in SMA mice.

scientific article published on 31 May 2013

The SMN complex is associated with snRNPs throughout their cytoplasmic assembly pathway

artículo científico publicado en 2002

The activity of the spinal muscular atrophy protein is regulated during development and cellular differentiation.

artículo científico publicado en 2005

The survival motor neuron protein of Schizosacharomyces pombe. Conservation of survival motor neuron interaction domains in divergent organisms

scientific article published on 01 August 2000

The survival of motor neurons (SMN) protein interacts with the snoRNP proteins fibrillarin and GAR1

artículo científico publicado en 2001

Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy

artículo científico publicado en 2007

Unrip is a component of SMN complexes active in snRNP assembly

artículo científico publicado en 2005

snRNAs contain specific SMN-binding domains that are essential for snRNP assembly

artículo científico publicado en 2004

Lista de obras de Livio Pellizzoni

A Stem Cell Model of the Motor Circuit Uncouples Motor Neuron Death from Hyperexcitability Induced by SMN Deficiency.

A cell system for phenotypic screening of modifiers of SMN2 gene expression and function

A functional interaction between the survival motor neuron complex and RNA polymerase II

A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing

A role for SMN exon 7 splicing in the selective vulnerability of motor neurons in spinal muscular atrophy

A systems view of spliceosomal assembly and branchpoints with iCLIP

AXenopus laevisHomologue of the La Autoantigen Binds the Pyrimidine Tract of the 5′ UTR of Ribosomal Protein mRNAsin Vitro: Implication of a Protein Factor in Complex Formation

Advances in modeling and treating spinal muscular atrophy

An SMN-dependent U12 splicing event essential for motor circuit function

Author Correction: A systems view of spliceosomal assembly and branchpoints with iCLIP

Cellular nucleic acid binding protein binds a conserved region of the 5' UTR of Xenopus laevis ribosomal protein mRNAs

Chaperoning ribonucleoprotein biogenesis in health and disease

Converging Mechanisms of p53 Activation Drive Motor Neuron Degeneration in Spinal Muscular Atrophy.

Different forms of U15 snoRNA are encoded in the introns of the ribosomal protein S1 gene of Xenopus laevis

Disease mechanisms and therapeutic approaches in spinal muscular atrophy

Dysregulation of Mdm2 and Mdm4 alternative splicing underlies motor neuron death in spinal muscular atrophy.

Effects of 2,4-diaminoquinazoline derivatives on SMN expression and phenotype in a mouse model for spinal muscular atrophy

Essential role for the SMN complex in the specificity of snRNP assembly

Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems

Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli

Gemin8 is a novel component of the survival motor neuron complex and functions in small nuclear ribonucleoprotein assembly

Gemin8 is required for the architecture and function of the survival motor neuron complex

Identification and characterization of Gemin7, a novel component of the survival of motor neuron complex

Involvement of the Xenopus laevis Ro60 autoantigen in the alternative interaction of La and CNBP proteins with the 5'UTR of L4 ribosomal protein mRNA

Pharmacokinetics, pharmacodynamics, and efficacy of a small-molecule SMN2 splicing modifier in mouse models of spinal muscular atrophy

Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy.

Protective effects of butyrate-based compounds on a mouse model for spinal muscular atrophy.

Purification of native survival of motor neurons complexes and identification of Gemin6 as a novel component

Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs

SMN control of RNP assembly: from post-transcriptional gene regulation to motor neuron disease.

SMN is essential for the biogenesis of U7 small nuclear ribonucleoprotein and 3'-end formation of histone mRNAs.

SMN is required for sensory-motor circuit function in Drosophila

SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins.

Sequence of the cDNA and gene coding for ribosomal protein S1 of Xenopus laevis

Sequence-specific interaction of U1 snRNA with the SMN complex

Stasimon/Tmem41b localizes to mitochondria-associated ER membranes and is essential for mouse embryonic development

The DcpS inhibitor RG3039 improves motor function in SMA mice.

The SMN complex is associated with snRNPs throughout their cytoplasmic assembly pathway

The activity of the spinal muscular atrophy protein is regulated during development and cellular differentiation.

The survival motor neuron protein of Schizosacharomyces pombe. Conservation of survival motor neuron interaction domains in divergent organisms

The survival of motor neurons (SMN) protein interacts with the snoRNP proteins fibrillarin and GAR1

Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy

Unrip is a component of SMN complexes active in snRNP assembly

snRNAs contain specific SMN-binding domains that are essential for snRNP assembly