Lista de obras - Wilfried Rossoll - Dominio Público Uruguay

A human pluripotent stem cell model of catecholaminergic polymorphic ventricular tachycardia recapitulates patient-specific drug responses.

artículo científico publicado en 2016

A role for the survival of motor neuron protein in mRNP assembly and transport

artículo científico publicado en 2016

Bag1 is essential for differentiation and survival of hematopoietic and neuronal cells

artículo científico publicado en 2005

Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1)

scientific journal article

Coaggregation of RNA-binding proteins in a model of TDP-43 proteinopathy with selective RGG motif methylation and a role for RRM1 ubiquitination

artículo científico publicado en 2012

Deficiency of the Survival of Motor Neuron Protein Impairs mRNA Localization and Local Translation in the Growth Cone of Motor Neurons.

artículo científico publicado en 2016

Dynamics of survival of motor neuron (SMN) protein interaction with the mRNA-binding protein IMP1 facilitates its trafficking into motor neuron axons

artículo científico publicado en 2013

Dysregulation of mRNA Localization and Translation in Genetic Disease

artículo científico publicado en 2016

Gene targeting of Gemin2 in mice reveals a correlation between defects in the biogenesis of U snRNPs and motoneuron cell death

artículo científico publicado en 2002

Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons

artículo científico publicado en 2006

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

artículo científico publicado en 2012

PABPN1 suppresses TDP-43 toxicity in ALS disease models.

artículo científico publicado en 2015

Post-transcriptional Inhibition of Hsc70-4/HSPA8 Expression Leads to Synaptic Vesicle Cycling Defects in Multiple Models of ALS.

artículo científico publicado en 2017

Proximity proteomics of C9orf72 dipeptide repeat proteins identifies molecular chaperones as modifiers of poly-GA aggregation

artículo científico publicado en 2022

Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons

scientific journal article

Sox10 regulates ciliary neurotrophic factor gene expression in Schwann cells

artículo científico publicado en 2006

Spatially and temporally regulating translation via mRNA-binding proteins in cellular and neuronal function.

artículo científico publicado en 2017

Spinal muscular atrophy and a model for survival of motor neuron protein function in axonal ribonucleoprotein complexes

artículo científico publicado en 2009

Spinal muscular atrophy: the role of SMN in axonal mRNA regulation.

artículo científico publicado en 2012

TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD.

artículo científico publicado en 2018

The ALS disease protein TDP-43 is actively transported in motor neuron axons and regulates axon outgrowth.

artículo científico publicado en 2012

The Survival of Motor Neuron Protein Acts as a Molecular Chaperone for mRNP Assembly

artículo científico publicado en 2017

The heterogeneous nuclear ribonucleoprotein-R is necessary for axonal beta-actin mRNA translocation in spinal motor neurons

artículo científico publicado en 2010

The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn / mice and results in a mouse with spinal muscular atrophy

article

The survival of motor neuron (SMN) protein interacts with the mRNA-binding protein HuD and regulates localization of poly(A) mRNA in primary motor neuron axons.

artículo científico publicado en 2011

Trehalose upregulates progranulin expression in human and mouse models of GRN haploinsufficiency: a novel therapeutic lead to treat frontotemporal dementia

artículo científico publicado en 2016

Lista de obras de Wilfried Rossoll

A human pluripotent stem cell model of catecholaminergic polymorphic ventricular tachycardia recapitulates patient-specific drug responses.

A role for the survival of motor neuron protein in mRNP assembly and transport

Bag1 is essential for differentiation and survival of hematopoietic and neuronal cells

Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1)

Coaggregation of RNA-binding proteins in a model of TDP-43 proteinopathy with selective RGG motif methylation and a role for RRM1 ubiquitination

Deficiency of the Survival of Motor Neuron Protein Impairs mRNA Localization and Local Translation in the Growth Cone of Motor Neurons.

Dynamics of survival of motor neuron (SMN) protein interaction with the mRNA-binding protein IMP1 facilitates its trafficking into motor neuron axons

Dysregulation of mRNA Localization and Translation in Genetic Disease

Gene targeting of Gemin2 in mice reveals a correlation between defects in the biogenesis of U snRNPs and motoneuron cell death

Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

PABPN1 suppresses TDP-43 toxicity in ALS disease models.

Post-transcriptional Inhibition of Hsc70-4/HSPA8 Expression Leads to Synaptic Vesicle Cycling Defects in Multiple Models of ALS.

Proximity proteomics of C9orf72 dipeptide repeat proteins identifies molecular chaperones as modifiers of poly-GA aggregation

Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons

Sox10 regulates ciliary neurotrophic factor gene expression in Schwann cells

Spatially and temporally regulating translation via mRNA-binding proteins in cellular and neuronal function.

Spinal muscular atrophy and a model for survival of motor neuron protein function in axonal ribonucleoprotein complexes

Spinal muscular atrophy: the role of SMN in axonal mRNA regulation.

TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD.

The ALS disease protein TDP-43 is actively transported in motor neuron axons and regulates axon outgrowth.

The Survival of Motor Neuron Protein Acts as a Molecular Chaperone for mRNP Assembly

The heterogeneous nuclear ribonucleoprotein-R is necessary for axonal beta-actin mRNA translocation in spinal motor neurons

The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn / mice and results in a mouse with spinal muscular atrophy

The survival of motor neuron (SMN) protein interacts with the mRNA-binding protein HuD and regulates localization of poly(A) mRNA in primary motor neuron axons.

Trehalose upregulates progranulin expression in human and mouse models of GRN haploinsufficiency: a novel therapeutic lead to treat frontotemporal dementia