Lista de obras - Cédric Raoul - Dominio Público Uruguay

Calreticulin levels determine onset of early muscle denervation by fast motoneurons of ALS model mice.

artículo científico publicado en 2014

Cerebrospinal fluid-targeted delivery of neutralizing anti-IFNγ antibody delays motor decline in an ALS mouse model.

artículo científico publicado en 2014

Chronic activation in presymptomatic amyotrophic lateral sclerosis (ALS) mice of a feedback loop involving Fas, Daxx, and FasL.

artículo científico publicado en 2006

Collapsin response mediator protein 4a (CRMP4a) is upregulated in motoneurons of mutant SOD1 mice and can trigger motoneuron axonal degeneration and cell death.

artículo científico publicado en 2010

Cytotoxic CD8 T lymphocytes expressing ALS-causing SOD1 mutant selectively trigger death of spinal motoneurons

article published in the Proceedings of the National Academy of Sciences of the United States of America

Death Receptors in the Selective Degeneration of Motoneurons in Amyotrophic Lateral Sclerosis

artículo científico publicado en 2013

Elevated levels of IFNγ and LIGHT in the spinal cord of patients with sporadic amyotrophic lateral sclerosis

artículo científico publicado en 2012

Enhanced neuronal Met signalling levels in ALS mice delay disease onset. ⬇️

artículo científico publicado en 2011

Expression of a dominant negative form of Daxx in vivo rescues motoneurons from Fas (CD95)-induced cell death.

artículo científico publicado en 2005

Fas/tumor necrosis factor receptor death signaling is required for axotomy-induced death of motoneurons in vivo

scientific journal article

Fxyd2 regulates Aδ- and C-fiber mechanosensitivity and is required for the maintenance of neuropathic pain.

artículo científico publicado en 2016

How Degeneration of Cells Surrounding Motoneurons Contributes to Amyotrophic Lateral Sclerosis

artículo científico publicado en 2020

IFNγ triggers a LIGHT-dependent selective death of motoneurons contributing to the non-cell-autonomous effects of mutant SOD1.

artículo científico publicado en 2010

Insulin-like growth factor-1 and neurotrophin-3 gene therapy prevents motor decline in an X-linked adrenoleukodystrophy mouse model.

artículo científico publicado en 2009

Lack of confirmation of anti-inward rectifying potassium channel 4.1 antibodies as reliable markers of multiple sclerosis

scientific article published on 22 April 2014

Liver X Receptor Genes Variants Modulate ALS Phenotype.

artículo científico publicado en 2017

Liver X receptors: from cholesterol regulation to neuroprotection-a new barrier against neurodegeneration in amyotrophic lateral sclerosis?

artículo científico publicado en 2016

Morphology and intrinsic excitability of regenerating sensory and motor neurons grown on a line micropattern

artículo científico publicado en 2014

Motoneuron death triggered by a specific pathway downstream of Fas. potentiation by ALS-linked SOD1 mutations.

artículo científico publicado en 2002

Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles

artículo científico publicado en 2022

Myotube elasticity of an amyotrophic lateral sclerosis mouse model.

artículo científico publicado en 2018

NSC-34 Motor Neuron-Like Cells Are Unsuitable as Experimental Model for Glutamate-Mediated Excitotoxicity.

artículo científico publicado en 2016

Neuroimmunity dynamics and the development of therapeutic strategies for amyotrophic lateral sclerosis

artículo científico publicado en 2013

Olesoxime delays muscle denervation, astrogliosis, microglial activation and motoneuron death in an ALS mouse model

artículo científico publicado en 2012

Pathogenic commonalities between spinal muscular atrophy and amyotrophic lateral sclerosis: Converging roads to therapeutic development.

artículo científico publicado en 2017

Programmed cell death of embryonic motoneurons triggered through the Fas death receptor

artículo científico publicado en 1999

ROCK inhibition as a therapy for spinal muscular atrophy: understanding the repercussions on multiple cellular targets

artículo científico publicado en 2014

Reduced calreticulin levels link endoplasmic reticulum stress and Fas-triggered cell death in motoneurons vulnerable to ALS.

artículo científico publicado en 2012

Regulation of Brain Cholesterol: What Role Do Liver X Receptors Play in Neurodegenerative Diseases?

scientific article published on 08 August 2019

Regulation of neuronal high-voltage activated Ca(V)2 Ca(2+) channels by the small GTPase RhoA.

artículo científico publicado en 2015

Somatic and axonal LIGHT signaling elicit degenerative and regenerative responses in motoneurons, respectively

artículo científico publicado en 2014

Systemic AAV6 delivery mediating RNA interference against SOD1: neuromuscular transduction does not alter disease progression in fALS mice.

artículo científico publicado en 2008

The Metabolic Disturbances of Motoneurons Exposed to Glutamate.

artículo científico publicado en 2018

Tweak regulates astrogliosis, microgliosis and skeletal muscle atrophy in a mouse model of amyotrophic lateral sclerosis.

artículo científico publicado en 2015

Viral-based modelling and correction of neurodegenerative diseases by RNA interference.

artículo científico publicado en 2006

Vitamin D confers protection to motoneurons and is a prognostic factor of amyotrophic lateral sclerosis

artículo científico publicado en 2013

Wildtype motoneurons, ALS-Linked SOD1 mutation and glutamate profoundly modify astrocyte metabolism and lactate shuttling.

artículo científico publicado en 2017

[Death of the motor neurones in amyotrophic lateral sclerosis: suicide or murder?]

artículo científico publicado en 2006

Lista de obras de Cédric Raoul

Calreticulin levels determine onset of early muscle denervation by fast motoneurons of ALS model mice.

Cerebrospinal fluid-targeted delivery of neutralizing anti-IFNγ antibody delays motor decline in an ALS mouse model.

Chronic activation in presymptomatic amyotrophic lateral sclerosis (ALS) mice of a feedback loop involving Fas, Daxx, and FasL.

Collapsin response mediator protein 4a (CRMP4a) is upregulated in motoneurons of mutant SOD1 mice and can trigger motoneuron axonal degeneration and cell death.

Cytotoxic CD8 T lymphocytes expressing ALS-causing SOD1 mutant selectively trigger death of spinal motoneurons

Death Receptors in the Selective Degeneration of Motoneurons in Amyotrophic Lateral Sclerosis

Elevated levels of IFNγ and LIGHT in the spinal cord of patients with sporadic amyotrophic lateral sclerosis

Enhanced neuronal Met signalling levels in ALS mice delay disease onset. ⬇️

Expression of a dominant negative form of Daxx in vivo rescues motoneurons from Fas (CD95)-induced cell death.

Fas/tumor necrosis factor receptor death signaling is required for axotomy-induced death of motoneurons in vivo

Fxyd2 regulates Aδ- and C-fiber mechanosensitivity and is required for the maintenance of neuropathic pain.

How Degeneration of Cells Surrounding Motoneurons Contributes to Amyotrophic Lateral Sclerosis

IFNγ triggers a LIGHT-dependent selective death of motoneurons contributing to the non-cell-autonomous effects of mutant SOD1.

Insulin-like growth factor-1 and neurotrophin-3 gene therapy prevents motor decline in an X-linked adrenoleukodystrophy mouse model.

Lack of confirmation of anti-inward rectifying potassium channel 4.1 antibodies as reliable markers of multiple sclerosis

Liver X Receptor Genes Variants Modulate ALS Phenotype.

Liver X receptors: from cholesterol regulation to neuroprotection-a new barrier against neurodegeneration in amyotrophic lateral sclerosis?

Morphology and intrinsic excitability of regenerating sensory and motor neurons grown on a line micropattern

Motoneuron death triggered by a specific pathway downstream of Fas. potentiation by ALS-linked SOD1 mutations.

Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles

Myotube elasticity of an amyotrophic lateral sclerosis mouse model.

NSC-34 Motor Neuron-Like Cells Are Unsuitable as Experimental Model for Glutamate-Mediated Excitotoxicity.

Neuroimmunity dynamics and the development of therapeutic strategies for amyotrophic lateral sclerosis

Olesoxime delays muscle denervation, astrogliosis, microglial activation and motoneuron death in an ALS mouse model

Pathogenic commonalities between spinal muscular atrophy and amyotrophic lateral sclerosis: Converging roads to therapeutic development.

Programmed cell death of embryonic motoneurons triggered through the Fas death receptor

ROCK inhibition as a therapy for spinal muscular atrophy: understanding the repercussions on multiple cellular targets

Reduced calreticulin levels link endoplasmic reticulum stress and Fas-triggered cell death in motoneurons vulnerable to ALS.

Regulation of Brain Cholesterol: What Role Do Liver X Receptors Play in Neurodegenerative Diseases?

Regulation of neuronal high-voltage activated Ca(V)2 Ca(2+) channels by the small GTPase RhoA.

Somatic and axonal LIGHT signaling elicit degenerative and regenerative responses in motoneurons, respectively

Systemic AAV6 delivery mediating RNA interference against SOD1: neuromuscular transduction does not alter disease progression in fALS mice.

The Metabolic Disturbances of Motoneurons Exposed to Glutamate.

Tweak regulates astrogliosis, microgliosis and skeletal muscle atrophy in a mouse model of amyotrophic lateral sclerosis.

Viral-based modelling and correction of neurodegenerative diseases by RNA interference.

Vitamin D confers protection to motoneurons and is a prognostic factor of amyotrophic lateral sclerosis

Wildtype motoneurons, ALS-Linked SOD1 mutation and glutamate profoundly modify astrocyte metabolism and lactate shuttling.

[Death of the motor neurones in amyotrophic lateral sclerosis: suicide or murder?]