Lista de obras -

Capucin does not modify the toxicity of a mutant Huntingtin fragment in vivo

artículo científico publicado en 2012

Correction: IRC-082451, a Novel Multitargeting Molecule, Reduces L-DOPA-Induced Dyskinesias in MPTP Parkinsonian Primates

artículo científico publicado en 2013

Dopamine determines the vulnerability of striatal neurons to the N-terminal fragment of mutant huntingtin through the regulation of mitochondrial complex II.

artículo científico publicado en 2008

IRC-082451, a novel multitargeting molecule, reduces L-DOPA-induced dyskinesias in MPTP Parkinsonian primates

artículo científico publicado en 2013

Impaired brain energy metabolism in the BACHD mouse model of Huntington's disease: critical role of astrocyte-neuron interactions

artículo científico publicado en 2014

Impairment of Glycolysis-Derived l-Serine Production in Astrocytes Contributes to Cognitive Deficits in Alzheimer's Disease

artículo científico publicado en 2020

Involvement of mitochondrial complex II defects in neuronal death produced by N-terminus fragment of mutated huntingtin

artículo científico publicado en 2006

Loss of the thyroid hormone-binding protein Crym renders striatal neurons more vulnerable to mutant huntingtin in Huntington's disease

artículo científico publicado en 2014

Modulation of astrocyte reactivity improves functional deficits in mouse models of Alzheimer's disease

artículo científico publicado en 2018

Preclinical Evaluation of a Lentiviral Vector for Huntingtin Silencing

artículo científico publicado en 2017

Progressive and selective striatal degeneration in primary neuronal cultures using lentiviral vector coding for a mutant huntingtin fragment

artículo científico publicado en 2005

Quantitative assessment of transcriptome differences between brain territories

artículo científico publicado en 2003

Quantitative gene expression profiling of mouse brain regions reveals differential transcripts conserved in human and affected in disease models

artículo científico publicado en 2008

SET translocation is associated with increase in caspase cleaved amyloid precursor protein in CA1 of Alzheimer and Down syndrome patients

artículo científico publicado en 2013

Striatal long noncoding RNA Abhd11os is neuroprotective against an N-terminal fragment of mutant huntingtin in vivo

artículo científico publicado en 2014

The C-terminal domain of LRRK2 with the G2019S mutation is sufficient to produce neurodegeneration of dopaminergic neurons in vivo

scientific article published on 09 October 2019

The striatal kinase DCLK3 produces neuroprotection against mutant huntingtin.

artículo científico publicado en 2018

Lista de obras de

Capucin does not modify the toxicity of a mutant Huntingtin fragment in vivo

Correction: IRC-082451, a Novel Multitargeting Molecule, Reduces L-DOPA-Induced Dyskinesias in MPTP Parkinsonian Primates

Dopamine determines the vulnerability of striatal neurons to the N-terminal fragment of mutant huntingtin through the regulation of mitochondrial complex II.

IRC-082451, a novel multitargeting molecule, reduces L-DOPA-induced dyskinesias in MPTP Parkinsonian primates

Impaired brain energy metabolism in the BACHD mouse model of Huntington's disease: critical role of astrocyte-neuron interactions

Impairment of Glycolysis-Derived l-Serine Production in Astrocytes Contributes to Cognitive Deficits in Alzheimer's Disease

Involvement of mitochondrial complex II defects in neuronal death produced by N-terminus fragment of mutated huntingtin

Loss of the thyroid hormone-binding protein Crym renders striatal neurons more vulnerable to mutant huntingtin in Huntington's disease

Modulation of astrocyte reactivity improves functional deficits in mouse models of Alzheimer's disease

Preclinical Evaluation of a Lentiviral Vector for Huntingtin Silencing

Progressive and selective striatal degeneration in primary neuronal cultures using lentiviral vector coding for a mutant huntingtin fragment

Quantitative assessment of transcriptome differences between brain territories

Quantitative gene expression profiling of mouse brain regions reveals differential transcripts conserved in human and affected in disease models

SET translocation is associated with increase in caspase cleaved amyloid precursor protein in CA1 of Alzheimer and Down syndrome patients

Striatal long noncoding RNA Abhd11os is neuroprotective against an N-terminal fragment of mutant huntingtin in vivo

The C-terminal domain of LRRK2 with the G2019S mutation is sufficient to produce neurodegeneration of dopaminergic neurons in vivo

The striatal kinase DCLK3 produces neuroprotection against mutant huntingtin.