Lista de obras - Magalie Lecourtois - Dominio Público Uruguay

Argyrophilic grain disease: synergistic component of dementia?

artículo científico publicado en 2010

Both cytoplasmic and nuclear accumulations of the protein are neurotoxic in Drosophila models of TDP-43 proteinopathies.

artículo científico publicado en 2010

Cytoskeleton proteins are modulators of mutant tau-induced neurodegeneration in Drosophila.

artículo científico publicado en 2007

Detection of all adult Tau isoforms in a 3D culture model of iPSC-derived neurons

artículo científico publicado en 2019

Drosophila models of human tauopathies indicate that Tau protein toxicity in vivo is mediated by soluble cytosolic phosphorylated forms of the protein.

artículo científico publicado en 2010

Enhancing Mitofusin/Marf ameliorates neuromuscular dysfunction in Drosophila models of TDP-43 proteinopathies.

artículo científico publicado en 2017

FTLD/ALS-linked TDP-43 mutations do not alter TDP-43's ability to self-regulate its expression in Drosophila

artículo científico publicado en 2018

Filamin-A and Myosin VI colocalize with fibrillary Tau protein in Alzheimer's disease and FTDP-17 brains

artículo científico publicado en 2010

Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype

artículo científico publicado en 2010

Identification of TCERG1 as a new genetic modulator of TDP-43 production in Drosophila

artículo científico publicado en 2018

Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease

artículo científico publicado en 2021

Important neuronal toxicity of microtubule-bound Tau in vivo in Drosophila.

artículo científico publicado en 2011

Inhibition of proteasome and Shaggy/Glycogen synthase kinase-3beta kinase prevents clearance of phosphorylated tau in Drosophila.

artículo científico publicado en 2006

Lack of miRNA Misregulation at Early Pathological Stages in Drosophila Neurodegenerative Disease Models.

artículo científico publicado en 2012

Molecular characterization of human stathmin expressed in Escherichia coli: site-directed mutagenesis of two phosphorylatable serines (Ser-25 and Ser-63)

artículo científico publicado en 1994

Neuron-to-Neuron Transfer of FUS in Drosophila Primary Neuronal Culture Is Enhanced by ALS-Associated Mutations.

artículo científico publicado en 2017

Protein kinase CK-1 inhibitors as new potential drugs for amyotrophic lateral sclerosis

artículo científico publicado en 2014

Regulated endocytic routing modulates wingless signaling in Drosophila embryos.

artículo científico publicado en 2001

Splicing factors act as genetic modulators of TDP-43 production in a new autoregulatory TDP-43 Drosophila model

artículo científico

The activity of Drosophila Hairless is required in pupae but not in embryos to inhibit Notch signal transduction.

artículo científico publicado en 1998

The neurogenic suppressor of hairless DNA-binding protein mediates the transcriptional activation of the enhancer of split complex genes triggered by Notch signaling.

artículo científico publicado en 1995

Transcriptional repression by suppressor of hairless involves the binding of a hairless-dCtBP complex in Drosophila.

artículo científico publicado en 2001

Trisomy for synaptojanin1 in Down syndrome is functionally linked to the enlargement of early endosomes

artículo científico

Vascular endothelial growth factor and its high-affinity receptor (VEGFR-2) are highly expressed in the human forebrain and cerebellum during development.

artículo científico publicado en 2010

Lista de obras de Magalie Lecourtois

Argyrophilic grain disease: synergistic component of dementia?

Both cytoplasmic and nuclear accumulations of the protein are neurotoxic in Drosophila models of TDP-43 proteinopathies.

Cytoskeleton proteins are modulators of mutant tau-induced neurodegeneration in Drosophila.

Detection of all adult Tau isoforms in a 3D culture model of iPSC-derived neurons

Drosophila models of human tauopathies indicate that Tau protein toxicity in vivo is mediated by soluble cytosolic phosphorylated forms of the protein.

Enhancing Mitofusin/Marf ameliorates neuromuscular dysfunction in Drosophila models of TDP-43 proteinopathies.

FTLD/ALS-linked TDP-43 mutations do not alter TDP-43's ability to self-regulate its expression in Drosophila

Filamin-A and Myosin VI colocalize with fibrillary Tau protein in Alzheimer's disease and FTDP-17 brains

Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype

Identification of TCERG1 as a new genetic modulator of TDP-43 production in Drosophila

Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease

Important neuronal toxicity of microtubule-bound Tau in vivo in Drosophila.

Inhibition of proteasome and Shaggy/Glycogen synthase kinase-3beta kinase prevents clearance of phosphorylated tau in Drosophila.

Lack of miRNA Misregulation at Early Pathological Stages in Drosophila Neurodegenerative Disease Models.

Molecular characterization of human stathmin expressed in Escherichia coli: site-directed mutagenesis of two phosphorylatable serines (Ser-25 and Ser-63)

Neuron-to-Neuron Transfer of FUS in Drosophila Primary Neuronal Culture Is Enhanced by ALS-Associated Mutations.

Protein kinase CK-1 inhibitors as new potential drugs for amyotrophic lateral sclerosis

Regulated endocytic routing modulates wingless signaling in Drosophila embryos.

Splicing factors act as genetic modulators of TDP-43 production in a new autoregulatory TDP-43 Drosophila model

The activity of Drosophila Hairless is required in pupae but not in embryos to inhibit Notch signal transduction.

The neurogenic suppressor of hairless DNA-binding protein mediates the transcriptional activation of the enhancer of split complex genes triggered by Notch signaling.

Transcriptional repression by suppressor of hairless involves the binding of a hairless-dCtBP complex in Drosophila.

Trisomy for synaptojanin1 in Down syndrome is functionally linked to the enlargement of early endosomes

Vascular endothelial growth factor and its high-affinity receptor (VEGFR-2) are highly expressed in the human forebrain and cerebellum during development.