about
Molecular characterization of human stathmin expressed in Escherichia coli: site-directed mutagenesis of two phosphorylatable serines (Ser-25 and Ser-63)Trisomy for synaptojanin1 in Down syndrome is functionally linked to the enlargement of early endosomesArgyrophilic grain disease: synergistic component of dementia?Protein kinase CK-1 inhibitors as new potential drugs for amyotrophic lateral sclerosis.Lack of miRNA Misregulation at Early Pathological Stages in Drosophila Neurodegenerative Disease Models.Splicing factors act as genetic modulators of TDP-43 production in a new autoregulatory TDP-43 Drosophila model.Neuron-to-Neuron Transfer of FUS in Drosophila Primary Neuronal Culture Is Enhanced by ALS-Associated Mutations.Regulated endocytic routing modulates wingless signaling in Drosophila embryos.Vascular endothelial growth factor and its high-affinity receptor (VEGFR-2) are highly expressed in the human forebrain and cerebellum during development.Transcriptional repression by suppressor of hairless involves the binding of a hairless-dCtBP complex in Drosophila.Drosophila models of human tauopathies indicate that Tau protein toxicity in vivo is mediated by soluble cytosolic phosphorylated forms of the protein.The neurogenic suppressor of hairless DNA-binding protein mediates the transcriptional activation of the enhancer of split complex genes triggered by Notch signaling.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.Enhancing Mitofusin/Marf ameliorates neuromuscular dysfunction in Drosophila models of TDP-43 proteinopathies.The activity of Drosophila Hairless is required in pupae but not in embryos to inhibit Notch signal transduction.Inhibition of proteasome and Shaggy/Glycogen synthase kinase-3beta kinase prevents clearance of phosphorylated tau in Drosophila.Cytoskeleton proteins are modulators of mutant tau-induced neurodegeneration in Drosophila.Both cytoplasmic and nuclear accumulations of the protein are neurotoxic in Drosophila models of TDP-43 proteinopathies.Important neuronal toxicity of microtubule-bound Tau in vivo in Drosophila.Identification of TCERG1 as a new genetic modulator of TDP-43 production in DrosophilaFTLD/ALS-linked TDP-43 mutations do not alter TDP-43's ability to self-regulate its expression in DrosophilaDetection of all adult Tau isoforms in a 3D culture model of iPSC-derived neurons
P50
Q24528804-10A8BED1-4FC9-4509-8E25-D9D4A860783CQ28118988-F4675A44-EAEC-457A-98C4-462240CB8813Q28266662-A4C71EF8-1984-4BE5-8D86-D90420515369Q30574827-C1D19B11-9157-49DA-AD23-DBA6F970A3B8Q36355055-66FB93FC-6FB7-49FD-AD4F-8395D871DC95Q38601956-40918B48-BA7B-4FA9-A019-D04AB6D652AFQ38827430-31E250A2-AA73-413A-9BC9-2033C3A19F31Q41919592-8F43E5B1-79DE-44C7-9F9A-E1999D972DB0Q42466026-67817ABA-71AC-46E8-8497-75E1984B20E2Q43621582-8A719526-FCB0-4B80-8172-B17E3D49789EQ47070820-5F4090E2-0A6F-43F4-9257-A8931B2470A2Q47072129-E678E1A5-69DE-40F5-9984-5A2FA15400F1Q48203102-E31A9DB6-73D9-4C18-8058-4EB5D3AFBED4Q48244551-2B797BBB-E94F-4957-9403-929DC0707164Q50784802-48D5F84B-B66B-4076-BDD6-826BC40D4942Q52562454-CB7D6F42-4590-4936-ADD3-A59FC001B5C9Q52670847-C4C2A881-7856-4417-9BD9-62D76478DFB9Q52677007-C62B5FEC-DD86-4B4A-9627-A6FE3B7F3561Q52710311-C3094EB0-3E4C-4F67-B204-36EE7E4579A2Q52723359-D941410A-90F4-44E4-9DF2-A66BE6F1B32AQ60045141-8BDB2A4B-8141-4840-B4B3-58E37FF506BFQ88737553-91FFE263-A544-466F-BFF5-996D5ED70FF8Q90110363-1BEE3F89-4C4F-49C2-977B-BCF51AF620F2
P50
description
Forscher
@de
chercheur
@fr
investigador
@es
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
研究者
@zh
name
Magalie Lecourtois
@ast
Magalie Lecourtois
@en
Magalie Lecourtois
@es
Magalie Lecourtois
@nl
type
label
Magalie Lecourtois
@ast
Magalie Lecourtois
@en
Magalie Lecourtois
@es
Magalie Lecourtois
@nl
prefLabel
Magalie Lecourtois
@ast
Magalie Lecourtois
@en
Magalie Lecourtois
@es
Magalie Lecourtois
@nl
P106
P1153
6603094942
P31
P496
0000-0002-4257-1974