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Claude-Alain Maurage

Showing results (91-100 of 141) with videos related to

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Acta Neuropathologica Communications|July 16, 2017
Cryptic amyloidogenic elements in mutant NEFH causing Charcot-Marie-Tooth 2 trigger aggresome formation and neuronal deathArnaud Jacquier, Cécile Delorme, Edwige Belotti, et al.
Acta Neuropathologica Communications|March 19, 2023
Clinicopathological and molecular characterization of a case classified by DNA‑methylation profiling as "CNS embryonal tumor with BRD4-LEUTX fusion"Laetitia Lebrun, Sacha Allard-Demoustiez, Nathalie Gilis, et al.
Molecular and Cellular Neurosciences|May 16, 2006
Pin1 allows for differential Tau dephosphorylation in neuronal cellsMalika Hamdane, Pierre Dourlen, Alexis Bretteville, et al.
Nature Communications|November 5, 2022
Spatial analysis of the glioblastoma proteome reveals specific molecular signatures and markers of survivalMarie Duhamel, Lauranne Drelich, Maxence Wisztorski, et al.
Brain : a Journal of Neurology|April 3, 2010
Beneficial effect of human anti-amyloid-beta active immunization on neurite morphology and tau pathologyAlberto Serrano-Pozo, Christopher M William, Isidro Ferrer, et al.
Cancers|April 3, 2021
The Implementation of DNA Methylation Profiling into a Multistep Diagnostic Process in Pediatric Neuropathology: A 2-Year Real-World Experience by the French Neuropathology NetworkMelanie Pages, Emmanuelle Uro-Coste, Carole Colin, et al.
Journal of Biomedical Science|June 16, 2026
Tau profiling of brain extracellular vesicles reveals PHF6 peptide as core for pathological tau seeding in Alzheimer's diseaseMarie Oosterlynck, Laura Fichter, Elodie Leroux, et al.
Journal of Molecular Neuroscience : MN|January 24, 2003
Pin1: a therapeutic target in Alzheimer neurodegenerationMalika Hamdane, Caroline Smet, Anne-Véronique Sambo, et al.
Human Mutation|August 27, 2019
Tubular aggregate myopathy and Stormorken syndrome: Mutation spectrum and genotype/phenotype correlationGilles Morin, Valérie Biancalana, Andoni Echaniz-Laguna, et al.
Journal of Neuropathology and Experimental Neurology|July 27, 2025
Autophagy impairment is associated with enhanced satellite cell activation in muscle biopsies from younger late-onset Pompe disease patientsGianmarco Severa, Sultan Bastu, Giovanni Umberto Borin, et al.
Pageof 15

Showing results (91-100 of 141) with videos related to

Sort By:
Pageof 15
Acta Neuropathologica Communications|July 16, 2017
Cryptic amyloidogenic elements in mutant NEFH causing Charcot-Marie-Tooth 2 trigger aggresome formation and neuronal deathArnaud Jacquier, Cécile Delorme, Edwige Belotti, et al.
Acta Neuropathologica Communications|March 19, 2023
Clinicopathological and molecular characterization of a case classified by DNA‑methylation profiling as "CNS embryonal tumor with BRD4-LEUTX fusion"Laetitia Lebrun, Sacha Allard-Demoustiez, Nathalie Gilis, et al.
Molecular and Cellular Neurosciences|May 16, 2006
Pin1 allows for differential Tau dephosphorylation in neuronal cellsMalika Hamdane, Pierre Dourlen, Alexis Bretteville, et al.
Nature Communications|November 5, 2022
Spatial analysis of the glioblastoma proteome reveals specific molecular signatures and markers of survivalMarie Duhamel, Lauranne Drelich, Maxence Wisztorski, et al.
Brain : a Journal of Neurology|April 3, 2010
Beneficial effect of human anti-amyloid-beta active immunization on neurite morphology and tau pathologyAlberto Serrano-Pozo, Christopher M William, Isidro Ferrer, et al.
Cancers|April 3, 2021
The Implementation of DNA Methylation Profiling into a Multistep Diagnostic Process in Pediatric Neuropathology: A 2-Year Real-World Experience by the French Neuropathology NetworkMelanie Pages, Emmanuelle Uro-Coste, Carole Colin, et al.
Journal of Biomedical Science|June 16, 2026
Tau profiling of brain extracellular vesicles reveals PHF6 peptide as core for pathological tau seeding in Alzheimer's diseaseMarie Oosterlynck, Laura Fichter, Elodie Leroux, et al.
Journal of Molecular Neuroscience : MN|January 24, 2003
Pin1: a therapeutic target in Alzheimer neurodegenerationMalika Hamdane, Caroline Smet, Anne-Véronique Sambo, et al.
Human Mutation|August 27, 2019
Tubular aggregate myopathy and Stormorken syndrome: Mutation spectrum and genotype/phenotype correlationGilles Morin, Valérie Biancalana, Andoni Echaniz-Laguna, et al.
Journal of Neuropathology and Experimental Neurology|July 27, 2025
Autophagy impairment is associated with enhanced satellite cell activation in muscle biopsies from younger late-onset Pompe disease patientsGianmarco Severa, Sultan Bastu, Giovanni Umberto Borin, et al.
Pageof 15