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Anne Rovelet-Lecrux, Sebastien Feuillette, Laetitia Miguel, Catherine Schramm, Ségolène Pernet, et al.. Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease. Acta Neuropathologica Communications, BioMed Central part of Springer Science, 2021, 9, ⟨10.1186/s40478-021-01294-4⟩. ⟨hal-03512083⟩

Laetitia Miguel, Thierry Frébourg, Dominique Campion, Magalie Lecourtois. Moderate Overexpression of Tau in Drosophila Exacerbates Amyloid-β-Induced Neuronal Phenotypes and Correlates with Tau Oligomerization. Journal of Alzheimer's Disease, IOS Press, 2020, pp.1-11. ⟨10.3233/JAD-190906⟩. ⟨hal-02484269⟩

Sébastien Feuillette, Camille Charbonnier, Thierry Frebourg, Dominique Campion, Magalie Lecourtois. A Connected Network of Interacting Proteins Is Involved in Human-Tau Toxicity in Drosophila. Frontiers in Neuroscience, Frontiers, 2020, 14, ⟨10.3389/fnins.2020.00068⟩. ⟨hal-02503970⟩

Sébastien Feuillette, Camille Charbonnier, Thierry Frebourg, Dominique Campion, Magalie Lecourtois. A Connected Network of Interacting Proteins Is Involved in Human-Tau Toxicity in Drosophila. Frontiers in Neuroscience, Frontiers, 2020, 14, ⟨10.3389/fnins.2020.00068⟩. ⟨hal-03080080⟩

Laetitia Miguel, Anne Rovelet-Lecrux, Maxime Feyeux, Thierry Frebourg, Pierre Nassoy, et al.. Detection of all adult Tau isoforms in a 3D culture model of iPSC-derived neurons. Stem Cell Research, Elsevier, 2019, 40, pp.101541. ⟨10.1016/j.scr.2019.101541⟩. ⟨hal-03038792⟩

Laetitia Miguel, Anne Rovelet-Lecrux, Maxime Feyeux, Thierry Frebourg, Pierre Nassoy, et al.. Detection of all adult Tau isoforms in a 3D culture model of iPSC-derived neurons. Stem Cell Research, Elsevier, 2019, 40, pp.101541. ⟨10.1016/j.scr.2019.101541⟩. ⟨hal-02329946⟩

Laetitia Miguel, Tracey Avequin, Marine Pons, Thierry Frébourg, Dominique Campion, et al.. FTLD/ALS-linked TDP-43 mutations do not alter TDP-43’s ability to self-regulate its expression in Drosophila. Brain Research, Elsevier, 2018, 1695, pp.1-9. ⟨10.1016/j.brainres.2018.05.021⟩. ⟨hal-02330526⟩

Marine Pons, Silvia Prieto, Laetitia Miguel, Thierry Frébourg, Dominique Campion, et al.. Identification of TCERG1 as a new genetic modulator of TDP-43 production in Drosophila. Acta Neuropathologica Communications, BioMed Central part of Springer Science, 2018, 6 (1), ⟨10.1186/s40478-018-0639-5⟩. ⟨hal-02330484⟩

Marine Pons, Laetitia Miguel, Camille Miel, Tracey Avequin, François Juge, et al.. Splicing factors act as genetic modulators of TDP-43 production in a new autoregulatory TDP-43 Drosophila model. Human Molecular Genetics, Oxford University Press (OUP), 2017, 26 (17), pp.3396-3408. ⟨10.1093/hmg/ddx229⟩. ⟨hal-02330529⟩

Bilal Khalil, Marie-Jeanne Cabirol-Pol, Laetitia Miguel, Alexander J. Whitworth, Magalie Lecourtois, et al.. Enhancing Mitofusin/Marf ameliorates neuromuscular dysfunction in Drosophila models of TDP-43 proteinopathies. Neurobiology of Aging, Elsevier, 2017, 54, pp.71--83. ⟨10.1016/j.neurobiolaging.2017.02.016⟩. ⟨hal-01994093⟩

Sébastien Feuillette, Morgane Delarue, Gaetan Riou, Anne-Lise Gaffuri, Jane Wu, et al.. Neuron-to-Neuron Transfer of FUS in Drosophila Primary Neuronal Culture Is Enhanced by ALS-Associated Mutations. Journal of Molecular Neuroscience, Humana Press, 2017, 62 (1), pp.114-122. ⟨10.1007/s12031-017-0908-y⟩. ⟨hal-02330532⟩

Irene Salado, Miriam Redondo, Murilo Bello, Concepción Pérez, Nicole Liachko, et al.. Protein Kinase CK-1 Inhibitors As New Potential Drugs for Amyotrophic Lateral Sclerosis. Journal of Medicinal Chemistry, American Chemical Society, 2014, 57 (6), pp.2755-2772. ⟨10.1021/jm500065f⟩. ⟨hal-02330558⟩

Anita Reinhardt, Sébastien Feuillette, Marlène Cassar, Céline Callens, Hélène Thomassin, et al.. Lack of miRNA Misregulation at Early Pathological Stages in Drosophila Neurodegenerative Disease Models. Frontiers in Genetics, Frontiers, 2012, 3 (226), 14 p. ⟨10.3389/fgene.2012.00226⟩. ⟨hal-02331191⟩

Jack-Christophe Cossec, Jeremie Lavaur, Diego Berman, Isabelle Rivals, Alexander Hoischen, et al.. Trisomy for synaptojanin1 in Down syndrome is functionally linked to the enlargement of early endosomes. Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (14), pp.3156-3172. ⟨10.1093/hmg/dds142⟩. ⟨hal-02332572⟩

Laetitia Miguel, Tracey Avequin, Morgane Delarue, Sébastien Feuillette, Thierry Frebourg, et al.. Accumulation of insoluble forms of FUS protein correlates with toxicity in Drosophila. Neurobiology of Aging, Elsevier, 2012, 33 (5), pp.1008.e1-1008.e15. ⟨10.1016/j.neurobiolaging.2011.10.008⟩. ⟨hal-02332201⟩

Anita Reinhardt, Sébastien Feuillette, Marlène Cassar, Céline Callens, Hélène Thomassin-Bourrel, et al.. Lack of miRNA Misregulation at Early Pathological Stages in Drosophila Neurodegenerative Disease Models. Frontiers in Genetics, Frontiers, 2012, 3, pp.226. ⟨10.3389/fgene.2012.00226⟩. ⟨hal-01537142⟩

Laetitia Miguel, Thierry Frebourg, Dominique Campion, Magalie Lecourtois. Both cytoplasmic and nuclear accumulations of the protein are neurotoxic in Drosophila models of TDP-43 proteinopathies. Neurobiology of Disease, Elsevier, 2011, 41 (2), pp.398-406. ⟨10.1016/j.nbd.2010.10.007⟩. ⟨hal-02332578⟩

Yasmina Talmat-Amar, Yoan Arribat, Christelle Redt-Clouet, Sébastien Feuillette, Anne-Laure Bouge, et al.. Important neuronal toxicity of microtubule-bound Tau in vivo in Drosophila. Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (19), pp.3738-3745. ⟨10.1093/hmg/ddr290⟩. ⟨hal-02332575⟩

Sébastien Feuillette, Laetitia Miguel, Thierry Frebourg, Dominique Campion, Magalie Lecourtois. Drosophila models of human tauopathies indicate that Tau protein toxicity in vivo is mediated by soluble cytosolic phosphorylated forms of the protein. Journal of Neurochemistry, Wiley, 2010, 113 (4), pp.895-903. ⟨10.1111/j.1471-4159.2010.06663.x⟩. ⟨hal-02332582⟩

Sébastien Feuillette, Vincent Deramecourt, Annie Laquérriere, Charles Duyckaerts, Marie-Bernadette Delisle, et al.. Filamin-A and Myosin VI colocalize with fibrillary Tau protein in Alzheimer's disease and FTDP-17 brains. Brain Research, Elsevier, 2010, 1345, pp.182-189. ⟨10.1016/j.brainres.2010.05.007⟩. ⟨hal-02329958⟩

Magalie Lecourtois, Karine Poirier, Gaëlle Friocourt, Xavier Jaglin, Alice Goldenberg, et al.. Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype. Acta Neuropathologica, Springer Verlag, 2010, 119 (6), pp.779-789. ⟨10.1007/s00401-010-0684-z⟩. ⟨hal-02332580⟩

Anne Rovelet-Lecrux, Magalie Lecourtois, Catherine Thomas-Antérion, Isabelle Le Ber, Alexis Brice, et al.. Partial deletion of the MAPT gene: A novel mechanism of FTDP-17. Human Mutation, Wiley, 2009, 30 (4), pp.E591-E602. ⟨10.1002/humu.20979⟩. ⟨hal-02332588⟩

Olivier Blard, Sébastien Feuillette, Jacqueline Bou, Boris Chaumette, Thierry Frebourg, et al.. Cytoskeleton proteins are modulators of mutant tau-induced neurodegeneration in Drosophila. Human Molecular Genetics, Oxford University Press (OUP), 2007, 16 (5), pp.555-566. ⟨10.1093/hmg/ddm011⟩. ⟨hal-02332593⟩

Olivier Blard, Thierry Frebourg, Dominique Campion, Magalie Lecourtois. Inhibition of proteasome and Shaggy/Glycogen synthase kinase-3β kinase prevents clearance of phosphorylated tau inDrosophila. Journal of Neuroscience Research, Wiley, 2006, 84 (5), pp.1107-1115. ⟨10.1002/jnr.21006⟩. ⟨hal-02332595⟩

Sébastien Feuillette, Olivier Blard, Magalie Lecourtois, Thierry Frebourg, Dominique Campion, et al.. Tau is not normally degraded by the proteasome. Journal of Neuroscience Research, Wiley, 2005, 80 (3), pp.400-405. ⟨10.1002/jnr.20414⟩. ⟨hal-02332598⟩

Magalie Lecourtois, Cyrille Alexandre, Laurence Dubois, Jean-Paul Vincent. Wingless Capture by Frizzled and Frizzled2 in Drosophila Embryos. Developmental Biology, Elsevier, 2001, 235 (2), pp.467-475. ⟨10.1006/dbio.2001.0320⟩. ⟨hal-02335777⟩