Questioning on the role of D amino acid oxidase in familial amyotrophic lateral sclerosis
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Published in Proceedings of the National Academy of Sciences - PNAS (29.06.2010)
Published in Proceedings of the National Academy of Sciences - PNAS (29.06.2010)
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Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis
Teyssou, Elisa, Chartier, Laura, Amador, Maria-Del-Mar, Lam, Roselina, Lautrette, Géraldine, Nicol, Marie, Machat, Selma, Da Barroca, Sandra, Moigneu, Carine, Mairey, Mathilde, Larmonier, Thierry, Saker, Safaa, Dussert, Christelle, Forlani, Sylvie, Fontaine, Bertrand, Seilhean, Danielle, Bohl, Delphine, Boillée, Séverine, Meininger, Vincent, Couratier, Philippe, Salachas, François, Stevanin, Giovanni, Millecamps, Stéphanie
Published in Neurobiology of aging (01.10.2017)
Published in Neurobiology of aging (01.10.2017)
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Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders
Lattante, Serena, Millecamps, Stéphanie, Stevanin, Giovanni, Rivaud-Péchoux, Sophie, Moigneu, Carine, Camuzat, Agnès, Da Barroca, Sandra, Mundwiller, Emeline, Couarch, Philippe, Salachas, François, Hannequin, Didier, Meininger, Vincent, Pasquier, Florence, Seilhean, Danielle, Couratier, Philippe, Danel-Brunaud, Véronique, Bonnet, Anne-Marie, Tranchant, Christine, LeGuern, Eric, Brice, Alexis, Le Ber, Isabelle, Kabashi, Edor
Published in Neurology (09.09.2014)
Published in Neurology (09.09.2014)
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Aggregation of Engineered Human β-Cells Into Pseudoislets: Insulin Secretion and Gene Expression Profile in Normoxic and Hypoxic Milieu
Lecomte, Marie-José, Pechberty, Séverine, Machado, Cécile, Da Barroca, Sandra, Ravassard, Philippe, Scharfmann, Raphaël, Czernichow, Paul, Duvillié, Bertrand
Published in Cell medicine (03.12.2016)
Published in Cell medicine (03.12.2016)
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