Sökresultat - Weber, Chantal

Transcriptional Activation of REST by Sp1 in Huntington's Disease Models av Ravache, Myriam, Weber, Chantal, Mérienne, Karine, Trottier, Yvon

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Development of a Social Communication Questionnaire (QSC-ID) for People With Intellectual Disability in a Deaf Sample: A Pilot and Feasibility Study av Weber, Chantal, Weber, Christoph, Fellinger, Johannes, Holzinger, Daniel

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PREVENTING POLYGLUTAMINE-INDUCED ACTIVATION OF C-JUN DELAYS NEURONAL DYSFUNCTION IN A MOUSE MODEL OF SCA7 RETINOPATHY av Merienne, Karine, Friedman, James, Akimoto, Masayuki, Abou-Sleymane, Gretta, Weber, Chantal, Swaroop, Anand, Trottier, Yvon

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Disease Progression Despite Early Loss of Polyglutamine Protein Expression in SCA7 Mouse Model av Helmlinger, Dominique, Abou-Sleymane, Gretta, Yvert, Gaël, Rousseau, Stéphane, Weber, Chantal, Trottier, Yvon, Mandel, Jean-Louis, Devys, Didier

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SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2 av Niewiadomska-Cimicka, Anna, Doussau, Frédéric, Perot, Jean-Baptiste, Roux, Michel J., Keime, Celine, Hache, Antoine, Piguet, Françoise, Novati, Ariana, Weber, Chantal, Yalcin, Binnaz, Meziane, Hamid, Champy, Marie-France, Grandgirard, Erwan, Karam, Alice, Messaddeq, Nadia, Eisenmann, Aurélie, Brouillet, Emmanuel, Nguyen, Hoa Huu Phuc, Flament, Julien, Isope, Philippe, Trottier, Yvon

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Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity av Asselin, Laure, Rivera Alvarez, José, Heide, Solveig, Bonnet, Camille S., Tilly, Peggy, Vitet, Hélène, Weber, Chantal, Bacino, Carlos A., Baranaño, Kristin, Chassevent, Anna, Dameron, Amy, Faivre, Laurence, Hanchard, Neil A., Mahida, Sonal, McWalter, Kirsty, Mignot, Cyril, Nava, Caroline, Rastetter, Agnès, Streff, Haley, Thauvin-Robinet, Christel, Weiss, Marjan M., Zapata, Gladys, Zwijnenburg, Petra J. G., Saudou, Frédéric, Depienne, Christel, Golzio, Christelle, Héron, Delphine, Godin, Juliette D.

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