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First PublishedTitleAuthor(s)Type
May-2011Identification of four functional NR3B isoforms in developing white matter reveals unexpected diversity among glutamate receptors.Domingues, AM; Neugebauer, KM; Fern, RJournal Article
Aug-2010Developmental expression of Synaptotagmin isoforms in single calyx of Held-generating neurons.Xiao, L; Han, Y; Runne, H; Murray, H; Kochubey, O; Luthi-Carter, R; Schneggenburger, RJournal Article
Jan-2012Neuroprotective role of Sirt1 in mammalian models of Huntington's disease through activation of multiple Sirt1 targets.Jiang, M; Wang, J; Fu, J; Du, L; Jeong, H; West, T; Xiang, L; Peng, Q; Hou, Z; Cai, H; Seredenina, T; Arbez, N; Zhu, S; Sommers, K; Qian, J; Zhang, J; Mori, S; Yang, XW; Tamashiro, KL; Aja, S; Moran, TH; Luthi-Carter, R; Martin, B; Maudsley, S; Mattson, MP; Cichewicz, RH; Ross, CA; Holtzman, DM; Krainc, D; Duan, WJournal Article
Jan-2009Implication of the JNK pathway in a rat model of Huntington's disease.Perrin, V; Dufour, N; Raoul, C; Hassig, R; Brouillet, E; Aebischer, P; Luthi-Carter, R; Déglon, NJournal Article
Mar-2009Sustained effects of nonallele-specific Huntingtin silencing.Drouet, V; Perrin, V; Hassig, R; Dufour, N; Auregan, G; Alves, S; Bonvento, G; Brouillet, E; Luthi-Carter, R; Hantraye, P; Déglon, NJournal Article
24-Sep-2008Dysregulation of gene expression in primary neuron models of Huntington's disease shows that polyglutamine-related effects on the striatal transcriptome may not be dependent on brain circuitry.Runne, H; Régulier, E; Kuhn, A; Zala, D; Gokce, O; Perrin, V; Sick, B; Aebischer, P; Déglon, N; Luthi-Carter, RJournal Article
Jan-2008Haloperidol protects striatal neurons from dysfunction induced by mutated huntingtin in vivo.Charvin, D; Roze, E; Perrin, V; Deyts, C; Betuing, S; Pagès, C; Régulier, E; Luthi-Carter, R; Brouillet, E; Déglon, N; Caboche, JJournal Article
2-Sep-2011Identification of human P2X1 receptor-interacting proteins reveals a role of the cytoskeleton in receptor regulation.Lalo, U; Roberts, JA; Evans, RJJournal Article
May-2007Neuroprotection by Hsp104 and Hsp27 in lentiviral-based rat models of Huntington's disease.Perrin, V.; Régulier, E.; Abbas-Terki, T.; Hassig, R.; Brouillet, E.; Aebischer, P.; Luthi-Carter, R.; Déglon, N.Journal Article
17-Jan-2013MicroRNA-22 (miR-22) Overexpression Is Neuroprotective via General Anti-Apoptotic Effects and May also Target Specific Huntington’s Disease-Related MechanismsJovicic, A.; Zaldivar Jolissaint, J. F.; Moser, R.; Silva Santos, Mariana de Fatima Silva; Luthi-Carter, RuthJournal Article