Neurotoxic Calcium Transfer from Endoplasmic Reticulum to Mitochondria Is Regulated by Cyclin-Dependent Kinase 5-Dependent Phosphorylation of Tau

per Darios, Frédéric, Muriel, Marie-Paule, Khondiker, Myriam Escobar, Brice, Alexis, Ruberg, Merle
Publicat a J Neurosci (2005)

Rescue of Mesencephalic Dopaminergic Neurons in Culture by Low-Level Stimulation of Voltage-Gated Sodium Channels

per Salthun-Lassalle, Bénédicte, Hirsch, Etienne C., Wolfart, Jakob, Ruberg, Merle, Michel, Patrick P.
Publicat a J Neurosci (2004)

Identification of genes involved in ceramide-dependent neuronal apoptosis using cDNA arrays

per Decraene, Charles, Brugg, Bernard, Ruberg, Merle, Eveno, Eric, Matingou, Christiane, Tahi, Fariza, Mariani, Jean, Auffray, Charles, Pietu, Geneviève
Publicat 2002

PML clastosomes prevent nuclear accumulation of mutant ataxin-7 and other polyglutamine proteins

per Janer, Alexandre, Martin, Elodie, Muriel, Marie-Paule, Latouche, Morwena, Fujigasaki, Hiroto, Ruberg, Merle, Brice, Alexis, Trottier, Yvon, Sittler, Annie
Publicat 2006

Consequences of Nigrostriatal Denervation on the Functioning of the Basal Ganglia in Human and Nonhuman Primates: An In Situ Hybridization Study of Cytochrome Oxidase Subunit I mRN...

per Vila, Miquel, Levy, Richard, Herrero, Maria-Trinidad, Ruberg, Merle, Faucheux, Baptiste, Obeso, José A., Agid, Yves, Hirsch, Etienne C.
Publicat a J Neurosci (1997)

Nuclear translocation of NF-κB is increased in dopaminergic neurons of patients with Parkinson disease

per Hunot, Stephane, Brugg, Bernard, Ricard, Damien, Michel, Patrick P., Muriel, Marie-Paule, Ruberg, Merle, Faucheux, Baptiste A., Agid, Yves, Hirsch, Etienne C.
Publicat 1997

REM Sleep Behavior Disorder in Patients With Guadeloupean Parkinsonism, a Tauopathy

per De Cock, Valérie Cochen, Lannuzel, Annie, Verhaeghe, Stéphane, Roze, Emmanuel, Ruberg, Merle, Derenne, Jean Philippe, Willer, Jean Claude, Vidailhet, Marie, Arnulf, Isabelle
Publicat 2007

Caspase-8 Is an Effector in Apoptotic Death of Dopaminergic Neurons in Parkinson's Disease, But Pathway Inhibition Results in Neuronal Necrosis

per Hartmann, Andreas, Troadec, Jean-Denis, Hunot, Stéphane, Kikly, Kristy, Faucheux, Baptiste A., Mouatt-Prigent, Annick, Ruberg, Merle, Agid, Yves, Hirsch, Etienne C.
Publicat a J Neurosci (2001)

Stimulation of subterritories of the subthalamic nucleus reveals its role in the integration of the emotional and motor aspects of behavior

per Mallet, Luc, Schüpbach, Michael, N'Diaye, Karim, Remy, Philippe, Bardinet, Eric, Czernecki, Virginie, Welter, Marie-Laure, Pelissolo, Antoine, Ruberg, Merle, Agid, Yves, Yelnik, Jérôme
Publicat 2007

Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia

per Depienne, Christel, Fedirko, Estelle, Forlani, Sylvie, Cazeneuve, Cécile, Ribaï, Pascale, Feki, Imed, Tallaksen, Chantal, Nguyen, Karine, Stankoff, Bruno, Ruberg, Merle, Stevanin, Giovanni, Durr, Alexandra, Brice, Alexis
Publicat 2007

Lentiviral vector-mediated overexpression of mutant ataxin-7 recapitulates SCA7 pathology and promotes accumulation of the FUS/TLS and MBNL1 RNA-binding proteins

per Alves, Sandro, Marais, Thibaut, Biferi, Maria-Grazia, Furling, Denis, Marinello, Martina, El Hachimi, Khalid, Cartier, Nathalie, Ruberg, Merle, Stevanin, Giovanni, Brice, Alexis, Barkats, Martine, Sittler, Annie
Publicat a Mol Neurodegener (2016)

A Conditional Pan-Neuronal Drosophila Model of Spinocerebellar Ataxia 7 with a Reversible Adult Phenotype Suitable for Identifying Modifier Genes

per Latouche, Morwena, Lasbleiz, Christelle, Martin, Elodie, Monnier, Véronique, Debeir, Thomas, Mouatt-Prigent, Annick, Muriel, Marie-Paule, Morel, Lydie, Ruberg, Merle, Brice, Alexis, Stevanin, Giovanni, Tricoire, Hérvé
Publicat a J Neurosci (2007)

Caspase-3: A vulnerability factor and final effector in apoptotic death of dopaminergic neurons in Parkinson's disease

per Hartmann, Andreas, Hunot, Stéphane, Michel, Patrick P., Muriel, Marie-Paule, Vyas, Sheela, Faucheux, Baptiste A., Mouatt-Prigent, Annick, Turmel, Hélène, Srinivasan, Anu, Ruberg, Merle, Evan, Gerard I., Agid, Yves, Hirsch, Etienne C.
Publicat 2000

A Third Locus for Autosomal Dominant Cerebellar Ataxia Type 1 Maps to Chromosome 14q24.3-qter: Evidence for the Existence of a Fourth Locus

per Stevanin, Giovanni, Le Guern, Eric, Ravisé, Nicole, Chneiweiss, Hervé, Dürr, Alexandra, Cancel, Géraldine, Vignal, Alain, Boch, Anne-Laure, Ruberg, Merle, Penet, Christiane, Pothin, Yolaine, Lagroua, Isabelle, Haguenau, Michel, Rancurel, Gérald, Weissenbach, Jean, Agid, Yves, Brice, Alexis
Publicat 1994

Annonacin, a Natural Mitochondrial Complex I Inhibitor, Causes Tau Pathology in Cultured Neurons

per Escobar-Khondiker, Myriam, Höllerhage, Matthias, Muriel, Marie-Paule, Champy, Pierre, Bach, Antoine, Depienne, Christel, Respondek, Gesine, Yamada, Elizabeth S., Lannuzel, Annie, Yagi, Takao, Hirsch, Etienne C., Oertel, Wolfgang H., Jacob, Ralf, Michel, Patrick P., Ruberg, Merle, Höglinger, Günter U.
Publicat a J Neurosci (2007)

Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders

per Nava, Caroline, Rupp, Johanna, Boissel, Jean-Paul, Mignot, Cyril, Rastetter, Agnès, Amiet, Claire, Jacquette, Aurélia, Dupuits, Céline, Bouteiller, Delphine, Keren, Boris, Ruberg, Merle, Faudet, Anne, Doummar, Diane, Philippe, Anne, Périsse, Didier, Laurent, Claudine, Lebrun, Nicolas, Guillemot, Vincent, Chelly, Jamel, Cohen, David, Héron, Delphine, Brice, Alexis, Closs, Ellen I., Depienne, Christel
Publicat a Amino Acids (2015)

Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

per Depienne, Christel, Bouteiller, Delphine, Keren, Boris, Cheuret, Emmanuel, Poirier, Karine, Trouillard, Oriane, Benyahia, Baya, Quelin, Chloé, Carpentier, Wassila, Julia, Sophie, Afenjar, Alexandra, Gautier, Agnès, Rivier, François, Meyer, Sophie, Berquin, Patrick, Hélias, Marie, Py, Isabelle, Rivera, Serge, Bahi-Buisson, Nadia, Gourfinkel-An, Isabelle, Cazeneuve, Cécile, Ruberg, Merle, Brice, Alexis, Nabbout, Rima, LeGuern, Eric
Publicat 2009

Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

per Depienne, Christel, Bouteiller, Delphine, Keren, Boris, Cheuret, Emmanuel, Poirier, Karine, Trouillard, Oriane, Benyahia, Baya, Quelin, Chloé, Carpentier, Wassila, Julia, Sophie, Afenjar, Alexandra, Gautier, Agnès, Rivier, François, Meyer, Sophie, Berquin, Patrick, Hélias, Marie, Py, Isabelle, Rivera, Serge, Bahi-Buisson, Nadia, Gourfinkel-An, Isabelle, Cazeneuve, Cécile, Ruberg, Merle, Brice, Alexis, Nabbout, Rima, LeGuern, Eric
Publicat 2009