Ngā hua rapu - Ruberg, Merle

  • E whakaatu ana i te 1 - 17 hua o te 17
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  1. 1
    Neurotoxic Calcium Transfer from Endoplasmic Reticulum to Mitochondria Is Regulated by Cyclin-Dependent Kinase 5-Dependent Phosphorylation of Tau

    Neurotoxic Calcium Transfer from Endoplasmic Reticulum to Mitochondria Is Regulated by Cyclin-Dependent Kinase 5-Dependent Phosphorylation of Tau mā Darios, Frédéric, Muriel, Marie-Paule, Khondiker, Myriam Escobar, Brice, Alexis, Ruberg, Merle

    I whakaputaina 2005
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  2. 2
    Rescue of Mesencephalic Dopaminergic Neurons in Culture by Low-Level Stimulation of Voltage-Gated Sodium Channels

    Rescue of Mesencephalic Dopaminergic Neurons in Culture by Low-Level Stimulation of Voltage-Gated Sodium Channels mā Salthun-Lassalle, Bénédicte, Hirsch, Etienne C., Wolfart, Jakob, Ruberg, Merle, Michel, Patrick P.

    I whakaputaina 2004
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  3. 3
    Identification of genes involved in ceramide-dependent neuronal apoptosis using cDNA arrays

    Identification of genes involved in ceramide-dependent neuronal apoptosis using cDNA arrays mā Decraene, Charles, Brugg, Bernard, Ruberg, Merle, Eveno, Eric, Matingou, Christiane, Tahi, Fariza, Mariani, Jean, Auffray, Charles, Pietu, Geneviève

    I whakaputaina 2002
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  4. 4
    PML clastosomes prevent nuclear accumulation of mutant ataxin-7 and other polyglutamine proteins

    PML clastosomes prevent nuclear accumulation of mutant ataxin-7 and other polyglutamine proteins mā Janer, Alexandre, Martin, Elodie, Muriel, Marie-Paule, Latouche, Morwena, Fujigasaki, Hiroto, Ruberg, Merle, Brice, Alexis, Trottier, Yvon, Sittler, Annie

    I whakaputaina 2006
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  5. 5
    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 mRNA

    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... mā Vila, Miquel, Levy, Richard, Herrero, Maria-Trinidad, Ruberg, Merle, Faucheux, Baptiste, Obeso, José A., Agid, Yves, Hirsch, Etienne C.

    I whakaputaina 1997
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  6. 6
    REM Sleep Behavior Disorder in Patients With Guadeloupean Parkinsonism, a Tauopathy

    REM Sleep Behavior Disorder in Patients With Guadeloupean Parkinsonism, a Tauopathy mā De Cock, Valérie Cochen, Lannuzel, Annie, Verhaeghe, Stéphane, Roze, Emmanuel, Ruberg, Merle, Derenne, Jean Philippe, Willer, Jean Claude, Vidailhet, Marie, Arnulf, Isabelle

    I whakaputaina 2007
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  7. 7
    Nuclear translocation of NF-κB is increased in dopaminergic neurons of patients with Parkinson disease

    Nuclear translocation of NF-κB is increased in dopaminergic neurons of patients with Parkinson disease mā Hunot, Stephane, Brugg, Bernard, Ricard, Damien, Michel, Patrick P., Muriel, Marie-Paule, Ruberg, Merle, Faucheux, Baptiste A., Agid, Yves, Hirsch, Etienne C.

    I whakaputaina 1997
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  8. 8
    Caspase-8 Is an Effector in Apoptotic Death of Dopaminergic Neurons in Parkinson's Disease, But Pathway Inhibition Results in Neuronal Necrosis

    Caspase-8 Is an Effector in Apoptotic Death of Dopaminergic Neurons in Parkinson's Disease, But Pathway Inhibition Results in Neuronal Necrosis mā Hartmann, Andreas, Troadec, Jean-Denis, Hunot, Stéphane, Kikly, Kristy, Faucheux, Baptiste A., Mouatt-Prigent, Annick, Ruberg, Merle, Agid, Yves, Hirsch, Etienne C.

    I whakaputaina 2001
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  9. 9
    Stimulation of subterritories of the subthalamic nucleus reveals its role in the integration of the emotional and motor aspects of behavior

    Stimulation of subterritories of the subthalamic nucleus reveals its role in the integration of the emotional and motor aspects of behavior mā Mallet, Luc, Schüpbach, Michael, N'Diaye, Karim, Remy, Philippe, Bardinet, Eric, Czernecki, Virginie, Welter, Marie-Laure, Pelissolo, Antoine, Ruberg, Merle, Agid, Yves, Yelnik, Jérôme

    I whakaputaina 2007
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  10. 10
    Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia

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

    I whakaputaina 2007
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  11. 11
    Lentiviral vector-mediated overexpression of mutant ataxin-7 recapitulates SCA7 pathology and promotes accumulation of the FUS/TLS and MBNL1 RNA-binding proteins

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

    I whakaputaina 2016
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  12. 12
    A Conditional Pan-Neuronal Drosophila Model of Spinocerebellar Ataxia 7 with a Reversible Adult Phenotype Suitable for Identifying Modifier Genes

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

    I whakaputaina 2007
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  13. 13
    Caspase-3: A vulnerability factor and final effector in apoptotic death of dopaminergic neurons in Parkinson's disease

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

    I whakaputaina 2000
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  14. 14
    A Third Locus for Autosomal Dominant Cerebellar Ataxia Type 1 Maps to Chromosome 14q24.3-qter: Evidence for the Existence of a Fourth Locus

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

    I whakaputaina 1994
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  15. 15
    Annonacin, a Natural Mitochondrial Complex I Inhibitor, Causes Tau Pathology in Cultured Neurons

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

    I whakaputaina 2007
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  16. 16
    Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

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

    I whakaputaina 2009
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  17. 17
    Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

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

    I whakaputaina 2009
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