खोज परिणाम - Ruberg, Merle

  • प्रदर्शित 1 - 17 परिणाम 17
परिणाम को परिष्कृत करें
  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 द्वारा Darios, Frédéric, Muriel, Marie-Paule, Khondiker, Myriam Escobar, Brice, Alexis, Ruberg, Merle

    प्रकाशित 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 द्वारा Salthun-Lassalle, Bénédicte, Hirsch, Etienne C., Wolfart, Jakob, Ruberg, Merle, Michel, Patrick P.

    प्रकाशित 2004
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा Decraene, Charles, Brugg, Bernard, Ruberg, Merle, Eveno, Eric, Matingou, Christiane, Tahi, Fariza, Mariani, Jean, Auffray, Charles, Pietu, Geneviève

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

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

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

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

    प्रकाशित 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 द्वारा Hartmann, Andreas, Troadec, Jean-Denis, Hunot, Stéphane, Kikly, Kristy, Faucheux, Baptiste A., Mouatt-Prigent, Annick, Ruberg, Merle, Agid, Yves, Hirsch, Etienne C.

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

    प्रकाशित 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 द्वारा 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

    प्रकाशित 2007
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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

    प्रकाशित 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 द्वारा 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

    प्रकाशित 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 द्वारा 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.

    प्रकाशित 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 द्वारा 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

    प्रकाशित 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 द्वारा 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.

    प्रकाशित 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 द्वारा 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

    प्रकाशित 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 द्वारा 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

    प्रकाशित 2009
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