Suchergebnisse - Karine Mérienne

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  1. 1
    Transcriptional Activation of REST by Sp1 in Huntington's Disease Models

    Transcriptional Activation of REST by Sp1 in Huntington's Disease Models von Myriam Ravache, C. R. Weber, Karine Mérienne, Yvon Trottier

    Veröffentlicht 2010
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  2. 2
    A phosphoserine-regulated docking site in the protein kinase RSK2 that recruits and activates PDK1

    A phosphoserine-regulated docking site in the protein kinase RSK2 that recruits and activates PDK1 von Morten Frödin, Claus J. Jensen, Karine Mérienne, Steen Gammeltoft

    Veröffentlicht 2000
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  3. 3
    Mitogen-Regulated RSK2-CBP Interaction Controls Their Kinase and Acetylase Activities

    Mitogen-Regulated RSK2-CBP Interaction Controls Their Kinase and Acetylase Activities von Karine Mérienne, Solange Pannetier, Annick Harel‐Bellan, Paolo Sassone–Corsi

    Veröffentlicht 2001
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  4. 4
    Contribution of Neuroepigenetics to Huntington’s Disease

    Contribution of Neuroepigenetics to Huntington’s Disease von Laetitia Francelle, Caroline Lotz, Tiago F. Outeiro, Emmanuel Brouillet, Karine Mérienne

    Veröffentlicht 2017
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  5. 5
    Transcription Elongation and Tissue-Specific Somatic CAG Instability

    Transcription Elongation and Tissue-Specific Somatic CAG Instability von Agathi-Vasiliki Goula, Agnieszka Styś, Jackson Ping Kei Chan, Yvon Trottier, Richard Festenstein, Karine Mérienne

    Veröffentlicht 2012
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  6. 6
    Stoichiometry of Base Excision Repair Proteins Correlates with Increased Somatic CAG Instability in Striatum over Cerebellum in Huntington's Disease Transgenic Mice

    Stoichiometry of Base Excision Repair Proteins Correlates with Increased Somatic CAG Instability in Striatum over Cerebellum in Huntington's Disease Transgenic Mice von Agathi-Vassiliki Goula, Brian R. Berquist, David M. Wilson, Vanessa C. Wheeler, Yvon Trottier, Karine Mérienne

    Veröffentlicht 2009
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  7. 7
    Mutation Analysis of the RSK2 Gene in Coffin-Lowry Patients: Extensive Allelic Heterogeneity and a High Rate of De Novo Mutations

    Mutation Analysis of the RSK2 Gene in Coffin-Lowry Patients: Extensive Allelic Heterogeneity and a High Rate of De Novo Mutations von Sylvie Jacquot, Karine Mérienne, Dario De Cesare, Solange Pannetier, Jean‐Louis Mandel, Paolo Sassone–Corsi, André Hanauer

    Veröffentlicht 1998
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  8. 8
    Neuronal identity genes regulated by super-enhancers are preferentially down-regulated in the striatum of Huntington's disease mice

    Neuronal identity genes regulated by super-enhancers are preferentially down-regulated in the striatum of Huntington's disease mice von M. Achour, Stéphanie Le Gras, Céline Keime, Frédéric Parmentier, François Lejeune, Anne‐Laurence Boutillier, Christian Néri, Irwin Davidson, Karine Mérienne

    Veröffentlicht 2015
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  9. 9
    Mutations in the X-linked RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome

    Mutations in the X-linked RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome von Jean‐Pierre Delaunoy, Fatima Abidi, Maria Zeniou, Sylvie Jacquot, Karine Mérienne, Solange Pannetier, Mich�le Schmitt, Charles E. Schwartz, Andr� Hanauer

    Veröffentlicht 2001
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  10. 10
    Altered enhancer transcription underlies Huntington’s disease striatal transcriptional signature

    Altered enhancer transcription underlies Huntington’s disease striatal transcriptional signature von Stéphanie Le Gras, Céline Keime, Anne Anthony, Caroline Lotz, Lucie de Longprez, Emmanuel Brouillet, Jean‐Christophe Cassel, Anne‐Laurence Boutillier, Karine Mérienne

    Veröffentlicht 2017
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  11. 11
    Polyglutamine expansion causes neurodegeneration by altering the neuronal differentiation program

    Polyglutamine expansion causes neurodegeneration by altering the neuronal differentiation program von Gretta Abou‐Sleymane, Frédéric Chalmel, Dominique Helmlinger, Aurélie Lardenois, Christelle Thibault-Carpentier, C. R. Weber, Karine Mérienne, Jean‐Louis Mandel, Olivier Poch, Didier Devys, Yvon Trottier

    Veröffentlicht 2006
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  12. 12
    Accelerated epigenetic aging in Huntington’s disease involves polycomb repressive complex 1

    Accelerated epigenetic aging in Huntington’s disease involves polycomb repressive complex 1 von Baptiste Brulé, Rafael Alcalá‐Vida, Noémie Penaud, Jil Scuto, Coline Mounier, Jonathan Séguin, Sina Vincent Khodaverdian, Brigitte Cosquer, Étienne Birmelé, Stéphanie Le Gras, Charles Decraene, Anne‐Laurence Boutillier, Karine Mérienne

    Veröffentlicht 2025
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  13. 13
    Cell-Type-Specific Gene Expression Profiling in Adult Mouse Brain Reveals Normal and Disease-State Signatures

    Cell-Type-Specific Gene Expression Profiling in Adult Mouse Brain Reveals Normal and Disease-State Signatures von Nicolas Mérienne, Cécile Meunier, Anne T. Schneider, Jonathan Séguin, Satish S. Nair, Anne B. Rocher, Stéphanie Le Gras, Céline Keime, Richard L. M. Faull, Luc Pellerin, Jean‐Yves Chatton, Christian Néri, Karine Mérienne, Nicole Déglon

    Veröffentlicht 2019
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  14. 14
    Reinstating plasticity and memory in a tauopathy mouse model with an acetyltransferase activator

    Reinstating plasticity and memory in a tauopathy mouse model with an acetyltransferase activator von Snehajyoti Chatterjee, Raphaelle Cassel, Anne Schneider‐Anthony, Karine Mérienne, Brigitte Cosquer, Laura Tzeplaeff, Sarmistha Halder Sinha, Manoj Kumar, Piyush Chaturbedy, Muthusamy Eswaramoorthy, Stéphanie Le Gras, Céline Keime, Olivier Bousiges, P. Dutar, Petnoï Petsophonsakul, Claire Rampon, Jean‐Christophe Cassel, Luc Buée, David Blum, Tapas K. Kundu, Anne‐Laurence Boutillier

    Veröffentlicht 2018
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