Hasil Pencarian - Evelyne Goillot

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  1. 1
    Wnt4 participates in the formation of vertebrate neuromuscular junction.

    Wnt4 participates in the formation of vertebrate neuromuscular junction. oleh Laure Strochlic, Julien Falk, Evelyne Goillot, Séverine Sigoillot, Francine Bourgeois, Perrine Delers, Jérôme Rouvière, Amanda Swain, Valérie Castellani, Laurent Schaeffer, Claire Legay

    Diterbitkan 2012-01-01
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  2. 2
    Lack of muscle mTOR kinase activity causes early onset myopathy and compromises whole‐body homeostasis

    Lack of muscle mTOR kinase activity causes early onset myopathy and compromises whole‐body homeostasis oleh Qing Zhang, Agnès Duplany, Vincent Moncollin, Sandrine Mouradian, Evelyne Goillot, Laetitia Mazelin, Karine Gauthier, Nathalie Streichenberger, Céline Angleraux, Jie Chen, Shuzhe Ding, Laurent Schaeffer, Yann‐Gaël Gangloff

    Diterbitkan 2019-02-01
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  3. 3
    LSD1 Controls Timely MyoD Expression via MyoD Core Enhancer Transcription

    LSD1 Controls Timely MyoD Expression via MyoD Core Enhancer Transcription oleh Isabella Scionti, Shinichiro Hayashi, Sandrine Mouradian, Emmanuelle Girard, Joana Esteves de Lima, Véronique Morel, Thomas Simonet, Maud Wurmser, Pascal Maire, Katia Ancelin, Eric Metzger, Roland Schüle, Evelyne Goillot, Frederic Relaix, Laurent Schaeffer

    Diterbitkan 2017-02-01
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  4. 4
    The AMPK-related kinase NUAK1 controls cortical axons branching by locally modulating mitochondrial metabolic functions

    The AMPK-related kinase NUAK1 controls cortical axons branching by locally modulating mitochondrial metabolic functions oleh Marine Lanfranchi, Sozerko Yandiev, Géraldine Meyer-Dilhet, Salma Ellouze, Martijn Kerkhofs, Raphael Dos Reis, Audrey Garcia, Camille Blondet, Alizée Amar, Anita Kneppers, Hélène Polvèche, Damien Plassard, Marc Foretz, Benoit Viollet, Kei Sakamoto, Rémi Mounier, Cyril F. Bourgeois, Olivier Raineteau, Evelyne Goillot, Julien Courchet

    Diterbitkan 2024-03-01
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  5. 5
    A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia.

    A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia. oleh Asma Ben Ammar, Payam Soltanzadeh, Stéphanie Bauché, Pascale Richard, Evelyne Goillot, Ruth Herbst, Karen Gaudon, Caroline Huzé, Laurent Schaeffer, Yuji Yamanashi, Osamu Higuchi, Antoine Taly, Jeanine Koenig, Jean-Paul Leroy, Fayçal Hentati, Hossein Najmabadi, Kimia Kahrizi, Manouchehr Ilkhani, Michel Fardeau, Bruno Eymard, Daniel Hantaï

    Diterbitkan 2013-01-01
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  6. 6
    Correction: A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia.

    Correction: A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia. oleh Asma Ben Ammar, Payam Soltanzadeh, Stéphanie Bauché, Pascale Richard, Evelyne Goillot, Ruth Herbst, Karen Gaudon, Caroline Huzé, Laurent Schaeffer, Yuji Yamanashi, Osamu Higuchi, Antoine Taly, Jeanine Koenig, Jean-Paul Leroy, Fayçal Hentati, Hossein Najmabadi, Kimia Kahrizi, Manouchehr Ilkhani, Michel Fardeau, Bruno Eymard, Daniel Hantaï

    Diterbitkan 2013-01-01
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  7. 7
    Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairment

    Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairment oleh Pascal Laforêt, Michio Inoue, Evelyne Goillot, Claire Lefeuvre, Umut Cagin, Nathalie Streichenberger, Sarah Leonard-Louis, Guy Brochier, Angeline Madelaine, Clemence Labasse, Carola Hedberg-Oldfors, Thomas Krag, Louisa Jauze, Julien Fabregue, Philippe Labrune, Jose Milisenda, Aleksandra Nadaj-Pakleza, Sabrina Sacconi, Federico Mingozzi, Giuseppe Ronzitti, François Petit, Benedikt Schoser, Anders Oldfors, John Vissing, Norma B. Romero, Ichizo Nishino, Edoardo Malfatti

    Diterbitkan 2019-10-01
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