Works by Girard, Emmanuelle


Results: 21
    1
    2
    3

    Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.

    Published in:
    Acta Neuropathologica, 2022, v. 144, n. 4, p. 707, doi. 10.1007/s00401-022-02475-8
    By:
    • Jacquier, Arnaud;
    • Risson, Valérie;
    • Simonet, Thomas;
    • Roussange, Florine;
    • Lacoste, Nicolas;
    • Ribault, Shams;
    • Carras, Julien;
    • Theuriet, Julian;
    • Girard, Emmanuelle;
    • Grosjean, Isabelle;
    • Le Goff, Laure;
    • Kröger, Stephan;
    • Meltoranta, Julia;
    • Bauché, Stéphanie;
    • Sternberg, Damien;
    • Fournier, Emmanuel;
    • Kostera-Pruszczyk, Anna;
    • O'Connor, Emily;
    • Eymard, Bruno;
    • Lochmüller, Hanns
    Publication type:
    Article
    4

    MACF1 controls skeletal muscle function through the microtubule-dependent localization of extra-synaptic myonuclei and mitochondria biogenesis.

    Published in:
    eLife, 2021, p. 1, doi. 10.7554/eLife.70490
    By:
    • Ghasemizadeh, Alireza;
    • Christin, Emilie;
    • Guiraud, Alexandre;
    • Couturier, Nathalie;
    • Abitbol, Marie;
    • Risson, Valerie;
    • Girard, Emmanuelle;
    • Jagla, Christophe;
    • Soler, Cedric;
    • Laddada, Lilia;
    • Sanchez, Colline;
    • Jaque-Fernandez, Francisco-Ignacio;
    • Jacquemond, Vincent;
    • Thomas, Jean-Luc;
    • Lanfranchi, Marine;
    • Courchet, Julien;
    • Gondin, Julien;
    • Schaeffer, Laurent;
    • Gache, Vincent
    Publication type:
    Article
    5
    6
    7
    8
    9
    10
    11
    12
    13

    Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progression.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 8, p. 2359, doi. 10.1093/brain/awt164
    By:
    • Bruneteau, Gaëlle;
    • Simonet, Thomas;
    • Bauché, Stéphanie;
    • Mandjee, Nathalie;
    • Malfatti, Edoardo;
    • Girard, Emmanuelle;
    • Tanguy, Marie-Laure;
    • Behin, Anthony;
    • Khiami, Frédéric;
    • Sariali, Elhadi;
    • Hell-Remy, Caroline;
    • Salachas, François;
    • Pradat, Pierre-François;
    • Fournier, Emmanuel;
    • Lacomblez, Lucette;
    • Koenig, Jeanine;
    • Romero, Norma Beatriz;
    • Fontaine, Bertrand;
    • Meininger, Vincent;
    • Schaeffer, Laurent
    Publication type:
    Article
    14
    15
    16

    Evidence of a dosage effect and a physiological endplate acetylcholinesterase deficiency in the first mouse models mimicking Schwartz–Jampel syndrome neuromyotonia.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 20, p. 3166, doi. 10.1093/hmg/ddn213
    By:
    • Stum, Morgane;
    • Girard, Emmanuelle;
    • Bangratz, Marie;
    • Bernard, Véronique;
    • Herbin, Marc;
    • Vignaud, Alban;
    • Ferry, Arnaud;
    • Davoine, Claire-Sophie;
    • Echaniz-Laguna, Andoni;
    • René, Frédérique;
    • Marcel, Christophe;
    • Molgó, Jordi;
    • Fontaine, Bertrand;
    • Krejci, Eric;
    • Nicole, Sophie
    Publication type:
    Article
    17
    18
    19

    H2A.Z is involved in premature aging and DSB repair initiation in muscle fibers.

    Published in:
    Nucleic Acids Research, 2024, v. 52, n. 6, p. 3031, doi. 10.1093/nar/gkae020
    By:
    • Belotti, Edwige;
    • Lacoste, Nicolas;
    • Iftikhar, Arslan;
    • Simonet, Thomas;
    • Papin, Christophe;
    • Osseni, Alexis;
    • Streichenberger, Nathalie;
    • Mari, Pierre-Olivier;
    • Girard, Emmanuelle;
    • Graies, Mohamed;
    • Giglia-Mari, Giuseppina;
    • Dimitrov, Stefan;
    • Hamiche, Ali;
    • Schaeffer, Laurent
    Publication type:
    Article
    20
    21