Works by Pichon, Jacques


Results: 17
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    Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by a BKCa channel opener molecule.

    Published in:
    Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/s13023-014-0124-6
    By:
    • Hebert, Betty;
    • Pietropaolo, Susanna;
    • Même, Sandra;
    • Laudier, Béatrice;
    • Laugeray, Anthony;
    • Doisne, Nicolas;
    • Quartier, Angélique;
    • Lefeuvre, Sandrine;
    • Got, Laurence;
    • Cahard, Dominique;
    • Laumonnier, Frédéric;
    • Crusio, Wim;
    • Pichon, Jacques;
    • Menuet, Arnaud;
    • Perche, Olivier;
    • Briault, Sylvain
    Publication type:
    Article
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    Early Retinal Defects in Fmr1<sup>-ly </sup>Mice: Toward a Critical Role of Visual Dys-Sensitivity in the Fragile X Syndrome Phenotype?

    Published in:
    Frontiers in Cellular Neuroscience, 2018, p. 1, doi. 10.3389/fncel.2018.00096
    By:
    • Perche, Olivier;
    • Felgerolle, Chloé;
    • Ardourel, Maryvonne;
    • Bazinet, Audrey;
    • Pâris, Arnaud;
    • Rossignol, Rafaëlle;
    • Meyer-Dilhet, Géraldine;
    • Mausset-Bonnefont, Anne-Laure;
    • Hébert, Betty;
    • Laurenceau, David;
    • Montécot-Dubourg, Céline;
    • Menuet, Arnaud;
    • Bizot, Jean-Charles;
    • Pichon, Jacques;
    • Ranchon-Cole, Isabelle;
    • Briault, Sylvain
    Publication type:
    Article
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