Works by Menuet, Arnaud


Results: 28
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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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    Detection of Chromosomal Breakpoints in Patients with Developmental Delay and Speech Disorders.

    Published in:
    PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0090852
    By:
    • Utami, Kagistia H.;
    • Hillmer, Axel M.;
    • Aksoy, Irene;
    • Chew, Elaine G. Y.;
    • Teo, Audrey S. M.;
    • Zhang, Zhenshui;
    • Lee, Charlie W. H.;
    • Chen, Pauline J.;
    • Seng, Chan Chee;
    • Ariyaratne, Pramila N.;
    • Rouam, Sigrid L.;
    • Soo, Lim Seong;
    • Yousoof, Saira;
    • Prokudin, Ivan;
    • Peters, Gregory;
    • Collins, Felicity;
    • Wilson, Meredith;
    • Kakakios, Alyson;
    • Haddad, Georges;
    • Menuet, Arnaud
    Publication type:
    Article
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    Dysregulation of FOXG1 pathway in a 14q12 microdeletion case.

    Published in:
    American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 12, p. 3072, doi. 10.1002/ajmg.a.36170
    By:
    • Perche, Olivier;
    • Haddad, Georges;
    • Menuet, Arnaud;
    • Callier, Patrick;
    • Marcos, Mélanie;
    • Briault, Sylvain;
    • Laudier, Béatrice
    Publication type:
    Article
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    FG syndrome: The FGS2 locus revisited.

    Published in:
    American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 6, p. 1489, doi. 10.1002/ajmg.a.35322
    By:
    • Perche, Olivier;
    • Laudier, Béatrice;
    • Menuet, Arnaud;
    • Odent, Sylvie;
    • Laumonnier, Frederic;
    • Briault, Sylvain
    Publication type:
    Article
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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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    Spinal cord oligodendrocyte-derived alarmin IL-33 mediates neuropathic pain.

    Published in:
    FASEB Journal, 2016, v. 30, n. 1, p. 54, doi. 10.1096/fj.14-267146
    By:
    • Zarpelon, Ana C.;
    • Rodrigues, Francielle C.;
    • Lopes, Alexandre H.;
    • Souza, Guilherme R.;
    • Carvalho, Thacyana T.;
    • Pinto, Larissa G.;
    • Damo Xu;
    • Ferreira, Sergio H.;
    • Alves-Filho, Jose C.;
    • McInnes, Iain B.;
    • Ryffel, Bernhard;
    • Quesniaux, Valérie F. J.;
    • Reverchon, Flora;
    • Mortaud, Stéphane;
    • Menuet, Arnaud;
    • Liew, Foo Y.;
    • Cunha, Fernando Q.;
    • Cunha, Thiago M.;
    • Verri Jr., Waldiceu A.
    Publication type:
    Article