Works matching IS 17574676 AND DT 2016 AND VI 8 AND IP 11


Results: 8
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    A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss.

    Published in:
    EMBO Molecular Medicine, 2016, v. 8, n. 11, p. 1289, doi. 10.15252/emmm.201505815
    By:
    • Servián‐Morilla, Emilia;
    • Takeuchi, Hideyuki;
    • Lee, Tom V;
    • Clarimon, Jordi;
    • Mavillard, Fabiola;
    • Area‐Gómez, Estela;
    • Rivas, Eloy;
    • Nieto‐González, Jose L;
    • Rivero, Maria C;
    • Cabrera‐Serrano, Macarena;
    • Gómez‐Sánchez, Leonardo;
    • Martínez‐López, Jose A;
    • Estrada, Beatriz;
    • Márquez, Celedonio;
    • Morgado, Yolanda;
    • Suárez‐Calvet, Xavier;
    • Pita, Guillermo;
    • Bigot, Anne;
    • Gallardo, Eduard;
    • Fernández‐Chacón, Rafael
    Publication type:
    Article
    3

    Targeting key angiogenic pathways with a bispecific Cross MAb optimized for neovascular eye diseases.

    Published in:
    EMBO Molecular Medicine, 2016, v. 8, n. 11, p. 1265, doi. 10.15252/emmm.201505889
    By:
    • Regula, Jörg T;
    • Lundh von Leithner, Peter;
    • Foxton, Richard;
    • Barathi, Veluchamy A;
    • Cheung, Chui Ming Gemmy;
    • Bo Tun, Sai Bo;
    • Wey, Yeo Sia;
    • Iwata, Daiju;
    • Dostalek, Miroslav;
    • Moelleken, Jörg;
    • Stubenrauch, Kay G;
    • Nogoceke, Everson;
    • Widmer, Gabriella;
    • Strassburger, Pamela;
    • Koss, Michael J;
    • Klein, Christian;
    • Shima, David T;
    • Hartmann, Guido
    Publication type:
    Article
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