Works matching DE "NONSENSE suppression (Genetics)"


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    Key clinical features to identify girls with CDKL5 mutations.

    Published in:
    Brain: A Journal of Neurology, 2008, v. 131, n. 10, p. 2647, doi. 10.1093/brain/awn197
    By:
    • Nadia Bahi-Buisson;
    • Juliette Nectoux;
    • Haydeé Rosas-Vargas;
    • Mathieu Milh;
    • Nathalie Boddaert;
    • Benoit Girard;
    • Claude Cances;
    • Dorothée Ville;
    • Alexandra Afenjar;
    • Marlène Rio;
    • Delphine Héron;
    • Marie Ange NGuyen Morel;
    • Alexis Arzimanoglou;
    • Christophe Philippe;
    • Philippe Jonveaux;
    • Jamel Chelly;
    • Thierry Bienvenu
    Publication type:
    Article
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    PTC124 targets genetic disorders caused by nonsense mutations.

    Published in:
    Nature, 2007, v. 447, n. 7140, p. 87, doi. 10.1038/nature05756
    By:
    • Welch, Ellen M.;
    • Barton, Elisabeth R.;
    • Jin Zhuo;
    • Tomizawa, Yuki;
    • Friesen, Westley J.;
    • Trifillis, Panayiota;
    • Paushkinv, Sergey;
    • Patel, Meenal;
    • Trotta, Christopher R.;
    • Seongwoo Hwang;
    • Wilde, Richard G.;
    • Karp, Gary;
    • Takasugi, James;
    • Guangming Chen;
    • Jones, Stephen;
    • Ren, Hongyu;
    • Young-Choon Moon;
    • Corsonv, Donald;
    • Turpoff, Anthony A.;
    • Campbell, Jeffrey A.
    Publication type:
    Article
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