Found: 5

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  • Mice Lacking Gpr179 with Complete Congenital Stationary Night Blindness Are a Good Model for Myopia.

    Published in:
    International Journal of Molecular Sciences, 2023, v. 24, n. 1, p. 219, doi. 10.3390/ijms24010219
    By:
    • Wilmet, Baptiste;
    • Callebert, Jacques;
    • Duvoisin, Robert;
    • Goulet, Ruben;
    • Tourain, Christophe;
    • Michiels, Christelle;
    • Frederiksen, Helen;
    • Schaeffel, Frank;
    • Marre, Olivier;
    • Sahel, José Alain;
    • Audo, Isabelle;
    • Picaud, Serge;
    • Zeitz, Christina
    Publication type:
    Article

  • Do differentially expressed genes explain high myopia in congenital stationary night blindness?

    Published in:
    Acta Ophthalmologica (1755375X), 2024, v. 102, p. N.PAG, doi. 10.1111/aos.16374
    By:
    • Zeitz, Christina;
    • Roger, Jerome E.;
    • Michiels, Christelle;
    • Sánchez‐Farías, Nuria;
    • Varin, Juliette;
    • Frederiksen, Helen;
    • Wilmet, Baptiste;
    • Gimenez, Marie‐Laure;
    • Bouzidi, Nassima;
    • Blond, Frederic;
    • Guilllonneau, Xavier;
    • Léveillard, Thierry;
    • Sahel, José‐Alain;
    • Picaud, Serge;
    • Audo, Isabelle
    Publication type:
    Article

  • Shedding light on myopia by studying complete congenital stationary night blindness.

    Published in:
    Acta Ophthalmologica (1755375X), 2022, v. 100, p. N.PAG, doi. 10.1111/j.1755-3768.2022.15380
    By:
    • Zeitz, Christina;
    • Roger, Jerome E.;
    • Michiels, Christelle;
    • Sánchez‐Farías, Nuria;
    • Varin, Juliette;
    • Frederiksen, Helen;
    • Wilmet, Baptiste;
    • Gimenez, Marie‐Laure;
    • Bouzidi, Nassima;
    • Blond, Frederic;
    • Guilllonneau, Xavier;
    • Léveillard, Thierry;
    • Sahel, José‐Alain;
    • Picaud, Serge;
    • Audo, Isabelle
    Publication type:
    Article

  • Establishment and measurement of myopia in mice with ON‐bipolar cell defects.

    Published in:
    Acta Ophthalmologica (1755375X), 2022, v. 100, p. N.PAG, doi. 10.1111/j.1755-3768.2022.0624
    By:
    • Baptiste, Wilmet;
    • Robert, Duvoisin;
    • Jacques, Callebert;
    • Ruben, Goulet;
    • Christophe, Tourain;
    • Christelle, Michiels;
    • Julie, Degardin;
    • Helen, Frederiksen;
    • Quenol, Cesar;
    • Manuel, Simonutti;
    • Olivier, Marre;
    • José‐Alain, Sahel;
    • Audo, Isabelle;
    • Serge, Picaud;
    • Zeitz, Christina
    Publication type:
    Article

  • CHM mutation spectrum and disease: An update at the time of human therapeutic trials.

    Published in:
    Human Mutation, 2021, v. 42, n. 4, p. 323, doi. 10.1002/humu.24174
    By:
    • Zeitz, Christina;
    • Nassisi, Marco;
    • Laurent‐Coriat, Caroline;
    • Andrieu, Camille;
    • Boyard, Fiona;
    • Condroyer, Christel;
    • Démontant, Vanessa;
    • Antonio, Aline;
    • Lancelot, Marie‐Elise;
    • Frederiksen, Helen;
    • Kloeckener‐Gruissem, Barbara;
    • El‐Shamieh, Said;
    • Zanlonghi, Xavier;
    • Meunier, Isabelle;
    • Roux, Anne‐Françoise;
    • Mohand‐Saïd, Saddek;
    • Sahel, José‐Alain;
    • Audo, Isabelle
    Publication type:
    Article