Found: 6

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  • iPSCs derived from infertile men carrying complex genetic abnormalities can generate primordial germ-like cells.

    Published in:
    Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-17337-2
    By:
    • Mouka, Aurélie;
    • Arkoun, Brahim;
    • Moison, Pauline;
    • Drévillon, Loïc;
    • Jarray, Rafika;
    • Brisset, Sophie;
    • Mayeur, Anne;
    • Bouligand, Jérôme;
    • Boland-Auge, Anne;
    • Deleuze, Jean-François;
    • Yates, Frank;
    • Lemonnier, Thomas;
    • Callier, Patrick;
    • Duffourd, Yannis;
    • Nitschke, Patrick;
    • Ollivier, Emmanuelle;
    • Bourdin, Arnaud;
    • De Vos, John;
    • Livera, Gabriel;
    • Tachdjian, Gérard
    Publication type:
    Article

  • Codon usage as a tool to predict the cellular location of eukaryotic ribosomal proteins and aminoacyl-tRNA synthetases.

    Published in:
    Nucleic Acids Research, 1999, v. 27, n. 14, p. 2848, doi. 10.1093/nar/27.14.2848
    By:
    • Chiapello, Hélène;
    • Ollivier, Emmanuelle;
    • Landès-Devauchelle, Claudine;
    • Nitschké, Patrick;
    • Risler, Jean-Loup;
    • Sharp, P.M.;
    • Gouy, M.;
    • Nakamura, Y.;
    • Stenico, M.;
    • Ikemura, T.;
    • Medigue, C.;
    • Hénaut, A.;
    • McInerney, J.O.;
    • Kerr, A.R.;
    • Chiapello, H.;
    • Bulmer, M.;
    • Eyre-Walker, A.;
    • Pan, A.;
    • Diaz-Lazcoz, Y.;
    • Grantham, R.
    Publication type:
    Article

  • NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal–Hreidarsson syndrome.

    Published in:
    Human Molecular Genetics, 2020, v. 29, n. 6, p. 907, doi. 10.1093/hmg/ddaa011
    By:
    • Benyelles, Maname;
    • O'Donohue, Marie-Françoise;
    • Kermasson, Laëtitia;
    • Lainey, Elodie;
    • Borie, Raphael;
    • Lagresle-Peyrou, Chantal;
    • Nunes, Hilario;
    • Cazelles, Clarisse;
    • Fourrage, Cécile;
    • Ollivier, Emmanuelle;
    • Marcais, Ambroise;
    • Gamez, Anne-Sophie;
    • Morice-Picard, Fanny;
    • Caillaud, Denis;
    • Pottier, Nicolas;
    • Ménard, Christelle;
    • Ba, Ibrahima;
    • Fernandes, Alicia;
    • Crestani, Bruno;
    • Villartay, Jean-Pierre de
    Publication type:
    Article

  • Hunting for the genetic basis of Susac syndrome.

    Published in:
    European Journal of Neurology, 2021, v. 28, n. 7, p. e57, doi. 10.1111/ene.14836
    By:
    • David, Clemence;
    • Papo, Thomas;
    • Ba, Ibrahima;
    • Ollivier, Emmanuelle;
    • Boileau, Catherine;
    • Dieudé, Philippe;
    • Keren, Boris;
    • Kannengiesser, Caroline;
    • Sacre, Karim
    Publication type:
    Article

  • Loss-of-Function Mutations in NR4A2 Cause Dopa-Responsive Dystonia Parkinsonism.

    Published in:
    2020
    By:
    • Wirth, Thomas;
    • Mariani, Louise Laure;
    • Bergant, Gaber;
    • Baulac, Michel;
    • Habert, Marie‐Odile;
    • Drouot, Nathalie;
    • Ollivier, Emmanuelle;
    • Hodžić, Alenka;
    • Rudolf, Gorazd;
    • Nitschke, Patrick;
    • Rudolf, Gabrielle;
    • Chelly, Jamel;
    • Tranchant, Christine;
    • Anheim, Mathieu;
    • Roze, Emmanuel;
    • Habert, Marie-Odile
    Publication type:
    journal article

  • Colethality studied as an asset against viral drugescape: the HIV protease case.

    Published in:
    Biology Direct, 2010, v. 5, p. 40, doi. 10.1186/1745-6150-5-40
    By:
    • Brouillet, Sophie;
    • Valere, Thomas;
    • Ollivier, Emmanuelle;
    • Marsan, Laurent;
    • Vanet, Anne
    Publication type:
    Article