Works by Petit, Christine

Results: 159
    1

    Consequences of Isostructural Main-Chain Modifications for the Design of Antimicrobial Foldamers: Helical Mimics of Host-Defense Peptides Based on a Heterogeneous Amide/Urea Backbone.

    Published in:
    Angewandte Chemie, 2010, v. 122, n. 2, p. 343, doi. 10.1002/ange.200905591
    By:
    • Claudon, Paul;
    • Violette, Aude;
    • Lamour, Karen;
    • Decossas, Marion;
    • Fournel, Sylvie;
    • Heurtault, Béatrice;
    • Godet, Julien;
    • Mély, Yves;
    • Jamart-Grégoire, Brigitte;
    • Averlant-Petit, Marie-Christine;
    • Briand, Jean-Paul;
    • Duportail, Guy;
    • Monteil, Henri;
    • Guichard, Gilles
    Publication type:
    Article
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    Re-assigning the DFNB33 locus to chromosome 10p11.23–q21.1.

    Published in:
    European Journal of Human Genetics, 2009, v. 17, n. 1, p. 122, doi. 10.1038/ejhg.2008.155
    By:
    • Belguith, Hanen;
    • Masmoudi, Saber;
    • Medlej-Hashim, Myrna;
    • Chouery, Eliane;
    • Weil, Dominique;
    • Ayadi, Hammadi;
    • Petit, Christine;
    • Mégarbané, André
    Publication type:
    Article
    14

    Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene.

    Published in:
    European Journal of Human Genetics, 2004, v. 12, n. 4, p. 279, doi. 10.1038/sj.ejhg.5201147
    By:
    • Feldmann, Delphine;
    • Denoyelle, Françoise;
    • Loundon, Natalie;
    • Weil, Dominique;
    • Garabedian, Erea-Noel;
    • Couderc, Remy;
    • Joannard, Alain;
    • Schmerber, Sébastien;
    • Delobel, Bruno;
    • Leman, Jacques;
    • Journel, Hubert;
    • Catros, Hélène;
    • Ferrec, Claude;
    • Drouin-Garraud, Valérie;
    • Obstoy, Marie-Françoise;
    • Moati, Lucien;
    • Petit, Christine;
    • Marlin, Sandrine
    Publication type:
    Article
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    Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 106, doi. 10.1038/ng.278
    By:
    • Lagresle-Peyrou, Chantal;
    • Six, Emmanuelle M.;
    • Picard, Capucine;
    • Rieux-Laucat, Frédéric;
    • Michel, Vincent;
    • Ditadi, Andrea;
    • Chappedelaine, Corinne Demerens-de;
    • Morillon, Estelle;
    • Valensi, Françoise;
    • Simon-Stoos, Karen L;
    • Mullikin, James C;
    • Noroski, Lenora M;
    • Besse, Céline;
    • Wulffraat, Nicolas M.;
    • Ferster, Alina;
    • Abecasis, Manuel M.;
    • Calvo, Fabien;
    • Petit, Christine;
    • Candotti, Fabio;
    • Abel, Laurent
    Publication type:
    Article
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    Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2.

    Published in:
    PLoS Genetics, 2006, v. 3, n. 4, p. 1648, doi. 10.1371/journal.pgen.0020175
    By:
    • Dodé, Catherine;
    • Teixeira, Luis;
    • Levilliers, Jacqueline;
    • Fouveaut, Corinne;
    • Bouchard, Philippe;
    • Kottler, Marie-Laure;
    • Lespinasse, James;
    • Lienhardt-Roussie, Anne;
    • Mathieu, Michèle;
    • Moerman, Alexandre;
    • Morgan, Graeme;
    • Murat, Arnaud;
    • Toublanc, Jean-Edmont;
    • Wolczynski, Slawomir;
    • Delpech, Marc;
    • Petit, Christine;
    • Young, Jacques;
    • Hardelin, Jean-Pierre
    Publication type:
    Article
    37

    Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome.

    Published in:
    2018
    By:
    • Dulon, Didier;
    • Papal, Samantha;
    • Patni, Pranav;
    • Cortese, Matteo;
    • Vincent, Philippe F. Y.;
    • Tertrais, Margot;
    • Emptoz, Alice;
    • Tlili, Abdelaziz;
    • Bouleau, Yohan;
    • Michel, Vincent;
    • Delmaghani, Sedigheh;
    • Aghaie, Alain;
    • Pepermans, Elise;
    • Alegria-Prevot, Olinda;
    • Akil, Omar;
    • Lustig, Lawrence;
    • Avan, Paul;
    • Safieddine, Saaid;
    • Petit, Christine;
    • El-Amraouiw, Aziz
    Publication type:
    journal article
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    Specific Aspects of Consanguinity: Some Examples from the Tunisian Population.

    Published in:
    Human Heredity, 2014, v. 77, n. 1-4, p. 167, doi. 10.1159/000362167
    By:
    • Romdhane, Lilia;
    • Ben Halim, Nizar;
    • Rejeb, Insaf;
    • Kefi, Rym;
    • Bouyacoub, Yosra;
    • Ben Rekaya, Mariem;
    • Messai, Habib;
    • Messaoud, Olfa;
    • Riahi, Zied;
    • Bonnet, Crystel;
    • Ben Rhouma, Faten;
    • Nagara, Majdi;
    • Petit, Christine;
    • McElreavey, Ken;
    • Romeo, Giovanni;
    • Abdelhak, Sonia
    Publication type:
    Article
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    Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome.

    Published in:
    PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0161893
    By:
    • Abdi, Samia;
    • Bahloul, Amel;
    • Behlouli, Asma;
    • Hardelin, Jean-Pierre;
    • Makrelouf, Mohamed;
    • Boudjelida, Kamel;
    • Louha, Malek;
    • Cheknene, Ahmed;
    • Belouni, Rachid;
    • Rous, Yahia;
    • Merad, Zahida;
    • Selmane, Djamel;
    • Hasbelaoui, Mokhtar;
    • Bonnet, Crystel;
    • Zenati, Akila;
    • Petit, Christine
    Publication type:
    Article
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    Consequences of Isostructural Main-Chain Modifications for the Design of Antimicrobial Foldamers: Helical Mimics of Host-Defense Peptides Based on a Heterogeneous Amide/Urea Backbone.

    Published in:
    Angewandte Chemie International Edition, 2010, v. 49, n. 2, p. 333, doi. 10.1002/anie.200905591
    By:
    • Claudon, Paul;
    • Violette, Aude;
    • Lamour, Karen;
    • Decossas, Marion;
    • Fournel, Sylvie;
    • Heurtault, Béatrice;
    • Godet, Julien;
    • Mély, Yves;
    • Jamart-Grégoire, Brigitte;
    • Averlant-Petit, Marie-Christine;
    • Briand, Jean-Paul;
    • Duportail, Guy;
    • Monteil, Henri;
    • Guichard, Gilles
    Publication type:
    Article
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    Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush.

    Published in:
    International Journal of Molecular Sciences, 2021, v. 22, n. 19, p. 10352, doi. 10.3390/ijms221910352
    By:
    • Fakin, Ana;
    • Bonnet, Crystel;
    • Kurtenbach, Anne;
    • Mohand-Said, Saddek;
    • Zobor, Ditta;
    • Stingl, Katarina;
    • Testa, Francesco;
    • Simonelli, Francesca;
    • Sahel, José-Alain;
    • Audo, Isabelle;
    • Zrenner, Eberhart;
    • Hawlina, Marko;
    • Petit, Christine
    Publication type:
    Article