Výsledky vyhledávání - Guylène Le Meur

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  1. 1
    Biodistribution of rAAV Vectors Following Intraocular Administration: Evidence for the Presence and Persistence of Vector DNA in the Optic Nerve and in the Brain

    Biodistribution of rAAV Vectors Following Intraocular Administration: Evidence for the Presence and Persistence of Vector DNA in the Optic Nerve and in the Brain Autor Nathalie Provost, Guylène Le Meur, Michel Weber, Alexandra Mendes-Madeira, Guillaume Podevin, Yan Chérel, Marie-Anne Colle, Jack‐Yves Deschamps, Philippe Moullier, Fabienne Rolling

    Vydáno 2004
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  2. 2
    Long-term doxycycline-regulated transgene expression in the retina of nonhuman primates following subretinal injection of recombinant AAV vectors

    Long-term doxycycline-regulated transgene expression in the retina of nonhuman primates following subretinal injection of recombinant AAV vectors Autor Knut Stieger, Guylène Le Meur, Françoise Lasne, Michel Weber, Jack‐Yves Deschamps, Delphine Nivard, Alexandra Mendes-Madeira, Nathalie Provost, Laurent Martin, Philippe Moullier, Fabienne Rolling

    Vydáno 2006
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  3. 3
    Detection of Intact rAAV Particles up to 6 Years After Successful Gene Transfer in the Retina of Dogs and Primates

    Detection of Intact rAAV Particles up to 6 Years After Successful Gene Transfer in the Retina of Dogs and Primates Autor Knut Stieger, Josef Schroeder, Nathalie Provost, Alexandra Mendes-Madeira, Brahim Belbellaa, Guylène Le Meur, Michel Weber, Jack‐Yves Deschamps, Birgit Lorenz, Philippe Moullier, Fabienne Rolling

    Vydáno 2008
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  4. 4
    Safety and Long-Term Efficacy of AAV4 Gene Therapy in Patients with RPE65 Leber Congenital Amaurosis

    Safety and Long-Term Efficacy of AAV4 Gene Therapy in Patients with RPE65 Leber Congenital Amaurosis Autor Guylène Le Meur, Pierre Lebranchu, Fanny Billaud, Oumeya Adjali, Sébastien Schmitt, Stéphane Bézieau, Yann Péréon, Romain Valabrègue, Catherine Ivan, Christophe Darmon, Philippe Moullier, Fabienne Rolling, Michel Weber

    Vydáno 2017
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  5. 5
    Restoration of Vision in the pde6β-deficient Dog, a Large Animal Model of Rod-cone Dystrophy

    Restoration of Vision in the pde6β-deficient Dog, a Large Animal Model of Rod-cone Dystrophy Autor Lolita Petit, Elsa Lhériteau, Michel Weber, Guylène Le Meur, Jack‐Yves Deschamps, Nathalie Provost, Alexandra Mendes-Madeira, Lyse Libeau, Caroline Guihal, Marie-Anne Colle, Philippe Moullier, Fabienne Rolling

    Vydáno 2012
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  6. 6
    Subretinal Delivery of Recombinant AAV Serotype 8 Vector in Dogs Results in Gene Transfer to Neurons in the Brain

    Subretinal Delivery of Recombinant AAV Serotype 8 Vector in Dogs Results in Gene Transfer to Neurons in the Brain Autor Knut Stieger, Marie-Anne Colle, Laurence Dubreil, Alexandra Mendes-Madeira, Michel Weber, Guylène Le Meur, Jack Yves Deschamps, Nathalie Provost, Delphine Nivard, Yan Chérel, Philippe Moullier, Fabienne Rolling

    Vydáno 2008
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  7. 7
    AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6β-deficient Dogs

    AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6β-deficient Dogs Autor Virginie Pichard, Nathalie Provost, Alexandra Mendes-Madeira, Lyse Libeau, Philippe Hulin, Kizito‐Tshitoko Tshilenge, Marine Biget, Baptiste Ameline, Jack‐Yves Deschamps, Michel Weber, Guylène Le Meur, Marie-Anne Colle, Philippe Moullier, Fabienne Rolling

    Vydáno 2016
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  8. 8
    Successful Gene Therapy in the RPGRIP1-deficient Dog: a Large Model of Cone–Rod Dystrophy

    Successful Gene Therapy in the RPGRIP1-deficient Dog: a Large Model of Cone–Rod Dystrophy Autor Elsa Lhériteau, Lolita Petit, Michel Weber, Guylène Le Meur, Jack‐Yves Deschamps, Lyse Libeau, Alexandra Mendes-Madeira, Caroline Guihal, Achille François, Richard Guyon, Nathalie Provost, F Lemoine, Samantha Papal, A. Amraoui, Marie-Anne Colle, Philippe Moullier, Fabienne Rolling

    Vydáno 2013
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  9. 9
    Mannose-coupled AAV2: A second-generation AAV vector for increased retinal gene therapy efficiency

    Mannose-coupled AAV2: A second-generation AAV vector for increased retinal gene therapy efficiency Autor Mathieu Mével, Virginie Pichard, Mohammed Bouzelha, Dimitri Álvarez‐Dorta, Pierre-Alban Lalys, Nathalie Provost, Marine Allais, Alexandra Mendes, Elodie Landagaray, Jean‐Baptiste Ducloyer, Estelle Toublanc, Anne Galy, Nicole Brument, G. Lefèvre, Sébastien G. Gouin, Carolina Isiegas, Guylène Le Meur, Thérèse Cronin, Caroline Le Guiner, Michel Weber, Philippe Moullier, Eduard Ayuso, David Deniaud, Oumeya Adjali

    Vydáno 2024
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  10. 10
    Mutations in IMPG1 Cause Vitelliform Macular Dystrophies

    Mutations in IMPG1 Cause Vitelliform Macular Dystrophies Autor Gaël Manès, Isabelle Meunier, Almudena Ávila‐Fernández, Sandro Banfi, Guylène Le Meur, Xavier Zanlonghi, Marta Cortón, Francesca Simonelli, Philippe Brabet, Gilles Labesse, Isabelle Audo, Saddek Mohand‐Saïd, Christina Zeitz, José‐Alain Sahel, Michel Weber, Hélène Dollfus, Claire‐Marie Dhaenens, Delphine Allorge, Elfride De Baere, Robert K. Koenekoop, Susanne Kohl, Frans P.M. Cremers, Joe G. Hollyfield, Audrey Sénéćhal, Maxime Hebrard, Béatrice Bocquet, Carmen Ayuso, Christian P. Hamel

    Vydáno 2013
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  11. 11
    Expanding the phenotype of the X-linked BCOR microphthalmia syndromes

    Expanding the phenotype of the X-linked BCOR microphthalmia syndromes Autor Nicola Ragge, Bertrand Isidor, Pierre Bitoun, Sylvie Odent, Irina Giurgea, Benjamin Cogné, Wallid Deb, Marie Vincent, Jessica Le Gall, Jenny Morton, Derek Lim, Guylène Le Meur, Celia Zazo Seco, Dimitra Zafeiropoulou, Dorine A. Bax, Petra Zwijnenburg, Ana Arteche‐López, Saoud Tahsin Swafiri, Ruth Cleaver, Meriel McEntagart, Usha Kini, William D. Newman, Carmen Ayuso, Marta Cortón, Yvan Herenger, Médéric Jeanne, Patrick Calvas, Nicolas Chassaing

    Vydáno 2018
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  12. 12
    Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

    Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness Autor Isabelle Audo, Kinga M. Bujakowska, Elise Orhan, Charlotte M. Poloschek, Sabine Defoort‐Dhellemmes, Isabelle Drumare, Susanne Kohl, Tien D. Luu, Odile Lecompte, Eberhart Zrenner, Marie‐Elise Lancelot, Aline Antonio, Aurore Germain, Christelle Michiels, Claire Audier, Mélanie Letexier, Jean‐Paul Saraiva, Bart P. Leroy, Francis L. Munier, Saddek Mohand‐Saïd, Birgit Lorenz, Christoph Friedburg, Markus N. Preising, Ulrich Kellner, Agnes B. Renner, Veselina Moskova‐Doumanova, Wolfgang Berger, Bernd Wissinger, Christian Hamel, Daniel F. Schorderet, Elfride De Baere, Dror Sharon, Eyal Banin, Samuel G. Jacobson, Dominique Bonneau, Xavier Zanlonghi, Guylène Le Meur, Ingele Casteels, Robert K. Koenekoop, Vernon Long, Françoise Meire, Katrina Prescott, Thomy de Ravel, Ian Simmons, Hoan Nguyen, Hélène Dollfus, Olivier Poch, Thierry Léveillard, Kim T. Nguyen-Ba-Charvet, José‐Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz

    Vydáno 2012
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  13. 13
    Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy

    Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy Autor Benjamin Cogné, Xénia Latypova, Lokuliyanage Dona Samudita Senaratne, Ludovic Martin, Daniel C. Koboldt, Georgios Kellaris, Lorraine Fievet, Guylène Le Meur, D. Caldari, Dominique Debray, Mathilde Nizon, Eirik Frengen, Sara J. Bowne, Elizabeth L. Cadena, Stephen P. Daiger, Kinga M. Bujakowska, Eric A. Pierce, Michael B. Gorin, Nicholas Katsanis, Stéphane Bézieau, Simon M. Petersen‐Jones, Laurence M. Occelli, Leslie A. Lyons, Laurence Legeai‐Mallet, Lori S. Sullivan, Erica E. Davis, Bertrand Isidor, Reuben M. Buckley, Danielle Aberdein, Paulo C. Alves, Gregory S. Barsh, Rebecca R. Bellone, Tomas F. Bergström, Adam R. Boyko, Jeffrey A. Brockman, Margret L. Casal, Marta G. Castelhano, O. Distl, Nicholas H. Dodman, N. Matthew Ellinwood, Jonathan E. Fogle, Oliver P. Forman, Dorian J. Garrick, Edward I. Ginns, Jens Häggström, Victoria L. Harvey, Daisuke Hasegawa, Bianca Haase, Chris R. Helps, Isabel Hernández, Marjo K. Hytönen, Maria Kaukonen, Christopher B. Kaelin, Tomoki Kosho, Emilie Leclerc, T.L. Lear, Tosso Leeb, Ronald H. L. Li, Hannes Lohi, M. Longeri, Mark A. Magnuson, Richard Malík, Shrinivasrao P. Mane, John S. Munday, William J. Murphy, Niels C. Pedersen, Max F. Rothschild, Clare Rusbridge, Beth Shapiro, Joshua A. Stern, William F. Swanson, Karen A. Terio, Rory J. Todhunter, Wesley C. Warren, Elizabeth A. Wilcox, Julia H Wildschutte, Yoshihiko Yu

    Vydáno 2020
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