Works by Léveillard, Thierry

Results: 44
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    Insulin inhibits inflammation-induced cone death in retinal detachment.

    Published in:
    2020
    By:
    • Conart, Jean-Baptiste;
    • Blot, Guillaume;
    • Augustin, Sébastien;
    • Millet-Puel, Géraldine;
    • Roubeix, Christophe;
    • Beguier, Fanny;
    • Charles-Messance, Hugo;
    • Touhami, Sara;
    • Sahel, José-Alain;
    • Berrod, Jean-Paul;
    • Léveillard, Thierry;
    • Guillonneau, Xavier;
    • Delarasse, Cécile;
    • Sennlaub, Florian
    Publication type:
    journal article
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    Spare the Rod, Spoil the Degeneration.

    Published in:
    Journal of Pediatric Ophthalmology & Strabismus, 2014, v. 51, n. 2, p. 74, doi. 10.3928/01913913-20140220-06
    By:
    • Léveillard, Thierry
    Publication type:
    Article
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    Identification of an Alternative Splicing Product of the Otx2 Gene Expressed in the Neural Retina and Retinal Pigmented Epithelial Cells.

    Published in:
    PLoS ONE, 2016, v. 11, n. 3, p. 1, doi. 10.1371/journal.pone.0150758
    By:
    • Kole, Christo;
    • Berdugo, Naomi;
    • Da Silva, Corinne;
    • Aït-Ali, Najate;
    • Millet-Puel, Géraldine;
    • Pagan, Delphine;
    • Blond, Frédéric;
    • Poidevin, Laetitia;
    • Ripp, Raymond;
    • Fontaine, Valérie;
    • Wincker, Patrick;
    • Zack, Donald J.;
    • Sahel, José-Alain;
    • Poch, Olivier;
    • Léveillard, Thierry
    Publication type:
    Article
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    Identification and characterization of rod-derived cone viability factor.

    Published in:
    Nature Genetics, 2004, v. 36, n. 7, p. 755, doi. 10.1038/ng1386
    By:
    • Léveillard, Thierry;
    • Mohand-Saïd, Saddek;
    • Lorentz, Olivier;
    • Hicks, David;
    • Fintz, Anne-Claire;
    • Clérin, Emmanuelle;
    • Simonutti, Manuel;
    • Forster, Valérie;
    • Cavusoglu, Nükhet;
    • Chalmel, Frédéric;
    • Dollé, Pascal;
    • Poch, Olivier;
    • Lambrou, George;
    • Sahel, José-Alain
    Publication type:
    Article
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    CRB1 mutations in inherited retinal dystrophies.

    Published in:
    Human Mutation, 2012, v. 33, n. 2, p. 306, doi. 10.1002/humu.21653
    By:
    • Bujakowska, Kinga;
    • Audo, Isabelle;
    • Mohand-Saïd, Saddek;
    • Lancelot, Marie-Elise;
    • Antonio, Aline;
    • Germain, Aurore;
    • Léveillard, Thierry;
    • Letexier, Mélanie;
    • Saraiva, Jean-Paul;
    • Lonjou, Christine;
    • Carpentier, Wassila;
    • Sahel, José-Alain;
    • Bhattacharya, Shomi S.;
    • Zeitz, Christina
    Publication type:
    Article
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    Assessing Photoreceptor Status in Retinal Dystrophies: From High-Resolution Imaging to Functional Vision.

    Published in:
    Transactions of the American Ophthalmological Society, 2021, v. 119, p. 12, doi. 10.1016/j.ajo.2021.04.013
    By:
    • SAHEL, JOSÉ-ALAIN;
    • GRIEVE, KATE;
    • PAGOT, CHLOÉ;
    • AUTHIÉ, COLAS;
    • MOHAND-SAID, SADDEK;
    • PAQUES, MICHEL;
    • AUDO, ISABELLE;
    • BECKER, KARINE;
    • CHAUMET-RIFFAUD, ANNE-ELISABETH;
    • AZOULAY, LINE;
    • GUTMAN, EMMANUEL;
    • LÉVEILLARD, THIERRY;
    • ZEITZ, CHRISTINA;
    • PICAUD, SERGE;
    • DALKARA, DENIZ;
    • MARAZOVA, KATIA
    Publication type:
    Article
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    Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy.

    Published in:
    International Journal of Molecular Sciences, 2021, v. 22, n. 15, p. 7875, doi. 10.3390/ijms22157875
    By:
    • Zeitz, Christina;
    • Méjécase, Cécile;
    • Michiels, Christelle;
    • Condroyer, Christel;
    • Wohlschlegel, Juliette;
    • Foussard, Marine;
    • Antonio, Aline;
    • Démontant, Vanessa;
    • Emmenegger, Lisa;
    • Schalk, Audrey;
    • Neuillé, Marion;
    • Orhan, Elise;
    • Augustin, Sébastien;
    • Bonnet, Crystel;
    • Estivalet, Amrit;
    • Blond, Frédéric;
    • Blanchard, Steven;
    • Andrieu, Camille;
    • Chantot-Bastaraud, Sandra;
    • Léveillard, Thierry
    Publication type:
    Article
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    WDR34, a candidate gene for non‐syndromic rod‐cone dystrophy.

    Published in:
    Clinical Genetics, 2021, v. 99, n. 2, p. 298, doi. 10.1111/cge.13872
    By:
    • Solaguren‐Beascoa, Maria;
    • Bujakowska, Kinga M.;
    • Méjécase, Cécile;
    • Emmenegger, Lisa;
    • Orhan, Elise;
    • Neuillé, Marion;
    • Mohand‐Saïd, Saddek;
    • Condroyer, Christel;
    • Lancelot, Marie‐Elise;
    • Michiels, Christelle;
    • Demontant, Vanessa;
    • Antonio, Aline;
    • Letexier, Mélanie;
    • Saraiva, Jean‐Paul;
    • Lonjou, Christine;
    • Carpentier, Wassila;
    • Léveillard, Thierry;
    • Pierce, Eric A.;
    • Dollfus, Hélène;
    • Sahel, José‐Alain
    Publication type:
    Article
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    The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 2, p. 491, doi. 10.1093/hmg/ddt439
    By:
    • Audo, Isabelle;
    • Bujakowska, Kinga;
    • Orhan, Elise;
    • El Shamieh, Said;
    • Sennlaub, Florian;
    • Guillonneau, Xavier;
    • Antonio, Aline;
    • Michiels, Christelle;
    • Lancelot, Marie-Elise;
    • Letexier, Melanie;
    • Saraiva, Jean-Paul;
    • Nguyen, Hoan;
    • Luu, Tien D.;
    • Léveillard, Thierry;
    • Poch, Olivier;
    • Dollfus, Hélène;
    • Paques, Michel;
    • Goureau, Olivier;
    • Mohand-Saïd, Saddek;
    • Bhattacharya, Shomi S.
    Publication type:
    Article
    24

    Nxnl2 splicing results in dual functions in neuronal cell survival and maintenance of cell integrity.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 10, p. 2298, doi. 10.1093/hmg/dds050
    By:
    • Jaillard, Céline;
    • Mouret, Aurélie;
    • Niepon, Marie-Laure;
    • Clérin, Emmanuelle;
    • Yang, Ying;
    • Lee-Rivera, Irene;
    • Aït-Ali, Najate;
    • Millet-Puel, Géraldine;
    • Cronin, Thérèse;
    • Sedmak, Tina;
    • Raffelsberger, Wolfgang;
    • Kinzel, Bernd;
    • Trembleau, Alain;
    • Poch, Olivier;
    • Bennett, Jean;
    • Wolfrum, Uwe;
    • Lledo, Pierre-Marie;
    • Sahel, José-Alain;
    • Léveillard, Thierry
    Publication type:
    Article
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    Genotypic and Phenotypic Characterization of P23H Line 1 Rat Model.

    Published in:
    PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0127319
    By:
    • Orhan, Elise;
    • Dalkara, Deniz;
    • Neuillé, Marion;
    • Lechauve, Christophe;
    • Michiels, Christelle;
    • Picaud, Serge;
    • Léveillard, Thierry;
    • Sahel, José-Alain;
    • Naash, Muna I.;
    • Lavail, Matthew M.;
    • Zeitz, Christina;
    • Audo, Isabelle
    Publication type:
    Article
    28

    Taurine Provides Neuroprotection against Retinal Ganglion Cell Degeneration.

    Published in:
    PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0042017
    By:
    • Froger, Nicolas;
    • Cadetti, Lucia;
    • Lorach, Henri;
    • Martins, Joao;
    • Bemelmans, Alexis-Pierre;
    • Dubus, Elisabeth;
    • Degardin, Julie;
    • Pain, Dorothée;
    • Forster, Valérie;
    • Chicaud, Laurent;
    • Ivkovic, Ivana;
    • Simonutti, Manuel;
    • Fouquet, Stéphane;
    • Jammoul, Firas;
    • Léveillard, Thierry;
    • Benosman, Ryad;
    • Sahel, José-Alain;
    • Picaud, Serge
    Publication type:
    Article
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    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
    38

    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
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    Functional rescue of cone photoreceptors in retinitis pigmentosa.

    Published in:
    Graefe's Archive of Clinical & Experimental Ophthalmology, 2013, v. 251, n. 7, p. 1669, doi. 10.1007/s00417-013-2314-7
    By:
    • Sahel, José-Alain;
    • Léveillard, Thierry;
    • Picaud, Serge;
    • Dalkara, Deniz;
    • Marazova, Katia;
    • Safran, Avinoam;
    • Paques, Michel;
    • Duebel, Jens;
    • Roska, Botond;
    • Mohand-Said, Saddek
    Publication type:
    Article
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