Rod-Derived Cone Viability Factor Promotes Cone Survival by Stimulating Aerobic Glycolysis
Aït-Ali, Najate, Fridlich, Ram, Millet-Puel, Géraldine, Clérin, Emmanuelle, Delalande, François, Jaillard, Céline, Blond, Frédéric, Perrocheau, Ludivine, Reichman, Sacha, Byrne, Leah C., Olivier-Bandini, Anne, Bellalou, Jacques, Moyse, Emmanuel, Bouillaud, Frédéric, Nicol, Xavier, Dalkara, Deniz, van Dorsselaer, Alain, Sahel, José-Alain, Léveillard, Thierry
Published in Cell (07.05.2015)
Published in Cell (07.05.2015)
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Viral-mediated RdCVF and RdCVFL expression protects cone and rod photoreceptors in retinal degeneration
Byrne, Leah C, Dalkara, Deniz, Luna, Gabriel, Fisher, Steven K, Clérin, Emmanuelle, Sahel, Jose-Alain, Léveillard, Thierry, Flannery, John G
Published in The Journal of clinical investigation (01.01.2015)
Published in The Journal of clinical investigation (01.01.2015)
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Assessing Photoreceptor Status in Retinal Dystrophies: From High-Resolution Imaging to Functional Vision
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
Published in American journal of ophthalmology (01.10.2021)
Published in American journal of ophthalmology (01.10.2021)
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The 10q26 Risk Haplotype of Age-Related Macular Degeneration Aggravates Subretinal Inflammation by Impairing Monocyte Elimination
Beguier, Fanny, Housset, Michael, Roubeix, Christophe, Augustin, Sebastien, Zagar, Yvrick, Nous, Caroline, Mathis, Thibaud, Eandi, Chiara, Benchaboune, Mustapha, Drame-Maigné, Adèle, Carpentier, Wassila, Chardonnet, Solenne, Touhami, Sara, Blot, Guillaume, Conart, Jean Baptiste, Charles-Messance, Hugo, Potey, Anaïs, Girmens, Jean-François, Paques, Michel, Blond, Fréderic, Leveillard, Thierry, Koertvely, Elod, Roger, Jerome E., Sahel, José-Alain, Sapieha, Przemyslaw, Delarasse, Cécile, Guillonneau, Xavier, Sennlaub, Florian
Published in Immunity (Cambridge, Mass.) (18.08.2020)
Published in Immunity (Cambridge, Mass.) (18.08.2020)
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Affinity-controlled release of rod-derived cone viability factor enhances cone photoreceptor survival
Teal, Carter J., Ho, Margaret T., Huo, Lia, Harada, Hidekiyo, Bahlmann, Laura C., Léveillard, Thierry, Monnier, Philippe P., Ramachandran, Arun, Shoichet, Molly S.
Published in Acta biomaterialia (15.04.2023)
Published in Acta biomaterialia (15.04.2023)
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Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases
Audo, Isabelle, Bujakowska, Kinga M, Léveillard, Thierry, Mohand-Saïd, Saddek, Lancelot, Marie-Elise, Germain, Aurore, Antonio, Aline, Michiels, Christelle, Saraiva, Jean-Paul, Letexier, Mélanie, Sahel, José-Alain, Bhattacharya, Shomi S, Zeitz, Christina
Published in Orphanet journal of rare diseases (25.01.2012)
Published in Orphanet journal of rare diseases (25.01.2012)
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Polyglutamine-expanded ATXN7 alters a specific epigenetic signature underlying photoreceptor identity gene expression in SCA7 mouse retinopathy
Niewiadomska-Cimicka, Anna, Hache, Antoine, Le Gras, Stéphanie, Keime, Céline, Ye, Tao, Eisenmann, Aurelie, Harichane, Imen, Roux, Michel J, Messaddeq, Nadia, Clérin, Emmanuelle, Léveillard, Thierry, Trottier, Yvon
Published in Journal of biomedical science (20.12.2022)
Published in Journal of biomedical science (20.12.2022)
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Genotypic and phenotypic characterization of P23H line 1 rat model
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
Published in PloS one (26.05.2015)
Published in PloS one (26.05.2015)
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Insulin inhibits inflammation-induced cone death in retinal detachment
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
Published in Journal of neuroinflammation (26.11.2020)
Published in Journal of neuroinflammation (26.11.2020)
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CRB1 mutations in inherited retinal dystrophies
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
Published in Human mutation (01.02.2012)
Published in Human mutation (01.02.2012)
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Taurine provides neuroprotection against retinal ganglion cell degeneration
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
Published in PloS one (24.10.2012)
Published in PloS one (24.10.2012)
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Shedding light on myopia by studying complete congenital stationary night blindness
Zeitz, Christina, Roger, Jérome E., Audo, Isabelle, Michiels, Christelle, Sánchez-Farías, Nuria, Varin, Juliette, Frederiksen, Helen, Wilmet, Baptiste, Callebert, Jacques, Gimenez, Marie-Laure, Bouzidi, Nassima, Blond, Frederic, Guilllonneau, Xavier, Fouquet, Stéphane, Léveillard, Thierry, Smirnov, Vasily, Vincent, Ajoy, Héon, Elise, Sahel, José-Alain, Kloeckener-Gruissem, Barbara, Sennlaub, Florian, Morgans, Catherine W., Duvoisin, Robert M., Tkatchenko, Andrei V., Picaud, Serge
Published in Progress in retinal and eye research (01.03.2023)
Published in Progress in retinal and eye research (01.03.2023)
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Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy
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, Mohand-Saïd, Saddek, Sahel, José-Alain, Audo, Isabelle
Published in International journal of molecular sciences (01.08.2021)
Published in International journal of molecular sciences (01.08.2021)
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Functional Cone Rescue by RdCVF Protein in a Dominant Model of Retinitis Pigmentosa
Yang, Ying, Mohand-Said, Saddek, Danan, Aude, Simonutti, Manuel, Fontaine, Valérie, Clerin, Emmanuelle, Picaud, Serge, Léveillard, Thierry, Sahel, José-Alain
Published in Molecular therapy (01.05.2009)
Published in Molecular therapy (01.05.2009)
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Identification and characterization of rod-derived cone viability factor
Poch, Olivier, Fintz, Anne-Claire, Léveillard, Thierry, Cavusoglu, Nükhet, Chalmel, Frédéric, Forster, Valérie, Dollé, Pascal, Lambrou, George, Mohand-Saïd, Saddek, Simonutti, Manuel, Sahel, José-Alain, Clérin, Emmanuelle, Lorentz, Olivier, Hicks, David
Published in Nature genetics (01.07.2004)
Published in Nature genetics (01.07.2004)
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The Thioredoxin Encoded by the Rod-Derived Cone Viability Factor Gene Protects Cone Photoreceptors Against Oxidative Stress
Mei, Xin, Chaffiol, Antoine, Kole, Christo, Yang, Ying, Millet-Puel, Géraldine, Clérin, Emmanuelle, Aït-Ali, Najate, Bennett, Jean, Dalkara, Deniz, Sahel, José-Alain, Duebel, Jens, Léveillard, Thierry
Published in Antioxidants & redox signaling (01.06.2016)
Published in Antioxidants & redox signaling (01.06.2016)
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The metabolic signaling of the nucleoredoxin-like 2 gene supports brain function
Jaillard, Céline, Ouechtati, Farah, Clérin, Emmanuelle, Millet-Puel, Géraldine, Corsi, Mariangela, Aït-Ali, Najate, Blond, Frédéric, Chevy, Quentin, Gales, Lara, Farinelli, Mélissa, Dalkara, Deniz, Sahel, José-Alain, Portais, Jean-Charles, Poncer, Jean-Christophe, Léveillard, Thierry
Published in Redox biology (01.12.2021)
Published in Redox biology (01.12.2021)
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Journal Article
TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness
Audo, Isabelle, Kohl, Susanne, Leroy, Bart P., Munier, Francis L., Guillonneau, Xavier, Mohand-Saïd, Saddek, Bujakowska, Kinga, Nandrot, Emeline F., Lorenz, Birgit, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Bernd, Antje, Antonio, Aline, Moskova-Doumanova, Veselina, Lancelot, Marie-Elise, Poloschek, Charlotte M., Drumare, Isabelle, Defoort-Dhellemmes, Sabine, Wissinger, Bernd, Léveillard, Thierry, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Berger, Wolfgang, Jacobson, Samuel G., Zrenner, Eberhart, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina
Published in American journal of human genetics (13.11.2009)
Published in American journal of human genetics (13.11.2009)
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Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration
Ratnapriya, Rinki, Zhan, Xiaowei, Fariss, Robert N, Branham, Kari E, Zipprer, David, Chakarova, Christina F, Sergeev, Yuri V, Campos, Maria M, Othman, Mohammad, Friedman, James S, Maminishkis, Arvydas, Waseem, Naushin H, Brooks, Matthew, Rajasimha, Harsha K, Edwards, Albert O, Lotery, Andrew, Klein, Barbara E, Truitt, Barbara J, Li, Bingshan, Schaumberg, Debra A, Morgan, Denise J, Morrison, Margaux A, Souied, Eric, Tsironi, Evangelia E, Grassmann, Felix, Fishman, Gerald A, Silvestri, Giuliana, Scholl, Hendrik P N, Kim, Ivana K, Ramke, Jacqueline, Tuo, Jingsheng, Merriam, Joanna E, Merriam, John C, Park, Kyu Hyung, Olson, Lana M, Farrer, Lindsay A, Johnson, Matthew P, Peachey, Neal S, Lathrop, Mark, Baron, Robert V, Igo, Jr, Robert P, Klein, Ronald, Hagstrom, Stephanie A, Kamatani, Yoichiro, Martin, Tammy M, Jiang, Yingda, Conley, Yvette, Sahel, Jose-Alan, Zack, Donald J, Chan, Chi-Chao, Pericak-Vance, Margaret A, Jacobson, Samuel G, Gorin, Michael B, Klein, Michael L, Allikmets, Rando, Iyengar, Sudha K, Weber, Bernhard H, Haines, Jonathan L, Léveillard, Thierry, Deangelis, Margaret M, Stambolian, Dwight, Weeks, Daniel E, Bhattacharya, Shomi S, Chew, Emily Y, Heckenlively, John R, Abecasis, Gonçalo R, Swaroop, Anand
Published in Human molecular genetics (01.11.2014)
Published in Human molecular genetics (01.11.2014)
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Whole-Exome Sequencing Identifies KIZ as a Ciliary Gene Associated with Autosomal-Recessive Rod-Cone Dystrophy
El Shamieh, Said, Neuillé, Marion, Terray, Angélique, Orhan, Elise, Condroyer, Christel, Démontant, Vanessa, Michiels, Christelle, Antonio, Aline, Boyard, Fiona, Lancelot, Marie-Elise, Letexier, Mélanie, Saraiva, Jean-Paul, Léveillard, Thierry, Mohand-Saïd, Saddek, Goureau, Olivier, Sahel, José-Alain, Zeitz, Christina, Audo, Isabelle
Published in American journal of human genetics (03.04.2014)
Published in American journal of human genetics (03.04.2014)
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