The Signalling Role of the αvβ5-Integrin Can Impact the Efficacy of AAV in Retinal Gene Therapy

por Cronin, Therese, Chung, Daniel C., Yang, Ying, Nandrot, Emeline F., Bennett, Jean
Publicado 2012

Lack of the antioxidant enzyme methionine sulfoxide reductase A in mice impairs RPE phagocytosis and causes photoreceptor cone dysfunction

por Mazzoni, Francesca, Dun, Ying, Vargas, Jade A., Nandrot, Emeline F., Finnemann, Silvia C.
Publicado 2021

Loss of Synchronized Retinal Phagocytosis and Age-related Blindness in Mice Lacking αvβ5 Integrin

por Nandrot, Emeline F., Kim, Yoonhee, Brodie, Scott E., Huang, Xiaozhu, Sheppard, Dean, Finnemann, Silvia C.
Publicado 2004

Pleiotropic Roles of Scavenger Receptors in Circadian Retinal Phagocytosis: A New Function for Lysosomal SR-B2/LIMP-2 at the RPE Cell Surface

por Rieu, Quentin, Bougoüin, Antoine, Zagar, Yvrick, Chatagnon, Jonathan, Hamieh, Abdallah, Enderlin, Julie, Huby, Thierry, Nandrot, Emeline F.
Publicado 2022

Preclinical safety studies of human embryonic stem cell‐derived retinal pigment epithelial cells for the treatment of age‐related macular degeneration

por Petrus‐Reurer, Sandra, Kumar, Pankaj, Padrell Sánchez, Sara, Aronsson, Monica, André, Helder, Bartuma, Hammurabi, Plaza Reyes, Alvaro, Nandrot, Emeline F., Kvanta, Anders, Lanner, Fredrik
Publicado 2020

A Splice Variant in SLC16A8 Gene Leads to Lactate Transport Deficit in Human iPS Cell-Derived Retinal Pigment Epithelial Cells

por Klipfel, Laurence, Cordonnier, Marie, Thiébault, Léa, Clérin, Emmanuelle, Blond, Frédéric, Millet-Puel, Géraldine, Mohand-Saïd, Saddek, Goureau, Olivier, Sahel, José-Alain, Nandrot, Emeline F., Léveillard, Thierry
Publicado 2021

Chronic exposure to tumor necrosis factor alpha induces retinal pigment epithelium cell dedifferentiation

por Touhami, Sara, Beguier, Fanny, Augustin, Sébastien, Charles-Messance, Hugo, Vignaud, Lucile, Nandrot, Emeline F., Reichman, Sacha, Forster, Valérie, Mathis, Thibaud, Sahel, José-Alain, Bodaghi, Bahram, Guillonneau, Xavier, Sennlaub, Florian
Publicado 2018

Disease-Causing Mutations in BEST1 Gene Are Associated with Altered Sorting of Bestrophin-1 Protein

por Doumanov, Jordan A., Zeitz, Christina, Gimenez, Paloma Dominguez, Audo, Isabelle, Krishna, Abhay, Alfano, Giovanna, Diaz, Maria Luz Bellido, Moskova-Doumanova, Veselina, Lancelot, Marie-Elise, Sahel, José-Alain, Nandrot, Emeline F., Bhattacharya, Shomi S.
Publicado 2013

Identification of cell surface markers and establishment of monolayer differentiation to retinal pigment epithelial cells

por Plaza Reyes, Alvaro, Petrus-Reurer, Sandra, Padrell Sánchez, Sara, Kumar, Pankaj, Douagi, Iyadh, Bartuma, Hammurabi, Aronsson, Monica, Westman, Sofie, Lardner, Emma, André, Helder, Falk, Anna, Nandrot, Emeline F., Kvanta, Anders, Lanner, Fredrik
Publicado 2020

Publisher Correction: Identification of cell surface markers and establishment of monolayer differentiation to retinal pigment epithelial cells

por Reyes, Alvaro Plaza, Petrus-Reurer, Sandra, Sánchez, Sara Padrell, Kumar, Pankaj, Douagi, Iyadh, Bartuma, Hammurabi, Aronsson, Monica, Westman, Sofie, Lardner, Emma, André, Helder, Falk, Anna, Nandrot, Emeline F., Kvanta, Anders, Lanner, Fredrik
Publicado 2020

Publisher Correction: Identification of cell surface markers and establishment of monolayer differentiation to retinal pigment epithelial cells

por Reyes, Alvaro Plaza, Petrus-Reurer, Sandra, Sánchez, Sara Padrell, Kumar, Pankaj, Douagi, Iyadh, Bartuma, Hammurabi, Aronsson, Monica, Westman, Sofie, Lardner, Emma, André, Helder, Falk, Anna, Nandrot, Emeline F., Kvanta, Anders, Lanner, Fredrik
Publicado 2020

Otx2-Genetically Modified Retinal Pigment Epithelial Cells Rescue Photoreceptors after Transplantation

por Kole, Christo, Klipfel, Laurence, Yang, Ying, Ferracane, Vanessa, Blond, Frederic, Reichman, Sacha, Millet-Puel, Géraldine, Clérin, Emmanuelle, Aït-Ali, Najate, Pagan, Delphine, Camara, Hawa, Delyfer, Marie-Noëlle, Nandrot, Emeline F., Sahel, Jose-Alain, Goureau, Olivier, Léveillard, Thierry
Publicado 2018

Modeling PRPF31 retinitis pigmentosa using retinal pigment epithelium and organoids combined with gene augmentation rescue

por Rodrigues, Amélie, Slembrouck-Brec, Amélie, Nanteau, Céline, Terray, Angélique, Tymoshenko, Yelyzaveta, Zagar, Yvrick, Reichman, Sacha, Xi, Zhouhuan, Sahel, José-Alain, Fouquet, Stéphane, Orieux, Gael, Nandrot, Emeline F., Byrne, Leah C., Audo, Isabelle, Roger, Jérôme E., Goureau, Olivier
Publicado 2022

Cohen Syndrome-Associated Cataract Is Explained by VPS13B Functions in Lens Homeostasis and Is Modified by Additional Genetic Factors

por Lhussiez, Vincent, Dubus, Elisabeth, Cesar, Quénol, Acar, Niyazi, Nandrot, Emeline F., Simonutti, Manuel, Audo, Isabelle, Lizé, Eléonore, Nguyen, Sylvie, Geissler, Audrey, Bouchot, André, Ansar, Muhammad, Picaud, Serge, Thauvin-Robinet, Christel, Olivier-Faivre, Laurence, Duplomb, Laurence, Da Costa, Romain
Publicado 2020

CCR2(+) monocytes infiltrate atrophic lesions in age-related macular disease and mediate photoreceptor degeneration in experimental subretinal inflammation in Cx3cr1 deficient mice

por Sennlaub, Florian, Auvynet, Constance, Calippe, Bertrand, Lavalette, Sophie, Poupel, Lucie, Hu, Shulong J, Dominguez, Elisa, Camelo, Serge, Levy, Olivier, Guyon, Elodie, Saederup, Noah, Charo, Israel F, Van Rooijen, Nico, Nandrot, Emeline, Bourges, Jean-Louis, Behar-Cohen, Francine, Sahel, José-Alain, Guillonneau, Xavier, Raoul, William, Combadiere, Christophe
Publicado 2013

Cystoid maculopathy is a frequent feature of Cohen syndrome-associated retinopathy

por Gabrielle, Pierre-Henry, Faivre, Laurence, Audo, Isabelle, Zanlonghi, Xavier, Dollfus, Hélène, Thiadens, Alberta A. H. J., Zeitz, Christina, Mancini, Grazia M. S., Perdomo, Yaumara, Mohand-Saïd, Saddek, Lizé, Eléonore, Lhussiez, Vincent, Nandrot, Emeline F., Acar, Niyazi, Creuzot-Garcher, Catherine, Sahel, José-Alain, Ansar, Muhammad, Thauvin-Robinet, Christel, Duplomb, Laurence, Da Costa, Romain
Publicado 2021