Function of the Retinal Pigment Epithelium in Patients With Neurofibromatosis Type 1

por Touzé, Romain, Abitbol, Marc M., Bremond-Gignac, Dominique, Robert, Matthieu P.
Publicado 2022

Nestin contributes to laser choroidal and retinal neovascularization

por Miloudi, Sofiane, Valensi, Maud, El Sanharawi, Mohamed, Abitbol, Marc M., Behar-Cohen, Francine, Versaux-Botteri, Claudine
Publicado 2022

ATM localization and gene expression in the adult mouse eye

por Leemput, Julia, Masson, Christel, Bigot, Karine, Errachid, Abdelmounaim, Dansault, Anouk, Provost, Alexandra, Gadin, Stéphanie, Aoufouchi, Said, Menasche, Maurice, Abitbol, Marc
Publicado 2009

Expression of 8-oxoguanine DNA glycosylase (Ogg1) in mouse retina

por Bigot, Karine, Leemput, Julia, Vacher, Monique, Campalans, Anna, Radicella, J. Pablo, Lacassagne, Emmanuelle, Provost, Alexandra, Masson, Christel, Menasche, Maurice, Abitbol, Marc
Publicado 2009

Phenotypic variability in a French family with a novel mutation in the BEST1 gene causing multifocal best vitelliform macular dystrophy

por Lacassagne, Emmanuelle, Dhuez, Aurore, Rigaudière, Florence, Dansault, Anouk, Vêtu, Christelle, Bigot, Karine, Vieira, Véronique, Puech, Bernard, Defoort-Dhellemmes, Sabine, Abitbol, Marc
Publicado 2011

Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report

por de la Houssaye, Guillaume, Bieche, Ivan, Roche, Olivier, Vieira, Véronique, Laurendeau, Ingrid, Arbogast, Laurence, Zeghidi, Hatem, Rapp, Philippe, Halimi, Philippe, Vidaud, Michel, Dufier, Jean-Louis, Menasche, Maurice, Abitbol, Marc
Publicado 2006

CX(3)CR1(+) CD115(+) CD135(+) common macrophage/DC precursors and the role of CX(3)CR1 in their response to inflammation

por Auffray, Cedric, Fogg, Darin K., Narni-Mancinelli, Emilie, Senechal, Brigitte, Trouillet, Celine, Saederup, Noah, Leemput, Julia, Bigot, Karine, Campisi, Laura, Abitbol, Marc, Molina, Thierry, Charo, Israel, Hume, David A., Cumano, Ana, Lauvau, Gregoire, Geissmann, Frederic
Publicado 2009

Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics

por Dinet, Virginie, Ciccotosto, Giuseppe D., Delaunay, Kimberley, Borras, Céline, Ranchon-Cole, Isabelle, Kostic, Corinne, Savoldelli, Michèle, El Sanharawi, Mohamed, Jonet, Laurent, Pirou, Caroline, An, Na, Abitbol, Marc, Arsenijevic, Yvan, Behar-Cohen, Francine, Cappai, Roberto, Mascarelli, Frédéric
Publicado 2016

Eight previously unidentified mutations found in the OA1 ocular albinism gene

por Mayeur, Hélène, Roche, Olivier, Vêtu, Christelle, Jaliffa, Carolina, Marchant, Dominique, Dollfus, Hélène, Bonneau, Dominique, Munier, Francis L, Schorderet, Daniel F, Levin, Alex V, Héon, Elise, Sutherland, Joanne, Lacombe, Didier, Said, Edith, Mezer, Eedy, Kaplan, Josseline, Dufier, Jean-Louis, Marsac, Cécile, Menasche, Maurice, Abitbol, Marc
Publicado 2006

Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities

por Dansault, Anouk, David, Gabriel, Schwartz, Claire, Jaliffa, Carolina, Vieira, Véronique, de la Houssaye, Guillaume, Bigot, Karine, Catin, Françise, Tattu, Laurent, Chopin, Catherine, Halimi, Philippe, Roche, Olivier, Van Regemorter, Nicole, Munier, Francis, Schorderet, Daniel, Dufier, Jean-Louis, Marsac, Cécile, Ricquier, Daniel, Menasche, Maurice, Penfornis, Alfred, Abitbol, Marc
Publicado 2007

A novel antiangiogenic and vascular normalization therapy targeted against human CD160 receptor

por Chabot, Sophie, Jabrane-Ferrat, Nabila, Bigot, Karine, Tabiasco, Julie, Provost, Alexandra, Golzio, Muriel, Noman, Muhammad Zaeem, Giustiniani, Jérôme, Bellard, Elisabeth, Brayer, Stéphanie, Aguerre-Girr, Maryse, Meggetto, Fabienne, Giuriato, Sylvie, Malecaze, François, Galiacy, Stéphane, Jaïs, Jean-Philippe, Chose, Olivier, Kadouche, Jean, Chouaib, Salem, Teissié, Justin, Abitbol, Marc, Bensussan, Armand, Le Bouteiller, Philippe
Publicado 2011