Guiding Lights in Genome Editing for Inherited Retinal Disorders: Implications for Gene and Cell Therapy

por Sanjurjo-Soriano, Carla, Kalatzis, Vasiliki
Publicado 2018

Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3

por Diakatou, Michalitsa, Dubois, Gregor, Erkilic, Nejla, Sanjurjo-Soriano, Carla, Meunier, Isabelle, Kalatzis, Vasiliki
Publicado 2021

Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles

por Sanjurjo-Soriano, Carla, Erkilic, Nejla, Baux, David, Mamaeva, Daria, Hamel, Christian P., Meunier, Isabelle, Roux, Anne-Françoise, Kalatzis, Vasiliki
Publicado 2019

USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids

por Sanjurjo-Soriano, Carla, Jimenez-Medina, Carla, Erkilic, Nejla, Cappellino, Luisina, Lefevre, Arnaud, Nagel-Wolfrum, Kerstin, Wolfrum, Uwe, Van Wijk, Erwin, Roux, Anne-Françoise, Meunier, Isabelle, Kalatzis, Vasiliki
Publicado 2023

Retinoic acid delays initial photoreceptor differentiation and results in a highly structured mature retinal organoid

por Sanjurjo-Soriano, Carla, Erkilic, Nejla, Damodar, Krishna, Boukhaddaoui, Hassan, Diakatou, Michalitsa, Garita-Hernandez, Marcela, Mamaeva, Daria, Dubois, Gregor, Jazouli, Zhour, Jimenez-Medina, Carla, Goureau, Olivier, Meunier, Isabelle, Kalatzis, Vasiliki
Publicado 2022

A Novel Chromosomal Translocation Identified due to Complex Genetic Instability in iPSC Generated for Choroideremia

por Erkilic, Nejla, Gatinois, Vincent, Torriano, Simona, Bouret, Pauline, Sanjurjo-Soriano, Carla, De Luca, Valerie, Damodar, Krishna, Cereso, Nicolas, Puechberty, Jacques, Sanchez-Alcudia, Rocio, Hamel, Christian P., Ayuso, Carmen, Meunier, Isabelle, Pellestor, Franck, Kalatzis, Vasiliki
Publicado 2019