Unravelling the networks dictating host resistance versus tolerance during pulmonary infections

por Meunier, Isabelle, Kaufmann, Eva, Downey, Jeffrey, Divangahi, Maziar
Publicado 2017

Genome Editing as a Treatment for the Most Prevalent Causative Genes of Autosomal Dominant Retinitis Pigmentosa

por Diakatou, Michalitsa, Manes, Gaël, Bocquet, Beatrice, Meunier, Isabelle, Kalatzis, Vasiliki
Publicado 2019

Deep learning model for automatic differentiation of EMAP from AMD in macular atrophy

por Chouraqui, Maxime, Crincoli, Emanuele, Miere, Alexandra, Meunier, Isabelle Anne, Souied, Eric H.
Publicado 2023

Infection with a Mouse-Adapted Strain of the 2009 Pandemic Virus Causes a Highly Severe Disease Associated with an Impaired T Cell Response

por Meunier, Isabelle, Morisseau, Olivier, Garneau, Émilie, Marois, Isabelle, Cloutier, Alexandre, Richter, Martin V.
Publicado 2015

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

Quantification of the early pupillary dilation kinetic to assess rod and cone activity

por Kostic, Corinne, Crippa, Sylvain V., Leon, Lorette, Hamel, Christian, Meunier, Isabelle, Kawasaki, Aki
Publicado 2021

Association of Reticular Pseudodrusen and Early Onset Drusen

por De Bats, Flore, Wolff, Benjamin, Mauget-Faÿsse, Martine, Meunier, Isabelle, Denis, Philippe, Kodjikian, Laurent
Publicado 2013

Inhibition of Influenza Virus Replication by Targeting Broad Host Cell Pathways

por Marois, Isabelle, Cloutier, Alexandre, Meunier, Isabelle, Weingartl, Hana M., Cantin, André M., Richter, Martin V.
Publicado 2014

Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutations

por Bocquet, Béatrice, Marzouka, Nour al Dain, Hebrard, Maxime, Manes, Gaël, Sénéchal, Audrey, Meunier, Isabelle, Hamel, Christian P.
Publicado 2013

Type I IFN Triggers RIG-I/TLR3/NLRP3-dependent Inflammasome Activation in Influenza A Virus Infected Cells

por Pothlichet, Julien, Meunier, Isabelle, Davis, Beckley K., Ting, Jenny P-Y., Skamene, Emil, von Messling, Veronika, Vidal, Silvia M.
Publicado 2013

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

Novel splice-site mutation in TTLL5 causes cone dystrophy in a consanguineous family

por Dias, Miguel de Sousa, Hamel, Christian P., Meunier, Isabelle, Varin, Juliette, Blanchard, Steven, Boyard, Fiona, Sahel, José-Alain, Zeitz, Christina
Publicado 2017

Cone dystrophy or macular dystrophy associated with novel autosomal dominant GUCA1A mutations

por Manes, Gaël, Mamouni, Sonia, Hérald, Emilie, Richard, Anne-Claire, Sénéchal, Audrey, Aouad, Karim, Bocquet, Béatrice, Meunier, Isabelle, Hamel, Christian P.
Publicado 2017

A ROD–CONE DYSTROPHY IS SYSTEMATICALLY ASSOCIATED TO THE RTN4IP1 RECESSIVE OPTIC ATROPHY

por Meunier, Isabelle, Bocquet, Béatrice, Charif, Majida, Dhaenens, Claire-Marie, Manes, Gael, Amati-Bonneau, Patrizia, Roubertie, Agathe, Zanlonghi, Xavier, Lenaers, Guy
Publicado 2021

A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1

por Manes, Gaël, Hebrard, Maxime, Bocquet, Béatrice, Meunier, Isabelle, Coustes-Chazalette, Delphine, Sénéchal, Audrey, Bolland-Augé, Anne, Zelenika, Diana, Hamel, Christian P
Publicado 2011

The effect of PTC124 on choroideremia fibroblasts and iPSC-derived RPE raises considerations for therapy

por Torriano, Simona, Erkilic, Nejla, Baux, David, Cereso, Nicolas, De Luca, Valerie, Meunier, Isabelle, Moosajee, Mariya, Roux, Anne-Francoise, Hamel, Christian P., Kalatzis, Vasiliki
Publicado 2018

Casitas B-lineage lymphoma Gene Mutation Ocular Phenotype

por Fardeau, Christine, Alafaleq, Munirah, Ferchaud, Marie-Adélaïde, Hié, Miguel, Besnard, Caroline, Meynier, Sonia, Rieux-Laucat, Frédéric, Roos-Weil, Damien, Cohen, Fleur, Meunier, Isabelle
Publicado 2022

RIPK3 interacts with MAVS to regulate type I IFN-mediated immunity to Influenza A virus infection

por Downey, Jeffrey, Pernet, Erwan, Coulombe, François, Allard, Benoit, Meunier, Isabelle, Jaworska, Joanna, Qureshi, Salman, Vinh, Donald C., Martin, James G., Joubert, Philippe, Divangahi, Maziar
Publicado 2017

Clinical and functional analyses of AIPL1 variants reveal mechanisms of pathogenicity linked to different forms of retinal degeneration

por Sacristan-Reviriego, Almudena, Le, Hoang Mai, Georgiou, Michalis, Meunier, Isabelle, Bocquet, Beatrice, Roux, Anne-Françoise, Prodromou, Chrisostomos, Bainbridge, James, Michaelides, Michel, van der Spuy, Jacqueline
Publicado 2020

A 4.6 Mb Inversion Leading to PCDH15-LINC00844 and BICC1-PCDH15 Fusion Transcripts as a New Pathogenic Mechanism Implicated in Usher Syndrome Type 1

por Vaché, Christel, Puechberty, Jacques, Faugère, Valérie, Darmaisin, Floriane, Liquori, Alessandro, Baux, David, Blanchet, Catherine, Garcia-Garcia, Gema, Meunier, Isabelle, Pellestor, Franck, Koenig, Michel, Roux, Anne-Françoise
Publicado 2020