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Isabelle Meunier

Showing results (21-30 of 148) with videos related to

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ISRN Ophthalmology|February 25, 2014
Association of reticular pseudodrusen and early onset drusenFlore De Bats, Benjamin Wolff, Martine Mauget-Faÿsse, et al.
Plos One|October 22, 2014
Inhibition of influenza virus replication by targeting broad host cell pathwaysIsabelle Marois, Alexandre Cloutier, Isabelle Meunier, et al.
JAMA Ophthalmology|August 10, 2013
Early-onset foveal involvement in retinitis punctata albescens with mutations in RLBP1Elodie Dessalces, Béatrice Bocquet, Jérôme Bourien, et al.
Stem Cell Research|March 6, 2022
Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosaCarla Sanjurjo-Soriano, Nejla Erkilic, Christel Vache, et al.
Stem Cell Research|November 20, 2018
Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosaCarla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, et al.
Stem Cell Research|November 24, 2018
Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2Carla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 26, 2024
Crossed VEP asymmetry in a patient with AHR-linked infantile nystagmus and foveal hypoplasiaVasily M Smirnov, Eulalie Lasseaux, Vincent Michaud, et al.
Retinal Cases & Brief Reports|May 21, 2016
LEBER CONGENITAL AMAUROSIS WITH LARGE RETINAL PIGMENT CLUMPS CAUSED BY COMPOUND HETEROZYGOUS MUTATIONS IN KCNJ13Sarah Perez-Roustit, Virginie Marquette, Béatrice Bocquet, et al.
Stem Cell Research|June 28, 2019
Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosisNejla Erkilic, Carla Sanjurjo-Soriano, Gaël Manes, et al.
Molecular Vision|December 17, 2013
Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutationsBéatrice Bocquet, Nour Al Dain Marzouka, Maxime Hebrard, et al.
Pageof 15

Showing results (21-30 of 148) with videos related to

Sort By:
Pageof 15
ISRN Ophthalmology|February 25, 2014
Association of reticular pseudodrusen and early onset drusenFlore De Bats, Benjamin Wolff, Martine Mauget-Faÿsse, et al.
Plos One|October 22, 2014
Inhibition of influenza virus replication by targeting broad host cell pathwaysIsabelle Marois, Alexandre Cloutier, Isabelle Meunier, et al.
JAMA Ophthalmology|August 10, 2013
Early-onset foveal involvement in retinitis punctata albescens with mutations in RLBP1Elodie Dessalces, Béatrice Bocquet, Jérôme Bourien, et al.
Stem Cell Research|March 6, 2022
Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosaCarla Sanjurjo-Soriano, Nejla Erkilic, Christel Vache, et al.
Stem Cell Research|November 20, 2018
Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosaCarla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, et al.
Stem Cell Research|November 24, 2018
Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2Carla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 26, 2024
Crossed VEP asymmetry in a patient with AHR-linked infantile nystagmus and foveal hypoplasiaVasily M Smirnov, Eulalie Lasseaux, Vincent Michaud, et al.
Retinal Cases & Brief Reports|May 21, 2016
LEBER CONGENITAL AMAUROSIS WITH LARGE RETINAL PIGMENT CLUMPS CAUSED BY COMPOUND HETEROZYGOUS MUTATIONS IN KCNJ13Sarah Perez-Roustit, Virginie Marquette, Béatrice Bocquet, et al.
Stem Cell Research|June 28, 2019
Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosisNejla Erkilic, Carla Sanjurjo-Soriano, Gaël Manes, et al.
Molecular Vision|December 17, 2013
Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutationsBéatrice Bocquet, Nour Al Dain Marzouka, Maxime Hebrard, et al.
Pageof 15