Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Isabelle Audo

Showing results (101-110 of 234) with videos related to

Pageof 24
Sort By:
Stem Cell Research|September 18, 2024
Generation of human induced pluripotent stem cell lines from a subject with UBAP1L-associated retinal dystrophy and CRISPR/cas9-corrected isogenic iPSC linesAndréa Amprou, Tasnim Ben Yacoub, Camille Letellier, et al.
Journal of Patient-Reported Outcomes|July 19, 2023
Qualitative exploration of the visual function impairments and impacts on vision-dependent activities of daily living in Retinitis Pigmentosa and Leber Congenital Amaurosis: content validation of the ViSIO-PRO and ViSIO-ObsRO measuresChristine Kay, Isabelle Audo, Christel Naujoks, et al.
International Journal of Molecular Sciences|January 8, 2023
Mice Lacking <i>Gpr179</i> with Complete Congenital Stationary Night Blindness Are a Good Model for MyopiaBaptiste Wilmet, Jacques Callebert, Robert Duvoisin, et al.
JAMA Ophthalmology|April 19, 2019
Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6BSamer Khateb, Marco Nassisi, Kinga M Bujakowska, et al.
Plos One|May 27, 2015
Genotypic and phenotypic characterization of P23H line 1 rat modelElise Orhan, Deniz Dalkara, Marion Neuillé, et al.
European Journal of Ophthalmology|October 31, 2018
A novel missense mutation of <i>GJA8</i> causes congenital cataract in a large Mauritanian familyMouna Hadrami, Crystel Bonnet, Fatimetou Veten, et al.
Investigative Ophthalmology & Visual Science|March 16, 2022
The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A GeneDavid G Birch, Lassana Samarakoon, Michele Melia, et al.
Investigative Ophthalmology & Visual Science|November 14, 2013
Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindnessElise Orhan, Laurent Prézeau, Said El Shamieh, et al.
Transactions of the American Ophthalmological Society|January 28, 2003
Toxicity and dose-response studies of 1 alpha-hydroxyvitamin D2 in LH beta-Tag transgenic miceDaniel G Dawson, Joel Gleiser, Michele L Zimbric, et al.
International Journal of Molecular Sciences|October 13, 2021
Characteristics of Retinitis Pigmentosa Associated with <i>ADGRV1</i> and Comparison with <i>USH2A</i> in Patients from a Multicentric Usher Syndrome Study TreatrushAna Fakin, Crystel Bonnet, Anne Kurtenbach, et al.
Pageof 24

Showing results (101-110 of 234) with videos related to

Sort By:
Pageof 24
Stem Cell Research|September 18, 2024
Generation of human induced pluripotent stem cell lines from a subject with UBAP1L-associated retinal dystrophy and CRISPR/cas9-corrected isogenic iPSC linesAndréa Amprou, Tasnim Ben Yacoub, Camille Letellier, et al.
Journal of Patient-Reported Outcomes|July 19, 2023
Qualitative exploration of the visual function impairments and impacts on vision-dependent activities of daily living in Retinitis Pigmentosa and Leber Congenital Amaurosis: content validation of the ViSIO-PRO and ViSIO-ObsRO measuresChristine Kay, Isabelle Audo, Christel Naujoks, et al.
International Journal of Molecular Sciences|January 8, 2023
Mice Lacking <i>Gpr179</i> with Complete Congenital Stationary Night Blindness Are a Good Model for MyopiaBaptiste Wilmet, Jacques Callebert, Robert Duvoisin, et al.
JAMA Ophthalmology|April 19, 2019
Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6BSamer Khateb, Marco Nassisi, Kinga M Bujakowska, et al.
Plos One|May 27, 2015
Genotypic and phenotypic characterization of P23H line 1 rat modelElise Orhan, Deniz Dalkara, Marion Neuillé, et al.
European Journal of Ophthalmology|October 31, 2018
A novel missense mutation of <i>GJA8</i> causes congenital cataract in a large Mauritanian familyMouna Hadrami, Crystel Bonnet, Fatimetou Veten, et al.
Investigative Ophthalmology & Visual Science|March 16, 2022
The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A GeneDavid G Birch, Lassana Samarakoon, Michele Melia, et al.
Investigative Ophthalmology & Visual Science|November 14, 2013
Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindnessElise Orhan, Laurent Prézeau, Said El Shamieh, et al.
Transactions of the American Ophthalmological Society|January 28, 2003
Toxicity and dose-response studies of 1 alpha-hydroxyvitamin D2 in LH beta-Tag transgenic miceDaniel G Dawson, Joel Gleiser, Michele L Zimbric, et al.
International Journal of Molecular Sciences|October 13, 2021
Characteristics of Retinitis Pigmentosa Associated with <i>ADGRV1</i> and Comparison with <i>USH2A</i> in Patients from a Multicentric Usher Syndrome Study TreatrushAna Fakin, Crystel Bonnet, Anne Kurtenbach, et al.
Pageof 24