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Molecular Vision|February 5, 2011
Phenotypic variability in a French family with a novel mutation in the BEST1 gene causing multifocal best vitelliform macular dystrophyEmmanuelle Lacassagne, Aurore Dhuez, Florence Rigaudière, et al.
Molecular Therapy. Methods & Clinical Development|November 19, 2025
Transcriptional changes in non-human primate tissues after intrathecal delivery of serotype 9 adeno-associated viral vector: Insights into organ toxicitiesFumiaki Aihara, Matthew Mardo, Vera Ruda, et al.
Investigative Ophthalmology & Visual Science|May 2, 2009
Sirt1 involvement in rd10 mouse retinal degenerationCarolina Jaliffa, Ilhame Ameqrane, Anouk Dansault, et al.
Stroke|November 3, 2007
Novel mouse model of monocular amaurosis fugaxDominique Claude Lelong, Ivan Bieche, Elodie Perez, et al.
Cell Death & Disease|February 21, 2018
Light action spectrum on oxidative stress and mitochondrial damage in A2E-loaded retinal pigment epithelium cellsMélanie Marie, Karine Bigot, Claire Angebault, et al.
International Journal of Molecular Sciences|November 11, 2022
Neuroprotective Effects of Transferrin in Experimental Glaucoma ModelsJenny Youale, Karine Bigot, Bindu Kodati, et al.
Plos One|September 24, 2013
Phototoxic action spectrum on a retinal pigment epithelium model of age-related macular degeneration exposed to sunlight normalized conditionsEmilie Arnault, Coralie Barrau, Céline Nanteau, et al.
Molecular Therapy. Nucleic Acids|January 25, 2013
AON-mediated Exon Skipping Restores Ciliation in Fibroblasts Harboring the Common Leber Congenital Amaurosis CEP290 MutationXavier Gerard, Isabelle Perrault, Sylvain Hanein, et al.
Cell Death & Disease|October 6, 2025
Transferrin is a drug candidate for the treatment of dry age-related macular degeneration (AMD)Jenny Youale, Karine Bigot, Thara Jaworski, et al.
Neurobiology of Aging|July 28, 2016
Longitudinal noninvasive magnetic resonance imaging of brain microhemorrhages in BACE inhibitor-treated APP transgenic miceNicolau Beckmann, Arno Doelemeyer, Stefan Zurbruegg, et al.
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