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Advances in Experimental Medicine and Biology|February 10, 2025
The Challenge of VUS in Inherited Retinal Degeneration: Insight from Functional StudiesLaura K Finnegan, Anna R Ridgeway, Naomi Chadderton, et al.Journal of Glaucoma|July 4, 2017
lncRNAs, DNA Methylation, and the Pathobiology of Exfoliation GlaucomaWilliam M Johnson, Laura K Finnegan, Michael A Hauser, et al.International Journal of Molecular Sciences|February 15, 2022
SARM1 Ablation Is Protective and Preserves Spatial Vision in an In Vivo Mouse Model of Retinal Ganglion Cell DegenerationLaura K Finnegan, Naomi Chadderton, Paul F Kenna, et al.Scientific Reports|October 6, 2020
Novel 199 base pair NEFH promoter drives expression in retinal ganglion cellsSophia Millington-Ward, Naomi Chadderton, Megan Berkeley, et al.Genes|June 26, 2026
First Exonic Cryptic Branchpoint Variant in an Inherited Retinal Degeneration Detected in an Irish <i>RPGR</i> Pedigree with X-Linked Retinitis PigmentosaElla Kopčić, Laura Whelan, Ciara Shortall, et al.International Journal of Molecular Sciences|February 25, 2023
RPE-Directed Gene Therapy Improves Mitochondrial Function in Murine Dry AMD ModelsSophia Millington-Ward, Naomi Chadderton, Laura K Finnegan, et al.International Journal of Molecular Sciences|August 29, 2024
AAV-NDI1 Therapy Provides Significant Benefit to Murine and Cellular Models of GlaucomaSophia Millington-Ward, Arpad Palfi, Ciara Shortall, et al.Pharmaceutics|February 25, 2023
Optimisation of AAV-NDI1 Significantly Enhances Its Therapeutic Value for Correcting Retinal Mitochondrial DysfunctionNaomi Chadderton, Arpad Palfi, Daniel M Maloney, et al.Genes|January 25, 2025
Novel Splice-Altering Variants in the <i>CHM</i> and <i>CACNA1F</i> Genes Causative of X-Linked Choroideremia and Cone DystrophyAnna R Ridgeway, Ciara Shortall, Laura K Finnegan, et al.Genetics in Medicine Open|July 6, 2026
The landscape of variants in pre-mRNA-processing factor genes in an Irish cohortLaura K Finnegan, Anna R Ridgeway, Matthew Carrigan, et al.Pageof 1