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Human Gene Therapy|October 15, 2009
Adeno-associated virus-mediated rhodopsin replacement provides therapeutic benefit in mice with a targeted disruption of the rhodopsin geneArpad Palfi, Sophia Millington-Ward, Naomi Chadderton, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 13, 2011
Suppression and replacement gene therapy for autosomal dominant disease in a murine model of dominant retinitis pigmentosaSophia Millington-Ward, Naomi Chadderton, Mary O'Reilly, et al.
Scientific Reports|August 17, 2016
microRNA regulatory circuits in a mouse model of inherited retinal degenerationArpad Palfi, Karsten Hokamp, Stefanie M Hauck, 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.
European Journal of Human Genetics : EJHG|June 7, 2012
Intravitreal delivery of AAV-NDI1 provides functional benefit in a murine model of Leber hereditary optic neuropathyNaomi Chadderton, Arpad Palfi, Sophia Millington-Ward, et al.
Stem Cell Reports|June 13, 2020
Modeling and Rescue of RP2 Retinitis Pigmentosa Using iPSC-Derived Retinal OrganoidsAmelia Lane, Katarina Jovanovic, Ciara Shortall, 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.
Developmental Cell|August 17, 2013
CHD5 is required for neurogenesis and has a dual role in facilitating gene expression and polycomb gene repressionChris M Egan, Ulrika Nyman, Julie Skotte, et al.
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