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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.
Genes|December 2, 2020
Properties and Therapeutic Implications of an Enigmatic D477G RPE65 Variant Associated with Autosomal Dominant Retinitis PigmentosaAnna-Sophia Kiang, Paul F Kenna, Marian M Humphries, et al.
Case Reports in Ophthalmology|January 6, 2023
MFRP-Associated Retinopathy and Nanophthalmos in Two Irish Probands: A Case ReportAnn O'Connell, Julia Zhu, Kirk A J Stephenson, et al.
Advances in Experimental Medicine and Biology|March 19, 2010
Protection of photoreceptors in a mouse model of RP10Lawrence C S Tam, Anna-Sophia Kiang, Naomi Chadderton, et al.
Human Molecular Genetics|September 7, 2010
Prevention of autosomal dominant retinitis pigmentosa by systemic drug therapy targeting heat shock protein 90 (Hsp90)Lawrence C S Tam, Anna-Sophia Kiang, Matthew Campbell, et al.
Human Molecular Genetics|September 10, 2002
Validation in mesenchymal progenitor cells of a mutation-independent ex vivo approach to gene therapy for osteogenesis imperfectaSophia Millington-Ward, Carolina Allers, Gearóid Tuohy, et al.
International Journal of Molecular Sciences|January 21, 2022
Clinical and Genetic Re-Evaluation of Inherited Retinal Degeneration Pedigrees following Initial Negative Findings on Panel-Based Next Generation SequencingKirk A J Stephenson, Julia Zhu, Adrian Dockery, et al.
European Journal of Human Genetics : EJHG|July 9, 2004
RNAi of COL1A1 in mesenchymal progenitor cellsSophia Millington-Ward, Helena P McMahon, Danny Allen, et al.
Vision Research|October 9, 2007
A transgenic mouse model for gene therapy of rhodopsin-linked Retinitis PigmentosaMary O'Reilly, Sophia Millington-Ward, Arpad Palfi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 29, 2009
Improved retinal function in a mouse model of dominant retinitis pigmentosa following AAV-delivered gene therapyNaomi Chadderton, Sophia Millington-Ward, Arpad Palfi, et al.
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