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Molecular Therapy. Methods & Clinical Development|April 27, 2019
CRISPR Activation Enhances In Vitro Potency of AAV Vectors Driven by Tissue-Specific PromotersDevin S McDougald, Thu T Duong, Katherine C Palozola, et al.Nature Communications|June 14, 2022
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disordersXinyuan Zhang, Anastasia M Lucas, Yogasudha Veturi, et al.Molecular Therapy. Methods & Clinical Development|June 4, 2016
Corrigendum to "Efficient gene delivery to photoreceptors using AAV2/rh10 and rescue of the Rho-/- mouse"Arpad Palfi, Naomi Chadderton, Mary O'Reilly, et al.Molecular Therapy. Methods & Clinical Development|June 2, 2015
Efficient gene delivery to photoreceptors using AAV2/rh10 and rescue of the Rho(-/-) mouseArpad Palfi, Naomi Chadderton, Mary O'Reilly, et al.Experimental Eye Research|August 25, 2004
Light damage induced changes in mouse retinal gene expressionLin Chen, Wayne Wu, Tzvete Dentchev, et al.Human Gene Therapy|March 12, 2005
Long-term inducible gene expression in the eye via adeno-associated virus gene transfer in nonhuman primatesCorinna Lebherz, Alberto Auricchio, Albert M Maguire, et al.Ophthalmic Genetics|March 17, 2021
Bardet-Biedl syndrome-7 (BBS7) shows treatment potential and a cone-rod dystrophy phenotype that recapitulates the non-human primate modelTomas S Aleman, Erin C O'Neil, Keli O'Connor, et al.Current Eye Research|March 15, 2005
Adeno-associated viruses containing bFGF or BDNF are neuroprotective against excitotoxicityFrank Schuettauf, Christian Vorwerk, Rita Naskar, et al.Molecular Therapy. Methods & Clinical Development|October 30, 2019
Safety of Same-Eye Subretinal Sequential Readministration of AAV2-hRPE65v2 in Non-human PrimatesLindsey Weed, Michael J Ammar, Shangzhen Zhou, et al.Clinical & Experimental Ophthalmology|July 12, 2017
Novel mobility test to assess functional vision in patients with inherited retinal dystrophiesDaniel C Chung, Sarah McCague, Zi-Fan Yu, et al.Pageof 20