Showing results (161-170 of 386) with videos related to

Sort By:
Pageof 39
Frontiers in Neuroscience|April 13, 2023
Comparison of different gene-therapy methods to treat Leber hereditary optic neuropathy in a mouse modelSindhu Velmurugan, Tsung-Han Chou, Jeremy D Eastwood, et al.
Investigative Ophthalmology & Visual Science|November 1, 2001
Noninvasive imaging by optical coherence tomography to monitor retinal degeneration in the mouseQ Li, A M Timmers, K Hunter, et al.
Human Gene Therapy|March 25, 2017
Overexpression of the X-Linked Inhibitor of Apoptosis Protects Against Retinal Degeneration in a Feline Model of Retinal DetachmentSarah J Wassmer, Brian C Leonard, Stuart G Coupland, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 21, 2015
Gene therapy with the caspase activation and recruitment domain reduces the ocular inflammatory responseCristhian J Ildefonso, Henrique Jaime, Manas R Biswal, et al.
Plos One|April 6, 2013
Evaluation of lateral spread of transgene expression following subretinal AAV-mediated gene delivery in dogsAshlee R Bruewer, Freya M Mowat, Joshua T Bartoe, et al.
Frontiers in Molecular Neuroscience|July 25, 2018
Cone Phosphodiesterase-6γ' Subunit Augments Cone PDE6 Holoenzyme Assembly and Stability in a Mouse Model Lacking Both Rod and Cone PDE6 Catalytic SubunitsWen-Tao Deng, Saravanan Kolandaivelu, Astra Dinculescu, et al.
Expert Opinion on Orphan Drugs|August 7, 2015
Improvement in vision: a new goal for treatment of hereditary retinal degenerationsSamuel G Jacobson, Artur V Cideciyan, Gustavo D Aguirre, et al.
Gene Therapy|June 24, 2011
Efficient cochlear gene transfection in guinea-pigs with adeno-associated viral vectors by partial digestion of round window membraneH Wang, R Murphy, D Taaffe, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 27, 2000
Ribozyme rescue of photoreceptor cells in P23H transgenic rats: long-term survival and late-stage therapyM M LaVail, D Yasumura, M T Matthes, et al.
Human Molecular Genetics|October 3, 2014
Viral-mediated vision rescue of a novel AIPL1 cone-rod dystrophy modelCristy A Ku, Vince A Chiodo, Sanford L Boye, et al.
Pageof 39