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Advances in Experimental Medicine and Biology|March 26, 2014
Gene therapy in the rd6 mouse model of retinal degenerationAstra Dinculescu, Seok-Hong Min, Wen-Tao Deng, et al.
Molecular Vision|May 10, 2011
Quantifying transduction efficiencies of unmodified and tyrosine capsid mutant AAV vectors in vitro using two ocular cell linesRenee C Ryals, Sanford L Boye, Astra Dinculescu, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 20, 2002
Adeno-associated virus type-2 expression of pigmented epithelium-derived factor or Kringles 1-3 of angiostatin reduce retinal neovascularizationBrian J Raisler, Kenneth I Berns, Maria B Grant, et al.
Investigative Ophthalmology & Visual Science|April 27, 2007
Increased sensitivity to light-induced damage in a mouse model of autosomal dominant retinal diseaseD Alan White, Jason J Fritz, William W Hauswirth, et al.
Investigative Ophthalmology & Visual Science|July 13, 2014
Gene therapy with mitochondrial heat shock protein 70 suppresses visual loss and optic atrophy in experimental autoimmune encephalomyelitisVenu Talla, Vittorio Porciatti, Vince Chiodo, et al.
Molecular Vision|September 8, 2005
Knockdown of wild-type mouse rhodopsin using an AAV vectored ribozyme as part of an RNA replacement approachM S Gorbatyuk, J J Pang, J Thomas, et al.
Investigative Ophthalmology & Visual Science|August 1, 2006
Human blue-opsin promoter preferentially targets reporter gene expression to rat s-cone photoreceptorsLyudmyla G Glushakova, Adrian M Timmers, Jijing Pang, et al.
Molecular Vision|February 5, 2019
Rescue of cone function in cone-only <i>Nphp5</i> knockout mouse model with Leber congenital amaurosis phenotypeChristin Hanke-Gogokhia, Vince A Chiodo, William W Hauswirth, et al.
Experimental Eye Research|December 20, 2023
rAAV-compatible human mini promoters enhance transgene expression in rat retinal ganglion cellsVictor G Araujo, Mariana S Dias, William W Hauswirth, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 15, 2010
Leber hereditary optic neuropathy gene therapy clinical trial recruitment: year 1Byron L Lam, William J Feuer, Fawzi Abukhalil, et al.
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