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Molecular Therapy : the Journal of the American Society of Gene Therapy|July 6, 2004
AAV-mediated intravitreal gene therapy reduces lysosomal storage in the retinal pigmented epithelium and improves retinal function in adult MPS VII miceAnne K Hennig, Judith Mosinger Ogilvie, Kevin K Ohlemiller, et al.
Neuroreport|June 25, 1999
Ischemia induces a selective biphasic response in brain mitochondrial mRNA levelsB A Bruckner, M P Otal, M E Rupp, et al.
Gene Therapy|July 18, 2008
Novel anti-VEGF chimeric molecules delivered by AAV vectors for inhibition of retinal neovascularizationP Pechan, H Rubin, M Lukason, et al.
Gene Therapy|September 29, 2019
Retina transduction by rAAV2 after intravitreal injection: comparison between mouse and ratMariana S Dias, Victor G Araujo, Taliane Vasconcelos, et al.
Advances in Experimental Medicine and Biology|October 3, 2015
Gene Therapy for MERTK-Associated Retinal DegenerationsMatthew M LaVail, Douglas Yasumura, Michael T Matthes, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 20, 2005
Expression of cell surface antigens on mast cells: mast cell phenotypingAlexander W Hauswirth, Stefan Florian, Gerit-Holger Schernthaner, et al.
Investigative Ophthalmology & Visual Science|December 9, 2008
XIAP effects on retinal detachment-induced photoreceptor apoptosis [corrected]Laura A Zadro-Lamoureux, David N Zacks, Adam N Baker, et al.
Cold Spring Harbor Perspectives in Medicine|October 11, 2014
Gene augmentation for X-linked retinitis pigmentosa caused by mutations in RPGRWilliam A Beltran, Artur V Cideciyan, Alfred S Lewin, et al.
Plos One|February 18, 2026
Correction: Inhibitor of Apoptosis-Stimulating Protein of p53 (iASPP) Is Required for Neuronal Survival after Axonal InjuryAriel M Wilson, Vince A Chiodo, Sanford L Boye, et al.
Advances in Experimental Medicine and Biology|March 26, 2014
Cone specific promoter for use in gene therapy of retinal degenerative diseasesFrank M Dyka, Sanford L Boye, Renee C Ryals, et al.
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