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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.
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2011
Long-term RNA interference gene therapy in a dominant retinitis pigmentosa mouse modelLi Jiang, Houbin Zhang, Alexander M Dizhoor, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 21, 2021
Disease mechanisms of X-linked cone dystrophy caused by missense mutations in the red and green cone opsinsPing Zhu, Frank Dyka, Xiaojie Ma, et al.
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