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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 1, 2015
Kinesin family 17 (osmotic avoidance abnormal-3) is dispensable for photoreceptor morphology and functionLi Jiang, Beatrice M Tam, Guoxing Ying, et al.
Vision Research|October 24, 2007
Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: effects of serotype and site of administrationJi-jing Pang, Amanda Lauramore, Wen-tao Deng, et al.
Plos One|May 23, 2012
Caspase inhibition with XIAP as an adjunct to AAV vector gene-replacement therapy: improving efficacy and prolonging the treatment windowJingyu Yao, Lin Jia, Naheed Khan, et al.
Human Molecular Genetics|September 2, 2011
Gene therapy using self-complementary Y733F capsid mutant AAV2/8 restores vision in a model of early onset Leber congenital amaurosisCristy A Ku, Vince A Chiodo, Sanford L Boye, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 19, 2012
Towards optogenetic sensory replacementM Mehdi Doroudchi, Kenneth P Greenberg, Anthony N Zorzos, et al.
Nature|September 18, 2009
Gene therapy for red-green colour blindness in adult primatesKatherine Mancuso, William W Hauswirth, Qiuhong Li, et al.
Molecular Vision|April 18, 2006
Does recombinant adeno-associated virus-vectored proximal region of mouse rhodopsin promoter support only rod-type specific expression in vivo?Lyudmyla G Glushakova, Adrian M Timmers, Tawfik M Issa, et al.
Advances in Experimental Medicine and Biology|May 4, 2018
Co-Expression of Wild-Type and Mutant S163R C1QTNF5 in Retinal Pigment EpitheliumAstra Dinculescu, Frank M Dyka, Seok-Hong Min, et al.
Molecular Vision|September 17, 2009
AAV retinal transduction in a large animal model species: comparison of a self-complementary AAV2/5 with a single-stranded AAV2/5 vectorS M Petersen-Jones, J T Bartoe, A J Fischer, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|September 11, 2014
Flicker cone function in normal and day blind sheep: a large animal model for human achromatopsia caused by CNGA3 mutationRaaya Ezra-Elia, Eyal Banin, Hen Honig, et al.
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