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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.
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.
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.
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.
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