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Proceedings of the National Academy of Sciences of the United States of America|April 24, 2012
Gene delivery to mitochondria by targeting modified adenoassociated virus suppresses Leber's hereditary optic neuropathy in a mouse modelHong Yu, Rajeshwari D Koilkonda, Tsung-Han Chou, et al.Investigative Ophthalmology & Visual Science|December 30, 2011
γ-Secretase inhibition of murine choroidal neovascularization is associated with reduction of superoxide and proinflammatory cytokinesXiaoping Qi, Jun Cai, Qing Ruan, et al.Plos One|February 25, 2011
Ab-externo AAV-mediated gene delivery to the suprachoroidal space using a 250 micron flexible microcatheterMarc C Peden, Jeff Min, Craig Meyers, et al.Human Gene Therapy|November 26, 2015
Cone-Specific Promoters for Gene Therapy of Achromatopsia and Other Retinal DiseasesGuo-Jie Ye, Ewa Budzynski, Peter Sonnentag, et al.Proceedings of the National Academy of Sciences of the United States of America|October 7, 2015
Consequences of zygote injection and germline transfer of mutant human mitochondrial DNA in miceHong Yu, Rajeshwari D Koilkonda, Tsung-Han Chou, et al.Translational Vision Science & Technology|January 29, 2021
Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in AchromatopsiaKatie M Litts, Erica N Woertz, Michalis Georgiou, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|July 20, 2005
Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of x-linked juvenile retinoschisisSeok H Min, Laurie L Molday, Mathias W Seeliger, et al.Molecular Vision|February 5, 2009
Gene therapy following subretinal AAV5 vector delivery is not affected by a previous intravitreal AAV5 vector administration in the partner eyeWensheng Li, Fansheng Kong, Xia Li, et al.Proceedings of the National Academy of Sciences of the United States of America|October 10, 2009
Functional interchangeability of rod and cone transducin alpha-subunitsWen-Tao Deng, Keisuke Sakurai, Jianwen Liu, et al.Human Gene Therapy|July 22, 2016
Highly Efficient Delivery of Adeno-Associated Viral Vectors to the Primate RetinaShannon E Boye, John J Alexander, C Douglas Witherspoon, et al.Pageof 39