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Nature Genetics|July 11, 2000
Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapyR R Ali, G M Sarra, C Stephens, et al.
Gene Therapy|March 31, 2006
EIAV vector-mediated delivery of endostatin or angiostatin inhibits angiogenesis and vascular hyperpermeability in experimental CNVK S Balaggan, K Binley, M Esapa, et al.
Gene Therapy|July 27, 2018
Correction: Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65A Georgiadis, Y Duran, J Ribeiro, et al.
Gene Therapy|September 23, 2016
Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65A Georgiadis, Y Duran, J Ribeiro, et al.
Gene Therapy|July 29, 2003
Stable rAAV-mediated transduction of rod and cone photoreceptors in the canine retinaJ W B Bainbridge, A Mistry, F C Schlichtenbrede, et al.
Nature Communications|April 21, 2022
Lateral gain is impaired in macular degeneration and can be targeted to restore vision in miceM Rizzi, K Powell, M R Robinson, et al.
Human Gene Therapy|April 3, 1998
Lipid-mediated enhancement of transfection by a nonviral integrin-targeting vectorS L Hart, C V Arancibia-Cárcamo, M A Wolfert, et al.
Gene Therapy|December 1, 2017
In situ regeneration of retinal pigment epithelium by gene transfer of E2F2: a potential strategy for treatment of macular degenerationsD Kampik, M Basche, U F O Luhmann, et al.
Gene Therapy|September 16, 2005
Permanent partial phenotypic correction and tolerance in a mouse model of hemophilia B by stem cell gene delivery of human factor IXB W Bigger, E K Siapati, A Mistry, et al.
Gene Therapy|October 3, 2007
Progress and prospects: gene therapy clinical trials (part 1)B L Alexander, R R Ali, E W F Alton, et al.
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