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AAV-mediated gene transfer for retinal diseases

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Pages 1279-1294 | Published online: 22 Nov 2006

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Joseph C Corbo. (2008) The role of cis-regulatory elements in the design of gene therapy vectors for inherited blindness. Expert Opinion on Biological Therapy 8:5, pages 599-608.
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Katherine P Ponder & Alberto Auricchio. (2010) Gene therapy for ocular problems in mucopolysaccharidosis: an experimental and promising approach with benefits in animal models - a review. Clinical & Experimental Ophthalmology 38, pages 43-51.
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Keryn A Williams & Douglas J Coster. (2010) Gene therapy for diseases of the cornea – a review. Clinical & Experimental Ophthalmology 38:2, pages 93-103.
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Bo Lei, Keqing Zhang, Yongping Yue, Arkasubhra Ghosh & Dongsheng Duan. 2010. Retinal Degenerative Diseases. Retinal Degenerative Diseases 671 678 .
M.A. Gamulescu, A.B. Renner & H. Helbig. (2009) Klinische Manifestationen von Funktionsstörungen des retinalen PigmentepithelsClinical manifestations of functional disturbances of the retinal pigment epithelium. Der Ophthalmologe 106:4, pages 305-310.
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Pasqualina Colella, Gabriella Cotugno & Alberto Auricchio. (2009) Ocular gene therapy: current progress and future prospects. Trends in Molecular Medicine 15:1, pages 23-31.
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J Kong, S-R Kim, K Binley, I Pata, K Doi, J Mannik, J Zernant-Rajang, O Kan, S Iqball, S Naylor, J R Sparrow, P Gouras & R Allikmets. (2008) Correction of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapy. Gene Therapy 15:19, pages 1311-1320.
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Shih-Wen Lin & Hildegund CJ Ertl. (2008) Safety of adeno-associated viral vectors. Future Virology 3:5, pages 491-503.
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Rajendra Kumar-Singh. (2008) Barriers for retinal gene therapy: Separating fact from fiction. Vision Research 48:16, pages 1671-1680.
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Cynthia L MontanaJoseph C Corbo. (2008) Inherited diseases of photoreceptors and prospects for gene therapy. Pharmacogenomics 9:3, pages 335-347.
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Shizuya Saika, Osamu Yamanaka, Takayoshi Sumioka, Takeshi Miyamoto, Ken-ichi Miyazaki, Yuka Okada, Ai Kitano, Kumi Shirai, Sai-ichi Tanaka & Kazuo Ikeda. (2008) Fibrotic disorders in the eye: Targets of gene therapy. Progress in Retinal and Eye Research 27:2, pages 177-196.
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Inchan Kwon & David V. Schaffer. (2007) Designer Gene Delivery Vectors: Molecular Engineering and Evolution of Adeno-Associated Viral Vectors for Enhanced Gene Transfer. Pharmaceutical Research 25:3.
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Enrico M. Surace & Alberto Auricchio. (2008) Versatility of AAV vectors for retinal gene transfer. Vision Research 48:3, pages 353-359.
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Xiaoming Liu, Meihui Luo, Cyndi Trygg, Ziying Yan, Diana CM Lei-Butters, Carolina I Smith, Anne C Fischer, Keith Munson, William B Guggino, Bruce A Bunnell & John F Engelhardt. (2007) Biological Differences in rAAV Transduction of Airway Epithelia in Humans and in Old World Non-human Primates. Molecular Therapy 15:12, pages 2114-2123.
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Mariacarmela Allocca, Claudio Mussolino, Maria Garcia-Hoyos, Daniela Sanges, Carolina Iodice, Marco Petrillo, Luk H. Vandenberghe, James M. Wilson, Valeria Marigo, Enrico M. Surace & Alberto Auricchio. (2007) Novel Adeno-Associated Virus Serotypes Efficiently Transduce Murine Photoreceptors. Journal of Virology 81:20, pages 11372-11380.
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