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Gene Therapy for Choroidal Neovascularization

Published:2020 Issue: Volume: Page:381-390
ISSN:
Container-title:Choroidal Neovascularization
language:
Short-container-title:

Author:

Lee Joo Yong,Yeo Joon Hyung

Publisher

Springer Singapore

Link

http://link.springer.com/content/pdf/10.1007/978-981-15-2213-0_28

Reference61 articles.

1. Bennett J. Taking stock of retinal gene therapy: looking back and moving forward. Mol Ther. 2017;25(5):1076–94.

2. Hafler BP. Clinical progress in inherited retinal degenerations: gene therapy clinical trials and advances in genetic sequencing. Retina. 2017;37(3):417–23.

3. Morral N, O'Neal W, Zhou H, Langston C, Beaudet A. Immune responses to reporter proteins and high viral dose limit duration of expression with adenoviral vectors: comparison of E2a wild type and E2a deleted vectors. Hum Gene Ther. 1997;8(10):1275–86.

4. Gao GP, Yang Y, Wilson JM. Biology of adenovirus vectors with E1 and E4 deletions for liver-directed gene therapy. J Virol. 1996;70(12):8934–43.

5. Morral N, O’Neal W, Rice K, Leland M, Kaplan J, Piedra PA, et al. Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons. Proc Natl Acad Sci USA. 1999;96(22):12816–21.

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