Characterization of integration frequency and insertion sites of adenovirus DNA into mouse liver genomic DNA following intravenous injection-Reference-Cited by-同舟云学术

Characterization of integration frequency and insertion sites of adenovirus DNA into mouse liver genomic DNA following intravenous injection

Published:2021-08-18 Issue: Volume: Page:
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Wang Zhibin^ORCID,Troilo Philip J.,Griffiths Thomas G.,Harper Laural B.,Barnum Amy B.,Pacchione Stephen J.,Pauley Cindy J.,Lebron Jose A.,Wolf Jayanthi^ORCID,Ledwith Brian J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

https://www.nature.com/articles/s41434-021-00278-2.pdf

Reference38 articles.

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3. St George JA. Gene therapy progress and prospects: adenoviral vectors. Gene Ther. 2003;10:1135–41.

4. Ginn SL, Anais K, Amaya AK, Ian E, Alexander IE, Edelstein M, et al. Gene therapy clinical trials worldwide to 2017: an update. J Gene Med. 2018;20:e3015. https://doi.org/10.1002/jgm.3015.

5. Morsy MA, Gu M, Motzel S, Zhao J, Jing Lin J, Su Q, et al. An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene. Proc Natl Acad Sci USA. 1998;95:7866–71.

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