A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear-Reference-Cited by-同舟云学术

A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear

Published:2017-02-06 Issue:3 Volume:35 Page:280-284
ISSN:1087-0156
Container-title:Nature Biotechnology
language:en
Short-container-title:Nat Biotechnol

Author:

Landegger Lukas D^ORCID,Pan Bifeng^ORCID,Askew Charles^ORCID,Wassmer Sarah J,Gluck Sarah D,Galvin Alice,Taylor Ruth,Forge Andrew,Stankovic Konstantina M,Holt Jeffrey R,Vandenberghe Luk H^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Link

http://www.nature.com/articles/nbt.3781.pdf

Reference39 articles.

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2. Géléoc, G.S. & Holt, J.R. Sound strategies for hearing restoration. Science 344, 1241062 (2014).

3. Zinn, E. et al. In silico reconstruction of the viral evolutionary lineage yields a potent gene therapy vector. Cell Rep. 12, 1056–1068 (2015).

4. Parker, M. & Bitner-Glindzicz, M. Genetic investigations in childhood deafness. Arch. Dis. Child. 100, 271–278 (2015).

5. Stamatiou, G.A. & Stankovic, K.M. A comprehensive network and pathway analysis of human deafness genes. Otol. Neurotol. 34, 961–970 (2013).

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