Systemic AAV vectors for widespread and targeted gene delivery in rodents-Reference-Cited by-同舟云学术

Systemic AAV vectors for widespread and targeted gene delivery in rodents

Published:2019-01-09 Issue:2 Volume:14 Page:379-414
ISSN:1754-2189
Container-title:Nature Protocols
language:en
Short-container-title:Nat Protoc

Author:

Challis Rosemary C.,Ravindra Kumar Sripriya,Chan Ken Y.,Challis Collin,Beadle Keith,Jang Min J.,Kim Hyun Min,Rajendran Pradeep S.^ORCID,Tompkins John D.,Shivkumar Kalyanam,Deverman Benjamin E.,Gradinaru Viviana^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology

Link

http://www.nature.com/articles/s41596-018-0097-3.pdf

Reference82 articles.

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2. Chan, K. Y. et al. Engineered AAVs for efficient noninvasive gene delivery to the central and peripheral nervous systems. Nat. Neurosci. 20, 1172–1179 (2017).

3. Deverman, B. E. et al. Cre-dependent selection yields AAV variants for widespread gene transfer to the adult brain. Nat. Biotechnol. 34, 204–209 (2016).

4. Bedbrook, C. N., Deverman, B. E. & Gradinaru, V. Viral strategies for targeting the central and peripheral nervous systems. Annu. Rev. Neurosci. 41, 323–348 (2018).

5. Reed, S. E., Staley, E. M., Mayginnes, J. P., Pintel, D. J. & Tullis, G. E. Transfection of mammalian cells using linear polyethylenimine is a simple and effective means of producing recombinant adeno-associated virus vectors. J. Virol. Methods 138, 85–98 (2006).

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