AAV9 transduction mediated by systemic delivery of vector via retro-orbital injection in newborn, neonatal and juvenile mice-Reference-Cited by-同舟云学术

AAV9 transduction mediated by systemic delivery of vector via retro-orbital injection in newborn, neonatal and juvenile mice

Published:2021 Issue:4 Volume:70 Page:450-458
ISSN:1341-1357
Container-title:Experimental Animals
language:en
Short-container-title:Exp. Anim.

Author:

Prabhakar Shilpa¹,Lule Sevda²,da Hora Cintia Carla²,Breakefield Xandra O.¹,Cheah Pike See¹

Affiliation:

1. Department of Neurology, Massachusetts General Hospital and Harvard Medical School, 149 13th Street, Charlestown, 02129, Boston, MA, USA

2. Center for Molecular Imaging Research, Department of Radiology, Massachusetts General Hospital, 149 13th Street, Charlestown, 02129, Boston, MA, USA

Publisher

Japanese Association for Laboratory Animal Science

Subject

General Veterinary,General Biochemistry, Genetics and Molecular Biology,Animal Science and Zoology,General Medicine

Link

https://www.jstage.jst.go.jp/article/expanim/70/4/70_20-0186/_pdf

Reference29 articles.

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2. 2. Gessler DJ, Tai PWL, Li J, Gao G. Intravenous Infusion of AAV for widespread gene delivery to the nervous system. Methods Mol Biol. 2019; 1950: 143–163.

3. 3. Jerebtsova M, Ye X, Ray PE. A simple technique to establish a long-term adenovirus mediated gene transfer to the heart of newborn mice. Cardiovasc Hematol Disord Drug Targets. 2009; 9: 136–140.

4. 4. Jerebtsova M, Liu XH, Ye X, Ray PE. Adenovirus-mediated gene transfer to glomerular cells in newborn mice. Pediatr Nephrol. 2005; 20: 1395–1400.

5. 5. Cheah PS, Prabhakar S, Yellen D, Beauchamp RL, Zhang X, Kasamatsu S, et al. Gene therapy for tuberous sclerosis complex type 2 in a mouse model by delivery of AAV9 encoding a condensed form of tuberin. Sci Adv. 2021; 7: eabb1703.

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