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AAV viral vector delivery to the brain by shape-conforming MR-guided infusions

  • Published:2016-10 Issue: Volume:240 Page:434-442
  • ISSN:0168-3659
  • Container-title:Journal of Controlled Release
  • language:en
  • Short-container-title:Journal of Controlled Release

Author:

Bankiewicz Krystof S.,Sudhakar Vivek,Samaranch Lluis,San Sebastian Waldy,Bringas John,Forsayeth John

Funder

Michael J. Fox Foundation

National Institute of Neurological Disorders and Stroke

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference64 articles.

1. Eight years of clinical improvement in MPTP-lesioned primates after gene therapy with AAV2-hAADC;Hadaczek;Mol. Ther.,2010

2. Gene therapy for Parkinson's disease: where are we now and where are we going?;Forsayeth;Expert Rev. Neurother.,2010

3. Future applications: gene therapy;Richardson;Neurosurg. Clin. N. Am.,2009

4. Efficient gene therapy-based method for the delivery of therapeutics to primate cortex;Kells;Proc. Natl. Acad. Sci. U. S. A.,2009

5. Axonal transport of adeno-associated viral vectors is serotype-dependent;Salegio;Gene Ther.,2012
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