Inhibition of antigen presentation during AAV gene therapy using virus peptides-Reference-Cited by-同舟云学术

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Inhibition of antigen presentation during AAV gene therapy using virus peptides

Published:2017-12-19 Issue:4 Volume:27 Page:601-613
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Shao Wenwei¹,Chen Xiaojing¹,Samulski Richard J¹²,Hirsch Matthew L¹³,Li Chengwen¹⁴

Affiliation:

1. Gene Therapy Center, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

2. Department of Pharmacology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

3. Department of Ophthalmology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

4. Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/27/4/601/24325813/ddx427.pdf

Reference90 articles.

1. Prednisone treatment in Duchenne muscular dystrophy. Long-term benefit;DeSilva;Arch. Neurol,1987

2. Gene therapy strategies for Duchenne muscular dystrophy utilizing recombinant adeno-associated virus vectors;Blankinship;Mol. Ther,2006

3. Adeno-associated virus serotype-9 microdystrophin gene therapy ameliorates electrocardiographic abnormalities in mdx mice;Bostick;Hum. Gene. Ther,2008

4. Body-wide gene therapy of Duchenne muscular dystrophy in the mdx mouse model;Denti;Proc. Natl. Acad. Sci. U S A,2006

5. Efficient whole-body transduction with trans-splicing adeno-associated viral vectors;Ghosh;Mol. Ther,2007

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