Mouse adenovirus (MAV-1) expression in primary human endothelial cells and generation of a full-length infectious plasmid-Reference-Cited by-同舟云学术

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Mouse adenovirus (MAV-1) expression in primary human endothelial cells and generation of a full-length infectious plasmid

Published:1999-07 Issue:7 Volume:6 Page:1291-1297
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Nguyen T T,Nery J P,Joseph S,Rocha C E,Carney G E,Spindler K R,Villarreal L P

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/3300949.pdf

Reference35 articles.

1. Graham FL, Prevec L . Methods for construction of adenovirus vectors Mol Biotechnol 1995 3: 207–220

2. Kochanek S et al. A new adenoviral vector: replacement of all viral coding sequences with 28 kb of DNA independently expressing both full-length dystrophin and β-galactosidase Proc Natl Acad Sci USA 1996 93: 5731–5736

3. Haecker SE et al. In vivo expression of full-length human dystrophin from adenoviral vectors deleted of all viral genes Hum Gene Ther 1996 7: 1907–1914

4. McGrory WJ, Bautista DS, Graham FL . A simple technique for the rescue of early region I mutations into infectious human adenovirus type 5 Virology 1988 163: 614–617

5. Chartier C et al. Efficient generation of recombinant adenovirus vectors by homologous recombination in Escherichia coli J Virol 1996 70: 4805–4810

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