Sustained Improvement of Muscle Function One Year After Full-Length Dystrophin Gene Transfer intomdxMice by a Gutted Helper-Dependent Adenoviral Vector-Reference-Cited by-同舟云学术

Sustained Improvement of Muscle Function One Year After Full-Length Dystrophin Gene Transfer intomdxMice by a Gutted Helper-Dependent Adenoviral Vector

Published:2004-02 Issue:2 Volume:15 Page:145-156
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

Dudley Roy W.R.¹,Lu Yifan²,Gilbert Rénald³,Matecki Stefan¹,Nalbantoglu Josephine²,Petrof Basil J.¹,Karpati George²

Affiliation:

1. Respiratory Division, McGill University Health Center and Meakins-Christie Laboratories, McGill University, Montréal, Québec, Canada, H3A 1A1

2. Neuromuscular Research Group, Montreal Neurological Institute, McGill University, Montréal, Québec, Canada, H3A 2B4

3. Biotechnology Research Institute, NRC, 6100 Royalmount Ave, Montréal, Québec, Canada, H4P 2R2

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/104303404772679959

Reference49 articles.

1. Dystrophin Expression in Muscles of mdx Mice After Adenovirus-MediatedIn VivoGene Transfer

2. Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for Duchenne muscular dystrophy

3. Function and Genetics of Dystrophin and Dystrophin-Related Proteins in Muscle

4. DNA from Both High-Capacity and First-Generation Adenoviral Vectors Remains Intact in Skeletal Muscle

5. Functional protection of dystrophic mouse (mdx) muscles after adenovirus-mediated transfer of a dystrophin minigene.

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