Therapeutic gene transfer to dystrophic diaphragm by an adenoviral vector deleted of all viral genes

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DOIResolve DOI: http://doi.org/10.1152/ajplung.00117.2004
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TypeArticle
Journal titleAmerican Journal of Physiology: Lung Cellular and Molecular Physiology
ISSN1040-0605
Volume287
Issue3
PagesL569L576; # of pages: 8
Subjectbio; Duchenne muscular dystrophy; gene therapy; dystrophin deficiency; viral vectors; mdx mouse; adenoviridae; animals; CD4-positive T-lymphocytes; CD8-positive T-lymphocytes; diaphragm; dystrophin; gene expression; gene transfer techniques; mice; mice, inbred C57BL; mice, inbred mdx; muscular dystrophy, animal; muscular dystrophy, duchenne
Abstract
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LanguageEnglish
AffiliationNRC Biotechnology Research Institute; National Research Council Canada
Peer reviewedNo
Identifier10462983
NRC number37733
NPARC number3539975
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Record identifierf76b6963-7dc0-45ff-9d55-662ddf4f6c14
Record created2009-03-01
Record modified2016-05-09
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