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Although recombinant adenoviruses are attractive vectors for gene transfer to airway epithelia, they have proven to be relatively inefficient. To investigate the mechanisms of adenovirus-mediated gene transfer to airway epithelia, we examined the rol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a25f8ade4613eea2d869d78d6b0f05ed
https://europepmc.org/articles/PMC508289/
https://europepmc.org/articles/PMC508289/
Autor:
Alan E. Smith, Larry A. Couture, Richard J. Gregory, Michael J. Welsh, Michael Lukason, Lynn D. Keyes, Judith A. St. George, Deanna M. Petersen, Joseph Zabner, Aurita P. Puga, Scott M. Graham
Publikováno v:
Nature genetics. 6(1)
Gene therapy for cystic fibrosis (CF) will require the safe transfer of CFTR cDNA to airway epithelia in vivo. We showed previously that a recombinant adenovirus, Ad2/ CFTR–1, expresses CFTR in vitro. As adenovirus rarely integrates, treatment will