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Autor:
Jin Kim, Michael Kaleko, Jennifer Marshall-Neff, Theodore Smith, Susan C. Stevenson, Neeraja Idamakanti, Kathy Mulgrew, Michele Rollence, Glen R. Nemerow
Publikováno v:
Human Gene Therapy. 14:777-787
Adenoviral vectors used in gene therapy are predominantly derived from adenovirus serotype 5 (Ad5), which infects a broad range of cells. Ad5 cell entry involves interactions with the coxsackie-adenovirus receptor (CAR) and integrins. To assess these