Adenoviral vectors (AdVs) have been regarded as one of the most efficient gene delivery vehicles in vivo, and have been used in human gene therapy protocols.1 2 Their virions are relatively stable, ...
Helper-dependent adenoviral (HD-Ad) vectors have great potential for gene therapy applications; however, their administration induces acute toxicity that impairs safe clinical applications. We ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback