Adenoviral Delivery of CRISPR/Cas9 Aims to Expand Genome Editing to Primary Cells
Type
Blog Post
... Journal of Controlled Release 298:128–141 . https://doi.org/10.1016/j.jconrel.2019.02.009
Wang D, Mou...efficient introduction of DNA into therapeutically relevant, non-transformed mammalian cells. These viral ... could be realized via simple switching of the relevant gRNAs and donor DNA
Adenoviral CRISPR/Cas9 genome...