Adenoviral Delivery of CRISPR/Cas9 Aims to Expand Genome Editing to Primary Cells
Type
Blog Post
...to deliver a standard AdV vector to the targeted organs or tissues with Cas9 and a gRNA designed to target...67
Ding Q, Strong A, Patel KM, Ng S-L, Gosis BS, Regan SN, Cowan CA, Rader DJ, Musunuru K (2014) Permanent... Kendall Morgan...