Adenoviral Delivery of CRISPR/Cas9 Aims to Expand Genome Editing to Primary Cells
Type
Blog Post
Published
Dec. 10, 2020, 1 p.m.
...used for many years for in vivo delivery and gene therapy and represent one of the most studied viruses. ...with a packaging capacity of about 6 kb, the 1st generation of AdVs have already a packaging capacity larger...presumably reduce the likelihood that donor DNA will interact with sporadic double-stranded chromosomal DNA ...and very efficient introduction of DNA into therapeutically relevant, non-transformed mammalian cells. ...developed and used AdV vectors to edit genes in several biological systems. It has been used for instance...deficiency (most widely used so far) or for cancer gene therapy such as nonalcoholic steatohepatitis cancer. In...Targeting. In: Applications of viruses for cancer therapy. Elsevier, pp 39–67
Ding Q, Strong A, Patel KM,...