Strategies to facilitate the long-term expression of transgenes for treatment of chronic liver disease by van Haasteren, J

Demonstrating therapeutic applicability of homologyindependent targeted integration (HITI) in a fluorescent reporter cell line by Van Haasteren, J, Hyde, S, Gill, D

Lessons learned from lung and liver in-vivo gene therapy: implications for the future by van Haasteren, J, Hyde, S, Gill, D

Genome editing of the liver for treatment of alpha-1 antitrypsin deficiency using homology-independent targeted integration (HITI) by Van Haasteren, J, Hyde, S, Gill, D

Genome-wide integration site detection using Cas9 enriched amplification-free long-range sequencing by van Haasteren, J, Munis, AM, Gill, DR