Adenoviral vector delivery of RNA-guided CRISPR/Cas9 nuclease complexes induces targeted mutagenesis in a diverse array of human cells

by Maggio, Ignazio, Holkers, Maarten, Liu, Jin, Janssen, Josephine M., Chen, Xiaoyu, Gonçalves, Manuel A. F. V.
Published 2014

Adenoviral vectors encoding CRISPR/Cas9 multiplexes rescue dystrophin synthesis in unselected populations of DMD muscle cells

by Maggio, Ignazio, Liu, Jin, Janssen, Josephine M., Chen, Xiaoyu, Gonçalves, Manuel A. F. V.
Published 2016

Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populations

by Maggio, Ignazio, Stefanucci, Luca, Janssen, Josephine M., Liu, Jin, Chen, Xiaoyu, Mouly, Vincent, Gonçalves, Manuel A.F.V.
Published 2016

Differential integrity of TALE nuclease genes following adenoviral and lentiviral vector gene transfer into human cells

by Holkers, Maarten, Maggio, Ignazio, Liu, Jin, Janssen, Josephine M., Miselli, Francesca, Mussolino, Claudio, Recchia, Alessandra, Cathomen, Toni, Gonçalves, Manuel A. F. V.
Published 2013