pAdSh.PGK.Cas9 Citations (3)

Originally described in: Adenoviral vector delivery of RNA-guided CRISPR/Cas9 nuclease complexes induces targeted mutagenesis in a diverse array of human cells.
Maggio I, Holkers M, Liu J, Janssen JM, Chen X, Goncalves MA Sci Rep. 2014 May 29;4:5105. doi: 10.1038/srep05105. PubMed Journal

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Articles Citing pAdSh.PGK.Cas9

Articles
Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populations. Maggio I, Stefanucci L, Janssen JM, Liu J, Chen X, Mouly V, Goncalves MA. Nucleic Acids Res. 2016 Jan 13. pii: gkv1540. PubMed
Adenoviral vectors encoding CRISPR/Cas9 multiplexes rescue dystrophin synthesis in unselected populations of DMD muscle cells. Maggio I, Liu J, Janssen JM, Chen X, Goncalves MA. Sci Rep. 2016 Nov 15;6:37051. doi: 10.1038/srep37051. PubMed
Induction of Brain Arteriovenous Malformation Through CRISPR/Cas9-Mediated Somatic Alk1 Gene Mutations in Adult Mice. Zhu W, Saw D, Weiss M, Sun Z, Wei M, Shaligram S, Wang S, Su H. Transl Stroke Res. 2018 Dec 3. pii: 10.1007/s12975-018-0676-1. doi: 10.1007/s12975-018-0676-1. PubMed

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