CRISPR/Cas9-loxP-Mediated Gene Editing as a Novel Site-Specific Genetic Manipulation Tool
Targeted gene therapy and cell reprogramming in Fanconi anemia | EMBO Molecular Medicine
Addgene: AAVS1-idCas9-vpr
Efficient viral delivery of Cas9 into human safe harbor | Scientific Reports
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Targeted Integration and High-Level Transgene Expression in AAVS1 Transgenic Mice after In Vivo HSC Transduction with HDAd5/35++ Vectors: Molecular Therapy
Quantification of transgene expression in GSH AAVS1 with a novel CRISPR/Cas9-based approach reveals high transcriptional variation: Molecular Therapy - Methods & Clinical Development
Targeted transgene insertion into the AAVS1 locus driven by baculoviral vector‐mediated zinc finger nuclease expression in human‐induced pluripotent stem cells - Tay - 2013 - The Journal of Gene Medicine - Wiley Online Library
Identification of the safe harbor locus, AAVS1, from porcine genome and site-specific integration of recombinase-mediated casset
Efficient viral delivery of Cas9 into human safe harbor | Scientific Reports
CRISPR Cas9 AAVS1 Safe Harbor Knockin System
a). Schematic of the AAVS1 locus and the AAV-CAGGS-GFP donor plasmid... | Download Scientific Diagram
Characterization of the Mouse Adeno-Associated Virus AAVS1 Ortholog | Journal of Virology
Detailed design of PITCh-TG in human AAVS1 locus. Black lines indicate... | Download Scientific Diagram
Targeted genome engineering in human induced pluripotent stem cells from patients with hemophilia B using the CRISPR-Cas9 system | Stem Cell Research & Therapy | Full Text