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

Lignende værker

• Adenoviral vectors encoding CRISPR/Cas9 multiplexes rescue dystrophin synthesis in unselected populations of DMD muscle cells
  af: Maggio, Ignazio, et al.
  Udgivet: (2016)
• Differential integrity of TALE nuclease genes following adenoviral and lentiviral vector gene transfer into human cells
  af: Holkers, Maarten, et al.
  Udgivet: (2013)
• Integrating gene delivery and gene-editing technologies by adenoviral vector transfer of optimized CRISPR-Cas9 components
  af: Maggio, Ignazio, et al.
  Udgivet: (2020)
• Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populations
  af: Maggio, Ignazio, et al.
  Udgivet: (2016)
• The Chromatin Structure Differentially Impacts High-Specificity CRISPR-Cas9 Nuclease Strategies
  af: Chen, Xiaoyu, et al.
  Udgivet: (2017)