Ignazio Maggio
Leiden, ZH 2300RC, Netherlands
Last Updated: 09/26/2026
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Found 12 publications
Intronic SMCHD1 variants in FSHD: testing the potential for CRISPR-Cas9 genome editing.
Journal: Journal of medical genetics
Published: June 27, 2019
In trans paired nicking triggers seamless genome editing without double-stranded DNA cutting.
Journal: Nature communications
Published: June 30, 2017
Adenoviral vectors encoding CRISPR/Cas9 multiplexes rescue dystrophin synthesis in unselected populations of DMD muscle cells.
Journal: Scientific reports
Published: June 17, 2016
The emerging role of viral vectors as vehicles for DMD gene editing.
Journal: Genome medicine
Published: May 25, 2016
Probing the impact of chromatin conformation on genome editing tools.
Journal: Nucleic acids research
Published: April 06, 2016
Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populations.
Journal: Nucleic acids research
Published: July 27, 2015
Genome editing at the crossroads of delivery, specificity, and fidelity.
Journal: Trends in biotechnology
Published: January 15, 2015
Adenoviral vector DNA for accurate genome editing with engineered nucleases.
Journal: Nature methods
Published: April 11, 2014
Adenoviral vector delivery of RNA-guided CRISPR/Cas9 nuclease complexes induces targeted mutagenesis in a diverse array of human cells.
Journal: Scientific reports
Published: January 21, 2014
Histone deacetylase inhibition rescues gene knockout levels achieved with integrase-defective lentiviral vectors encoding zinc-finger nucleases.
Journal: Human gene therapy methods
Published: September 25, 2013
Showing 1-12 of 12
Last Updated: 09/26/2026