Directed Evolution of an Enhanced and Highly Efficient FokI Cleavage Domain for Zinc Finger Nucleases
- 4 May 2010
- journal article
- Published by Elsevier in Journal of Molecular Biology
- Vol. 400 (1), 96-107
- https://doi.org/10.1016/j.jmb.2010.04.060
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Modular system for the construction of zinc-finger libraries and proteinsNature Protocols, 2010
- Synthesis of programmable integrasesProceedings of the National Academy of Sciences, 2009
- Expanding or Restricting the Target Site Repertoire of Zinc-finger Nucleases: The Inter-domain Linker as a Major Determinant of Target Site SelectivityMolecular Therapy, 2009
- Increasing cloning possibilities using artificial zinc finger nucleasesProceedings of the National Academy of Sciences, 2008
- Rapid “Open-Source” Engineering of Customized Zinc-Finger Nucleases for Highly Efficient Gene ModificationMolecular Cell, 2008
- Establishment of HIV-1 resistance in CD4+ T cells by genome editing using zinc-finger nucleasesNature Biotechnology, 2008
- Heritable targeted gene disruption in zebrafish using designed zinc-finger nucleasesNature Biotechnology, 2008
- Targeted gene inactivation in zebrafish using engineered zinc-finger nucleasesNature Biotechnology, 2008
- An improved zinc-finger nuclease architecture for highly specific genome editingNature Biotechnology, 2007
- Zinc Finger Tools: custom DNA-binding domains for transcription factors and nucleasesNucleic Acids Research, 2006