Highly efficient endogenous human gene correction using designed zinc-finger nucleases
By F. Urnov, Jeffrey C. Miller, Ya-Li Lee, C. Beauséjour, Jeremy M. Rock, S. Augustus, A. Jamieson, M. Porteus, P. Gregory, M. Holmes. Nature, 2005
1,689 citations recorded by the source corpus.
Subfields: Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/4828fda84d149846e9c896370bf86eff851eb176
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
- D. Carroll
- Jeffry D. Sander
- J. Keith Joung
- Daniel F. Voytas
- Feng Zhang
- A. Klug
- Jin-Soo Kim
- Nathan D. Lawson
In Oncology
Citations in the corpus
- Zinc finger nuclease-mediated CCR5 knockout hematopoietic stem cell transplantation controls HIV-1 in vivo (2010, positive): “Since DSB formation requires only transient expression of ZFNs, gene delivery methods that are suitable to express ZFNs include plasmid DNA nucleofection, integrase-defective lentiviral vectors and adenoviral vectors (16,19,21).”
- Targeted gene inactivation in zebrafish using engineered zinc-finger nucleases (2008, methodology): “In vertebrate cell lines, genomic lesions at a specific site have been introduced using zinc-finger nucleases (ZFNs”
- Targeting DNA Double-Strand Breaks with TAL Effector Nucleases (2010, background): “In theabsenceofa repair template, broken chromosomes are rejoined by nonhomologous end joining, which often introduces short DNA insertions or deletions that create targeted gene knockouts.”
- Rapid “open-source” engineering of customized zinc-finger nucleases for highly efficient gene modification (2008, positive): “…human cells (Alwin et al., 2005; Beumer et al., 2006; Bibikova et al., 2003; Bibikova et al., 2002; Lloyd et al., 2005; Lombardo et al., 2007; Miller et al., 2007; Moehle et al., 2007; Morton et al., 2006; Porteus and Baltimore, 2003; Szczepek et al., 2007; Urnov et al., 2005; Wright et al., 2005).”
- Efficient TALEN-mediated gene knockout in livestock (2012, background): “This finding has also been observed for cells treated with ZFN’s (11, 35, 36).”
- Engineering the Delivery System for CRISPR-based Genome Editing (2018, background): “By fusing these proteins to nucleases, it is possible to create a double-strand break at a specified site in the genome, which would then be repaired either through non-homologous end joining, usually leading to a small insertion or deletion and thus gene knockout, or homologous recombination with a”
- Distinct factors control histone variant H3.3 localization at specific genomic regions (2010, methodology): “, 2007) and correction (Urnov et al., 2005) modes to engineer a panel of heterozygous ES lines carrying one allele of wild-type H3.”