Pages that link to "Q37385910"
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The following pages link to Stimulation of homology-directed gene targeting at an endogenous human locus by a nicking endonuclease. (Q37385910):
Displaying 23 items.
- Rapid and sensitive lentivirus vector-based conditional gene expression assay to monitor and quantify cell fusion activity (Q28474202) (← links)
- Targeted gene addition to a predetermined site in the human genome using a ZFN-based nicking enzyme (Q29308378) (← links)
- Engineered zinc finger nickases induce homology-directed repair with reduced mutagenic effects (Q34257442) (← links)
- Performance of the Cas9 nickase system in Drosophila melanogaster (Q34352087) (← links)
- Natural and engineered nicking endonucleases--from cleavage mechanism to engineering of strand-specificity (Q34474076) (← links)
- Single-strand nicks induce homologous recombination with less toxicity than double-strand breaks using an AAV vector template (Q34559611) (← links)
- Generation of interleukin-2 receptor gamma gene knockout pigs from somatic cells genetically modified by zinc finger nuclease-encoding mRNA (Q35018520) (← links)
- Development of a lentivirus vector-based assay for non-destructive monitoring of cell fusion activity (Q35207565) (← links)
- Engineering a Nickase on the Homing Endonuclease I-DmoI Scaffold. (Q35883835) (← links)
- Precision genome engineering with programmable DNA-nicking enzymes (Q36093894) (← links)
- Differential integrity of TALE nuclease genes following adenoviral and lentiviral vector gene transfer into human cells. (Q36684758) (← links)
- Homologous recombination rescues ssDNA gaps generated by nucleotide excision repair and reduced translesion DNA synthesis in yeast G2 cells. (Q37068630) (← links)
- An update on targeted gene repair in mammalian cells: methods and mechanisms (Q37834094) (← links)
- Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populations. (Q38531000) (← links)
- Adenoviral vector DNA for accurate genome editing with engineered nucleases. (Q38963280) (← links)
- Concerted nicking of donor and chromosomal acceptor DNA promotes homology-directed gene targeting in human cells. (Q39424452) (← links)
- Nonspaced inverted DNA repeats are preferential targets for homology-directed gene repair in mammalian cells. (Q39443686) (← links)
- Site- and strand-specific nicking of DNA by fusion proteins derived from MutH and I-SceI or TALE repeats (Q39875872) (← links)
- In trans paired nicking triggers seamless genome editing without double-stranded DNA cutting (Q41689807) (← links)
- Inverted terminal repeats of adeno-associated virus decrease random integration of a gene targeting fragment in Saccharomyces cerevisiae. (Q41936505) (← links)
- DNA, RNA, and Protein Tools for Editing the Genetic Information in Human Cells (Q58800372) (← links)
- Efficiency and Specificity of Targeted Integration Mediated by the Adeno-Associated Virus Serotype 2 Rep 78 Protein (Q59359941) (← links)
- Expanding the editable genome and CRISPR-Cas9 versatility using DNA cutting-free gene targeting based on in trans paired nicking (Q91678555) (← links)