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dc.contributor.authorGupta, Ankit
dc.contributor.authorRayla, Amy L.
dc.contributor.authorLakshmanan, Abirami
dc.contributor.authorWolfe, Scot A.
dc.contributor.authorChristensen, Ryan G.
dc.contributor.authorStormo, Gary D.
dc.date2022-08-11T08:10:15.000
dc.date.accessioned2022-08-23T17:01:17Z
dc.date.available2022-08-23T17:01:17Z
dc.date.issued2012-04-29
dc.date.submitted2012-05-21
dc.identifier.citationNat Methods. 2012 Apr 29. doi: 10.1038/nmeth.1994. [Epub ahead of print]
dc.identifier.issn1548-7091 (Linking)
dc.identifier.doi10.1038/nmeth.1994
dc.identifier.pmid22543349
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43975
dc.description.abstractThe widespread use of zinc-finger nucleases (ZFNs) for genome engineering is hampered by the fact that only a subset of sequences can be efficiently recognized using published finger archives. We describe a set of validated two-finger modules that complement existing finger archives and expand the range of ZFN-accessible sequences threefold. Using this archive, we introduced lesions at 9 of 11 target sites in the zebrafish genome.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=22543349&dopt=Abstract">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1038/nmeth.1994
dc.subjectZinc Fingers
dc.subjectGene Targeting
dc.subjectGenetics and Genomics
dc.titleAn optimized two-finger archive for ZFN-mediated gene targeting
dc.typeJournal Article
dc.source.journaltitleNature methods
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/pgfe_pp/186
dc.identifier.contextkey2878935
html.description.abstract<p>The widespread use of zinc-finger nucleases (ZFNs) for genome engineering is hampered by the fact that only a subset of sequences can be efficiently recognized using published finger archives. We describe a set of validated two-finger modules that complement existing finger archives and expand the range of ZFN-accessible sequences threefold. Using this archive, we introduced lesions at 9 of 11 target sites in the zebrafish genome.</p>
dc.identifier.submissionpathpgfe_pp/186
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentProgram in Gene Function and Expression


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