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dc.contributor.authorKiani, Samira
dc.contributor.authorBeal, Jacob
dc.contributor.authorHuh, Jin
dc.contributor.authorXie, Zhen
dc.contributor.authorLi, Yinqing
dc.contributor.authorWeiss, Ron
dc.contributor.authorEbrahimkhani, Mohammad Reza
dc.contributor.authorHall, Richard N.
dc.date.accessioned2015-10-30T17:33:13Z
dc.date.available2015-10-30T17:33:13Z
dc.date.issued2014-05
dc.date.submitted2014-03
dc.identifier.issn1548-7091
dc.identifier.issn1548-7105
dc.identifier.urihttp://hdl.handle.net/1721.1/99528
dc.description.abstractA key obstacle to creating sophisticated genetic circuits has been the lack of scalable device libraries. Here we present a modular transcriptional repression architecture based on clustered regularly interspaced palindromic repeats (CRISPR) system and examine approaches for regulated expression of guide RNAs in human cells. Subsequently we demonstrate that CRISPR regulatory devices can be layered to create functional cascaded circuits, which provide a valuable toolbox for engineering purposes.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 5R01CA155320-04)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant P50 GM098792)en_US
dc.description.sponsorshipKorea (South). Ministry of Science, Information and Communication Technolgy. Intelligent Synthetic Biology Center of Global Frontier Project (2013M3A6A8073557)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/nmeth.2969en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleCRISPR transcriptional repression devices and layered circuits in mammalian cellsen_US
dc.typeArticleen_US
dc.identifier.citationKiani, Samira, Jacob Beal, Mohammad R Ebrahimkhani, Jin Huh, Richard N Hall, Zhen Xie, Yinqing Li, and Ron Weiss. “CRISPR Transcriptional Repression Devices and Layered Circuits in Mammalian Cells.” Nat Meth 11, no. 7 (May 5, 2014): 723–726.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Synthetic Biology Centeren_US
dc.contributor.mitauthorKiani, Samiraen_US
dc.contributor.mitauthorEbrahimkhani, Mohammad Rezaen_US
dc.contributor.mitauthorHuh, Jinen_US
dc.contributor.mitauthorHall, Richard N.en_US
dc.contributor.mitauthorWeiss, Ronen_US
dc.relation.journalNature Methodsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsKiani, Samira; Beal, Jacob; Ebrahimkhani, Mohammad R; Huh, Jin; Hall, Richard N; Xie, Zhen; Li, Yinqing; Weiss, Ronen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6351-7256
dc.identifier.orcidhttps://orcid.org/0000-0003-0396-2443
dc.identifier.orcidhttps://orcid.org/0000-0003-1736-0937
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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