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dc.contributor.authorEndo, Keien
dc.contributor.authorHayashi, Karinen
dc.contributor.authorSaito, Hirohideen
dc.contributor.alternative遠藤, 慧ja
dc.contributor.alternative林, 香倫ja
dc.contributor.alternative齊藤, 博英ja
dc.date.accessioned2019-09-02T00:10:32Z-
dc.date.available2019-09-02T00:10:32Z-
dc.date.issued2019-08-02-
dc.identifier.issn2375-2548-
dc.identifier.urihttp://hdl.handle.net/2433/243837-
dc.description細胞内の複数のマイクロRNAを同時に検知して細胞を生きたまま精密に分けることに成功. 京都大学プレスリリース. 2019-08-30.ja
dc.description.abstractIntegrated bioengineering systems can make executable decisions according to the cell state. To sense the state, multiple biomarkers are detected and processed via logic gates with synthetic biological devices. However, numerical operations have not been achieved. Here, we show a design principle for messenger RNA (mRNA) devices that recapitulates intracellular information by multivariate calculations in single living cells. On the basis of this principle and the collected profiles of multiple microRNA activities, we demonstrate that rationally programmed mRNA sets classify living human cells and track their change during differentiation. Our mRNA devices automatically perform multivariate calculation and function as a decision-maker in response to dynamic intracellular changes in living cells.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Association for the Advancement of Science (AAAS)en
dc.rightsCopyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). This is an open-access article distributed under the terms of the Creative Commons Attribution license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.titleNumerical operations in living cells by programmable RNA devicesen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleScience Advancesen
dc.identifier.volume5-
dc.identifier.issue8-
dc.relation.doi10.1126/sciadv.aax0835-
dc.textversionpublisher-
dc.identifier.artnumeaax0835-
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto University・Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyoen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.identifier.pmid31457099-
dc.relation.urlhttps://www.kyoto-u.ac.jp/ja/research-news/2019-08-30-0-
dcterms.accessRightsopen access-
datacite.awardNumber15H05722-
datacite.awardNumber25870355-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
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