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dc.contributor.authorNakagawa, Masatoen
dc.contributor.authorTaniguchi, Yukimasaen
dc.contributor.authorSenda, Shoen
dc.contributor.authorTakizawa, Nanakoen
dc.contributor.authorIchisaka, Tomokoen
dc.contributor.authorAsano, Kanakoen
dc.contributor.authorMorizane, Asukaen
dc.contributor.authorDoi, Daisukeen
dc.contributor.authorTakahashi, Junen
dc.contributor.authorNishizawa, Masatoshien
dc.contributor.authorYoshida, Yoshinorien
dc.contributor.authorToyoda, Taroen
dc.contributor.authorOsafune, Kenjien
dc.contributor.authorSekiguchi, Kiyotoshien
dc.contributor.authorYamanaka, Shinyaen
dc.contributor.alternative中川, 誠人ja
dc.date.accessioned2014-01-09T07:08:49Z-
dc.date.available2014-01-09T07:08:49Z-
dc.date.issued2014-01-08-
dc.identifier.issn2045-2322-
dc.identifier.urihttp://hdl.handle.net/2433/180092-
dc.description細胞移植に適した新しいヒトiPS細胞の樹立・維持培養法を確立. 京都大学プレスリリース. 2014-01-08.ja
dc.description.abstractIn order to apply human embryonic stem cells (hESCs) and induced pluripotent stem cells (hiPSCs) to regenerative medicine, the cells should be produced under restricted conditions conforming to GMP guidelines. Since the conventional culture system has some issues that need to be addressed to achieve this goal, we developed a novel culture system. We found that recombinant laminin-511 E8 fragments are useful matrices for maintaining hESCs and hiPSCs when used in combination with a completely xeno-free (Xf) medium, StemFit™. Using this system, hESCs and hiPSCs can be easily and stably passaged by dissociating the cells into single cells for long periods, without any karyotype abnormalities. Human iPSCs could be generated under feeder-free (Ff) and Xf culture systems from human primary fibroblasts and blood cells, and they possessed differentiation abilities. These results indicate that hiPSCs can be generated and maintained under this novel Ff and Xf culture system.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherNature Publishing Groupen
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.en
dc.subjectEmbryonic stem cellsen
dc.subjectInduced pluripotent stem cellsen
dc.titleA novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cellsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleScientific Reportsen
dc.identifier.volume4-
dc.relation.doi10.1038/srep03594-
dc.textversionpublisher-
dc.identifier.artnum3594-
dc.identifier.pmid24399248-
dc.relation.urlhttps://www.kyoto-u.ac.jp/static/ja/news_data/h/h1/news6/2013_1/140108_1.htm-
dcterms.accessRightsopen access-
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