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Highly efficient targeted mutagenesis in one-cell mouse embryos mediated by the TALEN and CRISPR/Cas systems

https://tokushima-u.repo.nii.ac.jp/records/2000333
https://tokushima-u.repo.nii.ac.jp/records/2000333
4167ff11-0dda-43f4-85fd-db2d83706922
名前 / ファイル ライセンス アクション
srep_4_5705.pdf srep_4_5705.pdf (2.6 MB)
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Item type 文献 / Documents(1)
公開日 2025-03-04
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版社版DOI
関連識別子 https://doi.org/10.1038/srep05705
関連名称 10.1038/srep05705
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
タイトル
タイトル Highly efficient targeted mutagenesis in one-cell mouse embryos mediated by the TALEN and CRISPR/Cas systems
著者 泰江, 章博

× 泰江, 章博

WEKO 1252
e-Rad_Researcher 80380046

ja 泰江, 章博

ja-Kana ヤスエ, アキヒロ

en Yasue, Akihiro

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Mitsui, Silvia Naomi

× Mitsui, Silvia Naomi

en Mitsui, Silvia Naomi

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Watanabe, Takahito

× Watanabe, Takahito

en Watanabe, Takahito

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Sakuma, Tetsushi

× Sakuma, Tetsushi

en Sakuma, Tetsushi

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親泊, 政一

× 親泊, 政一

WEKO 305
徳島大学 教育研究者総覧 172432/profile-ja.html
e-Rad_Researcher 90502534

ja 親泊, 政一

ja-Kana オヤドマリ, セイイチ

en Oyadomari, Seiichi

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Yamamoto, Takashi

× Yamamoto, Takashi

en Yamamoto, Takashi

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野地, 澄晴

× 野地, 澄晴

WEKO 120
徳島大学 教育研究者総覧 10787/profile-ja.html
e-Rad_Researcher 40156211

ja 野地, 澄晴

ja-Kana ノジ, スミハレ

en Noji, Sumihare

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三戸, 太郎

× 三戸, 太郎

WEKO 123
徳島大学 教育研究者総覧 10793/profile-ja.html
e-Rad_Researcher 80322254

ja 三戸, 太郎

ja-Kana ミト, タロウ

en Mito, Taro

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田中, 栄二

× 田中, 栄二

WEKO 323
徳島大学 教育研究者総覧 174876/profile-ja.html
e-Rad_Researcher 40273693

ja 田中, 栄二

ja-Kana タナカ, エイジ

en Tanaka, Eiji

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抄録
内容記述 Since the establishment of embryonic stem (ES) cell lines, the combined use of gene targeting with homologous recombination has aided in elucidating the functions of various genes. However, the ES cell technique is inefficient and time-consuming. Recently, two new gene-targeting technologies have been developed: the transcription activator-like effector nuclease (TALEN) system and the clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated protein (Cas) system. In addition to aiding researchers in solving conventional problems, these technologies can be used to induce site-specific mutations in various species for which ES cells have not been established. Here, by targeting the Fgf10 gene through RNA microinjection in one-cell mouse embryos with the TALEN and CRISPR/Cas systems, we produced the known limb-defect phenotypes of Fgf10-deficient embryos at the F0 generation. Compared to the TALEN system, the CRISPR/Cas system induced the limb-defect phenotypes with a strikingly higher efficiency. Our results demonstrate that although both gene-targeting technologies are useful, the CRISPR/Cas system more effectively elicits single-step biallelic mutations in mice.
書誌情報 en : Scientific Reports

巻 4, p. 5705, 発行日 2014-07-16
収録物ID
収録物識別子タイプ EISSN
収録物識別子 20452322
出版者
出版者 Springer Nature
権利情報
権利情報 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
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識別子 280333
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言語 eng
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