MiR-142 is required for Staphylococcus aureus clearance at skin wound sites via small GTPase-mediated regulation of the neutrophil actin cytoskeleton

• Material Type: 博士論文
• Title: MiR-142 is required for Staphylococcus aureus clearance at skin wound sites via small GTPase-mediated regulation of the neutrophil actin cytoskeleton
• Author/Editor: 田中, 克弥
• Author Heading: 田中, 克弥
• Publication, Distribution, etc.: Elsevier, Inc.
• Publication Date: 2017-03-21
• Publication Date (W3CDTF): 2017-03-21
• Alternative Title: miR-142はsmall GTPaseを介して好中球のアクチン細胞骨格を調節し皮膚感染創での黄色ブドウ球菌の排除に必要である
• Periodical title: Journal of Investigative Dermatology
• No. or year of volume/issue: 137 4
• Volume: 137
• Issue: 4
• Pages: 931-940
• ISSN (Periodical Title): ISSN : 0022202X
• Degree grantor/type: Nagasaki University (長崎大学)
• Date Granted: 2017-03-21
• Dissertation Number: 甲医歯薬第946号
• Degree Type: 博士(医学)
• Text Language Code: eng
• Target Audience: 一般
• Note (General): 長崎大学学位論文 学位記番号:博(医歯薬)甲第946号 学位授与年月日:平成29年3月21日; Author: Katsuya Tanaka, Sang Eun Kim, Hiroki Yano, Gaku Matsumoto, Ryoma Ohuchida, Yuhoko Ishikura, Masatake Araki, Kimi Araki, Seongjoon Park, Toshimitsu Komatsu, Hiroko Hayashi, Kazuya Ikematsu, Katsumi Tanaka, Akiyoshi Hirano, Paul Martin, Isao Shimokawa, Ryoichi Mori; Citation: Journal of Investigative Dermatology, 137(4), pp.931-940; 2017; Nagasaki University (長崎大学), 博士(医学) (2017-03-21)
• Format (IMT): application/pdf
• Source: ISYK946_Tanaka.pdf （fulltext）; https://nagasaki-u.repo.nii.ac.jp/record/3971/files/ISYK946_Tanaka.pdf
• Access Restrictions: インターネット公開
• Rights (production): c 2016 The Authors. Published by Elsevier, Inc. on behalf of the Society for Investigative Dermatology.
• Related Material (URI): HDL; http://hdl.handle.net/10069/37404
• Related Material (DOI): 10.1016/j.jid.2016.11.018
• Data Provider (Database): 国立情報学研究所 : 学術機関リポジトリデータベース（IRDB）（機関リポジトリ）; https://irdb.nii.ac.jp
• Original Data Provider (Database): 長崎大学 : 長崎大学学術研究成果リポジトリ

• Summary, etc.: MicroRNAs (miRNAs) are small noncoding RNAs that regulate protein translation by binding to complementary target mRNAs. We previously identified two m...