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Development of the nucleoside analogs to harmonize with in vivo molecular function

Development of the nucleoside analogs to harmonize with in vivo molecular function
开发核苷类似物以协调体内分子功能
批准号:
20790013
负责人:
TANIGUCHI Yosuke
金额:
$2.75万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Young Scientists (B)
财政年份:
2008
资助国家:
日本
项目状态:
已结题
起止时间:
2008 至 2009

项目摘要

项目成果

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中文摘要
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英文摘要
In this study, we designed and synthesized the nucleoside analogs which interact with duplex DNA. Moreover, we aimed to establish the basic technology of the regulation of the gene expression using these nucleoside analogs. We have found that oligonucleotide containing the nucleoside analogs formed the stable triplex DNA as a result of interaction between the nucleoside analogs and duplex DNA. And this oligonucleotide inhibited the gene expression in the cultured cell.
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Formation of a stable triplex incorporating a CG interrupting site by a new WNA derivative containing 3-aminopyrazole as a nucleobase.
通过含有 3-氨基吡唑作为核碱基的新型 WNA 衍生物形成包含 CG 中断位点的稳定三链体。
DOI: --
发表时间: 2008
期刊: Nucleic Acids Symp. Ser. 52
影响因子: --
作者: [Uchida Y., Taniguchi Y., Aoki E., Togo M., Sasaki S.]
通讯作者: Sasaki S.
小さな認識塩基をもつW字型人工核酸の合成と3本鎖形成能の評価
小识别碱基W型人工核酸的合成及三链形成能力评价
DOI: --
发表时间: 2009
期刊:
影响因子: --
作者: [Funakawa, S., Watanabe, T., Kosaki, T., 内田 祐子]
通讯作者: 内田 祐子
The Alkyl-Connected 2-Amino-6-Vinylprine (AVP) Crosslinking Agent for Improved Selectivity to the Cytosine Base in RNA
烷基连接的 2-氨基-6-乙烯基吡啶 (AVP) 交联剂可提高 RNA 中胞嘧啶碱基的选择性
DOI: --
发表时间: 2010
期刊: Bioorganic & Medicinal Chemistry (In press)
影响因子: --
作者: [Shigenaga, A., Yosuke Taniguchi]
通讯作者: Yosuke Taniguchi
Recognition of the CG interrupting site by W-shaped nucleoside analogs (WNA) having the pyrozole ring in an anti-parallel triplex DNA
通过反平行三链 DNA 中具有吡唑环的 W 形核苷类似物 (WNA) 识别 CG 中断位点
DOI: --
发表时间: 2009
期刊: Bioorg Med. Chem. 17
影响因子: --
作者: [Yosuke Taniguchi, Yuko Uchida, Tomoko Takaki, Eriko Aoki, Shigeki Sasaki]
通讯作者: Shigeki Sasaki
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