Luciferase assay system to monitor fibroblast growth factor signal disruption in human iPSCs
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- Kanno, Seiya
- Fac Engn, Yokohama National University Fac Engn, Ctr Biol Safety & Res, Div Cellular & Mol Toxicol, National Institute of Health Sciences - Japan
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- Mizota, Kashu
- Fac Engn, Yokohama National University
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- Okubo, Yusuke
- Fac Engn, Ctr Biol Safety & Res, Div Cellular & Mol Toxicol, National Institute of Health Sciences - Japan
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- Kageyama, Tatsuto
- Fac Engn, Yokohama National University Fac Engn, Ctr Biol Safety & Res, Div Cellular & Mol Toxicol, Kanagawa Inst Ind Sci & Technol KISTEC
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- Yan, Lei
- Fac Engn, Yokohama National University
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- Fukuda, Junji
- Fac Engn, Yokohama National University Fac Engn, Ctr Biol Safety & Res, Div Cellular & Mol Toxicol, Kanagawa Inst Ind Sci & Technol KISTEC
書誌事項
- 公開日
- 2022-06-17
- 資源種別
- journal article
- 権利情報
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- Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
- DOI
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- 10.1016/j.xpro.2022.101439
- 公開者
- Elsevier
この論文をさがす
説明
We describe a protocol for a live-cell luciferase assay system for continuously monitoring fibroblast growth factor (FGF) signal disruption in human-induced pluripotent stem cells (iPSCs). Signal disrupting effects of chemicals are used as an indicator to evaluate toxicity. The assay is reliably predictive of the effects of limb malformation chemicals (AUC = 0.93). The current approach is limited to FGF signal disruption, and combinations with other types of signaling will be required to detect the effects of different toxicants. For complete details on the use and execution of this protocol, please refer to Kanno et al. (2022a).
収録刊行物
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- STAR Protocols
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STAR Protocols 3 (2), 101439-, 2022-06-17
Elsevier
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キーワード
詳細情報 詳細情報について
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- CRID
- 1050583159613875712
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- HANDLE
- 10131/0002001274
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- ISSN
- 26661667
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- PubMed
- 35677614
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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- IRDB
- Crossref
- KAKEN
- OpenAIRE