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- Watanabe Takashi
- Department of Cell Pharmacology, Nagoya University, Graduate School of Medicine
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- Wang Shujie
- Department of Neural Regeneration and Cell Communication, Mie University, Graduate School of Medicine
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- Kaibuchi Kozo
- Department of Cell Pharmacology, Nagoya University, Graduate School of Medicine
この論文をさがす
抄録
The actin-cytoskeleton plays a critical role in various biological processes, including cell migration, development, tissue remodeling, and memory formation. Both extracellular and intracellular signals regulate reorganization of the actin-cytoskeleton to modulate tissue architecture and cellular morphology in a spatiotemporal manner. Since the discovery that activation of Rho family GTPases induces actin-cytoskeleton reorganization, the mode of action of Rho family GTPases has been extensively studied and individual effectors have been characterized. The actin-binding protein IQGAP1 was identified as an effector of Rac and Cdc42 and is the founding member of the IQGAP family with two additional isoforms. The IQGAP family shows conserved domain organization, and each member displays a specific expression pattern in mammalian tissues. IQGAPs regulate the actin-cytoskeleton alone and with their binding partners, thereby controlling diverse cellular processes, such as cell migration and adhesion. Here, we introduce IQGAPs as an actin-cytoskeleton regulator.
収録刊行物
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- Cell Structure and Function
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Cell Structure and Function 40 (2), 69-77, 2015
日本細胞生物学会
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詳細情報 詳細情報について
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- CRID
- 1390001204696979328
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- NII論文ID
- 130005088157
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- NII書誌ID
- AA0060007X
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- ISSN
- 13473700
- 03867196
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- NDL書誌ID
- 027281697
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- PubMed
- 26051604
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
- KAKEN
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- 抄録ライセンスフラグ
- 使用不可