• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Analysis of migration in primary ureteric bud epithelial cells.

作者信息

Kuure Satu

机构信息

Institute of Biotechnology, Viikki Biocenter, University of Helsinki, Helsinki, Finland.

出版信息

Methods Mol Biol. 2012;886:147-55. doi: 10.1007/978-1-61779-851-1_13.

DOI:10.1007/978-1-61779-851-1_13
PMID:22639258
Abstract

Kidney development has been widely used as a model system to study molecular control of inductive tissue interactions and mechanisms through which branching organs form. Due to lacking or poor methods, less focus has been in understanding details of cellular events that accomplish example ureteric bud (UB) branching. In order to form a branch point, cells need to proliferate, move in relation to each other, and change their shape as well as adhesive properties. In this chapter, detailed description is given how to set up primary UB epithelial cell cultures and study cell motility in these cells.

摘要

相似文献

1
Analysis of migration in primary ureteric bud epithelial cells.
Methods Mol Biol. 2012;886:147-55. doi: 10.1007/978-1-61779-851-1_13.
2
Patterning parameters associated with the branching of the ureteric bud regulated by epithelial-mesenchymal interactions.与输尿管芽分支相关的模式参数由上皮-间充质相互作用调控。
Int J Dev Biol. 2003 Feb;47(1):3-13.
3
Involvement of laminin binding integrins and laminin-5 in branching morphogenesis of the ureteric bud during kidney development.层粘连蛋白结合整合素和层粘连蛋白-5在肾脏发育过程中输尿管芽分支形态发生中的作用。
Dev Biol. 2001 Oct 15;238(2):289-302. doi: 10.1006/dbio.2001.0391.
4
Engineered tissues to quantify collective cell migration during morphogenesis.用于在形态发生过程中量化集体细胞迁移的工程组织。
Methods Mol Biol. 2012;886:173-82. doi: 10.1007/978-1-61779-851-1_16.
5
In vitro induction of nephrogenesis in mouse metanephric mesenchyme with lithium introduction and ureteric bud recombination.
Methods Mol Biol. 2012;886:23-30. doi: 10.1007/978-1-61779-851-1_3.
6
Spatiotemporal regulation of morphogenetic molecules during in vitro branching of the isolated ureteric bud: toward a model of branching through budding in the developing kidney.离体输尿管芽体外分支过程中形态发生分子的时空调控:构建发育中肾脏通过出芽进行分支的模型
Dev Biol. 2004 Nov 1;275(1):44-67. doi: 10.1016/j.ydbio.2004.07.022.
7
Dissecting and culturing and imaging the mouse urogenital system.
Methods Mol Biol. 2012;886:3-11. doi: 10.1007/978-1-61779-851-1_1.
8
Vegf as an epithelial cell morphogen modulates branching morphogenesis of embryonic kidney by directly acting on the ureteric bud.血管内皮生长因子作为一种上皮细胞形态发生素,通过直接作用于输尿管芽来调节胚胎肾的分支形态发生。
Mech Dev. 2009 Mar-Apr;126(3-4):91-8. doi: 10.1016/j.mod.2008.12.003. Epub 2008 Dec 25.
9
In vitro culture of embryonic kidney rudiments and isolated ureteric buds.胚胎肾原基和分离的输尿管芽的体外培养。
Methods Mol Biol. 2012;886:13-21. doi: 10.1007/978-1-61779-851-1_2.
10
Microinjection into the lumen of the ureteric tree.
Methods Mol Biol. 2012;886:311-9. doi: 10.1007/978-1-61779-851-1_28.

引用本文的文献

1
Comparative whole-genome transcriptome analysis in renal cell populations reveals high tissue specificity of MAPK/ERK targets in embryonic kidney.在肾细胞群体中的比较全基因组转录组分析表明 MAPK/ERK 靶点在胚胎肾中有很高的组织特异性。
BMC Biol. 2022 May 13;20(1):112. doi: 10.1186/s12915-022-01309-z.
2
Mitogen-activated protein kinase (MAPK) pathway regulates branching by remodeling epithelial cell adhesion.丝裂原活化蛋白激酶(MAPK)通路通过重塑上皮细胞黏附来调节分支。
PLoS Genet. 2014 Mar 6;10(3):e1004193. doi: 10.1371/journal.pgen.1004193. eCollection 2014 Mar.