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利用共聚焦延时显微镜成像技术观察小鼠发育过程。

Imaging mouse development with confocal time-lapse microscopy.

作者信息

Nowotschin Sonja, Ferrer-Vaquer Anna, Hadjantonakis Anna-Katerina

机构信息

Developmental Biology Program, Sloan-Kettering Institute, New York, USA.

出版信息

Methods Enzymol. 2010;476:351-77. doi: 10.1016/S0076-6879(10)76020-1.

DOI:10.1016/S0076-6879(10)76020-1
PMID:20691876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3448272/
Abstract

The gene expression, signaling, and cellular dynamics driving mouse embryo development have emerged through embryology and genetic studies. However, since mouse development is a temporally regulated three-dimensional process, any insight needs to be placed in this context of real-time visualization. Live imaging using genetically encoded fluorescent protein reporters is pushing the envelope of our understanding by uncovering unprecedented insights into mouse development and leading to the formulation of quantitative accurate models.

摘要

驱动小鼠胚胎发育的基因表达、信号传导和细胞动力学已通过胚胎学和遗传学研究得以揭示。然而,由于小鼠发育是一个受时间调控的三维过程,任何见解都需要置于实时可视化的背景下。使用基因编码荧光蛋白报告基因的活体成像通过揭示对小鼠发育前所未有的见解并促成定量准确模型的建立,正在拓展我们的理解边界。

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本文引用的文献

1
Imaging the cytoskeleton in live Xenopus laevis embryos.对非洲爪蟾活胚胎中的细胞骨架进行成像。
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Dual transgene strategy for live visualization of chromatin and plasma membrane dynamics in murine embryonic stem cells and embryonic tissues.用于在小鼠胚胎干细胞和胚胎组织中实时可视化染色质和质膜动态的双转基因策略。
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Live-imaging fluorescent proteins in mouse embryos: multi-dimensional, multi-spectral perspectives.小鼠胚胎中的活体成像荧光蛋白:多维、多光谱视角
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A membrane associated mCherry fluorescent reporter line for studying vascular remodeling and cardiac function during murine embryonic development.一种用于研究小鼠胚胎发育过程中血管重塑和心脏功能的膜相关mCherry荧光报告基因系。
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