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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.

Methods Mol Biol. 2009

[2]
Use of KikGR a photoconvertible green-to-red fluorescent protein for cell labeling and lineage analysis in ES cells and mouse embryos.

BMC Dev Biol. 2009-9-9

[3]
Transthyretin mouse transgenes direct RFP expression or Cre-mediated recombination throughout the visceral endoderm.

Genesis. 2009-7

[4]
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Genesis. 2009-5

[5]
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Trends Biotechnol. 2009-5

[6]
A membrane associated mCherry fluorescent reporter line for studying vascular remodeling and cardiac function during murine embryonic development.

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[7]
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Dev Dyn. 2008-10

[8]
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Curr Protoc Cell Biol. 2008-3

[9]
High-speed imaging of developing heart valves reveals interplay of morphogenesis and function.

Development. 2008-3

[10]
Fluorescent proteins for photoactivation experiments.

Methods Cell Biol. 2008

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