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Mouse Embryogenesis

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Cover of 'Mouse Embryogenesis'

Table of Contents

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    Book Overview
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    Chapter 1 Mouse Genotyping
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    Chapter 2 Visualizing the Vascular Network in the Mouse Embryo and Yolk Sac
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    Chapter 3 In Vivo Evaluation of the Cardiovascular System of Mouse Embryo and Fetus Using High Frequency Ultrasound
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    Chapter 4 Dynamic Imaging of Mouse Embryos and Cardiodynamics in Static Culture
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    Chapter 5 In Vivo Imaging of the Mouse Reproductive Organs, Embryo Transfer, and Oviduct Cilia Dynamics Using Optical Coherence Tomography
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    Chapter 6 Live Imaging of Fetal Intra-abdominal Organs Using Two-Photon Laser-Scanning Microscopy
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    Chapter 7 Embryonary Mouse Cardiac Fibroblast Isolation
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    Chapter 8 Explant Culture for Studying Lung Development
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    Chapter 9 Isolating Embryonic Cardiac Progenitors and Cardiac Myocytes by Fluorescence-Activated Cell Sorting
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    Chapter 10 Isolation and Culture of Mouse Placental Endothelial Cells
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    Chapter 11 Flow Cytometry and Lineage Tracing Study for Identification of Adipocyte Precursor Cell (APC) Populations
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    Chapter 12 Whole-Mount and Section In Situ Hybridization in Mouse Embryos for Detecting mRNA Expression and Localization
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    Chapter 13 Chromosome Painting of Mouse Chromosomes
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    Chapter 14 Chromatin Immunoprecipitation in Early Mouse Embryos
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    Chapter 15 Shaping Up the Embryo: The Role of Genome 3D Organization
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    Chapter 16 Genome Editing During Development Using the CRISPR-Cas Technology
Attention for Chapter 4: Dynamic Imaging of Mouse Embryos and Cardiodynamics in Static Culture
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Chapter title
Dynamic Imaging of Mouse Embryos and Cardiodynamics in Static Culture
Chapter number 4
Book title
Mouse Embryogenesis
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7714-7_4
Pubmed ID
Book ISBNs
978-1-4939-7713-0, 978-1-4939-7714-7
Authors

Andrew L. Lopez, Irina V. Larina, Andrew L. LopezIII

Abstract

The heart is a dynamic organ that quickly undergoes morphological and mechanical changes through early embryonic development. Characterizing these early moments is important for our understanding of proper embryonic development and the treatment of heart disease. Traditionally, tomographic imaging modalities and fluorescence-based microscopy are excellent approaches to visualize structural features and gene expression patterns, respectively, and connect aberrant gene programs to pathological phenotypes. However, these approaches usually require static samples or fluorescent markers, which can limit how much information we can derive from the dynamic and mechanical changes that regulate heart development. Optical coherence tomography (OCT) is unique in this circumstance because it allows for the acquisition of three-dimensional structural and four-dimensional (3D + time) functional images of living mouse embryos without fixation or contrast reagents. In this chapter, we focus on how OCT can visualize heart morphology at different stages of development and provide cardiodynamic information to reveal mechanical properties of the developing heart.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 3 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 3 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 33%
Researcher 1 33%
Lecturer 1 33%
Readers by discipline Count As %
Agricultural and Biological Sciences 1 33%
Psychology 1 33%
Unknown 1 33%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 23 March 2018.
All research outputs
#18,591,506
of 23,028,364 outputs
Outputs from Methods in molecular biology
#7,974
of 13,175 outputs
Outputs of similar age
#330,587
of 442,381 outputs
Outputs of similar age from Methods in molecular biology
#950
of 1,499 outputs
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