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RNAi and Small Regulatory RNAs in Stem Cells

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Cover of 'RNAi and Small Regulatory RNAs in Stem Cells'

Table of Contents

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    Book Overview
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    Chapter 1 RNAi Technique in Stem Cell Research: Current Status and Future Perspectives
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    Chapter 2 RNAi and MicroRNA-Mediated Gene Regulation in Stem Cells
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    Chapter 3 Forward RNAi Screens in Human Hematopoietic Stem Cells
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    Chapter 4 Silencing of ATP11B by RNAi-Induced Changes in Neural Stem Cell Morphology
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    Chapter 5 High-Efficiency Transfection of Glioblastoma Cells and a Simple Spheroid Migration Assay
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    Chapter 6 Construction and Application of Random dsRNA Interference Library for Functional Genetic Screens in Embryonic Stem Cells
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    Chapter 7 Efficient Depletion of Essential Gene Products for Loss-of-Function Studies in Embryonic Stem Cells
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    Chapter 8 Regulation and/or Repression of Cholinergic Differentiation of Murine Embryonic Stem Cells Using RNAi Directed Against Transcription Factor L3/Lhx8
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    Chapter 9 A Recessive Genetic Screen for Components of the RNA Interference Pathway Performed in Mouse Embryonic Stem Cells
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    Chapter 10 RNAi Knockdown of Ape1 Gene in the Differentiation of Mouse Embryonic Stem Cells
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    Chapter 11 An Efficient Transfection Method for Differentiation and Cell Proliferation of Mouse Embryonic Stem Cells
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    Chapter 12 Implanting Glioblastoma Spheroids into Rat Brains and Monitoring Tumor Growth by MRI Volumetry
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    Chapter 13 RNAi-Based Techniques for the Analysis of Gene Function in Drosophila Germline Stem Cells
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    Chapter 14 In vivo RNAi in the Drosophila Follicular Epithelium: Analysis of Stem Cell Maintenance, Proliferation, and Differentiation
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    Chapter 15 A Phenotype-Based RNAi Screening for Ras-ERK/MAPK Signaling-Associated Stem Cell Regulators in C. elegans
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    Chapter 16 Engineering Human Mesenchymal Stem Cells to Release Adenosine Using miRNA Technology
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    Chapter 17 Efficient Gene Knockdowns in Mouse Embryonic Stem Cells Using MicroRNA-Based shRNAs
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    Chapter 18 Using Quantitative Real-Time PCR to Detect MicroRNA Expression Profile During Embryonic Stem Cell Differentiation
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    Chapter 19 Genetic Tools for Self-Organizing Culture of Mouse Embryonic Stem Cells via Small Regulatory RNA-Mediated Technologies, CRISPR/Cas9, and Inducible RNAi
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    Chapter 20 CRISPR-Cas9-Mediated Gene Editing in Mouse Spermatogonial Stem Cells
Attention for Chapter 10: RNAi Knockdown of Ape1 Gene in the Differentiation of Mouse Embryonic Stem Cells
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Chapter title
RNAi Knockdown of Ape1 Gene in the Differentiation of Mouse Embryonic Stem Cells
Chapter number 10
Book title
RNAi and Small Regulatory RNAs in Stem Cells
Published in
Methods in molecular biology, July 2017
DOI 10.1007/978-1-4939-7108-4_10
Pubmed ID
Book ISBNs
978-1-4939-7106-0, 978-1-4939-7108-4
Authors

Gang-Ming Zou M.D., Ph.D., Jieqing Yu, Cynthia LeBron, Yumei Fu, Gang-Ming Zou

Editors

Baohong Zhang

Abstract

Murine embryonic stem cells (ES) are pluripotent cells and have the potential to become a wide variety of specialized cell types. Mouse ES cell differentiation can be regarded as a valuable biological tool that has led to major advances in our understanding of cell and developmental biology. In vitro differentiation of mouse ES cells can be directed to a specific lineage formation, such as hematopoietic lineage, by appropriate cytokine and/or growth factor stimulation. To study specific gene function in early developmental events, gene knockout approaches have been traditionally used, however, this is a time-consuming and expensive approach. Recently, we have shown that siRNA is an effective strategy to knock down target gene expression, such as Ape1, during ES cell differentiation, and consequently, one can alter cell fates in ES-derived differentiated cells. This approach will be applicable to test the function of a wide variety of gene products using the ES cell differentiation system.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 2 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 2 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 1 50%
Student > Doctoral Student 1 50%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 1 50%
Unknown 1 50%