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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 18: Using Quantitative Real-Time PCR to Detect MicroRNA Expression Profile During Embryonic Stem Cell Differentiation
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Chapter title
Using Quantitative Real-Time PCR to Detect MicroRNA Expression Profile During Embryonic Stem Cell Differentiation
Chapter number 18
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_18
Pubmed ID
Book ISBNs
978-1-4939-7106-0, 978-1-4939-7108-4
Authors

Pan, Xiaoping, Murashov, Alexander K., Stellwag, Edmund J., Zhang, Baohong, Xiaoping Pan, Alexander K. Murashov, Edmund J. Stellwag, Baohong Zhang

Editors

Baohong Zhang

Abstract

Quantitative real-time PCR (qRT-PCR) is a reliable method to determine and monitor microRNA (miRNA) expression profiles in different cells, tissues, and organisms. Although there are several different strategies in performing qRT-PCR to determine miRNA expression, all of them have two steps in common: reverse transcription for obtaining cDNA from mature miRNA sequencing and standard real-time PCR for amplification of cDNA. This chapter demonstrates the application of quantitative real-time PCR for determining miRNA expression profiles during mouse embryonic stem cell differentiation. In this method, a mature miRNA sequence is first reverse transcribed into a long cDNA with a 40-50 nt miRNA-specific stem-loop primer; then, a standard real-time PCR reaction is performed for determining miRNA expression using a forward miRNA-specific primer and a universal reverse primer.

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The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Unspecified 1 7%
Librarian 1 7%
Other 1 7%
Lecturer 1 7%
Student > Doctoral Student 1 7%
Other 4 27%
Unknown 6 40%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 13%
Agricultural and Biological Sciences 2 13%
Unspecified 1 7%
Pharmacology, Toxicology and Pharmaceutical Science 1 7%
Social Sciences 1 7%
Other 2 13%
Unknown 6 40%
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 05 July 2017.
All research outputs
#20,431,953
of 22,985,065 outputs
Outputs from Methods in molecular biology
#9,929
of 13,149 outputs
Outputs of similar age
#273,455
of 313,616 outputs
Outputs of similar age from Methods in molecular biology
#204
of 264 outputs
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