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Cellular Programming and Reprogramming

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Cover of 'Cellular Programming and Reprogramming'

Table of Contents

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    Book Overview
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    Chapter 1 Human embryonic stem cell derivation, maintenance, and differentiation to trophoblast.
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    Chapter 2 Isolation and maintenance of mouse epiblast stem cells.
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    Chapter 3 Functional assays for hematopoietic stem cell self-renewal.
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    Chapter 4 Isolation procedure and characterization of multipotent adult progenitor cells from rat bone marrow.
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    Chapter 5 Generation of functional insulin-producing cells from human embryonic stem cells in vitro.
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    Chapter 6 Mesoderm cell development from ES cells.
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    Chapter 7 Directed differentiation of red blood cells from human embryonic stem cells.
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    Chapter 8 Directed differentiation of neural-stem cells and subtype-specific neurons from hESCs.
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    Chapter 9 Directing human embryonic stem cells to a retinal fate.
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    Chapter 10 Bovine somatic cell nuclear transfer.
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    Chapter 11 Cell fusion-induced reprogramming.
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    Chapter 12 An improved method for generating and identifying human induced pluripotent stem cells.
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    Chapter 13 Using small molecules to improve generation of induced pluripotent stem cells from somatic cells.
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    Chapter 14 Reprogramming of committed lymphoid cells by enforced transcription factor expression.
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    Chapter 15 Reprogramming of B cells.
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    Chapter 16 Adult cell fate reprogramming: converting liver to pancreas.
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    Chapter 17 In vitro reprogramming of pancreatic cells to hepatocytes.
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    Chapter 18 Generation of novel rat and human pluripotent stem cells by reprogramming and chemical approaches.
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    Chapter 19 Small molecule screen in zebrafish and HSC expansion.
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    Chapter 20 Zebrafish small molecule screen in reprogramming/cell fate modulation.
Attention for Chapter 13: Using small molecules to improve generation of induced pluripotent stem cells from somatic cells.
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Chapter title
Using small molecules to improve generation of induced pluripotent stem cells from somatic cells.
Chapter number 13
Book title
Cellular Programming and Reprogramming
Published in
Methods in molecular biology, February 2010
DOI 10.1007/978-1-60761-691-7_13
Pubmed ID
Book ISBNs
978-1-60761-690-0, 978-1-60761-691-7
Authors

Desponts C, Ding S, Caroline Desponts, Sheng Ding

Editors

Sheng Ding

Abstract

Induction of pluripotent stem cells from somatic cells by defined factors was shown to be possible only recently, but already several laboratories have made tremendous strive toward improving and understanding the process. Originally, Oct4, Sox2, Klf4, and cMyc were identified as being the combination of genes necessary to induce reprogramming. It was later shown that cMyc was dispensable; however, in its absence the process was less efficient and took a considerably longer period of time to occur. Furthermore, others have shown that the combination of Oct4, Sox2, Nanog, and Lin28 could also induce reprogramming. One major caveat associated with these techniques remains the need for overexpression of several genes using viral systems. Until very recently, most studies were done using integrating viruses such as retroviruses and lentiviruses. This method ensured that the protein of interested would be expressed at a high concentration and for an adequate period of time necessary to induce reprogramming. Up to date, others have now been able to use different nonintegrative method such as adenovirus and plasmid transfection to induce reprogramming. Furthermore, piggyBac transposition was successfully used to induce reprogramming of murine cells. Most importantly, it was recently published that reprogramming can be induced in the absence of virus, with proteins and small molecules. All of the later methods are appealing since they do not require the integration of the virus or plasmid to exert its effect. However, one avenue that would be all the more therapeutically appealing would be to induce reprogramming in the absence of gene overexpression systems, using small molecules to modulate signaling pathways in the somatic cells. A few molecules have already been identified with the ability to either improve the process or replace one or two of the genes deemed necessary for reprogramming. We have screened successfully for compounds that can replace some of these factors, and share the methods developed following these screens.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 44 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 2%
Unknown 43 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 13 30%
Student > Bachelor 5 11%
Other 5 11%
Researcher 4 9%
Professor > Associate Professor 4 9%
Other 7 16%
Unknown 6 14%
Readers by discipline Count As %
Agricultural and Biological Sciences 17 39%
Medicine and Dentistry 10 23%
Biochemistry, Genetics and Molecular Biology 5 11%
Neuroscience 4 9%
Immunology and Microbiology 1 2%
Other 1 2%
Unknown 6 14%
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 14 January 2013.
All research outputs
#20,178,948
of 22,693,205 outputs
Outputs from Methods in molecular biology
#9,830
of 13,045 outputs
Outputs of similar age
#89,833
of 94,096 outputs
Outputs of similar age from Methods in molecular biology
#21
of 23 outputs
Altmetric has tracked 22,693,205 research outputs across all sources so far. This one is in the 1st percentile – i.e., 1% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,045 research outputs from this source. They receive a mean Attention Score of 3.3. This one is in the 1st percentile – i.e., 1% of its peers scored the same or lower than it.
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We're also able to compare this research output to 23 others from the same source and published within six weeks on either side of this one. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.