Literature DB >> 24362033

Small molecule screening in human induced pluripotent stem cell-derived terminal cell types.

Sandra J Engle1, Fabien Vincent.   

Abstract

A need for better clinical outcomes has heightened interest in the use of physiologically relevant human cells in the drug discovery process. Patient-specific human induced pluripotent stem cells may offer a relevant, robust, scalable, and cost-effective model of human disease physiology. Small molecule high throughput screening in human induced pluripotent stem cell-derived cells with the intent of identifying novel therapeutic compounds is starting to influence the drug discovery process; however, the use of these cells presents many high throughput screening development challenges. This technology has the potential to transform the way drug discovery is performed.

Entities:  

Keywords:  Drug Action; Drug Development; Drug Discovery; Drug Screening; Stem Cells

Mesh:

Substances:

Year:  2013        PMID: 24362033      PMCID: PMC3931017          DOI: 10.1074/jbc.R113.529156

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


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4.  The why and how of phenotypic small-molecule screens.

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5.  Low incidence of DNA sequence variation in human induced pluripotent stem cells generated by nonintegrating plasmid expression.

Authors:  Linzhao Cheng; Nancy F Hansen; Ling Zhao; Yutao Du; Chunlin Zou; Frank X Donovan; Bin-Kuan Chou; Guangyu Zhou; Shijie Li; Sarah N Dowey; Zhaohui Ye; Settara C Chandrasekharappa; Huanming Yang; James C Mullikin; P Paul Liu
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Review 7.  A Tox21 Approach to Altered Epigenetic Landscapes: Assessing Epigenetic Toxicity Pathways Leading to Altered Gene Expression and Oncogenic Transformation In Vitro.

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8.  Introduction to thematic minireview series: Development of human therapeutics based on induced pluripotent stem cell (iPSC) technology.

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10.  Identification of Mouse Mesenteric and Subcutaneous in vitro Adipogenic Cells.

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