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Human Molecular Genetics 2008 17(R1):R23-R27; doi:10.1093/hmg/ddn050
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© The Author 2008. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

This article appears in the following Human Molecular Genetics issue: Stem Cells and Regeneration [View the issue table of contents]

Molecular basis of pluripotency

Lingyi Chen1 and George Q. Daley1,2,3,4,5,*

1 Division of Pediatric Hematology/Oncology, Children's Hospital Boston and Dana Farber Cancer Institute, Boston, MA 02115, USA 2 Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA 3 Division of Hematology, Brigham and Women's Hospital, Boston, MA 02115, USA, 4 Harvard Stem Cell Institute, Boston, MA 02115, USA 5 Howard Hughes Medical Institute, MD, USA

* To whom correspondence should be addressed. Email: george.daley{at}childrens.harvard.edu

Received December 31, 2007; Accepted February 13, 2008

Embryonic stem (ES) cells are pluripotent and capable of self-renewal, thus holding promise for regenerative medicine. Recent studies have begun to provide insights into the molecular mechanisms underlying pluripotency and self-renewal. In this article, we discuss the roles of transcriptional regulation, epigenetic regulation and miRNAs in the maintenance of pluripotency and the differentiation of ES cells.


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