| The Epigenetics of Fragile X Syndrome. | |
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MedLine Citation:
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PMID: 18371387 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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In this issue of Cell Stem Cell, Eiges et al. (2007) generate a human ES cell line from an embryo identified by preimplantation genetic diagnosis, and shed light on the molecular pathology of fragile X syndrome. The discovery that, upon differentiation, epigenetic modifications likely trigger silencing of the FMR1 gene sets the stage for further studies. |
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Authors:
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Stephen T Warren |
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Publication Detail:
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Type: JOURNAL ARTICLE |
Journal Detail:
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Title: Cell stem cell Volume: 1 ISSN: 1875-9777 ISO Abbreviation: Cell Stem Cell Publication Date: 2007 Nov |
Date Detail:
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Created Date: 2008-3-28 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 101311472 Medline TA: Cell Stem Cell Country: - |
Other Details:
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Languages: ENG Pagination: 488-489 Citation Subset: - |
Affiliation:
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Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA; Department of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322, USA; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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