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Embryonic Stem Cells/Induced Pluripotent Stem Cells
Disease Modeling Using Embryonic Stem Cells: MeCP2 Regulates Nuclear Size and RNA Synthesis in Neurons†‡§
Article first published online: 20 SEP 2012
DOI: 10.1002/stem.1180
Copyright © 2012 AlphaMed Press
Additional Information
How to Cite
Yazdani, M., Deogracias, R., Guy, J., Poot, R. A., Bird, A. and Barde, Y.-A. (2012), Disease Modeling Using Embryonic Stem Cells: MeCP2 Regulates Nuclear Size and RNA Synthesis in Neurons. STEM CELLS, 30: 2128–2139. doi: 10.1002/stem.1180
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Authors contributions: M.Y., R.D., and Y.-A.B.: conception and design, collection and assembly of data, data analysis and interpretation, and manuscript writing; J.G. and A.B.: provision of material, data analysis, and manuscript writing; R.A.P.: data analysis and interpretation and manuscript writing. M.Y. and R.D. contributed equally to this article.
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Disclosure of potential conflicts of interest is found at the end of this article.
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First published online in STEM CELLSEXPRESS August 3, 2012.
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Telephone: +41612672230; Fax: +41612672208
Publication History
- Issue published online: 20 SEP 2012
- Article first published online: 20 SEP 2012
- Accepted manuscript online: 3 AUG 2012 02:15PM EST
- Manuscript Accepted: 30 JUN 2012
- Manuscript Received: 20 DEC 2011
Funded by
- Rett Syndrome Research Foundation
- Swiss National Foundation. Grant Number: CRSI33_130441
- International Rett Syndrome Foundation
Cited in:
- CrossRef
This article has been cited by:
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- 3, , Genetic syndromes caused by mutations in epigenetic genes, Human Genetics, 2013, 132, 4, 359
- 4, , , , , , , , , , , , Impaired in vivo binding of MeCP2 to chromatin in the absence of its DNA methyl-binding domain, Nucleic Acids Research, 2013, 41, 9, 4888
- 5, , , Neuronal morphology in MeCP2 mouse models is intrinsically variable and depends on age, cell type, and Mecp2 mutation, Neurobiology of Disease, 2013, 58, 3

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