DNA methylation reader MECP2: cell type- and differentiation stage-specific protein distribution-Reference-Cited by-同舟云学术

DNA methylation reader MECP2: cell type- and differentiation stage-specific protein distribution

Published:2014-08-03 Issue:1 Volume:7 Page:
ISSN:1756-8935
Container-title:Epigenetics & Chromatin
language:en
Short-container-title:Epigenetics & Chromatin

Author:

Song Congdi,Feodorova Yana,Guy Jacky,Peichl Leo,Jost Katharina Laurence,Kimura Hiroshi,Cardoso Maria Cristina,Bird Adrian,Leonhardt Heinrich,Joffe Boris,Solovei Irina

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology

Link

https://link.springer.com/content/pdf/10.1186/1756-8935-7-17.pdf

Reference69 articles.

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2. Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY: Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet. 1999, 23: 185-188.

3. Chahrour M, Zoghbi HY: The story of Rett syndrome: from clinic to neurobiology. Neuron. 2007, 56: 422-437.

4. Gonzales ML, LaSalle JM: The role of MeCP2 in brain development and neurodevelopmental disorders. Curr Psychiatry Rep. 2010, 12: 127-134.

5. Moretti P, Zoghbi HY: MeCP2 dysfunction in Rett syndrome and related disorders. Curr Opin Genet Dev. 2006, 16: 276-281.

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