Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice-Reference-Cited by-同舟云学术

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Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

Published:2009-02-10 Issue:6 Volume:106 Page:2029-2034
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:PNAS

Author:

Tropea Daniela,Giacometti Emanuela,Wilson Nathan R.,Beard Caroline,McCurry Cortina,Fu Dong Dong,Flannery Ruth,Jaenisch Rudolf,Sur Mriganka

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference49 articles.

1. The Story of Rett Syndrome: From Clinic to Neurobiology

2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

3. MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription

4. Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

5. Expression of MeCP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis

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