Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3-Reference-Cited by-同舟云学术

Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3

Published:2002-07 Issue:2 Volume:35 Page:243-254
ISSN:0896-6273
Container-title:Neuron
language:en
Short-container-title:Neuron

Author:

Shahbazian Mona D.,Young Juan I.,Yuva-Paylor Lisa A.,Spencer Corinne M.,Antalffy Barbara A.,Noebels Jeffrey L.,Armstrong Dawna L.,Paylor Richard,Zoghbi Huda Y.

Publisher

Elsevier BV

Subject

General Neuroscience

Reference40 articles.

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3. Selective dendritic alterations in the cortex of Rett syndrome;Armstrong;J. Neuropathol. Exp. Neurol.,1995

4. MECP2 mutations account for most cases of typical forms of Rett syndrome;Bienvenu;Hum. Mol. Genet.,2000

5. Functional divergence between histone deacetylases in fission yeast by distinct cellular localization and in vivo specificity;Bjerling;Mol. Cell. Biol.,2002

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