Mice lacking methyl-CpG binding protein 1 have deficits in adult neurogenesis and hippocampal function-Reference-Cited by-同舟云学术

Mice lacking methyl-CpG binding protein 1 have deficits in adult neurogenesis and hippocampal function

Published:2003-05-14 Issue:11 Volume:100 Page:6777-6782
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Zhao X.,Ueba T.,Christie B. R.,Barkho B.,McConnell M. J.,Nakashima K.,Lein E. S.,Eadie B. D.,Willhoite A. R.,Muotri A. R.,Summers R. G.,Chun J.,Lee K.-F.,Gage F. H.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference37 articles.

1. DNA methylation patterns and epigenetic memory

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

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

4. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

5. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

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