MECP2 impairs neuronal structure by regulating KIBRA-Reference-Cited by-同舟云学术

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MECP2 impairs neuronal structure by regulating KIBRA

Published:2016-07 Issue: Volume:91 Page:284-291
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Williams Alison A.,White Robin,Siniard Ashley,Corneveaux Jason,Huentelman Matt,Duch Carsten

Funder

German Science Foundation

Natural and Medical Sciences Research Center of the University of Medicine Mainz

National Institute of Health

Science Foundation Arizona

Publisher

Elsevier BV

Subject

Neurology

Reference58 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999

2. Can we relate MeCP2 deficiency to the structural and chemical abnormalities in the Rett brain?;Armstrong;Brain Dev.,2005

3. An AT-hook domain in MeCP2 determines the clinical course of Rett syndrome and related disorders;Baker;Cell,2013

4. Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus;Ben-Shachar;Hum. Mol. Genet.,2009

5. Cytosine DNA methylation is found in Drosophila melanogaster but absent in Saccharomyces cerevisiae, Schizosaccharomyces pombe, and other yeast species;Capuano;Anal. Chem.,2014

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A multi-model approach defines function altering MECP2 missense variants identified in individuals with autism spectrum disorder;2024-08-13

2. The Role of MeCP2 in Regulating Synaptic Plasticity in the Context of Stress and Depression;Cells;2022-02-21

3. Neuronal activation modulates enhancer activity of genes for excitatory synaptogenesis through de novo DNA methylation;Journal of Reproduction and Development;2021

4. Apoptotic Activity of MeCP2 Is Enhanced by C-Terminal Truncating Mutations;PLOS ONE;2016-07-21

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