Elevating expression of MeCP2 T158M rescues DNA binding and Rett syndrome–like phenotypes-Reference-Cited by-同舟云学术

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Elevating expression of MeCP2 T158M rescues DNA binding and Rett syndrome–like phenotypes

Published:2017-04-10 Issue:5 Volume:127 Page:1889-1904
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Lamonica Janine M.,Kwon Deborah Y.,Goffin Darren,Fenik Polina,Johnson Brian S.,Cui Yue,Guo Hengyi,Veasey Sigrid,Zhou Zhaolan

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://www.jci.org/articles/view/90967/files/pdf

Reference57 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. Purification, sequence, and cellular localization of a novel chromosomal protein that binds to Methylated DNA

4. MeCP2 Is a Transcriptional Repressor with Abundant Binding Sites in Genomic Chromatin

5. Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

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1. Differential dynamics specify MeCP2 function at nucleosomes and methylated DNA;Nature Structural & Molecular Biology;2024-08-20

2. Testing the PEST hypothesis using relevant Rett mutations in MeCP2 E1 and E2 isoforms;Human Molecular Genetics;2024-08-14

3. Early differential impact of MeCP2 mutations on functional networks in Rett syndrome patient-derived human cerebral organoids;2024-08-10

4. Potentiation of the muscarinic acetylcholine receptor 1 modulates neurophysiological features in a mouse model of Rett syndrome;Neurotherapeutics;2024-07

5. Unlock the potential: Auditory-evoked event-related potential (ERP) as a treatment-responsive biomarker for Rett syndrome;Neurotherapeutics;2024-07

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