MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/10/10/1085/9813451/101085.pdf
Cited by 67 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. TAT-MeCP2 protein variants rescue disease phenotypes in human and mouse models of Rett syndrome;International Journal of Biological Macromolecules;2022-06
2. Nuclear and Cytoplasmatic Players in Mitochondria-Related CNS Disorders: Chromatin Modifications and Subcellular Trafficking;Biomolecules;2022-04-23
3. Expression, Purification, Characterization and Cellular Uptake of MeCP2 Variants;The Protein Journal;2022-04
4. Epigenetics of Autism Spectrum Disorder: Histone Deacetylases;Biological Psychiatry;2021-12
5. DNA methylation signatures in autism spectrum disorders;The Nucleus;2021-08-31
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