Two Highly Related p66 Proteins Comprise a New Family of Potent Transcriptional Repressors Interacting with MBD2 and MBD3
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference38 articles.
1. The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome
2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
3. DNA Methyltransferases Dnmt3a and Dnmt3b Are Essential for De Novo Methylation and Mammalian Development
4. Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
5. Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n
Cited by 77 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. GATAD2B is required for pre‐implantation embryonic development by regulating zygotic genome activation;Cell Proliferation;2024-04-12
2. Analysis of the complex between MBD2 and the histone deacetylase core of NuRD reveals key interactions critical for gene silencing;Proceedings of the National Academy of Sciences;2023-08-08
3. De novo variants in GATAD2A in individuals with a neurodevelopmental disorder: GATAD2A-related neurodevelopmental disorder;Human Genetics and Genomics Advances;2023-07
4. GATA zinc finger protein p66β promotes breast cancer cell migration by acting as a co-activator of Snail;Cell Death & Disease;2023-06-28
5. Methyl‐CpG binding domain (MBD)2/3 specifically recognizes and binds to the genomic mCpG site with a β‐sheet in the MBD to affect embryonic development in Bombyx mori;Insect Science;2023-04-10
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3