
MECP2 - Wikipedia
MECP2 (methyl CpG binding protein 2) is a gene [5] that encodes the protein MECP2. [6] MECP2 appears to be essential for the normal function of nerve cells. The protein seems to be …
MECP2 duplication syndrome - Children's Hospital of Philadelphia
MECP2 duplication syndrome is a rare neurodevelopmental condition caused by an extra copy (duplication) of the MECP2 gene. The disorder can cause a wide range of symptoms with …
MECP2 Gene - GeneCards | MECP2 Protein | MECP2 Antibody
2024年12月25日 · MECP2 (Methyl-CpG Binding Protein 2) is a Protein Coding gene. Diseases associated with MECP2 include Rett Syndrome and Encephalopathy, Neonatal Severe, Due …
神经系统发育障碍疾病致病基因之MeCP2 - 知乎 - 知乎专栏
MeCP2基因研究概况. MeCP2对哺乳动物的学习记忆能力有着重要的影响,同时也是 Rett综合症 和 MeCP2重复综合症 的致病基因。MeCP2通过多种机制对基因的转录有显著影响,而且有 …
MECP2 gene - MedlinePlus
The MECP2 gene provides instructions for making a protein called MeCP2. This protein helps regulate gene activity (expression) by modifying chromatin, the complex of DNA and protein …
Differential dynamics specify MeCP2 function at nucleosomes and ...
2024年8月20日 · Methyl-CpG-binding protein 2 (MeCP2) is an essential chromatin-binding protein whose mutations cause Rett syndrome (RTT), a severe neurological disorder that primarily...
MeCP2 regulates gene expression through recognition of H3K27me3 …
2020年6月19日 · Our findings indicate that MeCP2 interacts with genomic loci via binding to DNA as well as histones, and that interaction between MeCP2 and histone proteins plays a key role …
Nature | MeCP2突变导致相分离发生紊乱进而引起Rett综合征
近日,来自MIT的Richard A. Young课题组在Nature杂志发表了题为MeCP2 links heterochromatin condensates and neurodevelopmental disease 的文章,从 相分离 的角度阐述了MeCP2突变导 …
MECP2基因及MECP2相关疾病 - PMC - PubMed Central (PMC)
MECP2转录后形成MECP2-e1和MECP2-e2两种剪切体 。MECP2有3个主要的功能域:CpG结合域(methyl-CpG-bingding domain, MBD)、转录抑制域(transcription repression domain, …
MeCP2 基因- 生物百科 - 生物行
MeCP2(Methyl-CpG Binding Protein 2)基因是位于X染色体上的一个重要基因,编码一种结合甲基化CpG二核苷酸的蛋白质。 这种蛋白质在调控基因表达、维持染色质结构和调控神经元功 …