| 1 |
34867203 | Rett Syndrome and Fragile X Syndrome: Different Etiology With Common Molecular Dysfunctions. | 2021 |
1 |
| 2 |
32782676 | A genome-wide analysis reveals the MeCP2-dependent regulation of genes in BGC-823 cells. | 2020 |
2 |
| 3 |
31327966 | Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome. | 2019 Summer |
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| 4 |
23351786 | MeCP2 modulates gene expression pathways in astrocytes. | 2013 Jan 25 |
1 |
| 5 |
21394759 | Brain region-specific expression of Fxyd1, an Mecp2 target gene, is regulated by epigenetic mechanisms. | 2011 Jun |
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| 6 |
20979427 | Impact of base analogues within a CpG dinucleotide on the binding of DNA by the methyl-binding domain of MeCP2 and methylation by DNMT1. | 2010 Nov 30 |
1 |
| 7 |
17371874 | Intrinsic disorder and autonomous domain function in the multifunctional nuclear protein, MeCP2. | 2007 May 18 |
1 |
| 8 |
15959553 | MeCP2: the chromatin connection and beyond. | 2005 Jun |
2 |
| 9 |
15322089 | MeCP2 behaves as an elongated monomer that does not stably associate with the Sin3a chromatin remodeling complex. | 2004 Nov 5 |
1 |
| 10 |
12427740 | The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation. | 2003 Feb 7 |
1 |
| 11 |
11861904 | Methylation-dependent silencing at the H19 imprinting control region by MeCP2. | 2002 Mar 1 |
1 |
| 12 |
12112735 | Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype. | 2002 |
1 |
| 13 |
10508514 | Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. | 1999 Oct |
1 |