| 1 | 8001979 | Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome. | Genomics | 1994 Aug |
1 |
| 2 | 9038338 | MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin. | Cell | 1997 Feb 21 |
1 |
| 3 | 9271441 | Chicken MAR-binding protein ARBP is homologous to rat methyl-CpG-binding protein MeCP2. | Mol Cell Biol | 1997 Sep |
1 |
| 4 | 9916800 | Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer. | Nat Genet | 1999 Jan |
2 |
| 5 | 10390525 | Cytosine methylation transforms an E2F site in the retinoblastoma gene promoter into a binding site for the general repressor methylcytosine-binding protein 2 (MeCP2). | Nucleic Acids Res | 1999 Jul 15 |
2 |
| 6 | 10508514 | Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. | Nat Genet | 1999 Oct |
1 |
| 7 | 11262731 | Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations. | Curr Opin Neurol | 2001 Apr |
1 |
| 8 | 11331619 | MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome. | Hum Mol Genet | 2001 May 1 |
1 |
| 9 | 11392517 | Occurrence of Rett syndrome in boys. | J Child Neurol | 2001 May |
1 |
| 10 | 11453972 | Rett syndrome from quintuple and triple deletions within the MECP2 deletion hotspot region. | Clin Genet | 2001 Jun |
4 |
| 11 | 11861904 | Methylation-dependent silencing at the H19 imprinting control region by MeCP2. | Nucleic Acids Res | 2002 Mar 1 |
1 |
| 12 | 11865062 | Precipitous release of methyl-CpG binding protein 2 and histone deacetylase 1 from the methylated human multidrug resistance gene (MDR1) on activation. | Mol Cell Biol | 2002 Mar |
1 |
| 13 | 12107440 | MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain. | Hum Genet | 2002 Jun |
1 |
| 14 | 12112735 | Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype. | Ment Retard Dev Disabil Res Rev | 2002 |
2 |
| 15 | 12427740 | The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation. | J Biol Chem | 2003 Feb 7 |
3 |
| 16 | 14598336 | MECP2 gene mutations in non-syndromic X-linked mental retardation: phenotype-genotype correlation. | Am J Med Genet A | 2003 Dec 1 |
2 |
| 17 | 14974082 | Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndrome. | Hum Mutat | 2004 Mar |
1 |
| 18 | 15247904 | Mechanisms underlying lack of insulin-like growth factor-binding protein-3 expression in non-small-cell lung cancer. | Oncogene | 2004 Aug 26 |
1 |
| 19 | 15322089 | MeCP2 behaves as an elongated monomer that does not stably associate with the Sin3a chromatin remodeling complex. | J Biol Chem | 2004 Nov 5 |
1 |
| 20 | 15549394 | The impact of MECP2 mutations in the expression patterns of Rett syndrome patients. | Hum Genet | 2005 Jan |
1 |
| 21 | 15591025 | DNA methylation affects cell proliferation, cortisol secretion and steroidogenic gene expression in human adrenocortical NCI-H295R cells. | J Mol Endocrinol | 2004 Dec |
1 |
| 22 | 15689352 | Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples. | Hum Mol Genet | 2005 Mar 15 |
1 |
| 23 | 15809347 | The essential role of histone H3 Lys9 di-methylation and MeCP2 binding in MGMT silencing with poor DNA methylation of the promoter CpG island. | J Biochem | 2005 Mar |
1 |
| 24 | 15917437 | 5-halogenated pyrimidine lesions within a CpG sequence context mimic 5-methylcytosine by enhancing the binding of the methyl-CpG-binding domain of methyl-CpG-binding protein 2 (MeCP2). | Nucleic Acids Res | 2005 |
4 |
| 25 | 15959553 | MeCP2: the chromatin connection and beyond. | Biochem Cell Biol | 2005 Jun |
2 |
| 26 | 16647848 | MeCP2 dysfunction in Rett syndrome and related disorders. | Curr Opin Genet Dev | 2006 Jun |
1 |
| 27 | 16786000 | CpG island promoter methylation and silencing of 14-3-3sigma gene expression in LNCaP and Tramp-C1 prostate cancer cell lines is associated with methyl-CpG-binding protein MBD2. | Oncogene | 2006 Aug 3 |
2 |
| 28 | 17036333 | SPAN-XB core promoter sequence is regulated in myeloma cells by specific CpG dinucleotides associated with the MeCP2 protein. | Int J Cancer | 2006 Dec 15 |
1 |
| 29 | 17046689 | Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation. | Neuron | 2006 Oct 19 |
2 |
| 30 | 17084570 | Low significance of MECP2 mutations as a cause of mental retardation in Brazilian males. | Brain Dev | 2007 Jun |
1 |
| 31 | 17171659 | Sequence variants within exon 1 of MECP2 occur in females with mental retardation. | Am J Med Genet B Neuropsychiatr Genet | 2007 Apr 5 |
2 |
| 32 | 17339270 | 15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders. | Hum Mol Genet | 2007 Mar 15 |
1 |
| 33 | 17363207 | Imprinting status of paternally imprinted DLX5 gene in Japanese patients with Rett syndrome. | Brain Dev | 2007 Sep |
2 |
| 34 | 17371874 | Intrinsic disorder and autonomous domain function in the multifunctional nuclear protein, MeCP2. | J Biol Chem | 2007 May 18 |
3 |
| 35 | 17698632 | Homocysteine inhibits endothelial cell growth via DNA hypomethylation of the cyclin A gene. | Blood | 2007 Nov 15 |
2 |
| 36 | 18204074 | Epigenetic silencing of O6-methylguanine DNA methyltransferase gene in NiS-transformed cells. | Carcinogenesis | 2008 Jun |
1 |
| 37 | 18302774 | Characterization of novel isoforms and evaluation of SNF2L/SMARCA1 as a candidate gene for X-linked mental retardation in 12 families linked to Xq25-26. | BMC Med Genet | 2008 Feb 26 |
1 |
| 38 | 18310117 | Homocysteine-induced extracellular superoxide dismutase and its epigenetic mechanisms in monocytes. | J Exp Biol | 2008 Mar |
6 |
| 39 | 18477000 | Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure. | Clin Genet | 2008 Aug |
1 |
| 40 | 18492797 | Transcriptional repression of O6-methylguanine DNA methyltransferase gene rendering cells hypersensitive to N,N'-bis(2-chloroethyl)-N-nitrosurea in camptothecin-resistant cells. | Mol Pharmacol | 2008 Aug |
1 |
| 41 | 18513492 | ING2 recruits histone methyltransferase activity with methylation site specificity distinct from histone H3 lysines 4 and 9. | Biochim Biophys Acta | 2008 Oct |
1 |
| 42 | 18550052 | Clinically relevant concentrations of valproic acid modulate melatonin MT(1) receptor, HDAC and MeCP2 mRNA expression in C6 glioma cells. | Eur J Pharmacol | 2008 Jul 28 |
3 |
| 43 | 18723031 | Comparison of global DNA methylation profiles in replicative versus premature senescence. | Life Sci | 2008 Sep 26 |
1 |
| 44 | 18773074 | Genetic modifiers of MeCP2 function in Drosophila. | PLoS Genet | 2008 Sep 5 |
1 |
| 45 | 18952054 | Activity-dependent NR2B expression is mediated by MeCP2-dependent epigenetic regulation. | Biochem Biophys Res Commun | 2008 Dec 19 |
2 |
| 46 | 19012748 | Neurochemical changes in a mouse model of Rett syndrome: changes over time and in response to perinatal choline nutritional supplementation. | J Neurochem | 2009 Jan |
2 |
| 47 | 19034540 | The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoform. | Neurogenetics | 2009 Apr |
1 |
| 48 | 19109157 | Epigenetic regulation of Foxp3 expression in regulatory T cells by DNA methylation. | J Immunol | 2009 Jan 1 |
1 |
| 49 | 19116135 | Temozolomide and carmustine cause large-scale heterochromatin reorganization in glioma cells. | Biochem Biophys Res Commun | 2009 Feb 6 |
1 |
| 50 | 19120127 | Human sympathetic nerve biology: parallel influences of stress and epigenetics in essential hypertension and panic disorder. | Ann N Y Acad Sci | 2008 Dec |
1 |