|
| |
MECP2
| Symbol: | MECP2 | | Name(s): | methyl CpG binding protein 2 (Rett syndrome) | | Type: | protein-coding | | Organism: | Homo sapiens | | Synonyms: | AUTSX3, DKFZp686A24160, MRX16, MRX79, MRXS13, MRXSL, PPMX, RTS, RTT | | Links: |
Pubmed,
Entrez Gene,
GeneCards,
Map Viewer.
|
Gene Information from Publications |
| Publication Link |
Summary of findings |
| 18310203 |
Observational study of gene-disease association. (HuGE Navigator) |
| 18320046 |
Observational study of gene-disease association. (HuGE Navigator) |
| 18332345 |
Observational study of gene-disease association. (HuGE Navigator) |
| 17881312 |
Homozygosity for MECP2 gene is associated with Rett syndrome |
| 18190595 |
This result suggests that mechanisms other than X chromosome inactivation may contribute to the phenotypic heterogeneity associated with MECP2 mutations. |
| 11055898 |
Observational study of genetic testing. (HuGE Navigator) |
| 12030010 |
Observational study of genotype prevalence. (HuGE Navigator) |
| 12075485 |
Observational study of gene-disease association. (HuGE Navigator) |
| 12111644 |
Observational study of genotype prevalence. (HuGE Navigator) |
| 12180070 |
Observational study of genotype prevalence. (HuGE Navigator) | →View more information from publications. |
Recent Publications on MECP2: |  |
Survival Motor Neuron Gene 2 Silencing by DNA Methylation Correlates with Spinal Muscular Atrophy Disease Severity and can be Bypassed by Histone Deacetylase Inhibition.
Spinal muscular atrophy (SMA), a common neuromuscular disorder, is caused... | 31st October, 2008
| Institute of Human Genetics; Institute of Genetics, and Center for
| Hum Mol Genet. 2008 Oct 29.
DOI Direct Link |
Specific association between the Methyl-CpG binding domain protein 2 and the hypermethylated region of the human telomerase reverse transcriptase promoter in cancer cells.
Human telomerase reverse transcriptase (hTERT) is expressed in most cancer... | 28th October, 2008
| INSERM, U590, Lyon, F-69008, France.
| Carcinogenesis. 2008 Oct 24.
DOI Direct Link |
Activity-dependent NR2B expression is mediated by MeCP2-dependent epigenetic regulation.
Different NR2 subunits (NR2A-D) of NMDA receptors confer distinct... | 28th October, 2008
| School of Life Sciences and Biotechnology, Korea University, Seoul
| Biochem Biophys Res Commun. 2008 Oct 23.
DOI Direct Link |
Rett Syndrome: From the Gene to the Disease.
Rett syndrome (RTT, MIM No. 312750) is a progressive neurodevelopmental... | 25th October, 2008
| Rudjer Boskovic Institute, Division of Molecular Medicine, Zagreb,
| Eur Neurol. 2008 Oct 24;61(1):3-10.
DOI Direct Link |
Gene symbol: MECP2. Disease: Rett syndrome.
Xq28 duplications encompassing MECP2 have been described in male patients... | 25th October, 2008
| First School of Medicine Charles University, Department of Pediatrics, Ke
| Hum Genet. 2008 Oct;124(3):315.
|
→View more research publications. |
MECP2 results (if any) from reagent suppliers | 
|
Search Bioportfolio and other Life Science Sites for MECP2
This page has been viewed 187 times
Recent Search Terms used to find this page: Activity-dependent NR2B expression is mediated by MeCP2-dependent epigenetic regulation | MeCP2 antibody phospho | MeCP2 antibody phospho | phospho mecp2 | rett syndrome human mecp2 immunohistochemistry | MECP2 phosphorylation antibody | RETT and MECP2 and methylation | mecp2 interaction | Phospho-MECP2 antibody | .
Resources from the NCBI used on this page, NCBI's standard disclaimer applies.
|
