scholarly article | Q13442814 |
retracted paper | Q45182324 |
P356 | DOI | 10.1016/S1097-2765(03)00276-4 |
P698 | PubMed publication ID | 14536082 |
P50 | author | Huda Zoghbi | Q1633764 |
Irina Stancheva | Q30505459 | ||
Richard Meehan | Q42846183 | ||
P2093 | author name string | Anne L Collins | |
Ingatia B Van den Veyver | |||
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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 | Q22337290 | ||
The Ski protein family is required for MeCP2-mediated transcriptional repression | Q24291417 | ||
Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex | Q24324026 | ||
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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome | Q28504458 | ||
MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin | Q28576622 | ||
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription | Q29547568 | ||
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice | Q29616328 | ||
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3 | Q29616516 | ||
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P433 | issue | 2 | |
P921 | main subject | Rett syndrome | Q917357 |
P304 | page(s) | 425-435 | |
P577 | publication date | 2003-08-01 | |
P1433 | published in | Molecular Cell | Q3319468 |
P1476 | title | A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos | |
P478 | volume | 12 |
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Q36238523 | Reading the DNA methylation signal |
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Q36434812 | Replication and translation of epigenetic information. |
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Q28588081 | The transcriptional repressor Mecp2 regulates terminal neuronal differentiation |
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Q39960021 | Transcriptional activation by the Kaposi's sarcoma-associated herpesvirus latency-associated nuclear antigen is facilitated by an N-terminal chromatin-binding motif. |
Q36053034 | Transcriptional activities of retinoic acid receptors |
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Q53465855 | Using Morpholinos to control gene expression. |
Q35789580 | When enough is enough: genetic diseases associated with transcriptional derepression |
Q56270643 | X-linked mental retardation |
Q46962711 | Xenopus embryos lacking specific isoforms of the corepressor SMRT develop abnormal heads. |
Q51988923 | Xenopus hairy2 functions in neural crest formation by maintaining cells in a mitotic and undifferentiated state. |
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