Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2
Mutations in MeCP2, which encodes a protein that has been proposed to function as a global transcriptional repressor, are the cause of Rett syndrome (RT T), an X-linked progressive neurological disorder. Although the selective inactivation of MeCP2 in neurons is sufficient to confer a Rett-like phen...
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Veröffentlicht in: | Science (American Association for the Advancement of Science) 2003-10, Vol.301 (5646), p.885-889 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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