Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function.
Mutations of MECP2 (Methyl-CpG Binding Protein 2) cause Rett syndrome. As a chromatin-associated multifunctional protein, how MeCP2 integrates external signals and regulates neuronal function remain unclear. Although neuronal activity-induced phosphorylation of MeCP2 at serine 421 (S421) has been re...
Autors principals: | Tao, J, Hu, K, Chang, Q, Wu, H, Sherman, N, Martinowich, K, Klose, R, Schanen, C, Jaenisch, R, Wang, W, Sun, Y |
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Format: | Journal article |
Idioma: | English |
Publicat: |
2009
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