Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor.

Autor: Lyst, Matthew J1, Ekiert, Robert1, Ebert, Daniel H2, Merusi, Cara1, Nowak, Jakub1, Selfridge, Jim1, Guy, Jacky1, Kastan, Nathaniel R2, Robinson, Nathaniel D2, de Lima Alves, Flavia1, Rappsilber, Juri1, Greenberg, Michael E2, Bird, Adrian1
Zdroj: Nature Neuroscience. Jul2013, Vol. 16 Issue 7, p898-902. 5p.
Databáze: Academic Search Ultimate