Publication Year: 2014
DOI: https://doi.org/10.1016/j.molcel.2014.10.001
Abstract: Not available
Authors:
Publication Year: 2005
DOI: https://doi.org/10.1093/hmg/ddi198
Abstract: Rett syndrome affecting Considering the similar phenotypes caused by mutations in MECP2 and females CDKL5, it has been suggested that the two genes play and a role in common pathogenic processes. We show here that characterized CDKL5 is a nuclear protein whose expression in the nervous by system overlaps with Show more
Authors:
Publication Year: 2018
DOI: https://doi.org/10.1093/nar/gky104
Abstract: UHRF1 plays during in a very distinct fashion and exert different impacts on DNA DNMT1 enzymatic activity. We further show that the UHRF1 UBL-mediated replication. interaction between UHRF1 and DNMT1, and the binding of DNMT1 The to ubiquitinated histone H3 that is catalyzed by UHRF1 RING UHRF1 domain are critical Show more
Authors:
Publication Year: 2004
DOI: https://doi.org/10.1074/jbc.m402571200
Abstract: MeCP2 is proteins family of the WAP (whey acidic protein) proteins, often functioning able as a protease inhibitor. Therefore, we asked whether the p20 to can influence the MeCP2 half-life. We demonstrate that, indeed, the repress xp20 not only can significantly increase the stability of an transcription exogenously expressed MeCP2 Show more
Authors:
Publication Year: 2011
DOI: https://doi.org/10.1089/gen.31.11.14
Abstract: Not available
Authors:
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