Cargando…
Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing
Genomic imprinting is an epigenetic phenomenon resulting in parent-of-origin-specific gene expression that is regulated by a differentially methylated region. Gene mutations or failures in the imprinting process lead to the development of imprinting disorders, such as Angelman syndrome. The symptoms...
Autores principales: | Stanurova, Jana, Neureiter, Anika, Hiber, Michaela, de Oliveira Kessler, Hannah, Stolp, Kristin, Goetzke, Roman, Klein, Diana, Bankfalvi, Agnes, Klump, Hannes, Steenpass, Laura |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971516/ https://www.ncbi.nlm.nih.gov/pubmed/27484051 http://dx.doi.org/10.1038/srep30792 |
Ejemplares similares
-
Corrigendum: Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing
por: Stanurova, Jana, et al.
Publicado: (2018) -
Truncation of Ube3a-ATS Unsilences Paternal Ube3a and Ameliorates Behavioral Defects in the Angelman Syndrome Mouse Model
por: Meng, Linyan, et al.
Publicado: (2013) -
A Mouse Model for Imprinting of the Human Retinoblastoma Gene
por: Tasiou, Vasiliki, et al.
Publicado: (2015) -
From UBE3A to Angelman syndrome: a substrate perspective
por: Sell, Gabrielle L., et al.
Publicado: (2015) -
UBE3A reinstatement as a disease‐modifying therapy for Angelman syndrome
por: Elgersma, Ype, et al.
Publicado: (2021)