Differential regulation of non-protein coding RNAs from Prader-Willi Syndrome locus

Prader-Willi Syndrome (PWS) is a neurogenetic disorder caused by the deletion of imprinted genes on the paternally inherited human chromosome 15q11-q13. This locus harbours a long non-protein-coding RNA (U-UBE3A-ATS) that contains six intron-encoded snoRNAs, including the SNORD116 and SNORD115 repet...

Descripción completa

Detalles Bibliográficos
Autores principales: Galiveti, Chenna R., Raabe, Carsten A., Konthur, Zoltán, Rozhdestvensky, Timofey S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171697/
https://www.ncbi.nlm.nih.gov/pubmed/25246219
http://dx.doi.org/10.1038/srep06445

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171697/
https://www.ncbi.nlm.nih.gov/pubmed/25246219
http://dx.doi.org/10.1038/srep06445

Ejemplares similares