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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...

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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

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