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Maternal transcription of non-protein coding RNAs from the PWS-critical region rescues growth retardation in mice

Prader-Willi syndrome (PWS) is a neurogenetic disorder caused by loss of paternally expressed genes on chromosome 15q11-q13. The PWS-critical region (PWScr) contains an array of non-protein coding IPW-A exons hosting intronic SNORD116 snoRNA genes. Deletion of PWScr is associated with PWS in humans...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Sci Rep
Prif Awduron: Rozhdestvensky, Timofey S., Robeck, Thomas, Galiveti, Chenna R., Raabe, Carsten A., Seeger, Birte, Wolters, Anna, Gubar, Leonid V., Brosius, Jürgen, Skryabin, Boris V.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group 2016
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4742849/
https://ncbi.nlm.nih.gov/pubmed/26848093
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep20398
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