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Dysregulation of the long non-coding RNA transcriptome in a Rett syndrome mouse model

Mecp2 is a transcriptional repressor protein that is mutated in Rett syndrome, a neurodevelopmental disorder that is the second most common cause of mental retardation in women. It has been shown that the loss of the Mecp2 protein in Rett syndrome cells alters the transcriptional silencing of coding...

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Bibliografiset tiedot
Päätekijät: Petazzi, Paolo, Sandoval, Juan, Szczesna, Karolina, Jorge, Olga C., Roa, Laura, Sayols, Sergi, Gomez, Antonio, Huertas, Dori, Esteller, Manel
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Landes Bioscience 2013
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3849168/
https://ncbi.nlm.nih.gov/pubmed/23611944
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/rna.24286
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