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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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| Päätekijät: | , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Landes Bioscience
2013
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| 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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