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Sustained expression of FMR1 mRNA from reactivated fragile X syndrome alleles after treatment with small molecules that prevent trimethylation of H3K27
Expansion of a CGG-repeat tract in the 5’-untranslated region of the FMR1 gene to >200 repeats results in epigenetic silencing of the gene by a mechanism that is still unknown. FMR1 gene silencing results in fragile X syndrome (FXS), the most common heritable cause of intellectual disability. We...
Kaydedildi:
| Yayımlandı: | Hum Mol Genet |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5216614/ https://ncbi.nlm.nih.gov/pubmed/27378697 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw215 |
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