Repeat-mediated epigenetic dysregulation of the FMR1 gene in the fragile X-related disorders
Author:
Publisher
Frontiers Media SA
Subject
Genetics(clinical),Genetics,Molecular Medicine
Reference91 articles.
1. FMR1 epigenetic silencing commonly occurs in undifferentiated fragile X-affected embryonic stem cells;Avitzour;Stem Cell Reports,2014
2. Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element;Beilina;Hum. Mol. Genet.,2004
3. Reduced C9orf72 gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood;Belzil;Acta Neupathol.,2013
4. SIRT1 inhibition alleviates gene silencing in fragile X mental retardation syndrome;Biacsi;PLoS Genet.,2008
5. Quiescence-induced LncRNAs trigger H4K20 trimethylation and transcriptional silencing;Bierhoff;Mol. Cell,2014
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