Molecular analysis of FMR1 reactivation in fragile-X induced pluripotent stem cells and their neuronal derivatives
Author:
Publisher
Oxford University Press (OUP)
Subject
Cell Biology,Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/jmcb/article-pdf/4/3/180/16836441/mjs007.pdf
Reference12 articles.
1. Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated fragile X full mutation;Brouwer;Exp. Cell Res.,2007
2. Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells;Coffee;Nat. Genet.,1999
3. FMR1 and the fragile X syndrome: human genome epidemiology review;Crawford;Genet. Med.,2001
4. Regulation of molecular pathways in the fragile X syndrome: insights into autism spectrum disorders;De Rubeis;J. Neurodev. Disord.,2011
5. Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos;Eiges;Cell Stem Cell,2007
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1. EZH2 inhibition reactivates epigenetically silenced FMR1 and normalizes molecular and electrophysiological abnormalities in fragile X syndrome neurons;Frontiers in Neuroscience;2024-02-21
2. Directly reprogrammed fragile X syndrome dorsal forebrain precursor cells generate cortical neurons exhibiting impaired neuronal maturation;Frontiers in Cellular Neuroscience;2023-09-21
3. Crosstalk between microRNAs and epigenetics during brain development and neurological diseases;Transcription and Translation in Health and Disease;2023
4. Across Dimensions: Developing 2D and 3D Human iPSC-Based Models of Fragile X Syndrome;Cells;2022-05-24
5. High Throughput Small Molecule Screen for Reactivation of FMR1 in Fragile X Syndrome Human Neural Cells;Cells;2021-12-27
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