Defining the role of the CGGBP1 protein in FMR1 gene expression
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/ejhg2015182.pdf
Reference27 articles.
1. Pirozzi F, Tabolacci E, Neri G : The FRAXopathies: definition, overview, and update. Am J Med Genet 2011; 155A: 1803–1816.
2. Bassell GJ, Warren ST : Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function. Neuron 2008; 60: 201–214.
3. Coffee B, Keith K, Albizua I et al: Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA. Am J Hum Genet 2009; 85: 503–514.
4. Crawford DC, Meadows KL, Newman JL et al: Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population. Am J Hum Genet 1999; 64: 495–507.
5. Sutcliffe JS, Nelson DL, Zhang F et al: DNA methylation represses FMR-1 transcription in fragile X syndrome. Hum Mol Genet 1992; 1: 397–400.
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1. The CGG triplet repeat binding protein 1 counteracts DNA secondary structure-induced transcription-replication conflicts;2023-03-09
2. DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome;Biomolecules;2021-02-16
3. CGGBP1-regulated cytosine methylation at CTCF-binding motifs resists stochasticity;BMC Genetics;2020-07-29
4. CGGBP1-regulated cytosine methylation at CTCF-binding motifs resists stochasticity;2020-02-14
5. Reactivation of the FMR1 Gene;Fragile X Syndrome;2017
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