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G quadruplex RNA structures in PSD-95 mRNA: potential regulators of miR-125a seed binding site accessibility
Fragile X syndrome (FXS) is the most common inherited form of intellectual disability caused by the CGG trinucleotide expansion in the 3′-untranslated region of the FMR1 gene on the X chromosome, that silences the expression of the Fragile X mental retardation protein (FMRP). FMRP has been shown to...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Cold Spring Harbor Laboratory Press
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274637/ https://www.ncbi.nlm.nih.gov/pubmed/25406362 http://dx.doi.org/10.1261/rna.046722.114 |