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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...
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| Publicado no: | RNA |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4274637/ https://ncbi.nlm.nih.gov/pubmed/25406362 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1261/rna.046722.114 |
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