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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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Detalles Bibliográficos
Publicado en:RNA
Main Authors: Stefanovic, Snezana, Bassell, Gary J., Mihailescu, Mihaela Rita
Formato: Artigo
Idioma:Inglês
Publicado: Cold Spring Harbor Laboratory Press 2015
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Acceso en liña: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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