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Biophysical characterization of G-quadruplex forming FMR1 mRNA and of its interactions with different fragile X mental retardation protein isoforms
Fragile X syndrome, the most common form of inherited mental impairment in humans, is caused by the absence of the fragile X mental retardation protein (FMRP) due to a CGG trinucleotide repeat expansion in the 5′-untranslated region (UTR) and subsequent translational silencing of the fragile x menta...
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| Autores principales: | , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Cold Spring Harbor Laboratory Press
2014
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| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3866639/ https://ncbi.nlm.nih.gov/pubmed/24249225 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1261/rna.041442.113 |
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