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Phosphorylation of FMRP inhibits association with Dicer
Fragile X syndrome is caused by an absence of the protein product of the fragile X mental retardation gene (FMR1). The fragile X mental retardation protein (FMRP) is an RNA-binding protein that regulates translation of associated mRNAs; however, the mechanism for this regulation remains unknown. Con...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2657015/ https://ncbi.nlm.nih.gov/pubmed/19155329 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1261/rna.1500809 |
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