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FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism
FMRP loss-of-function causes Fragile X Syndrome (FXS) and autistic features. FMRP is a polyribosome-associated neuronal RNA-binding protein, suggesting that it plays a key role in regulating neuronal translation, but there has been little consensus regarding either its RNA targets or mechanism of ac...
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| Main Authors: | , , , , , , , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2011
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3232425/ https://ncbi.nlm.nih.gov/pubmed/21784246 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2011.06.013 |
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