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DDX3X and specific initiation factors modulate FMR1 repeat‐associated non‐AUG‐initiated translation
A CGG trinucleotide repeat expansion in the 5′ UTR of FMR1 causes the neurodegenerative disorder Fragile X‐associated tremor/ataxia syndrome (FXTAS). This repeat supports a non‐canonical mode of protein synthesis known as repeat‐associated, non‐AUG (RAN) translation. The mechanism underlying RAN tra...
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| Vydáno v: | EMBO Rep |
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| Hlavní autoři: | , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6726903/ https://ncbi.nlm.nih.gov/pubmed/31347257 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/embr.201847498 |
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