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A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins
Fragile X syndrome is a common form of inherited mental retardation caused by the loss of FMR1 expression. The FMR1 gene encodes an RNA-binding protein that associates with translating ribosomes and acts as a negative translational regulator. In Drosophila, the fly homolog of the FMR1 protein (dFMR1...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2002
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC187455/ https://ncbi.nlm.nih.gov/pubmed/12368261 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gad.1022002 |
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