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Casein Kinase II Phosphorylates the Fragile X Mental Retardation Protein and Modulates Its Biological Properties
Fragile X syndrome is caused by loss of FMR1 protein expression. FMR1 binds RNA and associates with polysomes in the cytoplasm; thus, it has been proposed to function as a regulator of gene expression at the posttranscriptional level. Posttranslational modification of FMR1 had previously been sugges...
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| Huvudupphovsmän: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
American Society for Microbiology
2002
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC139871/ https://ncbi.nlm.nih.gov/pubmed/12446764 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.22.24.8438-8447.2002 |
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