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Quantitative Profiling of Brain Lipid Raft Proteome in a Mouse Model of Fragile X Syndrome
Fragile X Syndrome, a leading cause of inherited intellectual disability and autism, arises from transcriptional silencing of the FMR1 gene encoding an RNA-binding protein, Fragile X Mental Retardation Protein (FMRP). FMRP can regulate the expression of approximately 4% of brain transcripts through...
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| Publicat a: | PLoS One |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Public Library of Science
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4388542/ https://ncbi.nlm.nih.gov/pubmed/25849048 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0121464 |
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