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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Public Library of Science
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4388542/ https://www.ncbi.nlm.nih.gov/pubmed/25849048 http://dx.doi.org/10.1371/journal.pone.0121464 |