Učitavanje...

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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:PLoS One
Glavni autori: Kalinowska, Magdalena, Castillo, Catherine, Francesconi, Anna
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2015
Teme:
Online pristup: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
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!