Načítá se...

In vivo neuronal function of the fragile X mental retardation protein is regulated by phosphorylation

Fragile X syndrome (FXS), caused by loss of the Fragile X Mental Retardation 1 (FMR1) gene product (FMRP), is the most common heritable cause of intellectual disability and autism spectrum disorders. It has been long hypothesized that the phosphorylation of serine 500 (S500) in human FMRP controls i...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Coffee, R. Lane, Williamson, Ashley J., Adkins, Christopher M., Gray, Marisa C., Page, Terry L., Broadie, Kendal
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2012
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3263990/
https://ncbi.nlm.nih.gov/pubmed/22080836
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr527
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!