Načítá se...

The RNA-binding fragile-X mental retardation protein and its role beyond the brain

It is well-established that variations of a CGG repeat expansion in the gene FMR1, which encodes the fragile-X mental retardation protein (FMRP), cause the neurocognitive disorder, fragile-X syndrome (FXS). However, multiple observations suggest a general and complex regulatory role of FMRP in proce...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Biophys Rev
Hlavní autoři: Malecki, Cassandra, Hambly, Brett D., Jeremy, Richmond W., Robertson, Elizabeth N.
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer Berlin Heidelberg 2020
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7429658/
https://ncbi.nlm.nih.gov/pubmed/32654068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12551-020-00730-4
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!