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A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability

✍ Scribed by Zalfa, Francesca; Eleuteri, Boris; Dickson, Kirsten S; Mercaldo, Valentina; De Rubeis, Silvia; di Penta, Alessandra; Tabolacci, Elisabetta; Chiurazzi, Pietro; Neri, Giovanni; Grant, Seth G N


Book ID
109940986
Publisher
Nature Publishing Group
Year
2007
Tongue
English
Weight
586 KB
Volume
10
Category
Article
ISSN
1097-6256

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Heads-up: New roles for the fragile X me
✍ Matthew A. Callan; Daniela C. Zarnescu πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 484 KB

## Abstract Fragile X syndrome (FXS) is the most common form of inherited mental retardation and is caused by the loss of function for Fragile X Mental Retardation Protein (FMRP), a selective RNA‐binding protein with a demonstrated role in the localized translation of target mRNAs at synapses. Seve