Altered mTOR signaling and enhanced CYFIP2 expression levels in subjects with Fragile X syndrome

Fragile X Syndrome (FXS) is the most common form of inherited intellectual disability and autism. The protein (FMRP) encoded by the fragile X mental retardation gene (FMR1), is an RNA-binding protein linked to translational control. Recently, in the Fmr1 knockout mouse model of FXS, dysregulated tra...

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Bibliografiset tiedot
Päätekijät: Hoeffer, Charles A., Sanchez, Eleonora, Hagerman, Randi J., Mu, Yi, Nguyen, Danh V., Wong, Helen, Whelan, Ashley M., Zukin, R. Suzanne, Klann, Eric, Tassone, Flora
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2012
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3319643/
https://ncbi.nlm.nih.gov/pubmed/22268788
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1601-183X.2012.00768.x
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