4 results for author:"De Rubeis S." in Literature citations
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| Molecular and cellular aspects of mental retardation in the Fragile X syndrome: from gene mutation/s to spine dysmorphogenesis. De Rubeis S., Fernandez E., Buzzi A., Di Marino D., Bagni C. Adv. Exp. Med. Biol. 970:517-551(2012) · Mapped (8) |
| Differential usage of transcriptional start sites and polyadenylation sites in FMR1 premutation alleles. Tassone F., De Rubeis S., Carosi C., La Fata G., Serpa G., Raske C., Willemsen R., Hagerman P.J., Bagni C. Nucleic Acids Res. 39:6172-6185(2011) · Mapped (8) |
| The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP. Napoli I., Mercaldo V., Boyl P.P., Eleuteri B., Zalfa F., De Rubeis S., Di Marino D., Mohr E., Massimi M., Falconi M. et al. |
| A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability. Zalfa F., Eleuteri B., Dickson K.S., Mercaldo V., De Rubeis S., di Penta A., Tabolacci E., Chiurazzi P., Neri G., Grant S.G. et al. Nat. Neurosci. 10:578-587(2007) · Mapped (11) |