Publications
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“A novel function for fragile X mental retardation protein in translational activation.”, PLoS Biol, vol. 7, no. 1, p. e16, 2009.
, “The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules.”, Hum Mol Genet, vol. 16, no. 24, pp. 3047-58, 2007.
, “Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure.”, Nucleic Acids Res, vol. 35, no. 1, pp. 299-306, 2007.
, “The fragile X syndrome: exploring its molecular basis and seeking a treatment.”, Expert Rev Mol Med, vol. 8, no. 8, pp. 1-16, 2006.
, “The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons.”, Hum Mol Genet, vol. 15, no. 9, pp. 1525-38, 2006.
, “FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts.”, Hum Mol Genet, vol. 14, no. 6, pp. 835-44, 2005.
, “Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles.”, Proc Natl Acad Sci U S A, vol. 101, no. 36, pp. 13357-62, 2004.
, “82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization.”, Hum Mol Genet, vol. 12, no. 14, pp. 1689-98, 2003.
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