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“Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies.”, PLoS Genet, vol. 9, no. 10, p. e1003890, 2013.
, “Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].”, PLoS One, vol. 7, no. 6, p. e39338, 2012.
, “Manipulating the fragile X mental retardation proteins in the frog.”, Results Probl Cell Differ, vol. 54, pp. 165-79, 2012.
, “Fragile X related protein 1 clusters with ribosomes and messenger RNAs at a subset of dendritic spines in the mouse hippocampus.”, PLoS One, vol. 6, no. 10, p. e26120, 2011.
, “A novel function for fragile X mental retardation protein in translational activation.”, PLoS Biol, vol. 7, no. 1, p. e16, 2009.
, “On BC1 RNA and the fragile X mental retardation protein.”, Proc Natl Acad Sci U S A, vol. 105, no. 2, pp. 734-9, 2008.
, “Reply to Bagni: On BC1 RNA and the fragile X mental retardation protein.”, Proc Natl Acad Sci U S A, vol. 105, no. 22, p. E29, 2008.
, “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 fragile X syndrome: one protein missing and 1001 disoriented mRNAs].”, Med Sci (Paris), vol. 22, no. 1, pp. 41-6, 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.
, “Disordered RNA chaperone proteins: from functions to disease.”, Cell Mol Life Sci, vol. 62, no. 13, pp. 1409-17, 2005.
, “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.
, “Lost once, the Fragile X Mental Retardation protein is now back onto brain polyribosomes.”, RNA Biol, vol. 2, no. 1, pp. 1-3, 2005.
, “The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis.”, Mol Biol Cell, vol. 16, no. 9, pp. 4350-61, 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.
, “The fragile X mental retardation protein has nucleic acid chaperone properties.”, Nucleic Acids Res, vol. 32, no. 7, pp. 2129-37, 2004.
, “Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome.”, J Med Genet, vol. 41, no. 4, p. e43, 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.
, “Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs.”, Hum Mol Genet, vol. 12, no. 23, pp. 3087-96, 2003.
, “Biology of the fragile X mental retardation protein, an RNA-binding protein.”, Biochem Cell Biol, vol. 77, no. 4, pp. 331-42, 1999.
, “Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis.”, Hum Mol Genet, vol. 7, no. 13, pp. 2121-8, 1998.
, “The fragile X mental retardation protein is associated with poly(A)+ mRNA in actively translating polyribosomes.”, Hum Mol Genet, vol. 6, no. 9, pp. 1465-72, 1997.
, “Structural and functional characterization of the human FMR1 promoter reveals similarities with the hnRNP-A2 promoter region.”, Hum Mol Genet, vol. 6, no. 12, pp. 2051-60, 1997.
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