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“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.
, “Fragile X-related protein FXR1P regulates proinflammatory cytokine tumor necrosis factor expression at the post-transcriptional level.”, J Biol Chem, vol. 280, no. 7, pp. 5750-63, 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.
, “Differential changes in dopamine D2- and D1-receptor mRNA levels induced by hypoxia in the arterial chemoreflex pathway organs in one-day-old and adult rabbits.”, Biol Neonate, vol. 84, no. 3, pp. 222-31, 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.
, “Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression.”, Hum Mol Genet, vol. 11, no. 24, pp. 3007-17, 2002.
, “Developmental expression of the fragile X-related 1 proteins in mouse testis: association with microtubule elements.”, Hum Mol Genet, vol. 10, no. 24, pp. 2803-11, 2001.
, “Disruption of LT-antigen/p53 complex by heat treatment correlates with inhibition of DNA synthesis during transforming infection with SV40.”, Biochem Cell Biol, vol. 78, no. 4, pp. 437-45, 2000.
, “Muscle specific fragile X related protein 1 isoforms are sequestered in the nucleus of undifferentiated myoblast.”, BMC Genet, vol. 1, p. 4, 2000.
, “Biology of the fragile X mental retardation protein, an RNA-binding protein.”, Biochem Cell Biol, vol. 77, no. 4, pp. 331-42, 1999.
, “Expression of dopamine D1-receptor mRNA in the carotid body of adult rabbits, cats and rats.”, Neurosci Res, vol. 31, no. 2, pp. 147-54, 1998.
, “Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis.”, Hum Mol Genet, vol. 7, no. 13, pp. 2121-8, 1998.
, “Expression of dopamine D2 receptor mRNA isoforms in the carotid body of rat, cat and rabbit.”, Brain Res, vol. 760, no. 1-2, pp. 287-9, 1997.
, “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.
, “Dopamine D2 receptor mRNA isoforms expression in the carotid body and petrosal ganglion of developing rabbits.”, Adv Exp Med Biol, vol. 410, pp. 285-9, 1996.
, “Expression of dopamine D2-receptor mRNA isoforms at the peripheral chemoreflex afferent pathway in developing rabbits.”, Am J Respir Cell Mol Biol, vol. 15, no. 3, pp. 374-81, 1996.
, “The fragile X mental retardation protein is associated with ribosomes.”, Nat Genet, vol. 12, no. 1, pp. 91-3, 1996.
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