BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

387 related articles for article (PubMed ID: 20442204)

  • 1. Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P.
    Coffee RL; Tessier CR; Woodruff EA; Broadie K
    Dis Model Mech; 2010; 3(7-8):471-85. PubMed ID: 20442204
    [TBL] [Abstract][Full Text] [Related]  

  • 2. In vivo neuronal function of the fragile X mental retardation protein is regulated by phosphorylation.
    Coffee RL; Williamson AJ; Adkins CM; Gray MC; Page TL; Broadie K
    Hum Mol Genet; 2012 Feb; 21(4):900-15. PubMed ID: 22080836
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neural circuit architecture defects in a Drosophila model of Fragile X syndrome are alleviated by minocycline treatment and genetic removal of matrix metalloproteinase.
    Siller SS; Broadie K
    Dis Model Mech; 2011 Sep; 4(5):673-85. PubMed ID: 21669931
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Argonaute2 suppresses Drosophila fragile X expression preventing neurogenesis and oogenesis defects.
    Pepper AS; Beerman RW; Bhogal B; Jongens TA
    PLoS One; 2009 Oct; 4(10):e7618. PubMed ID: 19888420
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Temporal requirements of the fragile X mental retardation protein in the regulation of synaptic structure.
    Gatto CL; Broadie K
    Development; 2008 Aug; 135(15):2637-48. PubMed ID: 18579676
    [TBL] [Abstract][Full Text] [Related]  

  • 6. dFmr1 Plays Roles in Small RNA Pathways of Drosophila melanogaster.
    Specchia V; D'Attis S; Puricella A; Bozzetti MP
    Int J Mol Sci; 2017 May; 18(5):. PubMed ID: 28509881
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Wnd/DLK Is a Critical Target of FMRP Responsible for Neurodevelopmental and Behavior Defects in the Drosophila Model of Fragile X Syndrome.
    Russo A; DiAntonio A
    Cell Rep; 2019 Sep; 28(10):2581-2593.e5. PubMed ID: 31484070
    [TBL] [Abstract][Full Text] [Related]  

  • 8. MiR-219 represses expression of dFMR1 in Drosophila melanogaster.
    Wang C; Ge L; Wu J; Wang X; Yuan L
    Life Sci; 2019 Feb; 218():31-37. PubMed ID: 30528775
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Acamprosate rescues neuronal defects in the Drosophila model of Fragile X Syndrome.
    Hutson RL; Thompson RL; Bantel AP; Tessier CR
    Life Sci; 2018 Feb; 195():65-70. PubMed ID: 29317220
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Modulation of dADAR-dependent RNA editing by the Drosophila fragile X mental retardation protein.
    Bhogal B; Jepson JE; Savva YA; Pepper AS; Reenan RA; Jongens TA
    Nat Neurosci; 2011 Oct; 14(12):1517-24. PubMed ID: 22037499
    [TBL] [Abstract][Full Text] [Related]  

  • 11. GABAergic circuit dysfunction in the Drosophila Fragile X syndrome model.
    Gatto CL; Pereira D; Broadie K
    Neurobiol Dis; 2014 May; 65():142-59. PubMed ID: 24423648
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Activity-dependent FMRP requirements in development of the neural circuitry of learning and memory.
    Doll CA; Broadie K
    Development; 2015 Apr; 142(7):1346-56. PubMed ID: 25804740
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Metabotropic glutamate receptor-mediated use-dependent down-regulation of synaptic excitability involves the fragile X mental retardation protein.
    Repicky S; Broadie K
    J Neurophysiol; 2009 Feb; 101(2):672-87. PubMed ID: 19036865
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Drosophila fragile X mental retardation gene regulates sleep need.
    Bushey D; Tononi G; Cirelli C
    J Neurosci; 2009 Feb; 29(7):1948-61. PubMed ID: 19228950
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic background mutations drive neural circuit hyperconnectivity in a fragile X syndrome model.
    Kennedy T; Rinker D; Broadie K
    BMC Biol; 2020 Jul; 18(1):94. PubMed ID: 32731855
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Casein kinase II phosphorylates the fragile X mental retardation protein and modulates its biological properties.
    Siomi MC; Higashijima K; Ishizuka A; Siomi H
    Mol Cell Biol; 2002 Dec; 22(24):8438-47. PubMed ID: 12446764
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein.
    Wan L; Dockendorff TC; Jongens TA; Dreyfuss G
    Mol Cell Biol; 2000 Nov; 20(22):8536-47. PubMed ID: 11046149
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The fragile X mental retardation protein developmentally regulates the strength and fidelity of calcium signaling in Drosophila mushroom body neurons.
    Tessier CR; Broadie K
    Neurobiol Dis; 2011 Jan; 41(1):147-59. PubMed ID: 20843478
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins.
    Spencer CM; Serysheva E; Yuva-Paylor LA; Oostra BA; Nelson DL; Paylor R
    Hum Mol Genet; 2006 Jun; 15(12):1984-94. PubMed ID: 16675531
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Modeling Fragile X Syndrome in
    Drozd M; Bardoni B; Capovilla M
    Front Mol Neurosci; 2018; 11():124. PubMed ID: 29713264
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.