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Journal Abstract Search

311 related items for PubMed ID: 32997566

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  • 43. Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice.
    Iliff AJ, Renoux AJ, Krans A, Usdin K, Sutton MA, Todd PK.
    Hum Mol Genet; 2013 Mar 15; 22(6):1180-92. PubMed ID: 23250915
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  • 44. Fragile X mental retardation protein replacement restores hippocampal synaptic function in a mouse model of fragile X syndrome.
    Zeier Z, Kumar A, Bodhinathan K, Feller JA, Foster TC, Bloom DC.
    Gene Ther; 2009 Sep 15; 16(9):1122-9. PubMed ID: 19571888
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  • 45. Fragile X mental retardation protein controls synaptic vesicle exocytosis by modulating N-type calcium channel density.
    Ferron L, Nieto-Rostro M, Cassidy JS, Dolphin AC.
    Nat Commun; 2014 Apr 07; 5():3628. PubMed ID: 24709664
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  • 48. Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures.
    Myrick LK, Deng PY, Hashimoto H, Oh YM, Cho Y, Poidevin MJ, Suhl JA, Visootsak J, Cavalli V, Jin P, Cheng X, Warren ST, Klyachko VA.
    Proc Natl Acad Sci U S A; 2015 Jan 27; 112(4):949-56. PubMed ID: 25561520
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  • 49. Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortex.
    Kwan KY, Lam MM, Johnson MB, Dube U, Shim S, Rašin MR, Sousa AM, Fertuzinhos S, Chen JG, Arellano JI, Chan DW, Pletikos M, Vasung L, Rowitch DH, Huang EJ, Schwartz ML, Willemsen R, Oostra BA, Rakic P, Heffer M, Kostović I, Judaš M, Sestan N.
    Cell; 2012 May 11; 149(4):899-911. PubMed ID: 22579290
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  • 52. Fragile X mental retardation protein controls ion channel expression and activity.
    Ferron L.
    J Physiol; 2016 Oct 15; 594(20):5861-5867. PubMed ID: 26864773
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  • 53. Astroglial Kir4.1 potassium channel deficit drives neuronal hyperexcitability and behavioral defects in Fragile X syndrome mouse model.
    Bataveljic D, Pivonkova H, de Concini V, Hébert B, Ezan P, Briault S, Bemelmans AP, Pichon J, Menuet A, Rouach N.
    Nat Commun; 2024 Apr 27; 15(1):3583. PubMed ID: 38678030
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  • 54. Identification of a molecular locus for normalizing dysregulated GABA release from interneurons in the Fragile X brain.
    Yang YM, Arsenault J, Bah A, Krzeminski M, Fekete A, Chao OY, Pacey LK, Wang A, Forman-Kay J, Hampson DR, Wang LY.
    Mol Psychiatry; 2020 Sep 27; 25(9):2017-2035. PubMed ID: 30224722
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  • 55. Postsynaptic FMRP Regulates Synaptogenesis In Vivo in the Developing Cochlear Nucleus.
    Wang X, Zorio DAR, Schecterson L, Lu Y, Wang Y.
    J Neurosci; 2018 Jul 18; 38(29):6445-6460. PubMed ID: 29950504
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  • 56. Roles of fragile X mental retardation protein in dopaminergic stimulation-induced synapse-associated protein synthesis and subsequent alpha-amino-3-hydroxyl-5-methyl-4-isoxazole-4-propionate (AMPA) receptor internalization.
    Wang H, Kim SS, Zhuo M.
    J Biol Chem; 2010 Jul 09; 285(28):21888-901. PubMed ID: 20457613
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  • 57. Deletion of the KH1 Domain of Fmr1 Leads to Transcriptional Alterations and Attentional Deficits in Rats.
    Golden CEM, Breen MS, Koro L, Sonar S, Niblo K, Browne A, Burlant N, Di Marino D, De Rubeis S, Baxter MG, Buxbaum JD, Harony-Nicolas H.
    Cereb Cortex; 2019 May 01; 29(5):2228-2244. PubMed ID: 30877790
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  • 58. Excessive astrocyte-derived neurotrophin-3 contributes to the abnormal neuronal dendritic development in a mouse model of fragile X syndrome.
    Yang Q, Feng B, Zhang K, Guo YY, Liu SB, Wu YM, Li XQ, Zhao MG.
    PLoS Genet; 2012 May 01; 8(12):e1003172. PubMed ID: 23300470
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  • 59. Dopamine D1-class receptors selectively modulate a slowly inactivating potassium current in rat medial prefrontal cortex pyramidal neurons.
    Dong Y, White FJ.
    J Neurosci; 2003 Apr 01; 23(7):2686-95. PubMed ID: 12684454
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  • 60. Fragile X mental retardation protein regulates new neuron differentiation in the adult olfactory bulb.
    Scotto-Lomassese S, Nissant A, Mota T, Néant-Féry M, Oostra BA, Greer CA, Lledo PM, Trembleau A, Caillé I.
    J Neurosci; 2011 Feb 09; 31(6):2205-15. PubMed ID: 21307257
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