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Pubmed for Handhelds

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Journal Abstract Search

297 related items for PubMed ID: 25917509

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  • 4. Fragile X Mental Retardation Protein and Dendritic Local Translation of the Alpha Subunit of the Calcium/Calmodulin-Dependent Kinase II Messenger RNA Are Required for the Structural Plasticity Underlying Olfactory Learning.
    Daroles L, Gribaudo S, Doulazmi M, Scotto-Lomassese S, Dubacq C, Mandairon N, Greer CA, Didier A, Trembleau A, Caillé I.
    Biol Psychiatry; 2016 Jul 15; 80(2):149-159. PubMed ID: 26372002
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  • 7. 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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  • 8. ICAM5 as a Novel Target for Treating Cognitive Impairment in Fragile X Syndrome.
    Pei YP, Wang YY, Liu D, Lei HY, Yang ZH, Zhang ZW, Han M, Cheng K, Chen YS, Li JQ, Cheng GR, Xu L, Wu QM, McClintock SM, Yang Y, Zhang Y, Zeng Y.
    J Neurosci; 2020 Feb 05; 40(6):1355-1365. PubMed ID: 31882402
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  • 10. Synaptic vesicle dynamic changes in a model of fragile X.
    Broek JAC, Lin Z, de Gruiter HM, van 't Spijker H, Haasdijk ED, Cox D, Ozcan S, van Cappellen GWA, Houtsmuller AB, Willemsen R, de Zeeuw CI, Bahn S.
    Mol Autism; 2016 Feb 05; 7():17. PubMed ID: 26933487
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  • 11. Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse.
    Filippini A, Bonini D, Lacoux C, Pacini L, Zingariello M, Sancillo L, Bosisio D, Salvi V, Mingardi J, La Via L, Zalfa F, Bagni C, Barbon A.
    RNA Biol; 2017 Nov 02; 14(11):1580-1591. PubMed ID: 28640668
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  • 12. microRNAs and Fragile X Syndrome.
    Lin SL.
    Adv Exp Med Biol; 2015 Nov 02; 888():107-21. PubMed ID: 26663181
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  • 13. 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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  • 14. Expression of fragile X mental retardation-1 gene with nuclear export signal mutation changes the expression profiling of mouse cerebella immortal neuronal cell.
    Hu L, Chen Y, Evers S, Shen Y.
    Proteomics; 2005 Oct 27; 5(15):3979-90. PubMed ID: 16130171
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  • 15. Lack of FMRP in the retina: Evidence of a retinal specific transcriptomic profile.
    Attallah A, Ardourel M, Gallazzini F, Lesne F, De Oliveira A, Togbé D, Briault S, Perche O.
    Exp Eye Res; 2024 Sep 27; 246():110015. PubMed ID: 39089568
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  • 17. FMRP Expression Levels in Mouse Central Nervous System Neurons Determine Behavioral Phenotype.
    Arsenault J, Gholizadeh S, Niibori Y, Pacey LK, Halder SK, Koxhioni E, Konno A, Hirai H, Hampson DR.
    Hum Gene Ther; 2016 Dec 27; 27(12):982-996. PubMed ID: 27604541
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  • 18. Rescue of NMDAR-dependent synaptic plasticity in Fmr1 knock-out mice.
    Bostrom CA, Majaess NM, Morch K, White E, Eadie BD, Christie BR.
    Cereb Cortex; 2015 Jan 27; 25(1):271-9. PubMed ID: 23968838
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