These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

219 related items for PubMed ID: 38678030

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Voltage-Independent SK-Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus of Fmr1 Knock-Out Mice.
    Deng PY, Carlin D, Oh YM, Myrick LK, Warren ST, Cavalli V, Klyachko VA.
    J Neurosci; 2019 Jan 02; 39(1):28-43. PubMed ID: 30389838
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Disruption of GpI mGluR-Dependent Cav2.3 Translation in a Mouse Model of Fragile X Syndrome.
    Gray EE, Murphy JG, Liu Y, Trang I, Tabor GT, Lin L, Hoffman DA.
    J Neurosci; 2019 Sep 18; 39(38):7453-7464. PubMed ID: 31350260
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Astroglial FMRP-dependent translational down-regulation of mGluR5 underlies glutamate transporter GLT1 dysregulation in the fragile X mouse.
    Higashimori H, Morel L, Huth J, Lindemann L, Dulla C, Taylor A, Freeman M, Yang Y.
    Hum Mol Genet; 2013 May 15; 22(10):2041-54. PubMed ID: 23396537
    [Abstract] [Full Text] [Related]

  • 8. Kv7/M channel dysfunction produces hyperexcitability in hippocampal CA1 pyramidal cells of Fmr1 knockout mice.
    Luque MA, Morcuende S, Torres B, Herrero L.
    J Physiol; 2024 Aug 15; 602(15):3769-3791. PubMed ID: 38976504
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Astrocytic Contributions to Synaptic and Learning Abnormalities in a Mouse Model of Fragile X Syndrome.
    Hodges JL, Yu X, Gilmore A, Bennett H, Tjia M, Perna JF, Chen CC, Li X, Lu J, Zuo Y.
    Biol Psychiatry; 2017 Jul 15; 82(2):139-149. PubMed ID: 27865451
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Genetic upregulation of BK channel activity normalizes multiple synaptic and circuit defects in a mouse model of fragile X syndrome.
    Deng PY, Klyachko VA.
    J Physiol; 2016 Jan 01; 594(1):83-97. PubMed ID: 26427907
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Matrix metalloproteinase-9 deletion rescues auditory evoked potential habituation deficit in a mouse model of Fragile X Syndrome.
    Lovelace JW, Wen TH, Reinhard S, Hsu MS, Sidhu H, Ethell IM, Binder DK, Razak KA.
    Neurobiol Dis; 2016 May 01; 89():126-35. PubMed ID: 26850918
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome.
    Sheridan SD, Theriault KM, Reis SA, Zhou F, Madison JM, Daheron L, Loring JF, Haggarty SJ.
    PLoS One; 2011 May 01; 6(10):e26203. PubMed ID: 22022567
    [Abstract] [Full Text] [Related]

  • 20. Alterations in CA1 hippocampal synapses in a mouse model of fragile X syndrome.
    Jawaid S, Kidd GJ, Wang J, Swetlik C, Dutta R, Trapp BD.
    Glia; 2018 Apr 01; 66(4):789-800. PubMed ID: 29274095
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.