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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

398 related articles for article (PubMed ID: 23300470)

  • 1. 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; 8(12):e1003172. PubMed ID: 23300470
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Selective Deletion of Astroglial FMRP Dysregulates Glutamate Transporter GLT1 and Contributes to Fragile X Syndrome Phenotypes In Vivo.
    Higashimori H; Schin CS; Chiang MS; Morel L; Shoneye TA; Nelson DL; Yang Y
    J Neurosci; 2016 Jul; 36(27):7079-94. PubMed ID: 27383586
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 66(4):789-800. PubMed ID: 29274095
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 40(6):1355-1365. PubMed ID: 31882402
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dysregulated Purinergic Signalling in Fragile X Syndrome Cortical Astrocytes.
    Reynolds KE; Napier M; Fei F; Green K; Scott AL
    Neuromolecular Med; 2024 Sep; 26(1):36. PubMed ID: 39254908
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Astrocyte-secreted thrombospondin-1 modulates synapse and spine defects in the fragile X mouse model.
    Cheng C; Lau SK; Doering LC
    Mol Brain; 2016 Aug; 9(1):74. PubMed ID: 27485117
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Increased coupling of caveolin-1 and estrogen receptor α contributes to the fragile X syndrome.
    Yang Q; Yang L; Zhang K; Guo YY; Liu SB; Wu YM; Li XQ; Song Q; Zhuo M; Zhao MG
    Ann Neurol; 2015 Apr; 77(4):618-36. PubMed ID: 25611593
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Imbalance between Glutamate and GABA in Fmr1 Knockout Astrocytes Influences Neuronal Development.
    Wang L; Wang Y; Zhou S; Yang L; Shi Q; Li Y; Zhang K; Yang L; Zhao M; Yang Q
    Genes (Basel); 2016 Aug; 7(8):. PubMed ID: 27517961
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 82(2):139-149. PubMed ID: 27865451
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 22(6):1180-92. PubMed ID: 23250915
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fragile X-like behaviors and abnormal cortical dendritic spines in cytoplasmic FMR1-interacting protein 2-mutant mice.
    Han K; Chen H; Gennarino VA; Richman R; Lu HC; Zoghbi HY
    Hum Mol Genet; 2015 Apr; 24(7):1813-23. PubMed ID: 25432536
    [TBL] [Abstract][Full Text] [Related]  

  • 12. BDNF and TrkB in neuronal differentiation of Fmr1-knockout mouse.
    Louhivuori V; Vicario A; Uutela M; Rantamäki T; Louhivuori LM; Castrén E; Tongiorgi E; Akerman KE; Castrén ML
    Neurobiol Dis; 2011 Feb; 41(2):469-80. PubMed ID: 21047554
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 22(10):2041-54. PubMed ID: 23396537
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 89():126-35. PubMed ID: 26850918
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 16(9):1122-9. PubMed ID: 19571888
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 14(11):1580-1591. PubMed ID: 28640668
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evidence for a fragile X mental retardation protein-mediated translational switch in metabotropic glutamate receptor-triggered Arc translation and long-term depression.
    Niere F; Wilkerson JR; Huber KM
    J Neurosci; 2012 Apr; 32(17):5924-36. PubMed ID: 22539853
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Local functions for FMRP in axon growth cone motility and activity-dependent regulation of filopodia and spine synapses.
    Antar LN; Li C; Zhang H; Carroll RC; Bassell GJ
    Mol Cell Neurosci; 2006; 32(1-2):37-48. PubMed ID: 16631377
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deletion of Fmr1 in parvalbumin-expressing neurons results in dysregulated translation and selective behavioral deficits associated with fragile X syndrome.
    Kalinowska M; van der Lei MB; Kitiashvili M; Mamcarz M; Oliveira MM; Longo F; Klann E
    Mol Autism; 2022 Jun; 13(1):29. PubMed ID: 35768828
    [TBL] [Abstract][Full Text] [Related]  

  • 20. BDNF in fragile X syndrome.
    Castrén ML; Castrén E
    Neuropharmacology; 2014 Jan; 76 Pt C():729-36. PubMed ID: 23727436
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.