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 *

795 related articles for article (PubMed ID: 33402421)

  • 21. Delayed Maturation of Fast-Spiking Interneurons Is Rectified by Activation of the TrkB Receptor in the Mouse Model of Fragile X Syndrome.
    Nomura T; Musial TF; Marshall JJ; Zhu Y; Remmers CL; Xu J; Nicholson DA; Contractor A
    J Neurosci; 2017 Nov; 37(47):11298-11310. PubMed ID: 29038238
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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; 39(38):7453-7464. PubMed ID: 31350260
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular and cellular aspects of mental retardation in the Fragile X syndrome: from gene mutation/s to spine dysmorphogenesis.
    De Rubeis S; Fernández E; Buzzi A; Di Marino D; Bagni C
    Adv Exp Med Biol; 2012; 970():517-51. PubMed ID: 22351071
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Proteome profiling of the prefrontal cortex of Fmr1 knockout mouse reveals enhancement of complement and coagulation cascades.
    Gao MM; Shi H; Yan HJ; Long YS
    J Proteomics; 2023 Mar; 274():104822. PubMed ID: 36646274
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Reduced Lateral Inhibition Impairs Olfactory Computations and Behaviors in a Drosophila Model of Fragile X Syndrome.
    Franco LM; Okray Z; Linneweber GA; Hassan BA; Yaksi E
    Curr Biol; 2017 Apr; 27(8):1111-1123. PubMed ID: 28366741
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The molecular biology of FMRP: new insights into fragile X syndrome.
    Richter JD; Zhao X
    Nat Rev Neurosci; 2021 Apr; 22(4):209-222. PubMed ID: 33608673
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Multifarious Functions of the Fragile X Mental Retardation Protein.
    Davis JK; Broadie K
    Trends Genet; 2017 Oct; 33(10):703-714. PubMed ID: 28826631
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Hippocampal proteome comparison of infant and adult Fmr1 deficiency mice reveals adult-related changes associated with postsynaptic density.
    Yang C; Huang YT; Yao YF; Fu JY; Long YS
    J Proteomics; 2024 Jul; 303():105202. PubMed ID: 38797434
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The state of synapses in fragile X syndrome.
    Pfeiffer BE; Huber KM
    Neuroscientist; 2009 Oct; 15(5):549-67. PubMed ID: 19325170
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Kinase pathway inhibition restores PSD95 induction in neurons lacking fragile X mental retardation protein.
    Yang Y; Geng Y; Jiang D; Ning L; Kim HJ; Jeon NL; Lau A; Chen L; Lin MZ
    Proc Natl Acad Sci U S A; 2019 Jun; 116(24):12007-12012. PubMed ID: 31118285
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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; 594(1):83-97. PubMed ID: 26427907
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Glomerulus-Selective Regulation of a Critical Period for Interneuron Plasticity in the
    Chodankar A; Sadanandappa MK; VijayRaghavan K; Ramaswami M
    J Neurosci; 2020 Jul; 40(29):5549-5560. PubMed ID: 32532889
    [TBL] [Abstract][Full Text] [Related]  

  • 33. FMRP Sustains Presynaptic Function via Control of Activity-Dependent Bulk Endocytosis.
    Bonnycastle K; Kind PC; Cousin MA
    J Neurosci; 2022 Feb; 42(8):1618-1628. PubMed ID: 34996816
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Impaired activity-dependent neural circuit assembly and refinement in autism spectrum disorder genetic models.
    Doll CA; Broadie K
    Front Cell Neurosci; 2014; 8():30. PubMed ID: 24570656
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. 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]  

  • 38. microRNAs and Fragile X Syndrome.
    Lin SL
    Adv Exp Med Biol; 2015; 888():107-21. PubMed ID: 26663181
    [TBL] [Abstract][Full Text] [Related]  

  • 39.
    Trajković J; Makevic V; Pesic M; Pavković-Lučić S; Milojevic S; Cvjetkovic S; Hagerman R; Budimirovic DB; Protic D
    Genes (Basel); 2022 Dec; 14(1):. PubMed ID: 36672829
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 40.