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 *

459 related articles for article (PubMed ID: 26291156)

  • 1. Altered Neuronal and Circuit Excitability in Fragile X Syndrome.
    Contractor A; Klyachko VA; Portera-Cailliau C
    Neuron; 2015 Aug; 87(4):699-715. PubMed ID: 26291156
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Impaired GABA Neural Circuits Are Critical for Fragile X Syndrome.
    Gao F; Qi L; Yang Z; Yang T; Zhang Y; Xu H; Zhao H
    Neural Plast; 2018; 2018():8423420. PubMed ID: 30402088
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Metabotropic glutamate receptors and fragile x mental retardation protein: partners in translational regulation at the synapse.
    Ronesi JA; Huber KM
    Sci Signal; 2008 Feb; 1(5):pe6. PubMed ID: 18272470
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Imbalance of neocortical excitation and inhibition and altered UP states reflect network hyperexcitability in the mouse model of fragile X syndrome.
    Gibson JR; Bartley AF; Hays SA; Huber KM
    J Neurophysiol; 2008 Nov; 100(5):2615-26. PubMed ID: 18784272
    [TBL] [Abstract][Full Text] [Related]  

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

  • 9. Neuroanatomical, molecular genetic, and behavioral correlates of fragile X syndrome.
    Koukoui SD; Chaudhuri A
    Brain Res Rev; 2007 Jan; 53(1):27-38. PubMed ID: 16844227
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic deletion of regulator of G-protein signaling 4 (RGS4) rescues a subset of fragile X related phenotypes in the FMR1 knockout mouse.
    Pacey LK; Doss L; Cifelli C; van der Kooy D; Heximer SP; Hampson DR
    Mol Cell Neurosci; 2011 Mar; 46(3):563-72. PubMed ID: 21215802
    [TBL] [Abstract][Full Text] [Related]  

  • 11. GABAB receptor-mediated feed-forward circuit dysfunction in the mouse model of fragile X syndrome.
    Wahlstrom-Helgren S; Klyachko VA
    J Physiol; 2015 Nov; 593(22):5009-24. PubMed ID: 26282581
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cell-Type Specific Channelopathies in the Prefrontal Cortex of the fmr1-/y Mouse Model of Fragile X Syndrome.
    Kalmbach BE; Johnston D; Brager DH
    eNeuro; 2015; 2(6):. PubMed ID: 26601124
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function.
    Bassell GJ; Warren ST
    Neuron; 2008 Oct; 60(2):201-14. PubMed ID: 18957214
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fragile X syndrome: molecular mechanisms of cognitive dysfunction.
    Huber K
    Am J Psychiatry; 2007 Apr; 164(4):556. PubMed ID: 17403966
    [No Abstract]   [Full Text] [Related]  

  • 15. The fragile X-cerebellum connection.
    Huber KM
    Trends Neurosci; 2006 Apr; 29(4):183-5. PubMed ID: 16500716
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fragile X syndrome and epilepsy.
    Qiu LF; Hao YH; Li QZ; Xiong ZQ
    Neurosci Bull; 2008 Oct; 24(5):338-44. PubMed ID: 18839028
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The role of the postsynaptic density in the pathology of the fragile X syndrome.
    Kindler S; Kreienkamp HJ
    Results Probl Cell Differ; 2012; 54():61-80. PubMed ID: 22009348
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The developmental roles of FMRP.
    Till SM
    Biochem Soc Trans; 2010 Apr; 38(2):507-10. PubMed ID: 20298211
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dysregulation and restoration of translational homeostasis in fragile X syndrome.
    Richter JD; Bassell GJ; Klann E
    Nat Rev Neurosci; 2015 Oct; 16(10):595-605. PubMed ID: 26350240
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 5(15):3979-90. PubMed ID: 16130171
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.