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 *

118 related articles for article (PubMed ID: 36067823)

  • 1. FMRP-related retinal phenotypes: Evidence of glutamate-glutamine metabolic cycle impairment.
    Ardourel M; Pâris A; Felgerolle C; Lesne F; Ranchon-Cole I; Briault S; Perche O
    Exp Eye Res; 2022 Nov; 224():109238. PubMed ID: 36067823
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 246():110015. PubMed ID: 39089568
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. The translational regulator FMRP controls lipid and glucose metabolism in mice and humans.
    Leboucher A; Pisani DF; Martinez-Gili L; Chilloux J; Bermudez-Martin P; Van Dijck A; Ganief T; Macek B; Becker JAJ; Le Merrer J; Kooy RF; Amri EZ; Khandjian EW; Dumas ME; Davidovic L
    Mol Metab; 2019 Mar; 21():22-35. PubMed ID: 30686771
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Fragile X mental retardation protein regulates the levels of scaffold proteins and glutamate receptors in postsynaptic densities.
    Schütt J; Falley K; Richter D; Kreienkamp HJ; Kindler S
    J Biol Chem; 2009 Sep; 284(38):25479-87. PubMed ID: 19640847
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Alterations of amino acids and monoamine metabolism in male Fmr1 knockout mice: a putative animal model of the human fragile X mental retardation syndrome.
    Gruss M; Braun K
    Neural Plast; 2001; 8(4):285-98. PubMed ID: 12018775
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome.
    Till SM; Wijetunge LS; Seidel VG; Harlow E; Wright AK; Bagni C; Contractor A; Gillingwater TH; Kind PC
    Hum Mol Genet; 2012 May; 21(10):2143-56. PubMed ID: 22328088
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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(12):982-996. PubMed ID: 27604541
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fragile X Mental Retardation Protein (FMRP) controls diacylglycerol kinase activity in neurons.
    Tabet R; Moutin E; Becker JA; Heintz D; Fouillen L; Flatter E; Krężel W; Alunni V; Koebel P; Dembélé D; Tassone F; Bardoni B; Mandel JL; Vitale N; Muller D; Le Merrer J; Moine H
    Proc Natl Acad Sci U S A; 2016 Jun; 113(26):E3619-28. PubMed ID: 27233938
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A MicroRNA Profile in Fmr1 Knockout Mice Reveals MicroRNA Expression Alterations with Possible Roles in Fragile X Syndrome.
    Liu T; Wan RP; Tang LJ; Liu SJ; Li HJ; Zhao QH; Liao WP; Sun XF; Yi YH; Long YS
    Mol Neurobiol; 2015; 51(3):1053-63. PubMed ID: 24906954
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dysregulated metabotropic glutamate receptor-dependent translation of AMPA receptor and postsynaptic density-95 mRNAs at synapses in a mouse model of fragile X syndrome.
    Muddashetty RS; Kelić S; Gross C; Xu M; Bassell GJ
    J Neurosci; 2007 May; 27(20):5338-48. PubMed ID: 17507556
    [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. Fragile X syndrome: From protein function to therapy.
    Bagni C; Oostra BA
    Am J Med Genet A; 2013 Nov; 161A(11):2809-21. PubMed ID: 24115651
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Fragile X mental retardation protein induces synapse loss through acute postsynaptic translational regulation.
    Pfeiffer BE; Huber KM
    J Neurosci; 2007 Mar; 27(12):3120-30. PubMed ID: 17376973
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.