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 *

409 related articles for article (PubMed ID: 21108954)

  • 21. 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]  

  • 22. 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]  

  • 23. Fragile X syndrome: clinical presentation, pathology and treatment.
    Salcedo-Arellano MJ; Hagerman RJ; Martínez-Cerdeño V
    Gac Med Mex; 2020; 156(1):60-66. PubMed ID: 32026885
    [TBL] [Abstract][Full Text] [Related]  

  • 24. GABA receptor subunit distribution and FMRP-mGluR5 signaling abnormalities in the cerebellum of subjects with schizophrenia, mood disorders, and autism.
    Fatemi SH; Folsom TD
    Schizophr Res; 2015 Sep; 167(1-3):42-56. PubMed ID: 25432637
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. Abnormal neuronal morphology and neurochemistry in the auditory brainstem of Fmr1 knockout rats.
    Ruby K; Falvey K; Kulesza RJ
    Neuroscience; 2015 Sep; 303():285-98. PubMed ID: 26166728
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Protein expression of targets of the FMRP regulon is altered in brains of subjects with schizophrenia and mood disorders.
    Folsom TD; Thuras PD; Fatemi SH
    Schizophr Res; 2015 Jul; 165(2-3):201-11. PubMed ID: 25956630
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Fragile X Mental Retardation Protein positively regulates PKA anchor Rugose and PKA activity to control actin assembly in learning/memory circuitry.
    Sears JC; Choi WJ; Broadie K
    Neurobiol Dis; 2019 Jul; 127():53-64. PubMed ID: 30771457
    [TBL] [Abstract][Full Text] [Related]  

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

  • 31. 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]  

  • 32. Persistent astrocyte activation in the fragile X mouse cerebellum.
    Pacey LK; Guan S; Tharmalingam S; Thomsen C; Hampson DR
    Brain Behav; 2015 Oct; 5(10):e00400. PubMed ID: 26516618
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A sound-driven cortical phase-locking change in the Fmr1 KO mouse requires Fmr1 deletion in a subpopulation of brainstem neurons.
    Holley AJ; Shedd A; Boggs A; Lovelace J; Erickson C; Gross C; Jankovic M; Razak K; Huber K; Gibson JR
    Neurobiol Dis; 2022 Aug; 170():105767. PubMed ID: 35588990
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Fragile X Syndrome: from molecular pathology to therapy.
    Maurin T; Zongaro S; Bardoni B
    Neurosci Biobehav Rev; 2014 Oct; 46 Pt 2():242-55. PubMed ID: 24462888
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Human pluripotent stem cell models of Fragile X syndrome.
    Bhattacharyya A; Zhao X
    Mol Cell Neurosci; 2016 Jun; 73():43-51. PubMed ID: 26640241
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptors.
    Nakamoto M; Nalavadi V; Epstein MP; Narayanan U; Bassell GJ; Warren ST
    Proc Natl Acad Sci U S A; 2007 Sep; 104(39):15537-42. PubMed ID: 17881561
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour.
    Stoyanova M; Hachmeriyan M; Levkova M; Bichev S; Georgieva M; Mladenov V; Angelova L
    Folia Med (Plovdiv); 2022 Feb; 64(1):27-32. PubMed ID: 35851904
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Fragile X syndrome: An overview and update of the FMR1 gene.
    Mila M; Alvarez-Mora MI; Madrigal I; Rodriguez-Revenga L
    Clin Genet; 2018 Feb; 93(2):197-205. PubMed ID: 28617938
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Macro role(s) of microRNAs in fragile X syndrome?
    Li X; Jin P
    Neuromolecular Med; 2009; 11(3):200-7. PubMed ID: 19669947
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.