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 *

336 related articles for article (PubMed ID: 21389081)

  • 1. CGG-repeat length threshold for FMR1 RNA pathogenesis in a cellular model for FXTAS.
    Hoem G; Raske CR; Garcia-Arocena D; Tassone F; Sanchez E; Ludwig AL; Iwahashi CK; Kumar M; Yang JE; Hagerman PJ
    Hum Mol Genet; 2011 Jun; 20(11):2161-70. PubMed ID: 21389081
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fragile X-associated tremor/ataxia syndrome: influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles.
    Wang JY; Hessl D; Schneider A; Tassone F; Hagerman RJ; Rivera SM
    JAMA Neurol; 2013 Aug; 70(8):1022-9. PubMed ID: 23753897
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells.
    Arocena DG; Iwahashi CK; Won N; Beilina A; Ludwig AL; Tassone F; Schwartz PH; Hagerman PJ
    Hum Mol Genet; 2005 Dec; 14(23):3661-71. PubMed ID: 16239243
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males.
    Birch RC; Hocking DR; Cornish KM; Menant JC; Georgiou-Karistianis N; Godler DE; Wen W; Hackett A; Rogers C; Trollor JN
    Genes Brain Behav; 2015 Mar; 14(3):251-9. PubMed ID: 25689687
    [TBL] [Abstract][Full Text] [Related]  

  • 5. FMR1 CGG repeat lengths mediate different regulation of reporter gene expression in comparative transient and locus specific integration assays.
    Sølvsten C; Nielsen AL
    Gene; 2011 Oct; 486(1-2):15-22. PubMed ID: 21767618
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size.
    Ludwig AL; Espinal GM; Pretto DI; Jamal AL; Arque G; Tassone F; Berman RF; Hagerman PJ
    Hum Mol Genet; 2014 Jun; 23(12):3228-38. PubMed ID: 24463622
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Unstable mutations in the FMR1 gene and the phenotypes.
    Loesch D; Hagerman R
    Adv Exp Med Biol; 2012; 769():78-114. PubMed ID: 23560306
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome.
    Todd PK; Oh SY; Krans A; Pandey UB; Di Prospero NA; Min KT; Taylor JP; Paulson HL
    PLoS Genet; 2010 Dec; 6(12):e1001240. PubMed ID: 21170301
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Argonaute-2-dependent rescue of a Drosophila model of FXTAS by FRAXE premutation repeat.
    Sofola OA; Jin P; Botas J; Nelson DL
    Hum Mol Genet; 2007 Oct; 16(19):2326-32. PubMed ID: 17635840
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Astroglial-targeted expression of the fragile X CGG repeat premutation in mice yields RAN translation, motor deficits and possible evidence for cell-to-cell propagation of FXTAS pathology.
    Wenzel HJ; Murray KD; Haify SN; Hunsaker MR; Schwartzer JJ; Kim K; La Spada AR; Sopher BL; Hagerman PJ; Raske C; Severijnen LWFM; Willemsen R; Hukema RK; Berman RF
    Acta Neuropathol Commun; 2019 Feb; 7(1):27. PubMed ID: 30808398
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.
    Jarmolowicz AI; Baker EK; Bartlett E; Francis D; Ling L; Gamage D; Delatycki MB; Godler DE
    Am J Med Genet A; 2021 May; 185(5):1498-1503. PubMed ID: 33544979
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Expression of an expanded CGG-repeat RNA in a single pair of primary sensory neurons impairs olfactory adaptation in Caenorhabditis elegans.
    Juang BT; Ludwig AL; Benedetti KL; Gu C; Collins K; Morales C; Asundi A; Wittmann T; L'Etoile N; Hagerman PJ
    Hum Mol Genet; 2014 Sep; 23(18):4945-59. PubMed ID: 24821701
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Abnormal dendrite and spine morphology in primary visual cortex in the CGG knock-in mouse model of the fragile X premutation.
    Berman RF; Murray KD; Arque G; Hunsaker MR; Wenzel HJ
    Epilepsia; 2012 Jun; 53 Suppl 1(0 1):150-60. PubMed ID: 22612820
    [TBL] [Abstract][Full Text] [Related]  

  • 14. RAN translation at CGG repeats induces ubiquitin proteasome system impairment in models of fragile X-associated tremor ataxia syndrome.
    Oh SY; He F; Krans A; Frazer M; Taylor JP; Paulson HL; Todd PK
    Hum Mol Genet; 2015 Aug; 24(15):4317-26. PubMed ID: 25954027
    [TBL] [Abstract][Full Text] [Related]  

  • 15. FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.
    Leehey MA; Berry-Kravis E; Goetz CG; Zhang L; Hall DA; Li L; Rice CD; Lara R; Cogswell J; Reynolds A; Gane L; Jacquemont S; Tassone F; Grigsby J; Hagerman RJ; Hagerman PJ
    Neurology; 2008 Apr; 70(16 Pt 2):1397-402. PubMed ID: 18057320
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The fragile X-associated tremor ataxia syndrome.
    Tassone F; Hagerman R
    Results Probl Cell Differ; 2012; 54():337-57. PubMed ID: 22009361
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [FMR1 PREMUTATION CARRIERS - ARE THEY REALLY ASYMPTOMATIC?].
    Elizur S; Berkenstadt M; Ries-Levavi L; Gruber N; Pinhas-Hamiel O; Hassin-Baer S; Raas-Rothschild A; Raanani H; Cukierman-Yaffe T; Orvieto R; Cohen Y; Gabis L
    Harefuah; 2018 Apr; 157(4):241-244. PubMed ID: 29688643
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation.
    Brouwer JR; Mientjes EJ; Bakker CE; Nieuwenhuizen IM; Severijnen LA; Van der Linde HC; Nelson DL; Oostra BA; Willemsen R
    Exp Cell Res; 2007 Jan; 313(2):244-53. PubMed ID: 17150213
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Age- and CGG repeat-related slowing of manual movement in fragile X carriers: A prodrome of fragile X-associated tremor ataxia syndrome?
    Shickman R; Famula J; Tassone F; Leehey M; Ferrer E; Rivera SM; Hessl D
    Mov Disord; 2018 Apr; 33(4):628-636. PubMed ID: 29389022
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Study of telomere length in men who carry a fragile X premutation or full mutation allele.
    Albizua I; Chopra P; Allen EG; He W; Amin AS; Sherman SL
    Hum Genet; 2020 Dec; 139(12):1531-1539. PubMed ID: 32533363
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.