BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

432 related articles for article (PubMed ID: 17283214)

  • 1. Elevated FMR1 mRNA in premutation carriers is due to increased transcription.
    Tassone F; Beilina A; Carosi C; Albertosi S; Bagni C; Li L; Glover K; Bentley D; Hagerman PJ
    RNA; 2007 Apr; 13(4):555-62. PubMed ID: 17283214
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The role of AGG interruptions in the transcription of FMR1 premutation alleles.
    Yrigollen CM; Tassone F; Durbin-Johnson B; Tassone F
    PLoS One; 2011; 6(7):e21728. PubMed ID: 21818263
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Transcription of the FMR1 gene in individuals with fragile X syndrome.
    Tassone F; Hagerman RJ; Chamberlain WD; Hagerman PJ
    Am J Med Genet; 2000; 97(3):195-203. PubMed ID: 11449488
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.
    Tassone F; Hagerman RJ; Taylor AK; Gane LW; Godfrey TE; Hagerman PJ
    Am J Hum Genet; 2000 Jan; 66(1):6-15. PubMed ID: 10631132
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Altered expression of the FMR1 splicing variants landscape in premutation carriers.
    Tseng E; Tang HT; AlOlaby RR; Hickey L; Tassone F
    Biochim Biophys Acta Gene Regul Mech; 2017 Nov; 1860(11):1117-1126. PubMed ID: 28888471
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fibroblast phenotype in male carriers of FMR1 premutation alleles.
    Garcia-Arocena D; Yang JE; Brouwer JR; Tassone F; Iwahashi C; Berry-Kravis EM; Goetz CG; Sumis AM; Zhou L; Nguyen DV; Campos L; Howell E; Ludwig A; Greco C; Willemsen R; Hagerman RJ; Hagerman PJ
    Hum Mol Genet; 2010 Jan; 19(2):299-312. PubMed ID: 19864489
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Differential increases of specific FMR1 mRNA isoforms in premutation carriers.
    Pretto DI; Eid JS; Yrigollen CM; Tang HT; Loomis EW; Raske C; Durbin-Johnson B; Hagerman PJ; Tassone F
    J Med Genet; 2015 Jan; 52(1):42-52. PubMed ID: 25358671
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Altered neural activity of magnitude estimation processing in adults with the fragile X premutation.
    Kim SY; Hashimoto R; Tassone F; Simon TJ; Rivera SM
    J Psychiatr Res; 2013 Dec; 47(12):1909-16. PubMed ID: 24045061
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.
    Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; Hagerman PJ
    Am J Med Genet; 2000 Sep; 94(3):232-6. PubMed ID: 10995510
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation.
    Hessl D; Tassone F; Loesch DZ; Berry-Kravis E; Leehey MA; Gane LW; Barbato I; Rice C; Gould E; Hall DA; Grigsby J; Wegelin JA; Harris S; Lewin F; Weinberg D; Hagerman PJ; Hagerman RJ
    Am J Med Genet B Neuropsychiatr Genet; 2005 Nov; 139B(1):115-21. PubMed ID: 16184602
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population.
    Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; Brunberg JA; Zhang L; Jardini T; Gane LW; Harris SW; Herman K; Grigsby J; Greco CM; Berry-Kravis E; Tassone F; Hagerman PJ
    JAMA; 2004 Jan; 291(4):460-9. PubMed ID: 14747503
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Expression of the FMR1 gene.
    Tassone F; Hagerman PJ
    Cytogenet Genome Res; 2003; 100(1-4):124-8. PubMed ID: 14526172
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of FMR1 gene expression in female premutation carriers using robust segmented linear regression models.
    García-Alegría E; Ibáñez B; Mínguez M; Poch M; Valiente A; Sanz-Parra A; Martinez-Bouzas C; Beristain E; Tejada MI
    RNA; 2007 May; 13(5):756-62. PubMed ID: 17449730
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A neuropsychological investigation of male premutation carriers of fragile X syndrome.
    Moore CJ; Daly EM; Schmitz N; Tassone F; Tysoe C; Hagerman RJ; Hagerman PJ; Morris RG; Murphy KC; Murphy DG
    Neuropsychologia; 2004; 42(14):1934-47. PubMed ID: 15381024
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.
    Lorefice L; Tranquilli S; Fenu G; Murru MR; Frau J; Rolesu M; Coghe GC; Marrosu F; Marrosu MG; Cocco E
    Neurol Sci; 2015 Dec; 36(12):2213-20. PubMed ID: 26194536
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing.
    Ardui S; Race V; Zablotskaya A; Hestand MS; Van Esch H; Devriendt K; Matthijs G; Vermeesch JR
    Hum Mutat; 2017 Mar; 38(3):324-331. PubMed ID: 27883256
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carriage of One or Two FMR1 Premutation Alleles Seems to Have No Effect on Illness Severity in a FXTAS Female with an Autozygous FMR1 Premutation Allele.
    Rodriguez-Revenga L; Pagonabarraga J; Gómez-Anson B; López-Mourelo O; Izquierdo S; Alvarez-Mora MI; Granell E; Madrigal I; Milà M
    Cerebellum; 2016 Oct; 15(5):570-7. PubMed ID: 27315125
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.