BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

284 related articles for article (PubMed ID: 19927162)

  • 1. Examination of FMR1 transcript and protein levels among 74 premutation carriers.
    Peprah E; He W; Allen E; Oliver T; Boyne A; Sherman SL
    J Hum Genet; 2010 Jan; 55(1):66-8. PubMed ID: 19927162
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cerebral protein synthesis in a knockin mouse model of the fragile X premutation.
    Qin M; Huang T; Liu Z; Kader M; Burlin T; Xia Z; Zeidler Z; Hukema RK; Smith CB
    ASN Neuro; 2014; 6(5):. PubMed ID: 25290064
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Mosaicism for a full mutation, premutation, and deletion of the CGG repeats results in 22% FMRP and elevated FMR1 mRNA levels in a high-functioning fragile X male.
    Han XD; Powell BR; Phalin JL; Chehab FF
    Am J Med Genet A; 2006 Jul; 140(13):1463-71. PubMed ID: 16761284
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?
    Salat U; Bardoni B; Wöhrle D; Steinbach P
    J Med Genet; 2000 Nov; 37(11):842-50. PubMed ID: 11073538
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. CGG-repeat dynamics and
    Zhou Y; Kumari D; Sciascia N; Usdin K
    Mol Autism; 2016; 7():42. PubMed ID: 27713816
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Altered neural activity in the 'when' pathway during temporal processing in fragile X premutation carriers.
    Kim SY; Tassone F; Simon TJ; Rivera SM
    Behav Brain Res; 2014 Mar; 261():240-8. PubMed ID: 24398265
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations.
    Primerano B; Tassone F; Hagerman RJ; Hagerman P; Amaldi F; Bagni C
    RNA; 2002 Dec; 8(12):1482-8. PubMed ID: 12515381
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter.
    Chen LS; Tassone F; Sahota P; Hagerman PJ
    Hum Mol Genet; 2003 Dec; 12(23):3067-74. PubMed ID: 14519687
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model.
    Entezam A; Biacsi R; Orrison B; Saha T; Hoffman GE; Grabczyk E; Nussbaum RL; Usdin K
    Gene; 2007 Jun; 395(1-2):125-34. PubMed ID: 17442505
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maternal FMR1 premutation allele expansion and contraction in fraternal twins.
    Alfaro MP; Cohen M; Vnencak-Jones CL
    Am J Med Genet A; 2013 Oct; 161A(10):2620-5. PubMed ID: 23949867
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome.
    Sheridan SD; Theriault KM; Reis SA; Zhou F; Madison JM; Daheron L; Loring JF; Haggarty SJ
    PLoS One; 2011; 6(10):e26203. PubMed ID: 22022567
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.