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 *

1052 related articles for article (PubMed ID: 21767618)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene.
    Loesch DZ; Sherwell S; Kinsella G; Tassone F; Taylor A; Amor D; Sung S; Evans A
    Clin Genet; 2012 Jul; 82(1):88-92. PubMed ID: 21476992
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy.
    Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; Ng V; Chitnis X; McGuire P; Suckling J; Davies KE; Hagerman RJ; Hagerman PJ; Murphy KC; Murphy DG
    Brain; 2004 Dec; 127(Pt 12):2672-81. PubMed ID: 15483045
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A fragile balance: FMR1 expression levels.
    Oostra BA; Willemsen R
    Hum Mol Genet; 2003 Oct; 12 Spec No 2():R249-57. PubMed ID: 12952862
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Chromatin changes caused by CGG repeat expansion in fmr1 gene].
    Yudkin DV; Lemskaya NA; Grischenko IV; Dolskiy AA
    Mol Biol (Mosk); 2015; 49(2):205-11. PubMed ID: 26065250
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Altered hypothalamus-pituitary-adrenal gland axis regulation in the expanded CGG-repeat mouse model for fragile X-associated tremor/ataxia syndrome.
    Brouwer JR; Severijnen E; de Jong FH; Hessl D; Hagerman RJ; Oostra BA; Willemsen R
    Psychoneuroendocrinology; 2008 Jul; 33(6):863-73. PubMed ID: 18472227
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats.
    Loesch DZ; Bui QM; Huggins RM; Mitchell RJ; Hagerman RJ; Tassone F
    J Med Genet; 2007 Mar; 44(3):200-4. PubMed ID: 16905681
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Fragile X premutation: new insights and clinical consequences.
    Van Esch H
    Eur J Med Genet; 2006; 49(1):1-8. PubMed ID: 16473304
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome.
    Pastori C; Peschansky VJ; Barbouth D; Mehta A; Silva JP; Wahlestedt C
    Hum Genet; 2014 Jan; 133(1):59-67. PubMed ID: 24005575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 53.