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 *

265 related articles for article (PubMed ID: 21499798)

  • 1. Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1.
    Datta S; Alam MP; Majumdar SS; Mehta AK; Maiti S; Wadhwa N; Brahmachari V
    Chromosome Res; 2011 May; 19(4):445-55. PubMed ID: 21499798
    [TBL] [Abstract][Full Text] [Related]  

  • 2. AGG/CCT interruptions affect nucleosome formation and positioning of healthy-length CGG/CCG triplet repeats.
    Volle CB; Delaney S
    BMC Biochem; 2013 Nov; 14():33. PubMed ID: 24261641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Nucleosome assembly on methylated CGG triplet repeats in the fragile X mental retardation gene 1 promoter.
    Godde JS; Kass SU; Hirst MC; Wolffe AP
    J Biol Chem; 1996 Oct; 271(40):24325-8. PubMed ID: 8798682
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population.
    Garcia Arocena D; Breece KE; Hagerman PJ
    Hum Genet; 2003 Oct; 113(5):371-6. PubMed ID: 12905066
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Fragile X syndrome: the FMR1 CGG repeat distribution among world populations.
    Peprah E
    Ann Hum Genet; 2012 Mar; 76(2):178-91. PubMed ID: 22188182
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Instability of a (CGG)98 repeat in the Fmr1 promoter.
    Bontekoe CJ; Bakker CE; Nieuwenhuizen IM; van der Linde H; Lans H; de Lange D; Hirst MC; Oostra BA
    Hum Mol Genet; 2001 Aug; 10(16):1693-9. PubMed ID: 11487573
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Use of human-derived stem cells to create a novel, in vitro model designed to explore FMR1 CGG repeat instability amongst female premutation carriers.
    Gustin SLF; Wang G; Baker VM; Latham G; Sebastiano V
    J Assist Reprod Genet; 2018 Aug; 35(8):1443-1455. PubMed ID: 29926373
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene.
    Wang H; Zhu X; Gui B; Cheung WC; Shi M; Yang Z; Kwok KY; Lim R; Pietilä S; Zhu Y; Choy KW
    J Vis Exp; 2019 Sep; (151):. PubMed ID: 31566610
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expression.
    Grønskov K; Hjalgrim H; Bjerager MO; Brøndum-Nielsen K
    Am J Hum Genet; 1997 Oct; 61(4):961-7. PubMed ID: 9382110
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Instability of a premutation-sized CGG repeat in FMR1 YAC transgenic mice.
    Peier AM; Nelson DL
    Genomics; 2002 Oct; 80(4):423-32. PubMed ID: 12376097
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Instability of CGG repeats in transgenic mice.
    Baskaran S; Datta S; Mandal A; Gulati N; Totey S; Anand RR; Brahmachari V
    Genomics; 2002 Aug; 80(2):151-7. PubMed ID: 12160728
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diminished ovarian reserve is not observed in infertility patients with high normal CGG repeats on the fragile X mental retardation 1 (FMR1) gene.
    Schufreider A; McQueen DB; Lee SM; Allon R; Uhler ML; Davie J; Feinberg EC
    Hum Reprod; 2015 Nov; 30(11):2686-92. PubMed ID: 26345686
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene.
    Milà M; Castellví-Bel S; Sánchez A; Lázaro C; Villa M; Estivill X
    J Med Genet; 1996 Apr; 33(4):338-40. PubMed ID: 8730293
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Promoter-bound trinucleotide repeat mRNA drives epigenetic silencing in fragile X syndrome.
    Colak D; Zaninovic N; Cohen MS; Rosenwaks Z; Yang WY; Gerhardt J; Disney MD; Jaffrey SR
    Science; 2014 Feb; 343(6174):1002-5. PubMed ID: 24578575
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Establishment of FXS-A9 panel with a single human X chromosome from fragile X syndrome-associated individual.
    Nakayama Y; Adachi K; Shioda N; Maeta S; Nanba E; Kugoh H
    Exp Cell Res; 2021 Jan; 398(2):112419. PubMed ID: 33296661
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice.
    Lavedan C; Grabczyk E; Usdin K; Nussbaum RL
    Genomics; 1998 Jun; 50(2):229-40. PubMed ID: 9653650
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CGG trinucleotide repeat length modulates neural plasticity and spatiotemporal processing in a mouse model of the fragile X premutation.
    Hunsaker MR; Kim K; Willemsen R; Berman RF
    Hippocampus; 2012 Dec; 22(12):2260-75. PubMed ID: 22707411
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.