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 *

279 related articles for article (PubMed ID: 8825491)

  • 1. Trinucleotide repeat expansion and human disease.
    Ashley CT; Warren ST
    Annu Rev Genet; 1995; 29():703-28. PubMed ID: 8825491
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Medical pathology due to trinucleotide repeats].
    Arenas-Aranda D; Peñaloza R; Salamanca-Gómez F
    Gac Med Mex; 1999; 135(1):53-65. PubMed ID: 10204311
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Dynamic mutation and its molecular cytogenetics].
    Hori T; Tsuji S; Yamauchi M
    Nihon Rinsho; 1999 Apr; 57(4):771-7. PubMed ID: 10222764
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mechanism of trinucleotide repeats instabilities: the necessities of repeat non-B secondary structure formation and the roles of cellular trans-acting factors.
    Pan XF
    Yi Chuan Xue Bao; 2006 Jan; 33(1):1-11. PubMed ID: 16450581
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci.
    Pearson CE; Sinden RR
    Biochemistry; 1996 Apr; 35(15):5041-53. PubMed ID: 8664297
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein.
    Sarafidou T; Kahl C; Martinez-Garay I; Mangelsdorf M; Gesk S; Baker E; Kokkinaki M; Talley P; Maltby EL; French L; Harder L; Hinzmann B; Nobile C; Richkind K; Finnis M; Deloukas P; Sutherland GR; Kutsche K; Moschonas NK; Siebert R; Gécz J;
    Genomics; 2004 Jul; 84(1):69-81. PubMed ID: 15203205
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Trinucleotide repeats in neurogenetic disorders.
    Paulson HL; Fischbeck KH
    Annu Rev Neurosci; 1996; 19():79-107. PubMed ID: 8833437
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Human chromosome fragility.
    Lukusa T; Fryns JP
    Biochim Biophys Acta; 2008 Jan; 1779(1):3-16. PubMed ID: 18078840
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trinucleotide repeat expansion and human disease.
    Hummerich H; Lehrach H
    Electrophoresis; 1995 Sep; 16(9):1698-704. PubMed ID: 8582359
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Long CCG triplet repeat blocks exclude nucleosomes: a possible mechanism for the nature of fragile sites in chromosomes.
    Wang YH; Gellibolian R; Shimizu M; Wells RD; Griffith J
    J Mol Biol; 1996 Nov; 263(4):511-6. PubMed ID: 8918933
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis.
    Koshy BT; Zoghbi HY
    Brain Pathol; 1997 Jul; 7(3):927-42. PubMed ID: 9217976
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.
    Parrish JE; Oostra BA; Verkerk AJ; Richards CS; Reynolds J; Spikes AS; Shaffer LG; Nelson DL
    Nat Genet; 1994 Nov; 8(3):229-35. PubMed ID: 7874164
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Molecular cytogenetics of fragile X syndrome].
    Yamauchi M; Tsuji S; Hori T
    Nihon Rinsho; 1999 Apr; 57(4):943-9. PubMed ID: 10222794
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of CGG variation through 642 meioses in Fragile X families.
    Rifé M; Badenas C; Quintó L; Puigoriol E; Tazón B; Rodriguez-Revenga L; Jiménez L; Sánchez A; Milà M
    Mol Hum Reprod; 2004 Oct; 10(10):773-6. PubMed ID: 15322225
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial transmission of the FMR1 CGG repeat.
    Nolin SL; Lewis FA; Ye LL; Houck GE; Glicksman AE; Limprasert P; Li SY; Zhong N; Ashley AE; Feingold E; Sherman SL; Brown WT
    Am J Hum Genet; 1996 Dec; 59(6):1252-61. PubMed ID: 8940270
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Trinucleotide repeat expansion in neurological disease.
    La Spada AR; Paulson HL; Fischbeck KH
    Ann Neurol; 1994 Dec; 36(6):814-22. PubMed ID: 7998766
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Chromosomal fragile sites].
    Hori T; Yamauchi M; Tsuji S
    Tanpakushitsu Kakusan Koso; 1996 Nov; 41(15 Suppl):2315-24. PubMed ID: 8952394
    [No Abstract]   [Full Text] [Related]  

  • 20. [Genomic instability and neurodegenerative disease].
    Miki T; Yamagata H
    Rinsho Byori; 1999 Jan; 47(1):37-45. PubMed ID: 10067364
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.