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 *

135 related articles for article (PubMed ID: 9207038)

  • 1. Effect of in vitro promoter methylation and CGG repeat expansion on FMR-1 expression.
    Sandberg G; Schalling M
    Nucleic Acids Res; 1997 Jul; 25(14):2883-7. PubMed ID: 9207038
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Detection of FMR-1 gene expression by RT-PCR].
    Zheng L; Fan Y; Huang T; Zhu N; Shen Y; Wu G
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Dec; 17(6):407-11. PubMed ID: 9208564
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Methylation mosaicism of 5'-(CGG)(n)-3' repeats in fragile X, premutation and normal individuals.
    Genç B; Müller-Hartmann H; Zeschnigk M; Deissler H; Schmitz B; Majewski F; von Gontard A; Doerfler W
    Nucleic Acids Res; 2000 May; 28(10):2141-52. PubMed ID: 10773084
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Molecular diagnosis of fragile X syndrome and distribution of CGG repeats in the FMR-1 gene in Taiwanese.
    Wang YC; Li C; Lin ML; Lin WH; Li SY
    J Formos Med Assoc; 2000 May; 99(5):402-7. PubMed ID: 10870330
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects.
    Chen TA; Lu XF; Che PK; Ho WK
    Ann Clin Biochem; 1997 Sep; 34 ( Pt 5)():517-20. PubMed ID: 9293305
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families.
    Milà M; Kruyer H; Glover G; Sánchez A; Carbonell P; Castellví-Bell S; Volpini V; Rossell J; Gabarrón J; López I
    Hum Genet; 1994 Oct; 94(4):395-400. PubMed ID: 7927336
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Stable DNA methylation boundaries and expanded trinucleotide repeats: role of DNA insertions.
    Naumann A; Kraus C; Hoogeveen A; Ramirez CM; Doerfler W
    J Mol Biol; 2014 Jul; 426(14):2554-66. PubMed ID: 24816393
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes.
    Gurling HM; Bolton PF; Vincent J; Melmer G; Rutter M
    Hum Hered; 1997; 47(5):254-62. PubMed ID: 9358013
    [TBL] [Abstract][Full Text] [Related]  

  • 10. DNA methylation represses FMR-1 transcription in fragile X syndrome.
    Sutcliffe JS; Nelson DL; Zhang F; Pieretti M; Caskey CT; Saxe D; Warren ST
    Hum Mol Genet; 1992 Sep; 1(6):397-400. PubMed ID: 1301913
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. In vitro DNA methylation inhibits FMR-1 promoter.
    Hwu WL; Lee YM; Lee SC; Wang TR
    Biochem Biophys Res Commun; 1993 May; 193(1):324-9. PubMed ID: 8503923
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A methylation PCR approach for detection of fragile X syndrome.
    Panagopoulos I; Lassen C; Kristoffersson U; Aman P
    Hum Mutat; 1999; 14(1):71-9. PubMed ID: 10447261
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population.
    Jara L; Aspillaga M; Avendaño I; Obreque V; Blanco R; Valenzuela CY
    Am J Med Genet; 1998 Jan; 75(3):277-82. PubMed ID: 9475597
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.
    Chaudhary AG; Hussein IR; Abuzenadah A; Gari M; Bassiouni R; Sogaty S; Lary S; Al-Quaiti M; Al Balwi M; Al Qahtani M
    Pediatr Neurol; 2014 Apr; 50(4):368-76. PubMed ID: 24630283
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation.
    Burman RW; Popovich BW; Jacky PB; Turker MS
    Hum Mol Genet; 1999 Nov; 8(12):2293-302. PubMed ID: 10545610
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome.
    Wang YC; Lin ML; Lin SJ; Li YC; Li SY
    Hum Mutat; 1997; 10(5):393-9. PubMed ID: 9375856
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Segregation of the fragile X mutation from a male with a full mutation: unusual somatic instability in the FMR-1 locus.
    Kambouris M; Snow K; Thibodeau S; Bluhm D; Green M; Feldman GL
    Am J Med Genet; 1996 Aug; 64(2):404-7. PubMed ID: 8844092
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.