138 related articles for article (PubMed ID: 8798475)
1. Methylation of expanded CCG triplet repeat DNA from fragile X syndrome patients enhances nucleosome exclusion.
Wang YH; Griffith J
J Biol Chem; 1996 Sep; 271(38):22937-40. PubMed ID: 8798475
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome.
Mulvihill DJ; Nichol Edamura K; Hagerman KA; Pearson CE; Wang YH
J Biol Chem; 2005 Feb; 280(6):4498-503. PubMed ID: 15574425
[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. The [(G/C)3NN]n motif: a common DNA repeat that excludes nucleosomes.
Wang YH; Griffith JD
Proc Natl Acad Sci U S A; 1996 Aug; 93(17):8863-7. PubMed ID: 8799118
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Human fragile site FRA16B DNA excludes nucleosomes in the presence of distamycin.
Hsu YY; Wang YH
J Biol Chem; 2002 May; 277(19):17315-9. PubMed ID: 11880377
[TBL] [Abstract][Full Text] [Related]
8. 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]
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. Hairpin induced slippage and hyper-methylation of the fragile X DNA triplets.
Chen X; Mariappan SV; Moyzis RK; Bradbury EM; Gupta G
J Biomol Struct Dyn; 1998 Feb; 15(4):745-56. PubMed ID: 9514250
[TBL] [Abstract][Full Text] [Related]
11. Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins.
Richards RI; Holman K; Yu S; Sutherland GR
Hum Mol Genet; 1993 Sep; 2(9):1429-35. PubMed ID: 8242066
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Chromatin structure of repeating CTG/CAG and CGG/CCG sequences in human disease.
Wang YH
Front Biosci; 2007 May; 12():4731-41. PubMed ID: 17485409
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome.
Hornstra IK; Nelson DL; Warren ST; Yang TP
Hum Mol Genet; 1993 Oct; 2(10):1659-65. PubMed ID: 8268919
[TBL] [Abstract][Full Text] [Related]
16. Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats.
Wöhrle D; Salat U; Gläser D; Mücke J; Meisel-Stosiek M; Schindler D; Vogel W; Steinbach P
J Med Genet; 1998 Feb; 35(2):103-11. PubMed ID: 9507388
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Effects of DNA methylation on nucleosome stability.
Collings CK; Waddell PJ; Anderson JN
Nucleic Acids Res; 2013 Mar; 41(5):2918-31. PubMed ID: 23355616
[TBL] [Abstract][Full Text] [Related]
19. Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island.
Gu Y; Shen Y; Gibbs RA; Nelson DL
Nat Genet; 1996 May; 13(1):109-13. PubMed ID: 8673086
[TBL] [Abstract][Full Text] [Related]
20. Methylation analysis of CGG sites in the CpG island of the human FMR1 gene.
Hansen RS; Gartler SM; Scott CR; Chen SH; Laird CD
Hum Mol Genet; 1992 Nov; 1(8):571-8. PubMed ID: 1301165
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]