264 related articles for article (PubMed ID: 11487573)
1. 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]
2. 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]
3. 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]
4. A fragile gene.
Oostra BA; Willems PJ
Bioessays; 1995 Nov; 17(11):941-7. PubMed ID: 8526888
[TBL] [Abstract][Full Text] [Related]
5. FMR1 premutation allele (CGG)81 is stable in mice.
Bontekoe CJ; de Graaff E; Nieuwenhuizen IM; Willemsen R; Oostra BA
Eur J Hum Genet; 1997; 5(5):293-8. PubMed ID: 9412786
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome.
Meijer H; de Graaff E; Merckx DM; Jongbloed RJ; de Die-Smulders CE; Engelen JJ; Fryns JP; Curfs PM; Oostra BA
Hum Mol Genet; 1994 Apr; 3(4):615-20. PubMed ID: 8069307
[TBL] [Abstract][Full Text] [Related]
10. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.
Gunter C; Paradee W; Crawford DC; Meadows KA; Newman J; Kunst CB; Nelson DL; Schwartz C; Murray A; Macpherson JN; Sherman SL; Warren ST
Hum Mol Genet; 1998 Nov; 7(12):1935-46. PubMed ID: 9811938
[TBL] [Abstract][Full Text] [Related]
11. Triplet repeat polymorphism & fragile X syndrome in the Indian context.
Baskaran S; Naseerullah MK; Manjunatha KR; Chetan GK; Arthi R; Rao GV; Girimaji SR; Srinath S; Sheshadri S; Devi RR; Brahmachari V
Indian J Med Res; 1998 Jan; 107():29-36. PubMed ID: 9529778
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population.
Patsalis PC; Sismani C; Stylianou S; Ioannou P; Joseph G; Manoli P; Holden JJ; Hettinger JA
Am J Med Genet; 1999 May; 84(3):217-20. PubMed ID: 10331595
[TBL] [Abstract][Full Text] [Related]
16. Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.
Eichler EE; Macpherson JN; Murray A; Jacobs PA; Chakravarti A; Nelson DL
Hum Mol Genet; 1996 Mar; 5(3):319-30. PubMed ID: 8852655
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability.
Crawford DC; Zhang F; Wilson B; Warren ST; Sherman SL
Hum Mol Genet; 2000 Jul; 9(12):1759-69. PubMed ID: 10915764
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients.
de Graaff E; Rouillard P; Willems PJ; Smits AP; Rousseau F; Oostra BA
Hum Mol Genet; 1995 Jan; 4(1):45-9. PubMed ID: 7711733
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
