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Items: 1 to 20 of 111

1.

In vitro reactivation of the FMR1 gene involved in fragile X syndrome.

Chiurazzi P, Pomponi MG, Willemsen R, Oostra BA, Neri G.

Hum Mol Genet. 1998 Jan;7(1):109-13.

PMID:
9384610
2.

Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine.

Pietrobono R, Pomponi MG, Tabolacci E, Oostra B, Chiurazzi P, Neri G.

Nucleic Acids Res. 2002 Jul 15;30(14):3278-85.

3.

Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene.

Chiurazzi P, Pomponi MG, Pietrobono R, Bakker CE, Neri G, Oostra BA.

Hum Mol Genet. 1999 Nov;8(12):2317-23.

PMID:
10545613
4.

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 15;28(10):2141-52.

5.

Transcription of the FMR1 gene in individuals with fragile X syndrome.

Tassone F, Hagerman RJ, Chamberlain WD, Hagerman PJ.

Am J Med Genet. 2000 Fall;97(3):195-203.

PMID:
11449488
6.

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.

PMID:
1301165
7.

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.

PMID:
8069307
8.

Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments.

Tabolacci E, Pietrobono R, Moscato U, Oostra BA, Chiurazzi P, Neri G.

Eur J Hum Genet. 2005 May;13(5):641-8.

10.

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.

11.

Normal phenotype in two brothers with a full FMR1 mutation.

Smeets HJ, Smits AP, Verheij CE, Theelen JP, Willemsen R, van de Burgt I, Hoogeveen AT, Oosterwijk JC, Oostra BA.

Hum Mol Genet. 1995 Nov;4(11):2103-8.

PMID:
8589687
12.

Hypomethylation of an expanded FMR1 allele is not associated with a global DNA methylation defect.

Burman RW, Yates PA, Green LD, Jacky PB, Turker MS, Popovich BW.

Am J Hum Genet. 1999 Nov;65(5):1375-86.

13.

Rare variants in the promoter of the fragile X syndrome gene (FMR1).

Milà M, Castellví-Bel S, Sánchez A, Barceló A, Badenas C, Mallolas J, Estivill X.

Mol Cell Probes. 2000 Apr;14(2):115-9.

PMID:
10799273
14.

Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1.

Stöger R, Kajimura TM, Brown WT, Laird CD.

Hum Mol Genet. 1997 Oct;6(11):1791-801.

PMID:
9302255
15.

Expression of the FMR1 gene.

Tassone F, Hagerman PJ.

Cytogenet Genome Res. 2003;100(1-4):124-8. Review.

PMID:
14526172
16.

Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.

Taylor AK, Safanda JF, Fall MZ, Quince C, Lang KA, Hull CE, Carpenter I, Staley LW, Hagerman RJ.

JAMA. 1994 Feb 16;271(7):507-14.

PMID:
8301764
17.

Contribution of the FMR1 gene mutation to human intellectual dysfunction.

Reiss AL, Freund LS, Baumgardner TL, Abrams MT, Denckla MB.

Nat Genet. 1995 Nov;11(3):331-4.

PMID:
7581460
18.

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ.

Am J Med Genet. 2000 Sep 18;94(3):232-6.

PMID:
10995510
19.

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 15;486(1-2):15-22. doi: 10.1016/j.gene.2011.06.034. Epub 2011 Jul 13.

PMID:
21767618
20.

Loss of FMR1 hypermethylation in somatic cell heterokaryons.

Stoyanova V, Rossetti S, VAN Unen L, Oostra BA, Hoogeveen AT.

FASEB J. 2004 Dec;18(15):1964-6. Epub 2004 Sep 17.

PMID:
15377638

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