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Items: 1 to 20 of 68

1.

Gene silencing induced by oxidative DNA base damage: association with local decrease of histone H4 acetylation in the promoter region.

Khobta A, Anderhub S, Kitsera N, Epe B.

Nucleic Acids Res. 2010 Jul;38(13):4285-95. doi: 10.1093/nar/gkq170. Epub 2010 Mar 24.

2.

Potassium bromate, a potent DNA oxidizing agent, exacerbates germline repeat expansion in a fragile X premutation mouse model.

Entezam A, Lokanga AR, Le W, Hoffman G, Usdin K.

Hum Mutat. 2010 May;31(5):611-6. doi: 10.1002/humu.21237.

3.

Distinguishing epigenetic marks of developmental and imprinting regulation.

McEwen KR, Ferguson-Smith AC.

Epigenetics Chromatin. 2010 Jan 15;3(1):2. doi: 10.1186/1756-8935-3-2.

4.

Epigenetic changes and non-coding expanded repeats.

Nakamori M, Thornton C.

Neurobiol Dis. 2010 Jul;39(1):21-7. doi: 10.1016/j.nbd.2010.02.004. Epub 2010 Feb 18. Review.

5.

A distinct DNA-methylation boundary in the 5'- upstream sequence of the FMR1 promoter binds nuclear proteins and is lost in fragile X syndrome.

Naumann A, Hochstein N, Weber S, Fanning E, Doerfler W.

Am J Hum Genet. 2009 Nov;85(5):606-16. doi: 10.1016/j.ajhg.2009.09.018. Epub 2009 Oct 22. Erratum in: Am J Hum Genet. 2010 Jan;86(1):98-100.

6.

ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice.

Entezam A, Usdin K.

Nucleic Acids Res. 2009 Oct;37(19):6371-7. doi: 10.1093/nar/gkp666. Epub 2009 Aug 26.

7.
8.

The role of DNA damage response pathways in chromosome fragility in Fragile X syndrome.

Kumari D, Somma V, Nakamura AJ, Bonner WM, D'Ambrosio E, Usdin K.

Nucleic Acids Res. 2009 Jul;37(13):4385-92. doi: 10.1093/nar/gkp391. Epub 2009 May 21.

9.

Determination of enriched histone modifications in non-genic portions of the human genome.

Rosenfeld JA, Wang Z, Schones DE, Zhao K, DeSalle R, Zhang MQ.

BMC Genomics. 2009 Mar 31;10:143. doi: 10.1186/1471-2164-10-143.

10.

The epigenetics of fragile X syndrome.

Warren ST.

Cell Stem Cell. 2007 Nov;1(5):488-9. No abstract available.

11.

Double strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island.

O'Hagan HM, Mohammad HP, Baylin SB.

PLoS Genet. 2008 Aug 15;4(8):e1000155. doi: 10.1371/journal.pgen.1000155.

12.

Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations.

Tabolacci E, Moscato U, Zalfa F, Bagni C, Chiurazzi P, Neri G.

Eur J Hum Genet. 2008 Dec;16(12):1487-98. doi: 10.1038/ejhg.2008.130. Epub 2008 Jul 16.

13.
14.

Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos.

Eiges R, Urbach A, Malcov M, Frumkin T, Schwartz T, Amit A, Yaron Y, Eden A, Yanuka O, Benvenisty N, Ben-Yosef D.

Cell Stem Cell. 2007 Nov;1(5):568-77. doi: 10.1016/j.stem.2007.09.001.

15.

SIRT1 inhibition alleviates gene silencing in Fragile X mental retardation syndrome.

Biacsi R, Kumari D, Usdin K.

PLoS Genet. 2008 Mar 7;4(3):e1000017. doi: 10.1371/journal.pgen.1000017.

16.

A novel RNA transcript with antiapoptotic function is silenced in fragile X syndrome.

Khalil AM, Faghihi MA, Modarresi F, Brothers SP, Wahlestedt C.

PLoS One. 2008 Jan 23;3(1):e1486. doi: 10.1371/journal.pone.0001486.

17.

ATR protects the genome against CGG.CCG-repeat expansion in Fragile X premutation mice.

Entezam A, Usdin K.

Nucleic Acids Res. 2008 Feb;36(3):1050-6. Epub 2007 Dec 26.

18.

SIRT1 regulates the histone methyl-transferase SUV39H1 during heterochromatin formation.

Vaquero A, Scher M, Erdjument-Bromage H, Tempst P, Serrano L, Reinberg D.

Nature. 2007 Nov 15;450(7168):440-4.

PMID:
18004385
19.

An antisense transcript spanning the CGG repeat region of FMR1 is upregulated in premutation carriers but silenced in full mutation individuals.

Ladd PD, Smith LE, Rabaia NA, Moore JM, Georges SA, Hansen RS, Hagerman RJ, Tassone F, Tapscott SJ, Filippova GN.

Hum Mol Genet. 2007 Dec 15;16(24):3174-87. Epub 2007 Oct 6.

PMID:
17921506
20.

Active and repressive chromatin are interspersed without spreading in an imprinted gene cluster in the mammalian genome.

Regha K, Sloane MA, Huang R, Pauler FM, Warczok KE, Melikant B, Radolf M, Martens JH, Schotta G, Jenuwein T, Barlow DP.

Mol Cell. 2007 Aug 3;27(3):353-66.

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