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Results: 1 to 20 of 115

Similar articles for PubMed (Select 21326358)

1.

MeCP2: structure and function.

Adkins NL, Georgel PT.

Biochem Cell Biol. 2011 Feb;89(1):1-11. doi: 10.1139/O10-112. Review.

PMID:
21326358
2.

MeCP2 in Rett syndrome: transcriptional repressor or chromatin architectural protein?

Chadwick LH, Wade PA.

Curr Opin Genet Dev. 2007 Apr;17(2):121-5. Epub 2007 Feb 20. Review.

PMID:
17317146
3.

Rett syndrome: a surprising result of mutation in MECP2.

Dragich J, Houwink-Manville I, Schanen C.

Hum Mol Genet. 2000 Oct;9(16):2365-75. Review.

4.

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome.

Horike S, Cai S, Miyano M, Cheng JF, Kohwi-Shigematsu T.

Nat Genet. 2005 Jan;37(1):31-40. Epub 2004 Dec 19.

PMID:
15608638
5.
6.

MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome.

Wan M, Zhao K, Lee SS, Francke U.

Hum Mol Genet. 2001 May 1;10(10):1085-92.

7.

MeCP2-chromatin interactions include the formation of chromatosome-like structures and are altered in mutations causing Rett syndrome.

Nikitina T, Ghosh RP, Horowitz-Scherer RA, Hansen JC, Grigoryev SA, Woodcock CL.

J Biol Chem. 2007 Sep 21;282(38):28237-45. Epub 2007 Jul 27.

8.

Deciphering Rett syndrome with mouse genetics, epigenomics, and human neurons.

Tao J, Wu H, Sun YE.

Int Rev Neurobiol. 2009;89:147-60. doi: 10.1016/S0074-7742(09)89007-7. Review.

PMID:
19900619
9.

The neurobiology of Rett syndrome.

Akbarian S.

Neuroscientist. 2003 Feb;9(1):57-63. Review.

PMID:
12580340
10.

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice.

Chen RZ, Akbarian S, Tudor M, Jaenisch R.

Nat Genet. 2001 Mar;27(3):327-31.

PMID:
11242118
11.

MeCP2 Rett mutations affect large scale chromatin organization.

Agarwal N, Becker A, Jost KL, Haase S, Thakur BK, Brero A, Hardt T, Kudo S, Leonhardt H, Cardoso MC.

Hum Mol Genet. 2011 Nov 1;20(21):4187-95. doi: 10.1093/hmg/ddr346. Epub 2011 Aug 10.

13.

[Research progress of Rett syndrome causing gene MECP2--the structure, function and modulation of MECP2].

Zhang JJ, Bao XH.

Beijing Da Xue Xue Bao. 2009 Dec 18;41(6):712-5. Review. Chinese.

14.

A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos.

Stancheva I, Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR.

Mol Cell. 2003 Aug;12(2):425-35.

PMID:
14536082
15.

MeCP2 and other methyl-CpG binding proteins.

Jørgensen HF, Bird A.

Ment Retard Dev Disabil Res Rev. 2002;8(2):87-93. Review.

PMID:
12112733
16.

The impact of MECP2 mutations in the expression patterns of Rett syndrome patients.

Ballestar E, Ropero S, Alaminos M, Armstrong J, Setien F, Agrelo R, Fraga MF, Herranz M, Avila S, Pineda M, Monros E, Esteller M.

Hum Genet. 2005 Jan;116(1-2):91-104. Epub 2004 Nov 11.

PMID:
15549394
17.

DNA methylation and Rett syndrome.

Kriaucionis S, Bird A.

Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R221-7. Epub 2003 Aug 19. Review.

18.

Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls.

Evans JC, Archer HL, Whatley SD, Kerr A, Clarke A, Butler R.

Eur J Hum Genet. 2005 Jan;13(1):124-6.

20.

MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression.

Makedonski K, Abuhatzira L, Kaufman Y, Razin A, Shemer R.

Hum Mol Genet. 2005 Apr 15;14(8):1049-58. Epub 2005 Mar 9.

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