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Items: 1 to 20 of 25

1.

Adult neural function requires MeCP2.

McGraw CM, Samaco RC, Zoghbi HY.

Science. 2011 Jul 8;333(6039):186. doi: 10.1126/science.1206593. Epub 2011 Jun 2.

2.

Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome.

Filosa S, Pecorelli A, D'Esposito M, Valacchi G, Hajek J.

Free Radic Biol Med. 2015 Nov;88(Pt A):81-90. doi: 10.1016/j.freeradbiomed.2015.04.019. Epub 2015 May 8. Review.

PMID:
25960047
3.

The story of Rett syndrome: from clinic to neurobiology.

Chahrour M, Zoghbi HY.

Neuron. 2007 Nov 8;56(3):422-37. Review.

4.

The relationship of Rett syndrome and MECP2 disorders to autism.

Neul JL.

Dialogues Clin Neurosci. 2012 Sep;14(3):253-62. Review.

5.

Rett syndrome: a complex disorder with simple roots.

Lyst MJ, Bird A.

Nat Rev Genet. 2015 May;16(5):261-75. doi: 10.1038/nrg3897. Epub 2015 Mar 3. Review.

PMID:
25732612
6.

Rett syndrome and MeCP2.

Liyanage VR, Rastegar M.

Neuromolecular Med. 2014 Jun;16(2):231-64. doi: 10.1007/s12017-014-8295-9. Epub 2014 Mar 11. Review.

7.

Reversibility of functional deficits in experimental models of Rett syndrome.

Cobb S, Guy J, Bird A.

Biochem Soc Trans. 2010 Apr;38(2):498-506. doi: 10.1042/BST0380498. Review.

PMID:
20298210
8.

Experimental models of Rett syndrome based on Mecp2 dysfunction.

Calfa G, Percy AK, Pozzo-Miller L.

Exp Biol Med (Maywood). 2011 Jan;236(1):3-19. doi: 10.1258/ebm.2010.010261. Review.

9.

Rett syndrome: the complex nature of a monogenic disease.

Renieri A, Meloni I, Longo I, Ariani F, Mari F, Pescucci C, Cambi F.

J Mol Med (Berl). 2003 Jun;81(6):346-54. Epub 2003 May 16. Review.

PMID:
12750821
10.

MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution.

Kaufmann WE, Johnston MV, Blue ME.

Brain Dev. 2005 Nov;27 Suppl 1:S77-S87. Epub 2005 Sep 22. Review.

PMID:
16182491
11.

Regulation mechanism and research progress of MeCP2 in Rett syndrome.

Yang W, Pan H.

Yi Chuan. 2014 Jul;36(7):625-30. doi: 10.3724/SP.J.1005.2014.0625. Review.

PMID:
25076025
12.

Brain-derived neurotrophic factor and Rett syndrome.

Katz DM.

Handb Exp Pharmacol. 2014;220:481-95. doi: 10.1007/978-3-642-45106-5_18. Review.

PMID:
24668484
13.

MeCP2 and Rett syndrome: reversibility and potential avenues for therapy.

Gadalla KK, Bailey ME, Cobb SR.

Biochem J. 2011 Oct 1;439(1):1-14. doi: 10.1042/BJ20110648. Review.

PMID:
21916843
14.

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
15.

Rett syndrome: from the gene to the disease.

Matijevic T, Knezevic J, Slavica M, Pavelic J.

Eur Neurol. 2009;61(1):3-10. doi: 10.1159/000165342. Epub 2008 Oct 24. Review.

16.

Generation and analysis of the Rett syndrome-associated MeCP2- null rat model.

Zhai W, Hu HX, Le L, Zhuang FF, Wang KZ, Zhao Y, Wang K, Liu XM, Sun D, Wang XY, Kuang SH, Hu KP.

Yi Chuan. 2016 Nov 20;38(11):1004-1011. Review.

PMID:
27867150
17.

Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations.

Ravn K, Roende G, Duno M, Fuglsang K, Eiklid KL, Tümer Z, Nielsen JB, Skjeldal OH.

Orphanet J Rare Dis. 2011 Aug 30;6:58. doi: 10.1186/1750-1172-6-58. Review.

18.

Rett syndrome: from bed to bench.

Weng SM, Bailey ME, Cobb SR.

Pediatr Neonatol. 2011 Dec;52(6):309-16. doi: 10.1016/j.pedneo.2011.08.002. Epub 2011 Nov 6. Review.

19.

Rett syndrome: of girls and mice--lessons for regression in autism.

Glaze DG.

Ment Retard Dev Disabil Res Rev. 2004;10(2):154-8. Review.

PMID:
15362175
20.

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

Zhang JJ, Bao XH.

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

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