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Items: 8

1.

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice.

Tropea D, Giacometti E, Wilson NR, Beard C, McCurry C, Fu DD, Flannery R, Jaenisch R, Sur M.

Proc Natl Acad Sci U S A. 2009 Feb 10;106(6):2029-34. doi: 10.1073/pnas.0812394106.

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.

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.

4.

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
5.

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
6.

Mechanisms of disease: neurogenetics of MeCP2 deficiency.

Francke U.

Nat Clin Pract Neurol. 2006 Apr;2(4):212-21. Review.

PMID:
16932552
7.

Dendritic spine dysgenesis in Rett syndrome.

Xu X, Miller EC, Pozzo-Miller L.

Front Neuroanat. 2014 Sep 10;8:97. doi: 10.3389/fnana.2014.00097. eCollection 2014. Review.

8.

Recent advances in understanding synaptic abnormalities in Rett syndrome.

Johnston M, Blue ME, Naidu S.

F1000Res. 2015 Dec 22;4. pii: F1000 Faculty Rev-1490. doi: 10.12688/f1000research.6987.1. eCollection 2015. Review.

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