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Results: 19

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.

PMID:
21636743
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

The story of Rett syndrome: from clinic to neurobiology.

Chahrour M, Zoghbi HY.

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

PMID:
17988628
[PubMed - indexed for MEDLINE]
Free Article
3.

The relationship of Rett syndrome and MECP2 disorders to autism.

Neul JL.

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

PMID:
23226951
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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.

PMID:
21239731
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

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
[PubMed - indexed for MEDLINE]
6.

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
[PubMed - indexed for MEDLINE]
7.

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
[PubMed - indexed for MEDLINE]
8.

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
[PubMed - indexed for MEDLINE]
9.

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
[PubMed - indexed for MEDLINE]
10.

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.

PMID:
18948693
[PubMed - indexed for MEDLINE]
11.

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.

PMID:
22192257
[PubMed - indexed for MEDLINE]
12.

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.

PMID:
21878110
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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
[PubMed - indexed for MEDLINE]
14.

Autonomic dysfunction with mutations in the gene that encodes methyl-CpG-binding protein 2: insights into Rett syndrome.

Lioy DT, Wu WW, Bissonnette JM.

Auton Neurosci. 2011 Apr 26;161(1-2):55-62. doi: 10.1016/j.autneu.2011.01.006. Epub 2011 Feb 12. Review.

PMID:
21316312
[PubMed - indexed for MEDLINE]
15.

Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations.

Amir RE, Zoghbi HY.

Am J Med Genet. 2000 Summer;97(2):147-52. Review.

PMID:
11180222
[PubMed - indexed for MEDLINE]
16.

MeCP2 dysfunction in Rett syndrome and related disorders.

Moretti P, Zoghbi HY.

Curr Opin Genet Dev. 2006 Jun;16(3):276-81. Epub 2006 May 2. Review.

PMID:
16647848
[PubMed - indexed for MEDLINE]
17.

[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.

PMID:
20019788
[PubMed - indexed for MEDLINE]
Free Article
18.

Breathing dysfunction in Rett syndrome: understanding epigenetic regulation of the respiratory network.

Ogier M, Katz DM.

Respir Physiol Neurobiol. 2008 Dec 10;164(1-2):55-63. doi: 10.1016/j.resp.2008.04.005. Review.

PMID:
18534925
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Breathing disorders in Rett syndrome: progressive neurochemical dysfunction in the respiratory network after birth.

Katz DM, Dutschmann M, Ramirez JM, Hilaire G.

Respir Physiol Neurobiol. 2009 Aug 31;168(1-2):101-8. doi: 10.1016/j.resp.2009.04.017. Epub 2009 Apr 24. Review.

PMID:
19394452
[PubMed - indexed for MEDLINE]
Free PMC Article

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