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Items: 1 to 20 of 128

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.

Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome.

Moretti P, Levenson JM, Battaglia F, Atkinson R, Teague R, Antalffy B, Armstrong D, Arancio O, Sweatt JD, Zoghbi HY.

J Neurosci. 2006 Jan 4;26(1):319-27.

4.

Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis.

Alvarez-Saavedra M, Sáez MA, Kang D, Zoghbi HY, Young JI.

Hum Mol Genet. 2007 Oct 1;16(19):2315-25. Epub 2007 Jul 17.

PMID:
17635839
5.

Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndrome.

Kerr B, Silva PA, Walz K, Young JI.

PLoS One. 2010 Jul 12;5(7):e11534. doi: 10.1371/journal.pone.0011534.

6.

Synaptic maturation at cortical projections to the lateral amygdala in a mouse model of Rett syndrome.

Gambino F, Khelfaoui M, Poulain B, Bienvenu T, Chelly J, Humeau Y.

PLoS One. 2010 Jul 2;5(7):e11399. doi: 10.1371/journal.pone.0011399.

7.

The story of Rett syndrome: from clinic to neurobiology.

Chahrour M, Zoghbi HY.

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

8.

MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome.

Chen L, Chen K, Lavery LA, Baker SA, Shaw CA, Li W, Zoghbi HY.

Proc Natl Acad Sci U S A. 2015 Apr 28;112(17):5509-14. doi: 10.1073/pnas.1505909112. Epub 2015 Apr 13. Erratum in: Proc Natl Acad Sci U S A. 2015 Jun 2;112(22):E2982.

9.

Genome-wide analysis reveals methyl-CpG-binding protein 2-dependent regulation of microRNAs in a mouse model of Rett syndrome.

Wu H, Tao J, Chen PJ, Shahab A, Ge W, Hart RP, Ruan X, Ruan Y, Sun YE.

Proc Natl Acad Sci U S A. 2010 Oct 19;107(42):18161-6. doi: 10.1073/pnas.1005595107. Epub 2010 Oct 4.

10.

The relationship of Rett syndrome and MECP2 disorders to autism.

Neul JL.

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

11.

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
12.

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.

PMID:
24615633
13.

Neuronal morphology in MeCP2 mouse models is intrinsically variable and depends on age, cell type, and Mecp2 mutation.

Wang IT, Reyes AR, Zhou Z.

Neurobiol Dis. 2013 Oct;58:3-12. doi: 10.1016/j.nbd.2013.04.020. Epub 2013 May 6.

14.

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
15.

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.

16.

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
17.

Early environmental enrichment moderates the behavioral and synaptic phenotype of MeCP2 null mice.

Lonetti G, Angelucci A, Morando L, Boggio EM, Giustetto M, Pizzorusso T.

Biol Psychiatry. 2010 Apr 1;67(7):657-65. doi: 10.1016/j.biopsych.2009.12.022. Epub 2010 Feb 20.

PMID:
20172507
18.

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
19.

MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits.

Schaevitz LR, Gómez NB, Zhen DP, Berger-Sweeney JE.

Genes Brain Behav. 2013 Oct;12(7):732-40. doi: 10.1111/gbb.12070. Epub 2013 Aug 26.

20.

A BDNF loop-domain mimetic acutely reverses spontaneous apneas and respiratory abnormalities during behavioral arousal in a mouse model of Rett syndrome.

Kron M, Lang M, Adams IT, Sceniak M, Longo F, Katz DM.

Dis Model Mech. 2014 Sep;7(9):1047-55. doi: 10.1242/dmm.016030.

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