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Items: 1 to 20 of 228

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.

Oral treatment with desipramine improves breathing and life span in Rett syndrome mouse model.

Zanella S, Mebarek S, Lajard AM, Picard N, Dutschmann M, Hilaire G.

Respir Physiol Neurobiol. 2008 Jan 1;160(1):116-21. Epub 2007 Aug 26.

PMID:
17905670
3.

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.

Moretti P, Bouwknecht JA, Teague R, Paylor R, Zoghbi HY.

Hum Mol Genet. 2005 Jan 15;14(2):205-20. Epub 2004 Nov 17.

PMID:
15548546
4.

Functional recovery with recombinant human IGF1 treatment in a mouse model of Rett Syndrome.

Castro J, Garcia RI, Kwok S, Banerjee A, Petravicz J, Woodson J, Mellios N, Tropea D, Sur M.

Proc Natl Acad Sci U S A. 2014 Jul 8;111(27):9941-6. doi: 10.1073/pnas.1311685111. Epub 2014 Jun 23.

5.

The MeCP2-null mouse hippocampus displays altered basal inhibitory rhythms and is prone to hyperexcitability.

Zhang L, He J, Jugloff DG, Eubanks JH.

Hippocampus. 2008;18(3):294-309.

PMID:
18058824
6.

Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice.

Gemelli T, Berton O, Nelson ED, Perrotti LI, Jaenisch R, Monteggia LM.

Biol Psychiatry. 2006 Mar 1;59(5):468-76. Epub 2005 Sep 30.

PMID:
16199017
7.

Gene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndrome.

Kriaucionis S, Paterson A, Curtis J, Guy J, Macleod N, Bird A.

Mol Cell Biol. 2006 Jul;26(13):5033-42.

8.

Evidence for abnormal early development in a mouse model of Rett syndrome.

Santos M, Silva-Fernandes A, Oliveira P, Sousa N, Maciel P.

Genes Brain Behav. 2007 Apr;6(3):277-86. Epub 2006 Jul 17.

9.

Early postnatal behavioral changes in the Mecp2-308 truncation mouse model of Rett syndrome.

De Filippis B, Ricceri L, Laviola G.

Genes Brain Behav. 2010 Mar 1;9(2):213-23. doi: 10.1111/j.1601-183X.2009.00551.x. Epub 2009 Nov 2.

10.

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
11.

Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations.

Chapleau CA, Calfa GD, Lane MC, Albertson AJ, Larimore JL, Kudo S, Armstrong DL, Percy AK, Pozzo-Miller L.

Neurobiol Dis. 2009 Aug;35(2):219-33. doi: 10.1016/j.nbd.2009.05.001. Epub 2009 May 12.

12.

MeCP2-dependent transcriptional repression regulates excitatory neurotransmission.

Nelson ED, Kavalali ET, Monteggia LM.

Curr Biol. 2006 Apr 4;16(7):710-6.

13.

MeCP2 in neurons: closing in on the causes of Rett syndrome.

Caballero IM, Hendrich B.

Hum Mol Genet. 2005 Apr 15;14 Spec No 1:R19-26. Review. Erratum in: Hum Mol Genet. 2005 Jul 15;14(14):2089.

PMID:
15809268
14.

Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice.

Viemari JC, Roux JC, Tryba AK, Saywell V, Burnet H, Peña F, Zanella S, Bévengut M, Barthelemy-Requin M, Herzing LB, Moncla A, Mancini J, Ramirez JM, Villard L, Hilaire G.

J Neurosci. 2005 Dec 14;25(50):11521-30.

15.

Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation.

Jentarra GM, Olfers SL, Rice SG, Srivastava N, Homanics GE, Blue M, Naidu S, Narayanan V.

BMC Neurosci. 2010 Feb 17;11:19. doi: 10.1186/1471-2202-11-19.

16.

Environmental enrichment alters locomotor behaviour and ventricular volume in Mecp2 1lox mice.

Nag N, Moriuchi JM, Peitzman CG, Ward BC, Kolodny NH, Berger-Sweeney JE.

Behav Brain Res. 2009 Jan 3;196(1):44-8. doi: 10.1016/j.bbr.2008.07.008. Epub 2008 Jul 18.

PMID:
18687363
17.

Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice.

Pelka GJ, Watson CM, Radziewic T, Hayward M, Lahooti H, Christodoulou J, Tam PP.

Brain. 2006 Apr;129(Pt 4):887-98. Epub 2006 Feb 8.

PMID:
16467389
18.

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.

19.

Alterations of cortical and hippocampal EEG activity in MeCP2-deficient mice.

D'Cruz JA, Wu C, Zahid T, El-Hayek Y, Zhang L, Eubanks JH.

Neurobiol Dis. 2010 Apr;38(1):8-16. doi: 10.1016/j.nbd.2009.12.018. Epub 2010 Jan 4.

PMID:
20045053
20.

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