Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 514

1.

Improvement in motor and exploratory behavior in Rett syndrome mice with restricted ketogenic and standard diets.

Mantis JG, Fritz CL, Marsh J, Heinrichs SC, Seyfried TN.

Epilepsy Behav. 2009 Jun;15(2):133-41. doi: 10.1016/j.yebeh.2009.02.038. Epub 2009 Feb 26.

PMID:
19249385
2.

Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.

Stearns NA, Schaevitz LR, Bowling H, Nag N, Berger UV, Berger-Sweeney J.

Neuroscience. 2007 May 25;146(3):907-21. Epub 2007 Mar 23.

PMID:
17383101
3.

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.

4.

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
5.

Environmental enrichment ameliorates a motor coordination deficit in a mouse model of Rett syndrome--Mecp2 gene dosage effects and BDNF expression.

Kondo M, Gray LJ, Pelka GJ, Christodoulou J, Tam PP, Hannan AJ.

Eur J Neurosci. 2008 Jun;27(12):3342-50. doi: 10.1111/j.1460-9568.2008.06305.x. Epub 2008 Jun 14.

PMID:
18557922
6.

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
7.

Effects of postnatal dietary choline supplementation on motor regional brain volume and growth factor expression in a mouse model of Rett syndrome.

Nag N, Mellott TJ, Berger-Sweeney JE.

Brain Res. 2008 Oct 27;1237:101-9. doi: 10.1016/j.brainres.2008.08.042. Epub 2008 Aug 26.

PMID:
18778693
8.

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.

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.

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
11.

Social impairments in Rett syndrome: characteristics and relationship with clinical severity.

Kaufmann WE, Tierney E, Rohde CA, Suarez-Pedraza MC, Clarke MA, Salorio CF, Bibat G, Bukelis I, Naram D, Lanham DC, Naidu S.

J Intellect Disabil Res. 2012 Mar;56(3):233-47. doi: 10.1111/j.1365-2788.2011.01404.x. Epub 2011 Mar 8.

PMID:
21385260
12.

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
13.

Targeted delivery of an Mecp2 transgene to forebrain neurons improves the behavior of female Mecp2-deficient mice.

Jugloff DG, Vandamme K, Logan R, Visanji NP, Brotchie JM, Eubanks JH.

Hum Mol Genet. 2008 May 15;17(10):1386-96. doi: 10.1093/hmg/ddn026. Epub 2008 Jan 25.

PMID:
18223199
14.

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
15.

Mouse models of Rett syndrome: from behavioural phenotyping to preclinical evaluation of new therapeutic approaches.

Ricceri L, De Filippis B, Laviola G.

Behav Pharmacol. 2008 Sep;19(5-6):501-17. doi: 10.1097/FBP.0b013e32830c3645. Review.

PMID:
18690105
16.

Longitudinal brain MRI study in a mouse model of Rett Syndrome and the effects of choline.

Ward BC, Agarwal S, Wang K, Berger-Sweeney J, Kolodny NH.

Neurobiol Dis. 2008 Jul;31(1):110-9. doi: 10.1016/j.nbd.2008.03.009. Epub 2008 Apr 10.

PMID:
18571096
17.

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.

18.

Cognitive and social functions and growth factors in a mouse model of Rett syndrome.

Schaevitz LR, Moriuchi JM, Nag N, Mellot TJ, Berger-Sweeney J.

Physiol Behav. 2010 Jun 1;100(3):255-63. doi: 10.1016/j.physbeh.2009.12.025. Epub 2010 Jan 5.

PMID:
20045424
19.

The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression.

Chang Q, Khare G, Dani V, Nelson S, Jaenisch R.

Neuron. 2006 Feb 2;49(3):341-8.

20.

Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks.

Belichenko PV, Wright EE, Belichenko NP, Masliah E, Li HH, Mobley WC, Francke U.

J Comp Neurol. 2009 May 20;514(3):240-58. doi: 10.1002/cne.22009.

PMID:
19296534

Supplemental Content

Support Center