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Items: 1 to 20 of 99

1.

Long-term home cage activity scans reveal lowered exploratory behaviour in symptomatic female Rett mice.

Robinson L, Plano A, Cobb S, Riedel G.

Behav Brain Res. 2013 Aug 1;250:148-56. doi: 10.1016/j.bbr.2013.04.041. Epub 2013 May 1.

2.

Neonatal exposure to low dose corticosterone persistently modulates hippocampal mineralocorticoid receptor expression and improves locomotor/exploratory behaviour in a mouse model of Rett syndrome.

De Filippis B, Ricceri L, Fuso A, Laviola G.

Neuropharmacology. 2013 May;68:174-83. doi: 10.1016/j.neuropharm.2012.05.048. Epub 2012 Jun 16.

PMID:
22709945
3.

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.

4.

Correcting deregulated Fxyd1 expression ameliorates a behavioral impairment in a mouse model of Rett syndrome.

Matagne V, Budden S, Ojeda SR, Raber J.

Brain Res. 2013 Feb 16;1496:104-14. doi: 10.1016/j.brainres.2012.12.009. Epub 2012 Dec 14.

5.

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
6.

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
7.

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
8.
9.

MeCP2-mediated transcription repression in the basolateral amygdala may underlie heightened anxiety in a mouse model of Rett syndrome.

Adachi M, Autry AE, Covington HE 3rd, Monteggia LM.

J Neurosci. 2009 Apr 1;29(13):4218-27. doi: 10.1523/JNEUROSCI.4225-08.2009.

10.

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.

11.

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
12.

Open field locomotor activity and anxiety-related behaviors in mucopolysaccharidosis type IIIA mice.

Lau AA, Crawley AC, Hopwood JJ, Hemsley KM.

Behav Brain Res. 2008 Aug 5;191(1):130-6. doi: 10.1016/j.bbr.2008.03.024. Epub 2008 Mar 25.

PMID:
18453006
13.

Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome.

Santos M, Summavielle T, Teixeira-Castro A, Silva-Fernandes A, Duarte-Silva S, Marques F, Martins L, Dierssen M, Oliveira P, Sousa N, Maciel P.

Neuroscience. 2010 Oct 13;170(2):453-67. doi: 10.1016/j.neuroscience.2010.07.010. Epub 2010 Jul 13.

PMID:
20633611
14.

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.

15.

Reduced exploration, increased anxiety, and altered social behavior: Autistic-like features of euchromatin histone methyltransferase 1 heterozygous knockout mice.

Balemans MC, Huibers MM, Eikelenboom NW, Kuipers AJ, van Summeren RC, Pijpers MM, Tachibana M, Shinkai Y, van Bokhoven H, Van der Zee CE.

Behav Brain Res. 2010 Mar 17;208(1):47-55. doi: 10.1016/j.bbr.2009.11.008. Epub 2009 Nov 5.

PMID:
19896504
16.

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
17.

Characterization of the MeCP2R168X knockin mouse model for Rett syndrome.

Wegener E, Brendel C, Fischer A, Hülsmann S, Gärtner J, Huppke P.

PLoS One. 2014 Dec 26;9(12):e115444. doi: 10.1371/journal.pone.0115444. eCollection 2014.

18.

Circadian rhythm disruption in a mouse model of Rett syndrome circadian disruption in RTT.

Li Q, Loh DH, Kudo T, Truong D, Derakhshesh M, Kaswan ZM, Ghiani CA, Tsoa R, Cheng Y, Sun YE, Colwell CS.

Neurobiol Dis. 2015 May;77:155-64. doi: 10.1016/j.nbd.2015.03.009. Epub 2015 Mar 14.

PMID:
25779967
19.

Anxiety-related mechanisms of respiratory dysfunction in a mouse model of Rett syndrome.

Ren J, Ding X, Funk GD, Greer JJ.

J Neurosci. 2012 Nov 28;32(48):17230-40. doi: 10.1523/JNEUROSCI.2951-12.2012.

20.

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.

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