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Items: 1 to 20 of 125

1.

Developmental abnormalities of cortical interneurons precede symptoms onset in a mouse model of Rett syndrome.

Tomassy GS, Morello N, Calcagno E, Giustetto M.

J Neurochem. 2014 Oct;131(1):115-27. doi: 10.1111/jnc.12803. Epub 2014 Aug 5.

2.

MeCP2+/- mouse model of RTT reproduces auditory phenotypes associated with Rett syndrome and replicate select EEG endophenotypes of autism spectrum disorder.

Liao W, Gandal MJ, Ehrlichman RS, Siegel SJ, Carlson GC.

Neurobiol Dis. 2012 Apr;46(1):88-92. doi: 10.1016/j.nbd.2011.12.048. Epub 2012 Jan 9.

3.

Altered somatosensory barrel cortex refinement in the developing brain of Mecp2-null mice.

Moroto M, Nishimura A, Morimoto M, Isoda K, Morita T, Yoshida M, Morioka S, Tozawa T, Hasegawa T, Chiyonobu T, Yoshimoto K, Hosoi H.

Brain Res. 2013 Nov 6;1537:319-26. doi: 10.1016/j.brainres.2013.09.017. Epub 2013 Sep 21.

PMID:
24060648
4.

Excitation/inhibition imbalance and impaired synaptic inhibition in hippocampal area CA3 of Mecp2 knockout mice.

Calfa G, Li W, Rutherford JM, Pozzo-Miller L.

Hippocampus. 2015 Feb;25(2):159-68. doi: 10.1002/hipo.22360. Epub 2014 Sep 25.

5.

Cellular origins of auditory event-related potential deficits in Rett syndrome.

Goffin D, Brodkin ES, Blendy JA, Siegel SJ, Zhou Z.

Nat Neurosci. 2014 Jun;17(6):804-6. doi: 10.1038/nn.3710. Epub 2014 Apr 28.

6.

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
7.

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
8.

Loss of MeCP2 from forebrain excitatory neurons leads to cortical hyperexcitation and seizures.

Zhang W, Peterson M, Beyer B, Frankel WN, Zhang ZW.

J Neurosci. 2014 Feb 12;34(7):2754-63. doi: 10.1523/JNEUROSCI.4900-12.2014.

9.

Enhancement of postsynaptic GABAA and extrasynaptic NMDA receptor-mediated responses in the barrel cortex of Mecp2-null mice.

Lo FS, Blue ME, Erzurumlu RS.

J Neurophysiol. 2016 Mar;115(3):1298-306. doi: 10.1152/jn.00944.2015. Epub 2015 Dec 16.

10.

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.

Chao HT, Chen H, Samaco RC, Xue M, Chahrour M, Yoo J, Neul JL, Gong S, Lu HC, Heintz N, Ekker M, Rubenstein JL, Noebels JL, Rosenmund C, Zoghbi HY.

Nature. 2010 Nov 11;468(7321):263-9. doi: 10.1038/nature09582.

11.

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
12.

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.

13.

Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions.

Maezawa I, Swanberg S, Harvey D, LaSalle JM, Jin LW.

J Neurosci. 2009 Apr 22;29(16):5051-61. doi: 10.1523/JNEUROSCI.0324-09.2009.

14.

MeCP2-mediated alterations of striatal features accompany psychomotor deficits in a mouse model of Rett syndrome.

Kao FC, Su SH, Carlson GC, Liao W.

Brain Struct Funct. 2015 Jan;220(1):419-34. doi: 10.1007/s00429-013-0664-x. Epub 2013 Nov 12.

PMID:
24218106
15.

Defects in brainstem neurons associated with breathing and motor function in the Mecp2R168X/Y mouse model of Rett syndrome.

Johnson CM, Zhong W, Cui N, Wu Y, Xing H, Zhang S, Jiang C.

Am J Physiol Cell Physiol. 2016 Dec 1;311(6):C895-C909. doi: 10.1152/ajpcell.00132.2016. Epub 2016 Sep 21.

PMID:
27653984
16.

Astrocyte Transcriptome from the Mecp2(308)-Truncated Mouse Model of Rett Syndrome.

Delépine C, Nectoux J, Letourneur F, Baud V, Chelly J, Billuart P, Bienvenu T.

Neuromolecular Med. 2015 Dec;17(4):353-63. doi: 10.1007/s12017-015-8363-9. Epub 2015 Jul 25.

PMID:
26208914
17.

Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome.

Medrihan L, Tantalaki E, Aramuni G, Sargsyan V, Dudanova I, Missler M, Zhang W.

J Neurophysiol. 2008 Jan;99(1):112-21. Epub 2007 Nov 21.

18.

Ube3a expression is not altered in Mecp2 mutant mice.

Jordan C, Francke U.

Hum Mol Genet. 2006 Jul 15;15(14):2210-5. Epub 2006 Jun 5.

PMID:
16754645
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.

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.

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