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Items: 1 to 20 of 202

1.

Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome.

McCauley MD, Wang T, Mike E, Herrera J, Beavers DL, Huang TW, Ward CS, Skinner S, Percy AK, Glaze DG, Wehrens XH, Neul JL.

Sci Transl Med. 2011 Dec 14;3(113):113ra125. doi: 10.1126/scitranslmed.3002982.

2.

Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs.

Herrera JA, Ward CS, Pitcher MR, Percy AK, Skinner S, Kaufmann WE, Glaze DG, Wehrens XH, Neul JL.

Dis Model Mech. 2015 Apr;8(4):363-71. doi: 10.1242/dmm.020131. Epub 2015 Feb 20.

3.

Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.

Zhang X, Cui N, Wu Z, Su J, Tadepalli JS, Sekizar S, Jiang C.

Am J Physiol Cell Physiol. 2010 Mar;298(3):C635-46. doi: 10.1152/ajpcell.00442.2009. Epub 2009 Dec 30.

4.

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
5.

Autonomic cardiovascular control in methyl-CpG-binding protein 2 (Mecp2) deficient mice.

Bissonnette JM, Knopp SJ, Maylie J, Thong T.

Auton Neurosci. 2007 Oct 30;136(1-2):82-9. Epub 2007 Jun 4.

6.

Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome.

Asaka Y, Jugloff DG, Zhang L, Eubanks JH, Fitzsimonds RM.

Neurobiol Dis. 2006 Jan;21(1):217-27. Epub 2005 Aug 8.

PMID:
16087343
7.

The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis.

Forlani G, Giarda E, Ala U, Di Cunto F, Salani M, Tupler R, Kilstrup-Nielsen C, Landsberger N.

Hum Mol Genet. 2010 Aug 15;19(16):3114-23. doi: 10.1093/hmg/ddq214. Epub 2010 May 26.

8.

Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome.

De Felice C, Della Ragione F, Signorini C, Leoncini S, Pecorelli A, Ciccoli L, Scalabrì F, Marracino F, Madonna M, Belmonte G, Ricceri L, De Filippis B, Laviola G, Valacchi G, Durand T, Galano JM, Oger C, Guy A, Bultel-Poncé V, Guy J, Filosa S, Hayek J, D'Esposito M.

Neurobiol Dis. 2014 Aug;68:66-77. doi: 10.1016/j.nbd.2014.04.006. Epub 2014 Apr 24.

9.

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.

10.

Wild-type microglia arrest pathology in a mouse model of Rett syndrome.

Derecki NC, Cronk JC, Lu Z, Xu E, Abbott SB, Guyenet PG, Kipnis J.

Nature. 2012 Mar 18;484(7392):105-9. doi: 10.1038/nature10907.

11.

Impaired hippocampal Ca2+ homeostasis and concomitant K+ channel dysfunction in a mouse model of Rett syndrome during anoxia.

Kron M, Müller M.

Neuroscience. 2010 Nov 24;171(1):300-15. doi: 10.1016/j.neuroscience.2010.08.031. Epub 2010 Aug 21.

PMID:
20732392
12.

Postnatal changes in serotonergic innervation to the hippocampus of methyl-CpG-binding protein 2-null mice.

Isoda K, Morimoto M, Matsui F, Hasegawa T, Tozawa T, Morioka S, Chiyonobu T, Nishimura A, Yoshimoto K, Hosoi H.

Neuroscience. 2010 Feb 17;165(4):1254-60. doi: 10.1016/j.neuroscience.2009.11.036. Epub 2009 Nov 22.

PMID:
19932741
13.

Alterations in the cholinergic system of brain stem neurons in a mouse model of Rett syndrome.

Oginsky MF, Cui N, Zhong W, Johnson CM, Jiang C.

Am J Physiol Cell Physiol. 2014 Sep 15;307(6):C508-20. doi: 10.1152/ajpcell.00035.2014. Epub 2014 Jul 9.

14.

Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

Giacometti E, Luikenhuis S, Beard C, Jaenisch R.

Proc Natl Acad Sci U S A. 2007 Feb 6;104(6):1931-6. Epub 2007 Jan 31.

15.

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.

16.

Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X.

Bissonnette JM, Schaevitz LR, Knopp SJ, Zhou Z.

Neuroscience. 2014 May 16;267:166-76. doi: 10.1016/j.neuroscience.2014.02.043. Epub 2014 Mar 10.

17.

GABAergic synaptic inputs of locus coeruleus neurons in wild-type and Mecp2-null mice.

Jin X, Cui N, Zhong W, Jin XT, Jiang C.

Am J Physiol Cell Physiol. 2013 May 1;304(9):C844-57. doi: 10.1152/ajpcell.00399.2012. Epub 2013 Feb 7.

18.

Metabolic fingerprints of altered brain growth, osmoregulation and neurotransmission in a Rett syndrome model.

Viola A, Saywell V, Villard L, Cozzone PJ, Lutz NW.

PLoS One. 2007 Jan 17;2(1):e157.

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.

Enhanced hypoxia susceptibility in hippocampal slices from a mouse model of rett syndrome.

Fischer M, Reuter J, Gerich FJ, Hildebrandt B, Hägele S, Katschinski D, Müller M.

J Neurophysiol. 2009 Feb;101(2):1016-32. doi: 10.1152/jn.91124.2008. Epub 2008 Dec 10.

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