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Items: 1 to 20 of 78


MeCP2 is critical within HoxB1-derived tissues of mice for normal lifespan.

Ward CS, Arvide EM, Huang TW, Yoo J, Noebels JL, Neul JL.

J Neurosci. 2011 Jul 13;31(28):10359-70. doi: 10.1523/JNEUROSCI.0057-11.2011.


Progressive Changes in a Distributed Neural Circuit Underlie Breathing Abnormalities in Mice Lacking MeCP2.

Huang TW, Kochukov MY, Ward CS, Merritt J, Thomas K, Nguyen T, Arenkiel BR, Neul JL.

J Neurosci. 2016 May 18;36(20):5572-86. doi: 10.1523/JNEUROSCI.2330-15.2016.


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.


Selective preservation of MeCP2 in catecholaminergic cells is sufficient to improve the behavioral phenotype of male and female Mecp2-deficient mice.

Lang M, Wither RG, Brotchie JM, Wu C, Zhang L, Eubanks JH.

Hum Mol Genet. 2013 Jan 15;22(2):358-71. doi: 10.1093/hmg/dds433. Epub 2012 Oct 16.


Acute intermittent hypoxia-induced expression of brain-derived neurotrophic factor is disrupted in the brainstem of methyl-CpG-binding protein 2 null mice.

Vermehren-Schmaedick A, Jenkins VK, Knopp SJ, Balkowiec A, Bissonnette JM.

Neuroscience. 2012 Mar 29;206:1-6. doi: 10.1016/j.neuroscience.2012.01.017. Epub 2012 Jan 18.


MeCP2 in the rostral striatum maintains local dopamine content critical for psychomotor control.

Su SH, Kao FC, Huang YB, Liao W.

J Neurosci. 2015 Apr 15;35(15):6209-20. doi: 10.1523/JNEUROSCI.4624-14.2015.


Exogenous brain-derived neurotrophic factor rescues synaptic dysfunction in Mecp2-null mice.

Kline DD, Ogier M, Kunze DL, Katz DM.

J Neurosci. 2010 Apr 14;30(15):5303-10. doi: 10.1523/JNEUROSCI.5503-09.2010.


Remodelling of the respiratory network in a mouse model of Rett syndrome depends on brain-derived neurotrophic factor regulated slow calcium buffering.

Mironov SL, Skorova E, Hartelt N, Mironova LA, Hasan MT, Kügler S.

J Physiol. 2009 Jun 1;587(Pt 11):2473-85. doi: 10.1113/jphysiol.2009.169805. Epub 2009 Apr 9. Erratum in: J Physiol. 2011 Aug 1;589(Pt 15):3897.


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.


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.


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.


Pathophysiology of locus ceruleus neurons in a mouse model of Rett syndrome.

Taneja P, Ogier M, Brooks-Harris G, Schmid DA, Katz DM, Nelson SB.

J Neurosci. 2009 Sep 30;29(39):12187-95. doi: 10.1523/JNEUROSCI.3156-09.2009.


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.


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.


Effect of inspired oxygen on periodic breathing in methy-CpG-binding protein 2 (Mecp2) deficient mice.

Bissonnette JM, Knopp SJ.

J Appl Physiol (1985). 2008 Jan;104(1):198-204. Epub 2007 Nov 15.


Setdb1-mediated histone H3K9 hypermethylation in neurons worsens the neurological phenotype of Mecp2-deficient mice.

Jiang Y, Matevossian A, Guo Y, Akbarian S.

Neuropharmacology. 2011 Jun;60(7-8):1088-97. doi: 10.1016/j.neuropharm.2010.09.020. Epub 2010 Sep 30.


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.


Methyl CpG-binding protein 2 (a mutation of which causes Rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brains.

Itoh M, Ide S, Takashima S, Kudo S, Nomura Y, Segawa M, Kubota T, Mori H, Tanaka S, Horie H, Tanabe Y, Goto Y.

J Neuropathol Exp Neurol. 2007 Feb;66(2):117-23.


Early abnormalities of post-sigh breathing in a mouse model of Rett syndrome.

Voituron N, Zanella S, Menuet C, Lajard AM, Dutschmann M, Hilaire G.

Respir Physiol Neurobiol. 2010 Feb 28;170(2):173-82. doi: 10.1016/j.resp.2009.12.009. Epub 2009 Dec 28.


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