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Items: 1 to 20 of 317

1.
2.

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.

3.

Dysregulation of brain-derived neurotrophic factor expression and neurosecretory function in Mecp2 null mice.

Wang H, Chan SA, Ogier M, Hellard D, Wang Q, Smith C, Katz DM.

J Neurosci. 2006 Oct 18;26(42):10911-5.

4.

Glatiramer acetate (GA, Copolymer-1) an hypothetical treatment option for Rett syndrome.

Ben-Zeev B, Aharoni R, Nissenkorn A, Arnon R.

Med Hypotheses. 2011 Feb;76(2):190-3. doi: 10.1016/j.mehy.2010.09.015. Epub 2010 Oct 15.

PMID:
20951500
5.

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
6.

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
7.

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
8.

A BDNF loop-domain mimetic acutely reverses spontaneous apneas and respiratory abnormalities during behavioral arousal in a mouse model of Rett syndrome.

Kron M, Lang M, Adams IT, Sceniak M, Longo F, Katz DM.

Dis Model Mech. 2014 Sep;7(9):1047-55. doi: 10.1242/dmm.016030.

9.

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.

11.

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.

12.

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
13.

The ups and downs of BDNF in Rett syndrome.

Sun YE, Wu H.

Neuron. 2006 Feb 2;49(3):321-3. Review.

14.

Neural development of methyl-CpG-binding protein 2 null embryonic stem cells: a system for studying Rett syndrome.

Okabe Y, Kusaga A, Takahashi T, Mitsumasu C, Murai Y, Tanaka E, Higashi H, Matsuishi T, Kosai K.

Brain Res. 2010 Nov 11;1360:17-27. doi: 10.1016/j.brainres.2010.08.090. Epub 2010 Sep 25.

PMID:
20816763
15.

A TrkB small molecule partial agonist rescues TrkB phosphorylation deficits and improves respiratory function in a mouse model of Rett syndrome.

Schmid DA, Yang T, Ogier M, Adams I, Mirakhur Y, Wang Q, Massa SM, Longo FM, Katz DM.

J Neurosci. 2012 Feb 1;32(5):1803-10. doi: 10.1523/JNEUROSCI.0865-11.2012. Erratum in: J Neurosci. 2014 Jan 29;34(5):2012.

16.

RNAi-induced down-regulation of Mecp2 expression in the rat brain.

Jin J, Bao X, Wang H, Pan H, Zhang Y, Wu X.

Int J Dev Neurosci. 2008 Aug;26(5):457-65. doi: 10.1016/j.ijdevneu.2008.02.009. Epub 2008 Mar 4.

PMID:
18396005
17.

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.

PMID:
17278996
18.

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice.

Chen RZ, Akbarian S, Tudor M, Jaenisch R.

Nat Genet. 2001 Mar;27(3):327-31.

PMID:
11242118
19.

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
20.

Rett syndrome microglia damage dendrites and synapses by the elevated release of glutamate.

Maezawa I, Jin LW.

J Neurosci. 2010 Apr 14;30(15):5346-56. doi: 10.1523/JNEUROSCI.5966-09.2010.

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