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Items: 1 to 20 of 219

1.

The ups and downs of BDNF in Rett syndrome.

Sun YE, Wu H.

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

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.

The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome.

Nectoux J, Bahi-Buisson N, Guellec I, Coste J, De Roux N, Rosas H, Tardieu M, Chelly J, Bienvenu T.

Neurology. 2008 May 27;70(22 Pt 2):2145-51. doi: 10.1212/01.wnl.0000304086.75913.b2. Epub 2008 Apr 23.

PMID:
18434641
4.

MeCP2 dysfunction in Rett syndrome and related disorders.

Moretti P, Zoghbi HY.

Curr Opin Genet Dev. 2006 Jun;16(3):276-81. Epub 2006 May 2. Review.

PMID:
16647848
5.

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
6.

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
7.

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
8.
9.

MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution.

Kaufmann WE, Johnston MV, Blue ME.

Brain Dev. 2005 Nov;27 Suppl 1:S77-S87. Epub 2005 Sep 22. Review.

PMID:
16182491
10.

The story of Rett syndrome: from clinic to neurobiology.

Chahrour M, Zoghbi HY.

Neuron. 2007 Nov 8;56(3):422-37. Review.

11.

Mechanisms of disease: neurogenetics of MeCP2 deficiency.

Francke U.

Nat Clin Pract Neurol. 2006 Apr;2(4):212-21. Review.

PMID:
16932552
12.

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
13.

Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene.

Bartholdi D, Klein A, Weissert M, Koenig N, Baumer A, Boltshauser E, Schinzel A, Berger W, Mátyás G.

Clin Genet. 2006 Apr;69(4):319-26.

PMID:
16630165
14.

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
15.

Rett syndrome: from the gene to the disease.

Matijevic T, Knezevic J, Slavica M, Pavelic J.

Eur Neurol. 2009;61(1):3-10. doi: 10.1159/000165342. Epub 2008 Oct 24. Review.

16.

Epilepsy in Rett syndrome---the experience of a National Rett Center.

Nissenkorn A, Gak E, Vecsler M, Reznik H, Menascu S, Ben Zeev B.

Epilepsia. 2010 Jul;51(7):1252-8. doi: 10.1111/j.1528-1167.2010.02597.x. Epub 2010 May 13.

17.

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
18.

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.

19.

A methyl-CpG-binding protein 2-enhanced green fluorescent protein reporter mouse model provides a new tool for studying the neuronal basis of Rett syndrome.

Schmid RS, Tsujimoto N, Qu Q, Lei H, Li E, Chen T, Blaustein CS.

Neuroreport. 2008 Mar 5;19(4):393-8. doi: 10.1097/WNR.0b013e3282f5661c.

PMID:
18287934

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