509 related articles for article (PubMed ID: 19296534)
1. Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks.
Belichenko PV; Wright EE; Belichenko NP; Masliah E; Li HH; Mobley WC; Francke U
J Comp Neurol; 2009 May; 514(3):240-58. PubMed ID: 19296534
[TBL] [Abstract][Full Text] [Related]
2. Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome.
Belichenko NP; Belichenko PV; Li HH; Mobley WC; Francke U
J Comp Neurol; 2008 May; 508(1):184-95. PubMed ID: 18306326
[TBL] [Abstract][Full Text] [Related]
3. Evidence for both neuronal cell autonomous and nonautonomous effects of methyl-CpG-binding protein 2 in the cerebral cortex of female mice with Mecp2 mutation.
Belichenko NP; Belichenko PV; Mobley WC
Neurobiol Dis; 2009 Apr; 34(1):71-7. PubMed ID: 19167498
[TBL] [Abstract][Full Text] [Related]
4. Synaptic structural abnormalities in the Ts65Dn mouse model of Down Syndrome.
Belichenko PV; Masliah E; Kleschevnikov AM; Villar AJ; Epstein CJ; Salehi A; Mobley WC
J Comp Neurol; 2004 Dec; 480(3):281-98. PubMed ID: 15515178
[TBL] [Abstract][Full Text] [Related]
5. 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; 16(19):2315-25. PubMed ID: 17635839
[TBL] [Abstract][Full Text] [Related]
6. Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.
Stearns NA; Schaevitz LR; Bowling H; Nag N; Berger UV; Berger-Sweeney J
Neuroscience; 2007 May; 146(3):907-21. PubMed ID: 17383101
[TBL] [Abstract][Full Text] [Related]
7. Hippocampal CA1 pyramidal neurons of Mecp2 mutant mice show a dendritic spine phenotype only in the presymptomatic stage.
Chapleau CA; Boggio EM; Calfa G; Percy AK; Giustetto M; Pozzo-Miller L
Neural Plast; 2012; 2012():976164. PubMed ID: 22919518
[TBL] [Abstract][Full Text] [Related]
8. Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations.
Chapleau CA; Calfa GD; Lane MC; Albertson AJ; Larimore JL; Kudo S; Armstrong DL; Percy AK; Pozzo-Miller L
Neurobiol Dis; 2009 Aug; 35(2):219-33. PubMed ID: 19442733
[TBL] [Abstract][Full Text] [Related]
9. Rett syndrome: from the gene to the disease.
Matijevic T; Knezevic J; Slavica M; Pavelic J
Eur Neurol; 2009; 61(1):3-10. PubMed ID: 18948693
[TBL] [Abstract][Full Text] [Related]
10. 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; 59(5):468-76. PubMed ID: 16199017
[TBL] [Abstract][Full Text] [Related]
11. 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; 165(4):1254-60. PubMed ID: 19932741
[TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 18557922
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 17278996
[TBL] [Abstract][Full Text] [Related]
14. Mouse models of Rett syndrome: from behavioural phenotyping to preclinical evaluation of new therapeutic approaches.
Ricceri L; De Filippis B; Laviola G
Behav Pharmacol; 2008 Sep; 19(5-6):501-17. PubMed ID: 18690105
[TBL] [Abstract][Full Text] [Related]
15. 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; 17(10):1386-96. PubMed ID: 18223199
[TBL] [Abstract][Full Text] [Related]
16. MeCP2 mutation results in compartment-specific reductions in dendritic branching and spine density in layer 5 motor cortical neurons of YFP-H mice.
Stuss DP; Boyd JD; Levin DB; Delaney KR
PLoS One; 2012; 7(3):e31896. PubMed ID: 22412847
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 16087343
[TBL] [Abstract][Full Text] [Related]
18. 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; 1237():101-9. PubMed ID: 18778693
[TBL] [Abstract][Full Text] [Related]
19. Neuronal morphology in MeCP2 mouse models is intrinsically variable and depends on age, cell type, and Mecp2 mutation.
Wang IT; Reyes AR; Zhou Z
Neurobiol Dis; 2013 Oct; 58():3-12. PubMed ID: 23659895
[TBL] [Abstract][Full Text] [Related]
20. Mechanisms of disease: neurogenetics of MeCP2 deficiency.
Francke U
Nat Clin Pract Neurol; 2006 Apr; 2(4):212-21. PubMed ID: 16932552
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]