328 related articles for article (PubMed ID: 28670438)
1. Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.
Allemang-Grand R; Ellegood J; Spencer Noakes L; Ruston J; Justice M; Nieman BJ; Lerch JP
Mol Autism; 2017; 8():32. PubMed ID: 28670438
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 24283265
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 25960047
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Surface- and voxel-based brain morphologic study in Rett and Rett-like syndrome with MECP2 mutation.
Shiohama T; Levman J; Takahashi E
Int J Dev Neurosci; 2019 Apr; 73():83-88. PubMed ID: 30690146
[TBL] [Abstract][Full Text] [Related]
6. Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets.
Jordan C; Li HH; Kwan HC; Francke U
BMC Med Genet; 2007 Jun; 8():36. PubMed ID: 17584923
[TBL] [Abstract][Full Text] [Related]
7. Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene.
Pitcher MR; Herrera JA; Buffington SA; Kochukov MY; Merritt JK; Fisher AR; Schanen NC; Costa-Mattioli M; Neul JL
Hum Mol Genet; 2015 May; 24(9):2662-72. PubMed ID: 25634563
[TBL] [Abstract][Full Text] [Related]
8. MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning.
Zahorakova D; Lelkova P; Gregor V; Magner M; Zeman J; Martasek P
J Hum Genet; 2016 Jul; 61(7):617-25. PubMed ID: 26984561
[TBL] [Abstract][Full Text] [Related]
9. Sex differences in Mecp2-mutant Rett syndrome model mice and the impact of cellular mosaicism in phenotype development.
Ribeiro MC; MacDonald JL
Brain Res; 2020 Feb; 1729():146644. PubMed ID: 31904347
[TBL] [Abstract][Full Text] [Related]
10. Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with bone disease severity in Rett syndrome.
Caffarelli C; Gonnelli S; Pitinca MDT; Camarri S; Al Refaie A; Hayek J; Nuti R
BMC Med Genet; 2020 Jan; 21(1):21. PubMed ID: 32005172
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Tsix-Mecp2 female mouse model for Rett syndrome reveals that low-level MECP2 expression extends life and improves neuromotor function.
Carrette LLG; Blum R; Ma W; Kelleher RJ; Lee JT
Proc Natl Acad Sci U S A; 2018 Aug; 115(32):8185-8190. PubMed ID: 30038001
[TBL] [Abstract][Full Text] [Related]
13. 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; 267():166-76. PubMed ID: 24626160
[TBL] [Abstract][Full Text] [Related]
14. Ube3a expression is not altered in Mecp2 mutant mice.
Jordan C; Francke U
Hum Mol Genet; 2006 Jul; 15(14):2210-5. PubMed ID: 16754645
[TBL] [Abstract][Full Text] [Related]
15. MeCP2 isoform e1 mutant mice recapitulate motor and metabolic phenotypes of Rett syndrome.
Vogel Ciernia A; Yasui DH; Pride MC; Durbin-Johnson B; Noronha AB; Chang A; Knotts TA; Rutkowsky JR; Ramsey JJ; Crawley JN; LaSalle JM
Hum Mol Genet; 2018 Dec; 27(23):4077-4093. PubMed ID: 30137367
[TBL] [Abstract][Full Text] [Related]
16. Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome.
Santos M; Summavielle T; Teixeira-Castro A; Silva-Fernandes A; Duarte-Silva S; Marques F; Martins L; Dierssen M; Oliveira P; Sousa N; Maciel P
Neuroscience; 2010 Oct; 170(2):453-67. PubMed ID: 20633611
[TBL] [Abstract][Full Text] [Related]
17. Proteomic analysis of the Rett syndrome experimental model mecp2
Cortelazzo A; Pietri T; De Felice C; Leoncini S; Guerranti R; Signorini C; Timperio AM; Zolla L; Ciccoli L; Hayek J
J Proteomics; 2017 Feb; 154():128-133. PubMed ID: 28062374
[TBL] [Abstract][Full Text] [Related]
18. Brain lipid analysis in mice with Rett syndrome.
Seyfried TN; Heinecke KA; Mantis JG; Denny CA
Neurochem Res; 2009 Jun; 34(6):1057-65. PubMed ID: 19002580
[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. Protective role of mirtazapine in adult female Mecp2
Flores Gutiérrez J; De Felice C; Natali G; Leoncini S; Signorini C; Hayek J; Tongiorgi E
J Neurodev Disord; 2020 Sep; 12(1):26. PubMed ID: 32988385
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
