BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 20634955)

  • 1. Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndrome.
    Kerr B; Silva PA; Walz K; Young JI
    PLoS One; 2010 Jul; 5(7):e11534. PubMed ID: 20634955
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Early environmental enrichment moderates the behavioral and synaptic phenotype of MeCP2 null mice.
    Lonetti G; Angelucci A; Morando L; Boggio EM; Giustetto M; Pizzorusso T
    Biol Psychiatry; 2010 Apr; 67(7):657-65. PubMed ID: 20172507
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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; 26(1):319-27. PubMed ID: 16399702
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Adult neural function requires MeCP2.
    McGraw CM; Samaco RC; Zoghbi HY
    Science; 2011 Jul; 333(6039):186. PubMed ID: 21636743
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The relationship of Rett syndrome and MECP2 disorders to autism.
    Neul JL
    Dialogues Clin Neurosci; 2012 Sep; 14(3):253-62. PubMed ID: 23226951
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Affective dysfunction in a mouse model of Rett syndrome: Therapeutic effects of environmental stimulation and physical activity.
    Kondo MA; Gray LJ; Pelka GJ; Leang SK; Christodoulou J; Tam PP; Hannan AJ
    Dev Neurobiol; 2016 Feb; 76(2):209-24. PubMed ID: 26019053
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.
    Moretti P; Bouwknecht JA; Teague R; Paylor R; Zoghbi HY
    Hum Mol Genet; 2005 Jan; 14(2):205-20. PubMed ID: 15548546
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation.
    Jentarra GM; Olfers SL; Rice SG; Srivastava N; Homanics GE; Blue M; Naidu S; Narayanan V
    BMC Neurosci; 2010 Feb; 11():19. PubMed ID: 20163734
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Evidence for abnormal early development in a mouse model of Rett syndrome.
    Santos M; Silva-Fernandes A; Oliveira P; Sousa N; Maciel P
    Genes Brain Behav; 2007 Apr; 6(3):277-86. PubMed ID: 16848781
    [TBL] [Abstract][Full Text] [Related]  

  • 17. MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders.
    Psoni S; Sofocleous C; Traeger-Synodinos J; Kitsiou-Tzeli S; Kanavakis E; Fryssira-Kanioura H
    Brain Dev; 2012 Jun; 34(6):487-95. PubMed ID: 21982064
    [TBL] [Abstract][Full Text] [Related]  

  • 18. MeCP2 dysfunction in Rett syndrome and related disorders.
    Moretti P; Zoghbi HY
    Curr Opin Genet Dev; 2006 Jun; 16(3):276-81. PubMed ID: 16647848
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations.
    Amir RE; Zoghbi HY
    Am J Med Genet; 2000; 97(2):147-52. PubMed ID: 11180222
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reversibility of functional deficits in experimental models of Rett syndrome.
    Cobb S; Guy J; Bird A
    Biochem Soc Trans; 2010 Apr; 38(2):498-506. PubMed ID: 20298210
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.