These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

350 related articles for article (PubMed ID: 22207122)

  • 1. Early intervention with psychostimulants or antidepressants to increase methyl-CpG-binding protein 2 (MeCP2) expressions: a potential therapy for Rett syndrome.
    Pan CH; Tsai S
    Med Sci Monit; 2012 Jan; 18(1):HY1-3. PubMed ID: 22207122
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease.
    Pejhan S; Rastegar M
    Biomolecules; 2021 Jan; 11(1):. PubMed ID: 33429932
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation.
    Cheung AY; Horvath LM; Grafodatskaya D; Pasceri P; Weksberg R; Hotta A; Carrel L; Ellis J
    Hum Mol Genet; 2011 Jun; 20(11):2103-15. PubMed ID: 21372149
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Differential brain region-specific expression of MeCP2 and BDNF in Rett Syndrome patients: a distinct grey-white matter variation.
    Pejhan S; Siu VM; Ang LC; Del Bigio MR; Rastegar M
    Neuropathol Appl Neurobiol; 2020 Dec; 46(7):735-750. PubMed ID: 32246495
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Mirtazapine treatment in a young female mouse model of Rett syndrome identifies time windows for the rescue of early phenotypes.
    Flores Gutiérrez J; Natali G; Giorgi J; De Leonibus E; Tongiorgi E
    Exp Neurol; 2022 Jul; 353():114056. PubMed ID: 35358499
    [TBL] [Abstract][Full Text] [Related]  

  • 7. PTP1B inhibition suggests a therapeutic strategy for Rett syndrome.
    Krishnan N; Krishnan K; Connors CR; Choy MS; Page R; Peti W; Van Aelst L; Shea SD; Tonks NK
    J Clin Invest; 2015 Aug; 125(8):3163-77. PubMed ID: 26214522
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lithium and antidepressants: potential agents for the treatment of Rett syndrome.
    Tsai SJ
    Med Hypotheses; 2006; 67(3):626-9. PubMed ID: 16584849
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rett Syndrome in Males: The Different Clinical Course in Two Brothers with the Same Microduplication MECP2 Xq28.
    Pitzianti MB; Santamaria Palombo A; Esposito S; Pasini A
    Int J Environ Res Public Health; 2019 Aug; 16(17):. PubMed ID: 31450876
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fluoxetine increases brain MeCP2 immuno-positive cells in a female Mecp2 heterozygous mouse model of Rett syndrome through endogenous serotonin.
    Villani C; Carli M; Castaldo AM; Sacchetti G; Invernizzi RW
    Sci Rep; 2021 Jul; 11(1):14690. PubMed ID: 34282222
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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. PubMed ID: 20951500
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.
    Braunschweig D; Simcox T; Samaco RC; LaSalle JM
    Hum Mol Genet; 2004 Jun; 13(12):1275-86. PubMed ID: 15115765
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Adenosinergic System and BDNF Signaling Changes as a Cross-Sectional Feature of RTT: Characterization of
    Miranda-Lourenço C; Rosa J; Rei N; Belo RF; Lopes AL; Silva D; Vieira C; Magalhães-Cardoso T; Viais R; Correia-de-Sá P; Sebastião AM; Diógenes MJ
    Int J Mol Sci; 2023 Nov; 24(22):. PubMed ID: 38003438
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome].
    Zhu XW; Pan H; Li MR; Bao XH; Zhang JJ; Wu XR
    Zhonghua Er Ke Za Zhi; 2009 Aug; 47(8):565-9. PubMed ID: 19951486
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
    Amir RE; Van den Veyver IB; Wan M; Tran CQ; Francke U; Zoghbi HY
    Nat Genet; 1999 Oct; 23(2):185-8. PubMed ID: 10508514
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations.
    Ravn K; Roende G; Duno M; Fuglsang K; Eiklid KL; Tümer Z; Nielsen JB; Skjeldal OH
    Orphanet J Rare Dis; 2011 Aug; 6():58. PubMed ID: 21878110
    [TBL] [Abstract][Full Text] [Related]  

  • 17. MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome.
    Chen L; Chen K; Lavery LA; Baker SA; Shaw CA; Li W; Zoghbi HY
    Proc Natl Acad Sci U S A; 2015 Apr; 112(17):5509-14. PubMed ID: 25870282
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pharmacological reactivation of inactive X-linked
    Przanowski P; Wasko U; Zheng Z; Yu J; Sherman R; Zhu LJ; McConnell MJ; Tushir-Singh J; Green MR; Bhatnagar S
    Proc Natl Acad Sci U S A; 2018 Jul; 115(31):7991-7996. PubMed ID: 30012595
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 18.