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 *

236 related articles for article (PubMed ID: 34599184)

  • 1. Rett syndrome linked to defects in forming the MeCP2/Rbfox/LASR complex in mouse models.
    Jiang Y; Fu X; Zhang Y; Wang SF; Zhu H; Wang WK; Zhang L; Wu P; Wong CCL; Li J; Ma J; Guan JS; Huang Y; Hui J
    Nat Commun; 2021 Oct; 12(1):5767. PubMed ID: 34599184
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Misregulation of Alternative Splicing in a Mouse Model of Rett Syndrome.
    Li R; Dong Q; Yuan X; Zeng X; Gao Y; Chiao C; Li H; Zhao X; Keles S; Wang Z; Chang Q
    PLoS Genet; 2016 Jun; 12(6):e1006129. PubMed ID: 27352031
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Activity-dependent aberrations in gene expression and alternative splicing in a mouse model of Rett syndrome.
    Osenberg S; Karten A; Sun J; Li J; Charkowick S; Felice CA; Kritzer M; Nguyen MVC; Yu P; Ballas N
    Proc Natl Acad Sci U S A; 2018 Jun; 115(23):E5363-E5372. PubMed ID: 29769330
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rett syndrome and MeCP2.
    Liyanage VR; Rastegar M
    Neuromolecular Med; 2014 Jun; 16(2):231-64. PubMed ID: 24615633
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Methyl CpG-binding protein isoform MeCP2_e2 is dispensable for Rett syndrome phenotypes but essential for embryo viability and placenta development.
    Itoh M; Tahimic CG; Ide S; Otsuki A; Sasaoka T; Noguchi S; Oshimura M; Goto Y; Kurimasa A
    J Biol Chem; 2012 Apr; 287(17):13859-67. PubMed ID: 22375006
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.
    Young JI; Hong EP; Castle JC; Crespo-Barreto J; Bowman AB; Rose MF; Kang D; Richman R; Johnson JM; Berget S; Zoghbi HY
    Proc Natl Acad Sci U S A; 2005 Dec; 102(49):17551-8. PubMed ID: 16251272
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders.
    Kruusvee V; Lyst MJ; Taylor C; Tarnauskaitė Ž; Bird AP; Cook AG
    Proc Natl Acad Sci U S A; 2017 Apr; 114(16):E3243-E3250. PubMed ID: 28348241
    [TBL] [Abstract][Full Text] [Related]  

  • 11. MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation.
    Sheikh TI; de Paz AM; Akhtar S; Ausió J; Vincent JB
    Hum Mol Genet; 2017 Nov; 26(21):4132-4141. PubMed ID: 28973632
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rbfox Proteins Regulate Splicing as Part of a Large Multiprotein Complex LASR.
    Damianov A; Ying Y; Lin CH; Lee JA; Tran D; Vashisht AA; Bahrami-Samani E; Xing Y; Martin KC; Wohlschlegel JA; Black DL
    Cell; 2016 Apr; 165(3):606-19. PubMed ID: 27104978
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 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. 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]  

  • 16. Brain protein changes in Mecp2 mouse mutant models: Effects on disease progression of Mecp2 brain specific gene reactivation.
    Cortelazzo A; De Felice C; Guy J; Timperio AM; Zolla L; Guerranti R; Leoncini S; Signorini C; Durand T; Hayek J
    J Proteomics; 2020 Jan; 210():103537. PubMed ID: 31629059
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A comprehensive longitudinal study of magnetic resonance imaging identifies novel features of the Mecp2 deficient mouse brain.
    Carli S; Chaabane L; De Rocco G; Albizzati E; Sormonta I; Calligaro S; Bonizzi P; Frasca A; Landsberger N
    Neurobiol Dis; 2023 May; 180():106083. PubMed ID: 36931532
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Regulation mechanism and research progress of MeCP2 in Rett syndrome.
    Yang W; Pan H
    Yi Chuan; 2014 Jul; 36(7):625-30. PubMed ID: 25076025
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing.
    Long SW; Ooi JY; Yau PM; Jones PL
    Biosci Rep; 2011 Oct; 31(5):333-43. PubMed ID: 21070191
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.