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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

720 related items for PubMed ID: 25076025

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

  • 22. 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 17; 11():19. PubMed ID: 20163734
    [Abstract] [Full Text] [Related]

  • 23. The impact of MECP2 mutations in the expression patterns of Rett syndrome patients.
    Ballestar E, Ropero S, Alaminos M, Armstrong J, Setien F, Agrelo R, Fraga MF, Herranz M, Avila S, Pineda M, Monros E, Esteller M.
    Hum Genet; 2005 Jan 17; 116(1-2):91-104. PubMed ID: 15549394
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Selective preservation of cholinergic MeCP2 rescues specific Rett-syndrome-like phenotypes in MeCP2stop mice.
    Zhou H, Wu W, Zhang Y, He H, Yuan Z, Zhu Z, Zhao Z.
    Behav Brain Res; 2017 Mar 30; 322(Pt A):51-59. PubMed ID: 28093257
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. 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 05; 115(23):E5363-E5372. PubMed ID: 29769330
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. Rett syndrome: disruption of epigenetic control of postnatal neurological functions.
    Pohodich AE, Zoghbi HY.
    Hum Mol Genet; 2015 Oct 15; 24(R1):R10-6. PubMed ID: 26060191
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Rett syndrome: from the gene to the disease.
    Matijevic T, Knezevic J, Slavica M, Pavelic J.
    Eur Neurol; 2009 Oct 15; 61(1):3-10. PubMed ID: 18948693
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action.
    Bedogni F, Rossi RL, Galli F, Cobolli Gigli C, Gandaglia A, Kilstrup-Nielsen C, Landsberger N.
    Neurosci Biobehav Rev; 2014 Oct 15; 46 Pt 2():187-201. PubMed ID: 24594195
    [Abstract] [Full Text] [Related]

  • 37. Generation and analysis of the Rett syndrome-associated MeCP2- null rat model.
    Zhai W, Hu HX, Le L, Zhuang FF, Wang KZ, Zhao Y, Wang K, Liu XM, Sun D, Wang XY, Kuang SH, Hu KP.
    Yi Chuan; 2016 Nov 20; 38(11):1004-1011. PubMed ID: 27867150
    [Abstract] [Full Text] [Related]

  • 38. The molecular pathology of Rett syndrome: synopsis and update.
    Akbarian S, Jiang Y, Laforet G.
    Neuromolecular Med; 2006 Nov 20; 8(4):485-94. PubMed ID: 17028371
    [Abstract] [Full Text] [Related]

  • 39. Novel alterations in the epigenetic signature of MeCP2-targeted promoters in lymphocytes of Rett syndrome patients.
    Lilja T, Wallenborg K, Björkman K, Albåge M, Eriksson M, Lagercrantz H, Rohdin M, Hermanson O.
    Epigenetics; 2013 Mar 20; 8(3):246-51. PubMed ID: 23348913
    [Abstract] [Full Text] [Related]

  • 40. DNA methylation in the gene body influences MeCP2-mediated gene repression.
    Kinde B, Wu DY, Greenberg ME, Gabel HW.
    Proc Natl Acad Sci U S A; 2016 Dec 27; 113(52):15114-15119. PubMed ID: 27965390
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 36.