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 *

237 related articles for article (PubMed ID: 14734626)

  • 1. Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders.
    Samaco RC; Nagarajan RP; Braunschweig D; LaSalle JM
    Hum Mol Genet; 2004 Mar; 13(6):629-39. PubMed ID: 14734626
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
    Samaco RC; Hogart A; LaSalle JM
    Hum Mol Genet; 2005 Feb; 14(4):483-92. PubMed ID: 15615769
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry.
    LaSalle JM; Goldstine J; Balmer D; Greco CM
    Hum Mol Genet; 2001 Aug; 10(17):1729-40. PubMed ID: 11532982
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples.
    Thatcher KN; Peddada S; Yasui DH; Lasalle JM
    Hum Mol Genet; 2005 Mar; 14(6):785-97. PubMed ID: 15689352
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation.
    Nagarajan RP; Hogart AR; Gwye Y; Martin MR; LaSalle JM
    Epigenetics; 2006; 1(4):e1-11. PubMed ID: 17486179
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.
    Balmer D; Goldstine J; Rao YM; LaSalle JM
    J Mol Med (Berl); 2003 Jan; 81(1):61-8. PubMed ID: 12545250
    [TBL] [Abstract][Full Text] [Related]  

  • 8. MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression.
    Makedonski K; Abuhatzira L; Kaufman Y; Razin A; Shemer R
    Hum Mol Genet; 2005 Apr; 14(8):1049-58. PubMed ID: 15757975
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 116(1-2):91-104. PubMed ID: 15549394
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism.
    Swanberg SE; Nagarajan RP; Peddada S; Yasui DH; LaSalle JM
    Hum Mol Genet; 2009 Feb; 18(3):525-34. PubMed ID: 19000991
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Histone modifications in Rett syndrome lymphocytes: a preliminary evaluation.
    Kaufmann WE; Jarrar MH; Wang JS; Lee YJ; Reddy S; Bibat G; Naidu S
    Brain Dev; 2005 Aug; 27(5):331-9. PubMed ID: 16023547
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Survey of MeCP2 in the Rett syndrome and the non-Rett syndrome brain.
    Armstrong DD; Deguchi K; Antallfy B
    J Child Neurol; 2003 Oct; 18(10):683-7. PubMed ID: 14649549
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Another patient with MECP2 mutation without classic Rett syndrome phenotype.
    Milani D; Pantaleoni C; D'Arrigo S; Selicorni A; Riva D
    Pediatr Neurol; 2005 May; 32(5):355-7. PubMed ID: 15866439
    [TBL] [Abstract][Full Text] [Related]  

  • 14. MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.
    Balmer D; Arredondo J; Samaco RC; LaSalle JM
    Hum Genet; 2002 Jun; 110(6):545-52. PubMed ID: 12107440
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome.
    Van den Veyver IB; Zoghbi HY
    Brain Dev; 2001 Dec; 23 Suppl 1():S147-51. PubMed ID: 11738862
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification.
    Colantuoni C; Jeon OH; Hyder K; Chenchik A; Khimani AH; Narayanan V; Hoffman EP; Kaufmann WE; Naidu S; Pevsner J
    Neurobiol Dis; 2001 Oct; 8(5):847-65. PubMed ID: 11592853
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rett syndrome: of girls and mice--lessons for regression in autism.
    Glaze DG
    Ment Retard Dev Disabil Res Rev; 2004; 10(2):154-8. PubMed ID: 15362175
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome.
    Inui K; Akagi M; Ono J; Tsukamoto H; Shimono K; Mano T; Imai K; Yamada M; Muramatsu T; Sakai N; Okada S
    Brain Dev; 2001 Jul; 23(4):212-5. PubMed ID: 11376998
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The role of MeCP2 in brain development and neurodevelopmental disorders.
    Gonzales ML; LaSalle JM
    Curr Psychiatry Rep; 2010 Apr; 12(2):127-34. PubMed ID: 20425298
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.