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Journal Abstract Search

305 related items for PubMed ID: 12928486

  • 1. DNA methylation and Rett syndrome.
    Kriaucionis S, Bird A.
    Hum Mol Genet; 2003 Oct 15; 12 Spec No 2():R221-7. PubMed ID: 12928486
    [Abstract] [Full Text] [Related]

  • 2. MeCP2 and other methyl-CpG binding proteins.
    Jørgensen HF, Bird A.
    Ment Retard Dev Disabil Res Rev; 2002 Oct 15; 8(2):87-93. PubMed ID: 12112733
    [Abstract] [Full Text] [Related]

  • 3. MeCP2 in neurons: closing in on the causes of Rett syndrome.
    Caballero IM, Hendrich B.
    Hum Mol Genet; 2005 Apr 15; 14 Spec No 1():R19-26. PubMed ID: 15809268
    [Abstract] [Full Text] [Related]

  • 4. Rett syndrome model suggests MECP2 gives neurons the quiet they need to think.
    Carter AR, Segal RA.
    Nat Neurosci; 2001 Apr 15; 4(4):342-3. PubMed ID: 11276217
    [No Abstract] [Full Text] [Related]

  • 5. Expression pattern of the Rett syndrome gene MeCP2 in primate prefrontal cortex.
    Akbarian S, Chen RZ, Gribnau J, Rasmussen TP, Fong H, Jaenisch R, Jones EG.
    Neurobiol Dis; 2001 Oct 15; 8(5):784-91. PubMed ID: 11592848
    [Abstract] [Full Text] [Related]

  • 6. Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.
    Hoffbuhr KC, Moses LM, Jerdonek MA, Naidu S, Hoffman EP.
    Ment Retard Dev Disabil Res Rev; 2002 Oct 15; 8(2):99-105. PubMed ID: 12112735
    [Abstract] [Full Text] [Related]

  • 7. Altered methylation pattern of the G6 PD promoter in Rett syndrome.
    Huppke P, Bohlander S, Krämer N, Laccone F, Hanefeld F.
    Neuropediatrics; 2002 Apr 15; 33(2):105-8. PubMed ID: 12075494
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 32(5):355-7. PubMed ID: 15866439
    [Abstract] [Full Text] [Related]

  • 9. No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.
    Vourc'h P, Bienvenu T, Beldjord C, Chelly J, Barthélémy C, Müh JP, Andres C.
    Eur J Hum Genet; 2001 Jul 15; 9(7):556-8. PubMed ID: 11464249
    [Abstract] [Full Text] [Related]

  • 10. Methyl-CpG binding proteins in the nervous system.
    Fan G, Hutnick L.
    Cell Res; 2005 Apr 15; 15(4):255-61. PubMed ID: 15857580
    [Abstract] [Full Text] [Related]

  • 11. Rett syndrome: a prototypical neurodevelopmental disorder.
    Neul JL, Zoghbi HY.
    Neuroscientist; 2004 Apr 15; 10(2):118-28. PubMed ID: 15070486
    [Abstract] [Full Text] [Related]

  • 12. Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy.
    Topçu M, Akyerli C, Sayi A, Törüner GA, Koçoğlu SR, Cimbiş M, Ozçelik T.
    Eur J Hum Genet; 2002 Jan 15; 10(1):77-81. PubMed ID: 11896459
    [Abstract] [Full Text] [Related]

  • 13. Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls.
    Evans JC, Archer HL, Whatley SD, Kerr A, Clarke A, Butler R.
    Eur J Hum Genet; 2005 Jan 15; 13(1):124-6. PubMed ID: 15367913
    [Abstract] [Full Text] [Related]

  • 14. Mutations found within exon 1 of MECP2 in Danish patients with Rett syndrome.
    Ravn K, Nielsen JB, Schwartz M.
    Clin Genet; 2005 Jun 15; 67(6):532-3. PubMed ID: 15857422
    [No Abstract] [Full Text] [Related]

  • 15. [Recognition of methylated DNA].
    Shirakawa M, Ohki I.
    Tanpakushitsu Kakusan Koso; 2002 Aug 15; 47(10):1268-75. PubMed ID: 12184065
    [No Abstract] [Full Text] [Related]

  • 16. Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy.
    Bienvenu T, Souville I, Poirier K, Aquaviva C, Burglen L, Amiel J, Héron B, Kaminska A, Couvert P, Beldjord C, Chelly J.
    Hum Mutat; 2001 Sep 15; 18(3):251-2. PubMed ID: 11524737
    [Abstract] [Full Text] [Related]

  • 17. [Developmental disorder in girls due to Rett syndrome].
    Pruissen DM, Sinke RJ, Terhal PA, Beemer FA, Peters AC.
    Ned Tijdschr Geneeskd; 2003 Aug 09; 147(32):1560-3. PubMed ID: 12942847
    [Abstract] [Full Text] [Related]

  • 18. 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 09; 27(5):331-9. PubMed ID: 16023547
    [Abstract] [Full Text] [Related]

  • 19. MeCP2: the chromatin connection and beyond.
    Zlatanova J.
    Biochem Cell Biol; 2005 Jun 09; 83(3):251-62. PubMed ID: 15959553
    [Abstract] [Full Text] [Related]

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