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Journal Abstract Search

456 related items for PubMed ID: 16274727

  • 1. Juvenile Huntington's disease: does a dosage-effect pathogenic mechanism differ from the classical adult disease?
    Squitieri F, Frati L, Ciarmiello A, Lastoria S, Quarrell O.
    Mech Ageing Dev; 2006 Feb; 127(2):208-12. PubMed ID: 16274727
    [Abstract] [Full Text] [Related]

  • 2. Autopsy-proven Huntington's disease with 29 trinucleotide repeats.
    Kenney C, Powell S, Jankovic J.
    Mov Disord; 2007 Jan; 22(1):127-30. PubMed ID: 17115386
    [Abstract] [Full Text] [Related]

  • 3. Parent-of-origin differences of mutant HTT CAG repeat instability in Huntington's disease.
    Aziz NA, van Belzen MJ, Coops ID, Belfroid RD, Roos RA.
    Eur J Med Genet; 2011 Jan; 54(4):e413-8. PubMed ID: 21540131
    [Abstract] [Full Text] [Related]

  • 4. Juvenile onset Huntington's disease--clinical and research perspectives.
    Nance MA, Myers RH.
    Ment Retard Dev Disabil Res Rev; 2001 Jan; 7(3):153-7. PubMed ID: 11553930
    [Abstract] [Full Text] [Related]

  • 5. Centrosome disorganization in fibroblast cultures derived from R6/2 Huntington's disease (HD) transgenic mice and HD patients.
    Sathasivam K, Woodman B, Mahal A, Bertaux F, Wanker EE, Shima DT, Bates GP.
    Hum Mol Genet; 2001 Oct 01; 10(21):2425-35. PubMed ID: 11689489
    [Abstract] [Full Text] [Related]

  • 6. Polyglutamine expansions cause decreased CRE-mediated transcription and early gene expression changes prior to cell death in an inducible cell model of Huntington's disease.
    Wyttenbach A, Swartz J, Kita H, Thykjaer T, Carmichael J, Bradley J, Brown R, Maxwell M, Schapira A, Orntoft TF, Kato K, Rubinsztein DC.
    Hum Mol Genet; 2001 Aug 15; 10(17):1829-45. PubMed ID: 11532992
    [Abstract] [Full Text] [Related]

  • 7. Intergeneration CAG expansion and contraction in a Chinese HD family.
    Tang Y, Wang Y, Yang P, Liu Y, Wang B, Podolsky R, McIndoe R, Wang CY.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Apr 05; 141B(3):242-4. PubMed ID: 16526033
    [Abstract] [Full Text] [Related]

  • 8. Juvenile onset Huntington disease resulting from a very large maternal expansion.
    Nahhas FA, Garbern J, Krajewski KM, Roa BB, Feldman GL.
    Am J Med Genet A; 2005 Sep 01; 137A(3):328-31. PubMed ID: 16096998
    [Abstract] [Full Text] [Related]

  • 9. Paradoxical delay in the onset of disease caused by super-long CAG repeat expansions in R6/2 mice.
    Morton AJ, Glynn D, Leavens W, Zheng Z, Faull RL, Skepper JN, Wight JM.
    Neurobiol Dis; 2009 Mar 01; 33(3):331-41. PubMed ID: 19130884
    [Abstract] [Full Text] [Related]

  • 10. Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease?
    Kennedy L, Shelbourne PF.
    Hum Mol Genet; 2000 Oct 12; 9(17):2539-44. PubMed ID: 11030759
    [Abstract] [Full Text] [Related]

  • 11. The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease.
    Klempíř J, Zidovská J, Stochl J, Ing VK, Uhrová T, Roth J.
    Mov Disord; 2011 Jan 12; 26(1):125-9. PubMed ID: 21322024
    [Abstract] [Full Text] [Related]

  • 12. XL PCR for the detection of large trinucleotide expansions in juvenile Huntington's disease.
    Milunsky JM, Maher TA, Loose BA, Darras BT, Ito M.
    Clin Genet; 2003 Jul 12; 64(1):70-3. PubMed ID: 12791042
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  • 14. Identification and characterization of the miniature pig Huntington's disease gene homolog: evidence for conservation and polymorphism in the CAG triplet repeat.
    Matsuyama N, Hadano S, Onoe K, Osuga H, Showguchi-Miyata J, Gondo Y, Ikeda JE.
    Genomics; 2000 Oct 01; 69(1):72-85. PubMed ID: 11013077
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  • 16. How does the Huntington's disease mutation damage cells?
    Rubinsztein DC.
    Sci Aging Knowledge Environ; 2003 Sep 17; 2003(37):PE26. PubMed ID: 13679594
    [Abstract] [Full Text] [Related]

  • 17. Sensitive biochemical aggregate detection reveals aggregation onset before symptom development in cellular and murine models of Huntington's disease.
    Weiss A, Klein C, Woodman B, Sathasivam K, Bibel M, Régulier E, Bates GP, Paganetti P.
    J Neurochem; 2008 Feb 17; 104(3):846-58. PubMed ID: 17986219
    [Abstract] [Full Text] [Related]

  • 18. Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis.
    Fusilli C, Migliore S, Mazza T, Consoli F, De Luca A, Barbagallo G, Ciammola A, Gatto EM, Cesarini M, Etcheverry JL, Parisi V, Al-Oraimi M, Al-Harrasi S, Al-Salmi Q, Marano M, Vonsattel JG, Sabatini U, Landwehrmeyer GB, Squitieri F.
    Lancet Neurol; 2018 Nov 17; 17(11):986-993. PubMed ID: 30243861
    [Abstract] [Full Text] [Related]

  • 19. Excessive blinking as an initial manifestation of juvenile Huntington's disease.
    Xing S, Chen L, Chen X, Pei Z, Zeng J, Li J.
    Neurol Sci; 2008 Sep 17; 29(4):275-7. PubMed ID: 18810605
    [Abstract] [Full Text] [Related]

  • 20. Polyglutamine pathogenesis.
    Ross CA, Wood JD, Schilling G, Peters MF, Nucifora FC, Cooper JK, Sharp AH, Margolis RL, Borchelt DR.
    Philos Trans R Soc Lond B Biol Sci; 1999 Jun 29; 354(1386):1005-11. PubMed ID: 10434299
    [Abstract] [Full Text] [Related]

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