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Journal Abstract Search

219 related items for PubMed ID: 22342974

  • 21. Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS.
    Onodera O, Oyake M, Takano H, Ikeuchi T, Igarashi S, Tsuji S.
    Am J Hum Genet; 1995 Nov; 57(5):1050-60. PubMed ID: 7485154
    [Abstract] [Full Text] [Related]

  • 22. DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation.
    Komure O, Sano A, Nishino N, Yamauchi N, Ueno S, Kondoh K, Sano N, Takahashi M, Murayama N, Kondo I.
    Neurology; 1995 Jan; 45(1):143-9. PubMed ID: 7824105
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  • 24. Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice.
    Manley K, Shirley TL, Flaherty L, Messer A.
    Nat Genet; 1999 Dec; 23(4):471-3. PubMed ID: 10581038
    [Abstract] [Full Text] [Related]

  • 25. Dentatorubral-pallidoluysian atrophy (DRPLA): close correlation of CAG repeat expansions with the wide spectrum of clinical presentations and prominent anticipation.
    Ikeuchi T, Onodera O, Oyake M, Koide R, Tanaka H, Tsuji S.
    Semin Cell Biol; 1995 Feb; 6(1):37-44. PubMed ID: 7620120
    [Abstract] [Full Text] [Related]

  • 26. Adenovirus-mediated expression of mutant DRPLA proteins with expanded polyglutamine stretches in neuronally differentiated PC12 cells. Preferential intranuclear aggregate formation and apoptosis.
    Sato A, Shimohata T, Koide R, Takano H, Sato T, Oyake M, Igarashi S, Tanaka K, Inuzuka T, Nawa H, Tsuji S.
    Hum Mol Genet; 1999 Jun; 8(6):997-1006. PubMed ID: 10332031
    [Abstract] [Full Text] [Related]

  • 27. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
    Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H.
    Arch Neurol; 2004 Feb; 61(2):209-12. PubMed ID: 14967767
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  • 28. Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p.
    Nagafuchi S, Yanagisawa H, Sato K, Shirayama T, Ohsaki E, Bundo M, Takeda T, Tadokoro K, Kondo I, Murayama N.
    Nat Genet; 1994 Jan; 6(1):14-8. PubMed ID: 8136826
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  • 29. A SCA7 CAG/CTG repeat expansion is stable in Drosophila melanogaster despite modulation of genomic context and gene dosage.
    Jackson SM, Whitworth AJ, Greene JC, Libby RT, Baccam SL, Pallanck LJ, La Spada AR.
    Gene; 2005 Feb 28; 347(1):35-41. PubMed ID: 15715978
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  • 31. Dentatorubral-pallidoluysian atrophy or Naito-Oyanagi disease.
    Kanazawa I.
    Neurogenetics; 1998 Dec 28; 2(1):1-17. PubMed ID: 9933295
    [Abstract] [Full Text] [Related]

  • 32. Differential pattern in tissue-specific somatic mosaicism of expanded CAG trinucleotide repeats in dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and X-linked recessive spinal and bulbar muscular atrophy.
    Tanaka F, Sobue G, Doyu M, Ito Y, Yamamoto M, Shimada N, Yamamoto K, Riku S, Hshizume Y, Mitsuma T.
    J Neurol Sci; 1996 Jan 28; 135(1):43-50. PubMed ID: 8926495
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  • 33. Sharing of polyglutamine localization by the neuronal nucleus and cytoplasm in CAG-repeat diseases.
    Yamada M, Tan CF, Inenaga C, Tsuji S, Takahashi H.
    Neuropathol Appl Neurobiol; 2004 Dec 28; 30(6):665-75. PubMed ID: 15541006
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  • 34. [Does the ataxo-choreic form of DRPLA exist in Europe? Search of mutation in 120 families].
    Dubourg O, Dürr A, Chneiweiss H, Stevanin G, Cancel G, Penet C, Agid Y, Brice A.
    Rev Neurol (Paris); 1995 Nov 28; 151(11):657-60. PubMed ID: 8745629
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  • 36. [Molecular pathogenesis of motor neuron diseases].
    Sobue G.
    Nihon Shinkei Seishin Yakurigaku Zasshi; 2001 Feb 28; 21(1):21-25. PubMed ID: 11400322
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  • 37. Neuronal atrophy and synaptic alteration in a mouse model of dentatorubral-pallidoluysian atrophy.
    Sakai K, Yamada M, Sato T, Yamada M, Tsuji S, Takahashi H.
    Brain; 2006 Sep 28; 129(Pt 9):2353-62. PubMed ID: 16891319
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  • 40. Age-dependent and tissue-specific CAG repeat instability occurs in mouse knock-in for a mutant Huntington's disease gene.
    Ishiguro H, Yamada K, Sawada H, Nishii K, Ichino N, Sawada M, Kurosawa Y, Matsushita N, Kobayashi K, Goto J, Hashida H, Masuda N, Kanazawa I, Nagatsu T.
    J Neurosci Res; 2001 Aug 15; 65(4):289-97. PubMed ID: 11494364
    [Abstract] [Full Text] [Related]

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