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Journal Abstract Search

425 related items for PubMed ID: 9020849

  • 1. Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.
    Mangiarini L, Sathasivam K, Mahal A, Mott R, Seller M, Bates GP.
    Nat Genet; 1997 Feb; 15(2):197-200. PubMed ID: 9020849
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  • 2. 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; 135(1):43-50. PubMed ID: 8926495
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  • 4. Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph disease.
    Cancel G, Gourfinkel-An I, Stevanin G, Didierjean O, Abbas N, Hirsch E, Agid Y, Brice A.
    Hum Mutat; 1998 Jan; 11(1):23-7. PubMed ID: 9450899
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  • 9. 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
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  • 10. Transgenic models of Huntington's disease.
    Bates GP, Mangiarini L, Mahal A, Davies SW.
    Hum Mol Genet; 1997 Aug 15; 6(10):1633-7. PubMed ID: 9300654
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  • 14. Somatic mosaicism of the expanded CAG trinucleotide repeat in mRNAs for the responsible gene of Machado-Joseph disease (MJD), dentatorubral-pallidoluysian atrophy (DRPLA), and spinal and bulbar muscular atrophy (SBMA).
    Ito Y, Tanaka F, Yamamoto M, Doyu M, Nagamatsu M, Riku S, Mitsuma T, Sobue G.
    Neurochem Res; 1998 Jan 15; 23(1):25-32. PubMed ID: 9482263
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  • 15. Mouse models of human CAG repeat disorders.
    Burright EN, Orr HT, Clark HB.
    Brain Pathol; 1997 Jul 15; 7(3):965-77. PubMed ID: 9217978
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  • 17. Transgenic mice expressing mutated full-length HD cDNA: a paradigm for locomotor changes and selective neuronal loss in Huntington's disease.
    Reddy PH, Charles V, Williams M, Miller G, Whetsell WO, Tagle DA.
    Philos Trans R Soc Lond B Biol Sci; 1999 Jun 29; 354(1386):1035-45. PubMed ID: 10434303
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  • 18. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
    Pujana MA, Corral J, Gratacòs M, Combarros O, Berciano J, Genís D, Banchs I, Estivill X, Volpini V.
    Hum Genet; 1999 Jun 29; 104(6):516-22. PubMed ID: 10453742
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  • 20. Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene.
    Sułek-Piatkowska A, Krysa W, Zdzienicka E, Szirkowiec W, Hoffman-Zacharska D, Rajkiewicz M, Fidziańska E, Kowalska G, Zaremba J.
    Neurol Neurochir Pol; 2008 Jun 29; 42(3):203-9. PubMed ID: 18651325
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