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Journal Abstract Search

542 related items for PubMed ID: 7998766

  • 1.
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  • 2. [Growing genes cause neurological diseases].
    Johansson J, Holmgren G, Forsgren L, Holmberg M.
    Lakartidningen; 1999 Feb 24; 96(8):897-900. PubMed ID: 10089735
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  • 6. Trinucleotide repeat expansions and human genetic disease.
    Bates G, Lehrach H.
    Bioessays; 1994 Apr 24; 16(4):277-84. PubMed ID: 8031305
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  • 8. The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis.
    Koshy BT, Zoghbi HY.
    Brain Pathol; 1997 Jul 24; 7(3):927-42. PubMed ID: 9217976
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  • 9. CAG repeat disorder models and human neuropathology: similarities and differences.
    Yamada M, Sato T, Tsuji S, Takahashi H.
    Acta Neuropathol; 2008 Jan 24; 115(1):71-86. PubMed ID: 17786457
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  • 10. DNA trinucleotide repeat expansion in neuropsychiatric patients.
    Mohmood S, Sherwani A, Khan F, Khan RH, Azfer A.
    Med Sci Monit; 2003 Sep 24; 9(9):RA237-45. PubMed ID: 12960939
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  • 11. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).
    Koide R, Ikeuchi T, Onodera O, Tanaka H, Igarashi S, Endo K, Takahashi H, Kondo R, Ishikawa A, Hayashi T.
    Nat Genet; 1994 Jan 24; 6(1):9-13. PubMed ID: 8136840
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  • 13. Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat.
    Ikeuchi T, Koide R, Tanaka H, Onodera O, Igarashi S, Takahashi H, Kondo R, Ishikawa A, Tomoda A, Miike T.
    Ann Neurol; 1995 Jun 24; 37(6):769-75. PubMed ID: 7778850
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  • 15. [Molecular pathogenesis of motor neuron diseases].
    Sobue G.
    Nihon Shinkei Seishin Yakurigaku Zasshi; 2001 Feb 24; 21(1):21-25. PubMed ID: 11400322
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  • 16. Dentatorubral-pallidoluysian atrophy (DRPLA). Molecular basis for wide clinical features of DRPLA.
    Ikeuchi T, Koide R, Onodera O, Tanaka H, Oyake M, Takano H, Tsuji S.
    Clin Neurosci; 1995 Feb 24; 3(1):23-7. PubMed ID: 7614090
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  • 17. [Expansion of triplet repeat and neurodegenerative disorders].
    Kanazawa I.
    Rinsho Shinkeigaku; 1994 Dec 24; 34(12):1224-6. PubMed ID: 7774118
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  • 18. [A new mechanism of mutation in man: expansion of trinucleotide repeats].
    Illarioshkin SN, Ivanova-Smolenskaia IA, Markova ED.
    Genetika; 1995 Nov 24; 31(11):1478-89. PubMed ID: 8666217
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  • 19. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1.
    Hashida H, Goto J, Kurisaki H, Mizusawa H, Kanazawa I.
    Ann Neurol; 1997 Apr 24; 41(4):505-11. PubMed ID: 9124808
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  • 20. Spinocerebellar ataxia type 1.
    Zoghbi HY.
    Clin Neurosci; 1995 Apr 24; 3(1):5-11. PubMed ID: 7614095
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