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Journal Abstract Search

416 related items for PubMed ID: 8896556

  • 1. Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.
    Sanpei K, Takano H, Igarashi S, Sato T, Oyake M, Sasaki H, Wakisaka A, Tashiro K, Ishida Y, Ikeuchi T, Koide R, Saito M, Sato A, Tanaka T, Hanyu S, Takiyama Y, Nishizawa M, Shimizu N, Nomura Y, Segawa M, Iwabuchi K, Eguchi I, Tanaka H, Takahashi H, Tsuji S.
    Nat Genet; 1996 Nov; 14(3):277-84. PubMed ID: 8896556
    [Abstract] [Full Text] [Related]

  • 2. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
    Pulst SM, Nechiporuk A, Nechiporuk T, Gispert S, Chen XN, Lopes-Cendes I, Pearlman S, Starkman S, Orozco-Diaz G, Lunkes A, DeJong P, Rouleau GA, Auburger G, Korenberg JR, Figueroa C, Sahba S.
    Nat Genet; 1996 Nov; 14(3):269-76. PubMed ID: 8896555
    [Abstract] [Full Text] [Related]

  • 3. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats.
    Imbert G, Saudou F, Yvert G, Devys D, Trottier Y, Garnier JM, Weber C, Mandel JL, Cancel G, Abbas N, Dürr A, Didierjean O, Stevanin G, Agid Y, Brice A.
    Nat Genet; 1996 Nov; 14(3):285-91. PubMed ID: 8896557
    [Abstract] [Full Text] [Related]

  • 4. Spinocerebellar ataxia type 1.
    Zoghbi HY.
    Clin Neurosci; 1995 Nov; 3(1):5-11. PubMed ID: 7614095
    [Abstract] [Full Text] [Related]

  • 5. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion.
    David G, Abbas N, Stevanin G, Dürr A, Yvert G, Cancel G, Weber C, Imbert G, Saudou F, Antoniou E, Drabkin H, Gemmill R, Giunti P, Benomar A, Wood N, Ruberg M, Agid Y, Mandel JL, Brice A.
    Nat Genet; 1997 Sep; 17(1):65-70. PubMed ID: 9288099
    [Abstract] [Full Text] [Related]

  • 6. Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA.
    Koob MD, Benzow KA, Bird TD, Day JW, Moseley ML, Ranum LP.
    Nat Genet; 1998 Jan; 18(1):72-5. PubMed ID: 9425905
    [Abstract] [Full Text] [Related]

  • 7. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
    Orr HT, Chung MY, Banfi S, Kwiatkowski TJ, Servadio A, Beaudet AL, McCall AE, Duvick LA, Ranum LP, Zoghbi HY.
    Nat Genet; 1993 Jul; 4(3):221-6. PubMed ID: 8358429
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q.
    Ikeuchi T, Sanpei K, Takano H, Sasaki H, Tashiro K, Cancel G, Brice A, Bird TD, Schellenberg GD, Pericak-Vance MA, Welsh-Bohmer KA, Clark LN, Wilhelmsen K, Tsuji S.
    Genomics; 1998 Apr 15; 49(2):321-6. PubMed ID: 9598323
    [Abstract] [Full Text] [Related]

  • 10. Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.
    Chung MY, Ranum LP, Duvick LA, Servadio A, Zoghbi HY, Orr HT.
    Nat Genet; 1993 Nov 15; 5(3):254-8. PubMed ID: 8275090
    [Abstract] [Full Text] [Related]

  • 11. Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease.
    Lopes-Cendes I, Maciel P, Kish S, Gaspar C, Robitaille Y, Clark HB, Koeppen AH, Nance M, Schut L, Silveira I, Coutinho P, Sequeiros J, Rouleau GA.
    Ann Neurol; 1996 Aug 15; 40(2):199-206. PubMed ID: 8773601
    [Abstract] [Full Text] [Related]

  • 12. Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1.
    Goldfarb LG, Vasconcelos O, Platonov FA, Lunkes A, Kipnis V, Kononova S, Chabrashvili T, Vladimirtsev VA, Alexeev VP, Gajdusek DC.
    Ann Neurol; 1996 Apr 15; 39(4):500-6. PubMed ID: 8619528
    [Abstract] [Full Text] [Related]

  • 13. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8).
    Koob MD, Moseley ML, Schut LJ, Benzow KA, Bird TD, Day JW, Ranum LP.
    Nat Genet; 1999 Apr 15; 21(4):379-84. PubMed ID: 10192387
    [Abstract] [Full Text] [Related]

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  • 16. [Molecular analyses of intergenerational instability of CAG repeat in SCA2 gene].
    Igarashi S, Tsuji S.
    Nihon Rinsho; 1999 Apr 15; 57(4):811-7. PubMed ID: 10222771
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  • 18. Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.
    Ikeuchi T, Takano H, Koide R, Horikawa Y, Honma Y, Onishi Y, Igarashi S, Tanaka H, Nakao N, Sahashi K, Tsukagoshi H, Inoue K, Takahashi H, Tsuji S.
    Ann Neurol; 1997 Dec 15; 42(6):879-84. PubMed ID: 9403480
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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 15; 41(4):505-11. PubMed ID: 9124808
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