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570 related items for PubMed ID: 8896555

  • 1. 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]

  • 2. 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]

  • 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. 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]

  • 5. Genomic structure of the human gene for spinocerebellar ataxia type 2 (SCA2) on chromosome 12q24.1.
    Sahba S, Nechiporuk A, Figueroa KP, Nechiporuk T, Pulst SM.
    Genomics; 1998 Feb 01; 47(3):359-64. PubMed ID: 9480749
    [Abstract] [Full Text] [Related]

  • 6. 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 01; 17(1):65-70. PubMed ID: 9288099
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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]

  • 9. 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 15; 61(2):209-12. PubMed ID: 14967767
    [Abstract] [Full Text] [Related]

  • 10. Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1-2 polymorphism and contribution to founder effect.
    Mizushima K, Watanabe M, Kondo I, Okamoto K, Shizuka M, Abe K, Aoki M, Shoji M.
    J Med Genet; 1999 Feb 15; 36(2):112-4. PubMed ID: 10051008
    [Abstract] [Full Text] [Related]

  • 11. [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
    [Abstract] [Full Text] [Related]

  • 12. [The phenotype variation correlates with the size of CAG repeat in SCA2].
    Sasaki H, Sanpei K.
    Nihon Rinsho; 1999 Apr 15; 57(4):818-21. PubMed ID: 10222772
    [Abstract] [Full Text] [Related]

  • 13. [Molecular analysis of the CAG repeat among patients with Type-2 spinocerebellar ataxia in the Mexican population].
    Magaña JJ, Vergara MD, Sierra-Martínez M, García-Jiménez E, Rodríguez-Antonio F, Gómez Mdel R, Valdés-Flores M, Cisneros B.
    Gac Med Mex; 2008 Apr 15; 144(5):413-8. PubMed ID: 19043961
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. A high-resolution PAC and BAC map of the SCA2 region.
    Nechiporuk T, Nechiporuk A, Sahba S, Figueroa K, Shibata H, Chen XN, Korenberg JR, de Jong P, Pulst SM.
    Genomics; 1997 Sep 15; 44(3):321-9. PubMed ID: 9325053
    [Abstract] [Full Text] [Related]

  • 16. 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 15; 18(1):72-5. PubMed ID: 9425905
    [Abstract] [Full Text] [Related]

  • 17. CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms.
    Choudhry S, Mukerji M, Srivastava AK, Jain S, Brahmachari SK.
    Hum Mol Genet; 2001 Oct 01; 10(21):2437-46. PubMed ID: 11689490
    [Abstract] [Full Text] [Related]

  • 18. Linkage disequilibrium at the SCA2 locus.
    Didierjean O, Cancel G, Stevanin G, Dürr A, Bürk K, Benomar A, Lezin A, Belal S, Abada-Bendid M, Klockgether T, Brice A.
    J Med Genet; 1999 May 01; 36(5):415-7. PubMed ID: 10353790
    [Abstract] [Full Text] [Related]

  • 19. The effect of CAT trinucleotide interruptions on the age at onset of spinocerebellar ataxia type 1 (SCA1).
    Matsuyama Z, Izumi Y, Kameyama M, Kawakami H, Nakamura S.
    J Med Genet; 1999 Jul 01; 36(7):546-8. PubMed ID: 10424816
    [Abstract] [Full Text] [Related]

  • 20. Identification and characterization of the gene causing type 1 spinocerebellar ataxia.
    Banfi S, Servadio A, Chung MY, Kwiatkowski TJ, McCall AE, Duvick LA, Shen Y, Roth EJ, Orr HT, Zoghbi HY.
    Nat Genet; 1994 Aug 01; 7(4):513-20. PubMed ID: 7951322
    [Abstract] [Full Text] [Related]

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