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Journal Abstract Search

222 related items for PubMed ID: 7951322

  • 1. 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; 7(4):513-20. PubMed ID: 7951322
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  • 2. Spinocerebellar ataxia type 1.
    Zoghbi HY.
    Clin Neurosci; 1995 Aug; 3(1):5-11. PubMed ID: 7614095
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  • 6. 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
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  • 9. 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
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  • 10. 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
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  • 11. Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1.
    Chong SS, McCall AE, Cota J, Subramony SH, Orr HT, Hughes MR, Zoghbi HY.
    Nat Genet; 1995 Jul; 10(3):344-50. PubMed ID: 7670474
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  • 12. Interruptions in the triplet repeats of SCA1 and FRAXA reduce the propensity and complexity of slipped strand DNA (S-DNA) formation.
    Pearson CE, Eichler EE, Lorenzetti D, Kramer SF, Zoghbi HY, Nelson DL, Sinden RR.
    Biochemistry; 1998 Feb 24; 37(8):2701-8. PubMed ID: 9485421
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  • 15. Bovine CACNA1A gene and comparative analysis of the CAG repeats associated to human spinocerebellar ataxia type-6.
    Andrés-Mateos E, Cruces J, Renart J, Solís-Garrido LM, Serantes R, de Lucas-Cerrillo AM, Montiel C.
    Gene; 2006 Sep 15; 380(1):54-61. PubMed ID: 16876337
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  • 16. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
    Lee PL, Gelbart T, West C, Halloran C, Beutler E.
    Blood Cells Mol Dis; 1998 Jun 15; 24(2):199-215. PubMed ID: 9642100
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  • 17. Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan.
    Kameya T, Abe K, Aoki M, Sahara M, Tobita M, Konno H, Itoyama Y.
    Neurology; 1995 Aug 15; 45(8):1587-94. PubMed ID: 7543989
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  • 19. Extracellular superoxide dismutase (SOD3): tissue-specific expression, genomic characterization, and computer-assisted sequence analysis of the human EC SOD gene.
    Folz RJ, Crapo JD.
    Genomics; 1994 Jul 01; 22(1):162-71. PubMed ID: 7959763
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