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Journal Abstract Search

218 related items for PubMed ID: 9598323

  • 1. 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]

  • 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 15; 14(3):269-76. PubMed ID: 8896555
    [Abstract] [Full Text] [Related]

  • 3. [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]

  • 4. 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 15; 14(3):277-84. PubMed ID: 8896556
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Molecular interpretation of expanded RED products in bipolar disorder by CAG/CTG repeats located at chromosomes 17q and 18q.
    Verheyen GR, Del-Favero J, Mendlewicz J, Lindblad K, Van Zand K, Aalbregtse M, Schalling M, Souery D, Van Broeckhoven C.
    Neurobiol Dis; 1999 Oct 15; 6(5):424-32. PubMed ID: 10527808
    [Abstract] [Full Text] [Related]

  • 7.
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  • 8. 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 15; 4(3):221-6. PubMed ID: 8358429
    [Abstract] [Full Text] [Related]

  • 9. Genome-wide scan for CAG/CTG repeat expansions in Pimas with early onset of type 2 diabetes mellitus.
    Wolford JK, Bogardus C, Prochazka M.
    Mol Genet Metab; 1999 Jan 15; 66(1):62-7. PubMed ID: 9973549
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 17(1):65-70. PubMed ID: 9288099
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases.
    Tachikawa M, Nagai Y, Nakamura K, Kobayashi K, Fujiwara T, Han HJ, Nakabayashi Y, Ichikawa Y, Goto J, Kanazawa I, Nakamura Y, Toda T.
    J Hum Genet; 2002 Apr 15; 47(6):275-8. PubMed ID: 12111376
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. No evidence for the involvement of CAG/CTG repeats from within 18q21.33-q23 in bipolar disorder.
    Goossens D, Villafuerte S, Tissir F, Van Gestel S, Claes S, Souery D, Massat I, Van den Bossche D, Van Zand K, Mendlewicz J, Van Broeckhoven C, Del-Favero J.
    Eur J Hum Genet; 2000 May 15; 8(5):385-8. PubMed ID: 10854100
    [Abstract] [Full Text] [Related]

  • 15. Development of a screening set for new (CAG/CTG)n dynamic mutations.
    Gastier JM, Brody T, Pulido JC, Businga T, Sunden S, Hu X, Maitra S, Buetow KH, Murray JC, Sheffield VC, Boguski M, Duyk GM, Hudson TJ.
    Genomics; 1996 Feb 15; 32(1):75-85. PubMed ID: 8786123
    [Abstract] [Full Text] [Related]

  • 16. [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]

  • 17. Exclusion of CAG/CTG trinucleotide repeat loci which map to chromosome 4 in bipolar disorder and schizophrenia.
    Speight G, Guy C, Bowen T, Asherson P, McGuffin P, Craddock N, Owen MJ, O'Donovan MC.
    Am J Med Genet; 1997 Apr 18; 74(2):204-6. PubMed ID: 9129726
    [Abstract] [Full Text] [Related]

  • 18. A SCA7 CAG/CTG repeat expansion is stable in Drosophila melanogaster despite modulation of genomic context and gene dosage.
    Jackson SM, Whitworth AJ, Greene JC, Libby RT, Baccam SL, Pallanck LJ, La Spada AR.
    Gene; 2005 Feb 28; 347(1):35-41. PubMed ID: 15715978
    [Abstract] [Full Text] [Related]

  • 19. An integrated map of chromosome 18 CAG trinucleotide repeat loci.
    Grierson AJ, van Groenigen M, Groot NP, Lindblad K, Hoovers JM, Schalling M, de Belleroche J, Baas F.
    Eur J Hum Genet; 1999 Jan 28; 7(1):12-9. PubMed ID: 10094186
    [Abstract] [Full Text] [Related]

  • 20. Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization.
    Haaf T, Sirugo G, Kidd KK, Ward DC.
    Nat Genet; 1996 Feb 28; 12(2):183-5. PubMed ID: 8563757
    [Abstract] [Full Text] [Related]

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