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Journal Abstract Search


255 related items for PubMed ID: 9425905

  • 1. 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]

  • 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 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]

  • 4. 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]

  • 5. Analysis of ERDA1, CTG18.1, and uncloned CAG/CTG repeat sequences in familial Parkinson's disease with anticipation.
    Schraen-Maschke S, Brique S, Chartier-Harlin MC, Brique E, Destée A, Sablonnière B.
    Am J Med Genet; 1999 Dec 15; 88(6):738-41. PubMed ID: 10581499
    [Abstract] [Full Text] [Related]

  • 6. Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy.
    Michalik A, Martin JJ, Van Broeckhoven C.
    Eur J Hum Genet; 2004 Jan 15; 12(1):2-15. PubMed ID: 14571264
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Direct detection of expanded trinucleotide repeats using PCR and DNA hybridization techniques.
    Petronis A, Heng HH, Tatuch Y, Shi XM, Klempan TA, Tsui LC, Ashizawa T, Surh LC, Holden JJ, Kennedy JL.
    Am J Med Genet; 1996 Feb 16; 67(1):85-91. PubMed ID: 8678121
    [Abstract] [Full Text] [Related]

  • 9. Analysis of thirteen trinucleotide repeat loci as candidate genes for schizophrenia and bipolar affective disorder.
    Jain S, Leggo J, DeLisi LE, Crow TJ, Margolis RL, Li SH, Goodburn S, Walsh C, Paykel ES, Ferguson-Smith MA, Ross CA, Rubinsztein DC.
    Am J Med Genet; 1996 Apr 09; 67(2):139-46. PubMed ID: 8723040
    [Abstract] [Full Text] [Related]

  • 10. 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 09; 4(3):221-6. PubMed ID: 8358429
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Detection and isolation of trinucleotide repeat expansions using the RED method.
    Yuan QP, Schalling M.
    Methods Mol Biol; 2004 Feb 28; 277():47-59. PubMed ID: 15201448
    [Abstract] [Full Text] [Related]

  • 13. [Genomic instability and neurodegenerative disease].
    Miki T, Yamagata H.
    Rinsho Byori; 1999 Jan 28; 47(1):37-45. PubMed ID: 10067364
    [Abstract] [Full Text] [Related]

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  • 15. Sequence analysis of genomic regions containing trinucleotide repeats isolated by a novel cloning method.
    Inoue S, Takahashi K, Ohta M.
    Genomics; 1999 Apr 01; 57(1):169-72. PubMed ID: 10191099
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 21(4):379-84. PubMed ID: 10192387
    [Abstract] [Full Text] [Related]

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  • 18. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
    Tang B, Xia J, Wang D, Tang X, Shen L, Liu C, Dai H, Yan X, Pan Q, Xiao J, Zhang B, Ou Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct 01; 16(5):281-4. PubMed ID: 10514531
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