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Journal Abstract Search

136 related items for PubMed ID: 10551541

  • 1. No evidence of linkage disequilibrium between a CAG repeat in the SCA1 gene and schizophrenia in Caucasian and Chinese schizophrenic subjects.
    Li T, Breen G, Brown J, Liu X, Murray RM, Shaw DJ, Sham PC, St Clair D, Collier DA.
    Psychiatr Genet; 1999 Sep; 9(3):123-7. PubMed ID: 10551541
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  • 7. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.
    Tsai HF, Liu CS, Leu TM, Wen FC, Lin SJ, Liu CC, Yang DK, Li C, Hsieh M.
    Acta Neurol Scand; 2004 May; 109(5):355-60. PubMed ID: 15080863
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  • 8. Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 families.
    Zhou YX, Qiao WH, Gu WH, Xie H, Tang BS, Zhou LS, Yang BX, Takiyama Y, Tsuji S, He HY, Deng CX, Goldfarb LG, Wang GX.
    Arch Neurol; 2001 May; 58(5):789-94. PubMed ID: 11346374
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  • 9. Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?
    Savić D, Topisirović I, Keckarević M, Keckarević D, Major T, Culjković B, Stojković O, Rakocević-Stojanović V, Mladenović J, Todorović S, Apostolski S, Romac S.
    Psychiatr Genet; 2001 Dec; 11(4):201-5. PubMed ID: 11807410
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  • 10. [Analysis and application of SCA1 and SCA3/MJD gene CAG repeats in Han population in Northeastern China].
    Jiang M, Jin CL, Lin CK, Qiu GR, Liu ZL, Wang CX, Sun KL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):83-5. PubMed ID: 14767919
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  • 12. Genetic association study of a polymorphic CAG repeats array of calcium-activated potassium channel (KCNN3) gene and schizophrenia among the Chinese population from Taiwan.
    Tsai MT, Shaw CK, Hsiao KJ, Chen CH.
    Mol Psychiatry; 1999 May; 4(3):271-3. PubMed ID: 10395218
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  • 15. [Association study of an (AC)n dinucleotide repeat and schizophrenia in Asian and European populations].
    Ma J, Fan JB, Wu SN, Zhang CS, Ji BH, Wang L, Li XW, Gu NF, Feng GY, St Clair D, He L.
    Yi Chuan; 2007 Oct; 29(10):1207-13. PubMed ID: 17905710
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  • 17. Insights into the mutational history and prevalence of SCA1 in the Indian population through anchored polymorphisms.
    Mittal U, Sharma S, Chopra R, Dheeraj K, Pal PK, Srivastava AK, Mukerji M.
    Hum Genet; 2005 Oct; 118(1):107-14. PubMed ID: 16133185
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  • 18. Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations.
    Takano H, Cancel G, Ikeuchi T, Lorenzetti D, Mawad R, Stevanin G, Didierjean O, Dürr A, Oyake M, Shimohata T, Sasaki R, Koide R, Igarashi S, Hayashi S, Takiyama Y, Nishizawa M, Tanaka H, Zoghbi H, Brice A, Tsuji S.
    Am J Hum Genet; 1998 Oct; 63(4):1060-6. PubMed ID: 9758625
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  • 20. [Studies on the CAG repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese Han].
    Wang J, Xu Q, Lei L, Shen L, Jiang H, Li X, Zhou Y, Yi J, Zhou J, Yan X, Pan Q, Xia K, Tang B.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):620-5. PubMed ID: 19953482
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