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436 related items for PubMed ID: 23051704

  • 1. Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.
    Agostinho Lde A, Rocha CF, Medina-Acosta E, Barboza HN, da Silva AF, Pereira SP, da Silva Idos S, Paradela ER, Figueiredo AL, Nogueira Ede M, Alvarenga RM, Hernan Cabello P, dos Santos SR, Paiva CL.
    J Hum Genet; 2012 Dec; 57(12):796-803. PubMed ID: 23051704
    [Abstract] [Full Text] [Related]

  • 2. Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India.
    Pramanik S, Basu P, Gangopadhaya PK, Sinha KK, Jha DK, Sinha S, Das SK, Maity BK, Mukherjee SC, Roychoudhuri S, Majumder PP, Bhattacharyya NP.
    Eur J Hum Genet; 2000 Sep; 8(9):678-82. PubMed ID: 10980573
    [Abstract] [Full Text] [Related]

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  • 4. DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients.
    Wang CK, Wu YR, Hwu WL, Chen CM, Ro LS, Chen ST, Gwinn-Hardy K, Yang CC, Wu RM, Chen TF, Wang HC, Chao MC, Chiu MJ, Lu CJ, Lee-Chen GJ.
    Eur Neurol; 2004 Sep; 52(2):96-100. PubMed ID: 15273431
    [Abstract] [Full Text] [Related]

  • 5. Linkage disequilibrium between the expanded (CAG)n repeat and an allele of the adjacent (CCG)n repeat in Huntington's disease patients of Greek origin.
    Yapijakis C, Vassilopoulos D, Tzagournisakis M, Maris T, Fesdjian C, Papageorgiou C, Plaitakis A.
    Eur J Hum Genet; 1995 Sep; 3(4):228-34. PubMed ID: 8528671
    [Abstract] [Full Text] [Related]

  • 6. The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease.
    Klempíř J, Zidovská J, Stochl J, Ing VK, Uhrová T, Roth J.
    Mov Disord; 2011 Jan; 26(1):125-9. PubMed ID: 21322024
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  • 8. [Molecular genetics of Huntington's disease].
    Goto J, Masuda N, Watanabe M, Kanazawa I.
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1529-31. PubMed ID: 8752453
    [Abstract] [Full Text] [Related]

  • 9. Null alleles at the Huntington disease locus: implications for diagnostics and CAG repeat instability.
    Williams LC, Hegde MR, Nagappan R, Faull RL, Giles J, Winship I, Snow K, Love DR.
    Genet Test; 2000 Dec; 4(1):55-60. PubMed ID: 10794362
    [Abstract] [Full Text] [Related]

  • 10. Investigation of intermediate CAG alleles of the HTT in the general population of Rio de Janeiro, Brazil, in comparison with a sample of Huntington disease-affected families.
    Apolinário TA, da Silva IDS, Agostinho LA, Paiva CLA.
    Mol Genet Genomic Med; 2020 Apr; 8(4):e1181. PubMed ID: 32067426
    [Abstract] [Full Text] [Related]

  • 11. The genetic analysis of Turkish patients with Huntington's disease.
    Ataç FB, Elibol B, Schaefer F.
    Acta Neurol Scand; 1999 Sep; 100(3):195-8. PubMed ID: 10478585
    [Abstract] [Full Text] [Related]

  • 12. Molecular analysis of Huntington's disease and linked polymorphisms in the Indian population.
    Saleem Q, Roy S, Murgood U, Saxena R, Verma IC, Anand A, Muthane U, Jain S, Brahmachari SK.
    Acta Neurol Scand; 2003 Oct; 108(4):281-6. PubMed ID: 12956863
    [Abstract] [Full Text] [Related]

  • 13. Huntington disease mutation in Venezuela: age of onset, haplotype analyses and geographic aggregation.
    Paradisi I, Hernández A, Arias S.
    J Hum Genet; 2008 Oct; 53(2):127-135. PubMed ID: 18157708
    [Abstract] [Full Text] [Related]

  • 14. Genetic background of Huntington disease in Croatia: Molecular analysis of CAG, CCG, and Delta2642 (E2642del) polymorphisms.
    Hećimović S, Klepac N, Vlasić J, Vojta A, Janko D, Skarpa-Prpić I, Canki-Klain N, Marković D, Bozikov J, Relja M, Pavelić K.
    Hum Mutat; 2002 Sep; 20(3):233. PubMed ID: 12204002
    [Abstract] [Full Text] [Related]

  • 15. Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population.
    Ma M, Yang Y, Shang H, Su D, Zhang H, Ma Y, Liu Y, Tao D, Zhang S.
    J Neurol Sci; 2010 Nov 15; 298(1-2):57-60. PubMed ID: 20864123
    [Abstract] [Full Text] [Related]

  • 16. Genetic polymorphisms adjacent to the CAG repeat influence clinical features at onset in Huntington's disease.
    Vuillaume I, Vermersch P, Destée A, Petit H, Sablonnière B.
    J Neurol Neurosurg Psychiatry; 1998 Jun 15; 64(6):758-62. PubMed ID: 9647305
    [Abstract] [Full Text] [Related]

  • 17. Biallelic mutations in huntington disease: A new case with just one affected parent, review of the literature and terminology.
    Uhlmann WR, Peñaherrera MS, Robinson WP, Milunsky JM, Nicholson JM, Albin RL.
    Am J Med Genet A; 2015 May 15; 167A(5):1152-60. PubMed ID: 25736541
    [Abstract] [Full Text] [Related]

  • 18. Analysis of CCG repeats in Huntingtin gene among HD patients and normal populations in Japan.
    Morovvati S, Nakagawa M, Osame M, Karami A.
    Arch Med Res; 2008 Jan 15; 39(1):131-3. PubMed ID: 18068007
    [Abstract] [Full Text] [Related]

  • 19. A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing.
    Andrew SE, Goldberg YP, Theilmann J, Zeisler J, Hayden MR.
    Hum Mol Genet; 1994 Jan 15; 3(1):65-7. PubMed ID: 8162053
    [Abstract] [Full Text] [Related]

  • 20. [Study of the association of genotype and phenotype features of the pathogenesis of Huntington's chorea].
    Hryshchenko NV, Kucherenko AM, Patskun EI, Livshyts' LA.
    Tsitol Genet; 2009 Jan 15; 43(3):42-7. PubMed ID: 19938636
    [Abstract] [Full Text] [Related]

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