These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 7981682)

  • 1. Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease.
    Novelletto A; Persichetti F; Sabbadini G; Mandich P; Bellone E; Ajmar F; Squitieri F; Campanella G; Bozza A; MacDonald ME
    Hum Mol Genet; 1994 Jul; 3(7):1129-32. PubMed ID: 7981682
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease.
    Masuda N; Goto J; Murayama N; Watanabe M; Kondo I; Kanazawa I
    J Med Genet; 1995 Sep; 32(9):701-5. PubMed ID: 8544189
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 39(1):131-3. PubMed ID: 18068007
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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; 43(3):42-7. PubMed ID: 19938636
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Relationships of the 2642 deletion polymorphism (delta 2642) in the huntingtin gene with the CAG repeat expansion length and age at onset of the disease.
    Lucotte G; Gérard N; Roubertoux P; Schmitt I; Riess O
    Genet Couns; 1996; 7(4):297-302. PubMed ID: 8985734
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 298(1-2):57-60. PubMed ID: 20864123
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomes.
    Pêcheux C; Mouret JF; Dürr A; Agid Y; Feingold J; Brice A; Dodé C; Kaplan JC
    J Med Genet; 1995 May; 32(5):399-400. PubMed ID: 7616551
    [TBL] [Abstract][Full Text] [Related]  

  • 10. New Huntington disease mutation arising from a paternal CAG34 allele showing somatic length variation in serially passaged lymphoblasts.
    Cannella M; Maglione V; Martino T; Simonelli M; Ragona G; Squitieri F
    Am J Med Genet B Neuropsychiatr Genet; 2005 Feb; 133B(1):127-30. PubMed ID: 15546151
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.
    García-Planells J; Burguera JA; Solís P; Millán JM; Ginestar D; Palau F; Espinós C
    Hum Mutat; 2005 May; 25(5):453-9. PubMed ID: 15832309
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 4(1):55-60. PubMed ID: 10794362
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 3(1):65-7. PubMed ID: 8162053
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 3(4):228-34. PubMed ID: 8528671
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CCG polymorphisms in the huntingtin gene have no effect on the pathogenesis of patients with Huntington's disease in mainland Chinese families.
    Zhang BR; Tian J; Yan YP; Yin XZ; Zhao GH; Wu ZY; Gu WH; Xia K; Tang BS
    J Neurol Sci; 2012 Jan; 312(1-2):92-6. PubMed ID: 21875723
    [TBL] [Abstract][Full Text] [Related]  

  • 17. HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism.
    Seong IS; Ivanova E; Lee JM; Choo YS; Fossale E; Anderson M; Gusella JF; Laramie JM; Myers RH; Lesort M; MacDonald ME
    Hum Mol Genet; 2005 Oct; 14(19):2871-80. PubMed ID: 16115812
    [TBL] [Abstract][Full Text] [Related]  

  • 18. DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence.
    Squitieri F; Andrew SE; Goldberg YP; Kremer B; Spence N; Zeisler J; Nichol K; Theilmann J; Greenberg J; Goto J
    Hum Mol Genet; 1994 Dec; 3(12):2103-14. PubMed ID: 7881406
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Analysis of the IT15 gene in Huntington's disease families].
    Genetika; 2004 Aug; 40(8):1123-30. PubMed ID: 15523851
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Factors associated with HD CAG repeat instability in Huntington disease.
    Wheeler VC; Persichetti F; McNeil SM; Mysore JS; Mysore SS; MacDonald ME; Myers RH; Gusella JF; Wexler NS;
    J Med Genet; 2007 Nov; 44(11):695-701. PubMed ID: 17660463
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.