BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 10522893)

  • 1. Evidence for the GluR6 gene associated with younger onset age of Huntington's disease.
    MacDonald ME; Vonsattel JP; Shrinidhi J; Couropmitree NN; Cupples LA; Bird ED; Gusella JF; Myers RH
    Neurology; 1999 Oct; 53(6):1330-2. PubMed ID: 10522893
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease.
    Rubinsztein DC; Leggo J; Chiano M; Dodge A; Norbury G; Rosser E; Craufurd D
    Proc Natl Acad Sci U S A; 1997 Apr; 94(8):3872-6. PubMed ID: 9108071
    [TBL] [Abstract][Full Text] [Related]  

  • 3. TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease.
    Lee JH; Lee JM; Ramos EM; Gillis T; Mysore JS; Kishikawa S; Hadzi T; Hendricks AE; Hayden MR; Morrison PJ; Nance M; Ross CA; Margolis RL; Squitieri F; Gellera C; Gomez-Tortosa E; Ayuso C; Suchowersky O; Trent RJ; McCusker E; Novelletto A; Frontali M; Jones R; Ashizawa T; Frank S; Saint-Hilaire MH; Hersch SM; Rosas HD; Lucente D; Harrison MB; Zanko A; Abramson RK; Marder K; Sequeiros J; Landwehrmeyer GB; ; Shoulson I; ; Myers RH; MacDonald ME; Gusella JF
    Biochem Biophys Res Commun; 2012 Aug; 424(3):404-8. PubMed ID: 22771793
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds.
    Andresen JM; Gayán J; Cherny SS; Brocklebank D; Alkorta-Aranburu G; Addis EA; ; Cardon LR; Housman DE; Wexler NS
    J Med Genet; 2007 Jan; 44(1):44-50. PubMed ID: 17018562
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India.
    Chattopadhyay B; Ghosh S; Gangopadhyay PK; Das SK; Roy T; Sinha KK; Jha DK; Mukherjee SC; Chakraborty A; Singhal BS; Bhattacharya AK; Bhattacharyya NP
    Neurosci Lett; 2003 Jul; 345(2):93-6. PubMed ID: 12821179
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The gender effect in juvenile Huntington disease patients of Italian origin.
    Cannella M; Gellera C; Maglione V; Giallonardo P; Cislaghi G; Muglia M; Quattrone A; Pierelli F; Di Donato S; Squitieri F
    Am J Med Genet B Neuropsychiatr Genet; 2004 Feb; 125B(1):92-8. PubMed ID: 14755452
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Experimental basis for the putative role of GluR6/kainate glutamate receptor subunit in Huntington's disease natural history.
    Diguet E; Fernagut PO; Normand E; Centelles L; Mulle C; Tison F
    Neurobiol Dis; 2004 Apr; 15(3):667-75. PubMed ID: 15056475
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutation analysis and association studies of the ubiquitin carboxy-terminal hydrolase L1 gene in Huntington's disease.
    Nazé P; Vuillaume I; Destée A; Pasquier F; Sablonnière B
    Neurosci Lett; 2002 Aug; 328(1):1-4. PubMed ID: 12123845
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic analysis of the GRIK2 modifier effect in Huntington's disease.
    Zeng W; Gillis T; Hakky M; Djoussé L; Myers RH; MacDonald ME; Gusella JF
    BMC Neurosci; 2006 Sep; 7():62. PubMed ID: 16959037
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease.
    Andrew SE; Goldberg YP; Kremer B; Telenius H; Theilmann J; Adam S; Starr E; Squitieri F; Lin B; Kalchman MA
    Nat Genet; 1993 Aug; 4(4):398-403. PubMed ID: 8401589
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease.
    Metzger S; Bauer P; Tomiuk J; Laccone F; Didonato S; Gellera C; Mariotti C; Lange HW; Weirich-Schwaiger H; Wenning GK; Seppi K; Melegh B; Havasi V; Balikó L; Wieczorek S; Zaremba J; Hoffman-Zacharska D; Sulek A; Basak AN; Soydan E; Zidovska J; Kebrdlova V; Pandolfo M; Ribaï P; Kadasi L; Kvasnicova M; Weber BH; Kreuz F; Dose M; Stuhrmann M; Riess O
    Hum Genet; 2006 Sep; 120(2):285-92. PubMed ID: 16847693
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Polymorphism of HD and UCHL-1 genes in Huntington's disease.
    Xu EH; Tang Y; Li D; Jia JP
    J Clin Neurosci; 2009 Nov; 16(11):1473-7. PubMed ID: 19683447
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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; 64(6):758-62. PubMed ID: 9647305
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington's Disease Symptoms.
    Chheda P; Chanekar M; Salunkhe Y; Dama T; Pais A; Pande S; Bendre R; Shah N
    Mol Diagn Ther; 2018 Jun; 22(3):353-359. PubMed ID: 29619771
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A genetic variation in the ADORA2A gene modifies age at onset in Huntington's disease.
    Dhaenens CM; Burnouf S; Simonin C; Van Brussel E; Duhamel A; Defebvre L; Duru C; Vuillaume I; Cazeneuve C; Charles P; Maison P; Debruxelles S; Verny C; Gervais H; Azulay JP; Tranchant C; Bachoud-Levi AC; Dürr A; Buée L; Krystkowiak P; Sablonnière B; Blum D;
    Neurobiol Dis; 2009 Sep; 35(3):474-6. PubMed ID: 19591938
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.
    De Rooij KE; De Koning Gans PA; Skraastad MI; Belfroid RD; Vegter-Van Der Vlis M; Roos RA; Bakker E; Van Ommen GJ; Den Dunnen JT; Losekoot M
    J Med Genet; 1993 Dec; 30(12):996-1002. PubMed ID: 8133511
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Huntington's disease in Grampian region: correlation of the CAG repeat number and the age of onset of the disease.
    Simpson SA; Davidson MJ; Barron LH
    J Med Genet; 1993 Dec; 30(12):1014-7. PubMed ID: 8133498
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.