BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 20528910)

  • 1. Association of the glucocerebrosidase N370S allele with Parkinson's disease in two separate Chinese Han populations of mainland China.
    Hu FY; Xi J; Guo J; Yu LH; Liu L; He XH; Liu ZL; Zou XY; Xu YM
    Eur J Neurol; 2010 Dec; 17(12):1476-8. PubMed ID: 20528910
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Glucocerebrosidase L444P mutation confers genetic risk for Parkinson's disease in central China.
    Wang Y; Liu L; Xiong J; Zhang X; Chen Z; Yu L; Chen C; Huang J; Zhang Z; Mohmed AA; Lin Z; Xiong N; Wang T
    Behav Brain Funct; 2012 Dec; 8():57. PubMed ID: 23227814
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel p.L216I mutation in the glucocerebrosidase gene is associated with Parkinson's disease in Han Chinese patients.
    Jin H; Chen J; Li K; Zhang JR; Gu CC; Mao CJ; Yang YP; Wang F; Liu CF
    Neurosci Lett; 2018 May; 674():66-69. PubMed ID: 29530815
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Association of Common Variants in the Glucocerebrosidase Gene with High Susceptibility to Parkinson's Disease among Chinese.
    Zhang X; Bao QQ; Zhuang XS; Gan SR; Zhao D; Liu Y; Hu Q; Chen Y; Zhu F; Wang L; Wang N
    Chin J Physiol; 2012 Dec; 55(6):398-404. PubMed ID: 23286447
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association between GBA L444P mutation and sporadic Parkinson's disease from Mainland China.
    Mao XY; Burgunder JM; Zhang ZJ; An XK; Zhang JH; Yang Y; Li T; Wang YC; Chang XL; Peng R
    Neurosci Lett; 2010 Jan; 469(2):256-9. PubMed ID: 20004703
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Contribution of glucocerebrosidase mutation in a large cohort of sporadic Parkinson's disease in Taiwan.
    Huang CL; Wu-Chou YH; Lai SC; Chang HC; Yeh TH; Weng YH; Chen RS; Huang YZ; Lu CS
    Eur J Neurol; 2011 Oct; 18(10):1227-32. PubMed ID: 21338444
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity.
    Clark LN; Nicolai A; Afridi S; Harris J; Mejia-Santana H; Strug L; Cote LJ; Louis ED; Andrews H; Waters C; Ford B; Frucht S; Fahn S; Mayeux R; Ottman R; Marder K
    Mov Disord; 2005 Jan; 20(1):100-3. PubMed ID: 15517591
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in the glucocerebrosidase gene are responsible for Chinese patients with Parkinson's disease.
    Yu Z; Wang T; Xu J; Wang W; Wang G; Chen C; Zheng L; Pan L; Gong D; Li X; Qu H; Li F; Zhang B; Le W; Han F
    J Hum Genet; 2015 Feb; 60(2):85-90. PubMed ID: 25518742
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Glucocerebrosidase gene mutations associated with Parkinson's disease: a meta-analysis in a Chinese population.
    Chen J; Li W; Zhang T; Wang YJ; Jiang XJ; Xu ZQ
    PLoS One; 2014; 9(12):e115747. PubMed ID: 25535748
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CD33 polymorphisms and Parkinson's disease Parkinson's disease in northern Chinese Han population: A case-control study.
    Tian Q; Sun X; Li C; Yang Y; Hou B; Xie A
    Neurosci Lett; 2023 Aug; 812():137400. PubMed ID: 37479176
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in the glucocerebrosidase gene are common in patients with Parkinson's disease from Eastern Canada.
    Han F; Grimes DA; Li F; Wang T; Yu Z; Song N; Wu S; Racacho L; Bulman DE
    Int J Neurosci; 2016; 126(5):415-21. PubMed ID: 26000814
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations of glucocerebrosidase gene and susceptibility to Parkinson's disease: An updated meta-analysis in a European population.
    Zhao F; Bi L; Wang W; Wu X; Li Y; Gong F; Lu S; Feng F; Qian Z; Hu C; Wu Y; Sun Y
    Neuroscience; 2016 Apr; 320():239-46. PubMed ID: 26868973
    [TBL] [Abstract][Full Text] [Related]  

  • 13. β-Glucocerebrosidase gene mutations in two cohorts of Greek patients with sporadic Parkinson's disease.
    Moraitou M; Hadjigeorgiou G; Monopolis I; Dardiotis E; Bozi M; Vassilatis D; Vilageliu L; Grinberg D; Xiromerisiou G; Stefanis L; Michelakakis H
    Mol Genet Metab; 2011; 104(1-2):149-52. PubMed ID: 21745757
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Glucocerebrosidase gene L444P mutation is a risk factor for Parkinson's disease in Chinese population.
    Sun QY; Guo JF; Wang L; Yu RH; Zuo X; Yao LY; Pan Q; Xia K; Tang BS
    Mov Disord; 2010 Jun; 25(8):1005-11. PubMed ID: 20131388
    [TBL] [Abstract][Full Text] [Related]  

  • 15. HLA-DRB1 alleles are associated with the susceptibility to sporadic Parkinson's disease in Chinese Han population.
    Sun C; Wei L; Luo F; Li Y; Li J; Zhu F; Kang P; Xu R; Xiao L; Liu Z; Xu P
    PLoS One; 2012; 7(11):e48594. PubMed ID: 23139797
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An assessment of the frequency of mutations in the GBA and VPS35 genes in Hungarian patients with sporadic Parkinson's disease.
    Török R; Zádori D; Török N; Csility É; Vécsei L; Klivényi P
    Neurosci Lett; 2016 Jan; 610():135-8. PubMed ID: 26547032
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease.
    Clark LN; Ross BM; Wang Y; Mejia-Santana H; Harris J; Louis ED; Cote LJ; Andrews H; Fahn S; Waters C; Ford B; Frucht S; Ottman R; Marder K
    Neurology; 2007 Sep; 69(12):1270-7. PubMed ID: 17875915
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Glucocerebrosidase mutations in a Serbian Parkinson's disease population.
    Kumar KR; Ramirez A; Göbel A; Kresojević N; Svetel M; Lohmann K; M Sue C; Rolfs A; Mazzulli JR; Alcalay RN; Krainc D; Klein C; Kostic V; Grünewald A
    Eur J Neurol; 2013 Feb; 20(2):402-5. PubMed ID: 22812582
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of mutations in the glucocerebrosidase gene with Parkinson disease in a Korean population.
    Choi JM; Kim WC; Lyoo CH; Kang SY; Lee PH; Baik JS; Koh SB; Ma HI; Sohn YH; Lee MS; Kim YJ
    Neurosci Lett; 2012 Apr; 514(1):12-5. PubMed ID: 22387070
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Revisiting the non-Gaucher-GBA-E326K carrier state: Is it sufficient to increase Parkinson's disease risk?
    Goldstein O; Gana-Weisz M; Cohen-Avinoam D; Shiner T; Thaler A; Cedarbaum JM; John S; Lalioti M; Gurevich T; Bar-Shira A; Mirelman A; Giladi N; Orr-Urtreger A
    Mol Genet Metab; 2019 Dec; 128(4):470-475. PubMed ID: 31662221
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.