BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 20146068)

  • 1. Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism.
    Guo JF; Zhang XW; Nie LL; Zhang HN; Liao B; Li J; Wang L; Yan XX; Tang BS
    J Neurol; 2010 Jul; 257(7):1170-5. PubMed ID: 20146068
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutation analysis for DJ-1 in sporadic and familial parkinsonism: screening strategy in parkinsonism.
    Tomiyama H; Li Y; Yoshino H; Mizuno Y; Kubo S; Toda T; Hattori N
    Neurosci Lett; 2009 May; 455(3):159-61. PubMed ID: 19429112
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism.
    Guo JF; Xiao B; Liao B; Zhang XW; Nie LL; Zhang YH; Shen L; Jiang H; Xia K; Pan Q; Yan XX; Tang BS
    Mov Disord; 2008 Oct; 23(14):2074-9. PubMed ID: 18785233
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism.
    Lee MJ; Mata IF; Lin CH; Tzen KY; Lincoln SJ; Bounds R; Lockhart PJ; Hulihan MM; Farrer MJ; Wu RM
    Mov Disord; 2009 Jan; 24(1):104-8. PubMed ID: 19006224
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease.
    Yonova-Doing E; Atadzhanov M; Quadri M; Kelly P; Shawa N; Musonda ST; Simons EJ; Breedveld GJ; Oostra BA; Bonifati V
    Parkinsonism Relat Disord; 2012 Jun; 18(5):567-71. PubMed ID: 22445250
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease.
    Kilarski LL; Pearson JP; Newsway V; Majounie E; Knipe MD; Misbahuddin A; Chinnery PF; Burn DJ; Clarke CE; Marion MH; Lewthwaite AJ; Nicholl DJ; Wood NW; Morrison KE; Williams-Gray CH; Evans JR; Sawcer SJ; Barker RA; Wickremaratchi MM; Ben-Shlomo Y; Williams NM; Morris HR
    Mov Disord; 2012 Oct; 27(12):1522-9. PubMed ID: 22956510
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exon dosage variations in Brazilian patients with Parkinson's disease: analysis of SNCA, PARKIN, PINK1 and DJ-1 genes.
    Moura KC; Junior MC; de Rosso AL; Nicaretta DH; Pereira JS; José Silva D; Santos-Rebouças CB; Pimentel MM
    Dis Markers; 2012; 32(3):173-8. PubMed ID: 22377733
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease.
    Choi JM; Woo MS; Ma HI; Kang SY; Sung YH; Yong SW; Chung SJ; Kim JS; Shin HW; Lyoo CH; Lee PH; Baik JS; Kim SJ; Park MY; Sohn YH; Kim JH; Kim JW; Lee MS; Lee MC; Kim DH; Kim YJ
    Neurogenetics; 2008 Oct; 9(4):263-9. PubMed ID: 18704525
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pink1, Parkin, DJ-1 and mitochondrial dysfunction in Parkinson's disease.
    Dodson MW; Guo M
    Curr Opin Neurobiol; 2007 Jun; 17(3):331-7. PubMed ID: 17499497
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients.
    Koziorowski D; Hoffman-Zacharska D; Sławek J; Jamrozik Z; Janik P; Potulska-Chromik A; Roszmann A; Tataj R; Bal J; Friedman A
    Neurol Neurochir Pol; 2013; 47(4):319-24. PubMed ID: 23986421
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism.
    Li Y; Tomiyama H; Sato K; Hatano Y; Yoshino H; Atsumi M; Kitaguchi M; Sasaki S; Kawaguchi S; Miyajima H; Toda T; Mizuno Y; Hattori N
    Neurology; 2005 Jun; 64(11):1955-7. PubMed ID: 15955953
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Parkinsonism due to mutations in PINK1, parkin, and DJ-1 and oxidative stress and mitochondrial pathways.
    Cookson MR
    Cold Spring Harb Perspect Med; 2012 Sep; 2(9):a009415. PubMed ID: 22951446
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence for a common biological pathway linking three Parkinson's disease-causing genes: parkin, PINK1 and DJ-1.
    van der Merwe C; Jalali Sefid Dashti Z; Christoffels A; Loos B; Bardien S
    Eur J Neurosci; 2015 May; 41(9):1113-25. PubMed ID: 25761903
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease.
    Macedo MG; Verbaan D; Fang Y; van Rooden SM; Visser M; Anar B; Uras A; Groen JL; Rizzu P; van Hilten JJ; Heutink P
    Mov Disord; 2009 Jan; 24(2):196-203. PubMed ID: 18973254
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements.
    Scarciolla O; Brancati F; Valente EM; Ferraris A; De Angelis MV; Valbonesi S; Garavaglia B; Uncini A; Palka G; Stuppia L; Dallapiccola B
    Mov Disord; 2007 Nov; 22(15):2274-8. PubMed ID: 17914726
    [TBL] [Abstract][Full Text] [Related]  

  • 16. PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutations.
    Ghazavi F; Fazlali Z; Banihosseini SS; Hosseini SR; Kazemi MH; Shojaee S; Parsa K; Sadeghi H; Sina F; Rohani M; Shahidi GA; Ghaemi N; Ronaghi M; Elahi E
    Mov Disord; 2011 Jan; 26(1):80-9. PubMed ID: 21322020
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heterozygous PINK1 mutations: a susceptibility factor for Parkinson disease?
    Djarmati A; Hedrich K; Svetel M; Lohnau T; Schwinger E; Romac S; Pramstaller PP; Kostić V; Klein C
    Mov Disord; 2006 Sep; 21(9):1526-30. PubMed ID: 16755580
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Parkin, PINK1, and DJ-1 form a ubiquitin E3 ligase complex promoting unfolded protein degradation.
    Xiong H; Wang D; Chen L; Choo YS; Ma H; Tang C; Xia K; Jiang W; Ronai Z; Zhuang X; Zhang Z
    J Clin Invest; 2009 Mar; 119(3):650-60. PubMed ID: 19229105
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DJ-1 acts in parallel to the PINK1/parkin pathway to control mitochondrial function and autophagy.
    Thomas KJ; McCoy MK; Blackinton J; Beilina A; van der Brug M; Sandebring A; Miller D; Maric D; Cedazo-Minguez A; Cookson MR
    Hum Mol Genet; 2011 Jan; 20(1):40-50. PubMed ID: 20940149
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial Parkinsonism with digenic parkin and PINK1 mutations.
    Funayama M; Li Y; Tsoi TH; Lam CW; Ohi T; Yazawa S; Uyama E; Djaldetti R; Melamed E; Yoshino H; Imamichi Y; Takashima H; Nishioka K; Sato K; Tomiyama H; Kubo S; Mizuno Y; Hattori N
    Mov Disord; 2008 Jul; 23(10):1461-5. PubMed ID: 18546294
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.