BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 18688798)

  • 1. Lrrk2 R1628P in non-Chinese Asian races.
    Tan EK; Tang M; Tan LC; Wu YR; Wu RM; Ross OA; Zhao Y
    Ann Neurol; 2008 Oct; 64(4):472-3. PubMed ID: 18688798
    [No Abstract]   [Full Text] [Related]  

  • 2. LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.
    Zhang Z; Burgunder JM; An X; Wu Y; Chen W; Zhang J; Wang Y; Xu Y; Gou Y; Yuan G; Mao X; Peng R
    Mov Disord; 2009 Oct; 24(13):1902-5. PubMed ID: 19672984
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Uniting Chinese across Asia: the LRRK2 Gly2385Arg risk variant.
    Tan EK; Schapira AH
    Eur J Neurol; 2008 Mar; 15(3):203-4. PubMed ID: 18290841
    [No Abstract]   [Full Text] [Related]  

  • 4. LRRK2 G2385R and LRRK2 R1628P increase risk of Parkinson's disease in a Han Chinese population from Southern Mainland China.
    Fu X; Zheng Y; Hong H; He Y; Zhou S; Guo C; Liu Y; Xian W; Zeng J; Li J; Liu Z; Chen L; Pei Z
    Parkinsonism Relat Disord; 2013 Mar; 19(3):397-8. PubMed ID: 22981185
    [No Abstract]   [Full Text] [Related]  

  • 5. Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease.
    Ross OA; Wu YR; Lee MC; Funayama M; Chen ML; Soto AI; Mata IF; Lee-Chen GJ; Chen CM; Tang M; Zhao Y; Hattori N; Farrer MJ; Tan EK; Wu RM
    Ann Neurol; 2008 Jul; 64(1):88-92. PubMed ID: 18412265
    [TBL] [Abstract][Full Text] [Related]  

  • 6. LRRK2 G2019S founder haplotype in the Chinese population.
    Tan EK; Skipper L; Tan L; Liu JJ
    Mov Disord; 2007 Jan; 22(1):105-7. PubMed ID: 17083102
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Confirmation of the association between LRRK2 R1628P variant and susceptibility to Parkinson's disease in the Thai population.
    Pulkes T; Papsing C; Thakkinstian A; Pongpakdee S; Kulkantrakorn K; Hanchaiphiboolkul S; Tiamkao S; Boonkongchuen P
    Parkinsonism Relat Disord; 2014 Sep; 20(9):1018-21. PubMed ID: 24997548
    [TBL] [Abstract][Full Text] [Related]  

  • 8. LRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson's disease in the Malaysian population.
    Gopalai AA; Lim SY; Chua JY; Tey S; Lim TT; Mohamed Ibrahim N; Tan AH; Eow GB; Abdul Aziz Z; Puvanarajah SD; Viswanathan S; Looi I; Lim SK; Tan LP; Chong YB; Tan CT; Zhao Y; Tan EK; Ahmad-Annuar A
    Biomed Res Int; 2014; 2014():867321. PubMed ID: 25243190
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variants.
    Wang C; Cai Y; Zheng Z; Tang BS; Xu Y; Wang T; Ma J; Chen SD; Langston JW; Tanner CM; Chan P;
    Parkinsonism Relat Disord; 2012 Sep; 18(8):958-63. PubMed ID: 22658533
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Parkinson-Related LRRK2 Mutation R1628P Enables Cdk5 Phosphorylation of LRRK2 and Upregulates Its Kinase Activity.
    Shu Y; Ming J; Zhang P; Wang Q; Jiao F; Tian B
    PLoS One; 2016; 11(3):e0149739. PubMed ID: 26930193
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study.
    Tan EK; Peng R; Teo YY; Tan LC; Angeles D; Ho P; Chen ML; Lin CH; Mao XY; Chang XL; Prakash KM; Liu JJ; Au WL; Le WD; Jankovic J; Burgunder JM; Zhao Y; Wu RM
    Hum Mutat; 2010 May; 31(5):561-8. PubMed ID: 20186690
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Relationship between LRRK2 R1628P polymorphism and Parkinson's disease in Asian populations.
    Zhao H; Kong Z
    Oncotarget; 2016 Jul; 7(30):46890-46898. PubMed ID: 27384489
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Comparing LRRK2 Gly2385Arg carriers with noncarriers.
    Tan EK; Fook-Chong S; Yi Z
    Mov Disord; 2007 Apr; 22(5):749-50. PubMed ID: 17290460
    [No Abstract]   [Full Text] [Related]  

  • 14. Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia.
    Farrer MJ; Stone JT; Lin CH; Dächsel JC; Hulihan MM; Haugarvoll K; Ross OA; Wu RM
    Parkinsonism Relat Disord; 2007 Mar; 13(2):89-92. PubMed ID: 17222580
    [TBL] [Abstract][Full Text] [Related]  

  • 15. LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.
    An XK; Peng R; Li T; Burgunder JM; Wu Y; Chen WJ; Zhang JH; Wang YC; Xu YM; Gou YR; Yuan GG; Zhang ZJ
    Eur J Neurol; 2008 Mar; 15(3):301-5. PubMed ID: 18201193
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The association between the LRRK2 R1628P variant and the risk of Parkinson's disease in Asian: a meta-analysis.
    Wang X; Zhang X; Xue L; Xie A
    Neurosci Lett; 2016 Jun; 623():22-7. PubMed ID: 27133195
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Non-motor symptoms in Chinese Parkinson's disease patients with and without LRRK2 G2385R and R1628P variants.
    Li DW; Gu Z; Wang C; Ma J; Tang BS; Chen SD; Chan P
    J Neural Transm (Vienna); 2015 May; 122(5):661-7. PubMed ID: 25062988
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The LRRK2 G2385R variant is a risk factor for sporadic Parkinson's disease in the Korean population.
    Kim JM; Lee JY; Kim HJ; Kim JS; Shin ES; Cho JH; Park SS; Jeon BS
    Parkinsonism Relat Disord; 2010 Feb; 16(2):85-8. PubMed ID: 19854095
    [TBL] [Abstract][Full Text] [Related]  

  • 19. LRRK2 R1398H polymorphism is associated with decreased risk of Parkinson's disease in a Han Chinese population.
    Chen L; Zhang S; Liu Y; Hong H; Wang H; Zheng Y; Zhou H; Chen J; Xian W; He Y; Li J; Liu Z; Pei Z; Zeng J
    Parkinsonism Relat Disord; 2011 May; 17(4):291-2. PubMed ID: 21159540
    [No Abstract]   [Full Text] [Related]  

  • 20. LRRK2 R1628P increases risk of Parkinson's disease: replication evidence.
    Tan EK; Tan LC; Lim HQ; Li R; Tang M; Yih Y; Pavanni R; Prakash KM; Fook-Chong S; Zhao Y
    Hum Genet; 2008 Oct; 124(3):287-8. PubMed ID: 18781329
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.