BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

81 related articles for article (PubMed ID: 19482505)

  • 1. GIGYF2 mutations are not a frequent cause of familial Parkinson's disease.
    Di Fonzo A; Fabrizio E; Thomas A; Fincati E; Marconi R; Tinazzi M; Breedveld GJ; Simons EJ; Chien HF; Ferreira JJ; Horstink MW; Abbruzzese G; Borroni B; Cossu G; Dalla Libera A; Fabbrini G; Guidi M; De Mari M; Lopiano L; Martignoni E; Marini P; Onofrj M; Padovani A; Stocchi F; Toni V; Sampaio C; Barbosa ER; Meco G; ; Oostra BA; Bonifati V
    Parkinsonism Relat Disord; 2009 Nov; 15(9):703-5. PubMed ID: 19482505
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Follow-up study of the GIGYF2 gene in French families with Parkinson's disease.
    Lesage S; Condroyer C; Lohman E; Troiano A; Tison F; Viallet F; Damier P; Tranchant C; Vidhaillet M; Ouvrard-Hernandez AM; Dürr A; Brice A;
    Neurobiol Aging; 2010 Jun; 31(6):1069-71; discussion 1072-4. PubMed ID: 20004041
    [TBL] [Abstract][Full Text] [Related]  

  • 3. GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population.
    Meeus B; Nuytemans K; Crosiers D; Engelborghs S; Pals P; Pickut B; Peeters K; Mattheijssens M; Corsmit E; Cras P; De Deyn PP; Theuns J; Van Broeckhoven C
    Neurobiol Aging; 2011 Feb; 32(2):308-12. PubMed ID: 19321232
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease.
    Lautier C; Goldwurm S; Dürr A; Giovannone B; Tsiaras WG; Pezzoli G; Brice A; Smith RJ
    Am J Hum Genet; 2008 Apr; 82(4):822-33. PubMed ID: 18358451
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Reported mutations in GIGYF2 are not a common cause of Parkinson's disease.
    Vilariño-Güell C; Ross OA; Soto AI; Farrer MJ; Haugarvoll K; Aasly JO; Uitti RJ; Wszolek ZK
    Mov Disord; 2009 Mar; 24(4):619-20. PubMed ID: 19133664
    [No Abstract]   [Full Text] [Related]  

  • 6. GIGYF2 Asn56Ser mutation is rare in Chinese Parkinson's disease patients.
    Zhang Y; Zheng L; Zhang T; Wang Y; Xiao Q; Fei QZ; Cui PJ; Cao L; Chen SD
    Neurosci Lett; 2009 Oct; 463(3):172-5. PubMed ID: 19638301
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese population.
    Wang L; Guo JF; Zhang WW; Xu Q; Zuo X; Shi CH; Luo LZ; Liu J; Hu L; Hu YC; She L; Jiang H; Yan XX; Xia K; Pan Q; Tang BS
    Neurosci Lett; 2010 Apr; 473(2):131-5. PubMed ID: 20178831
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Low frequency of alpha-synuclein mutations in familial Parkinson's disease.
    Farrer M; Wavrant-De Vrieze F; Crook R; Boles L; Perez-Tur J; Hardy J; Johnson WG; Steele J; Maraganore D; Gwinn K; Lynch T
    Ann Neurol; 1998 Mar; 43(3):394-7. PubMed ID: 9506559
    [TBL] [Abstract][Full Text] [Related]  

  • 9. No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients.
    Li L; Funayama M; Tomiyama H; Li Y; Yoshino H; Sasaki R; Kokubo Y; Kuzuhara S; Mizuno Y; Hattori N
    Neurosci Lett; 2010 Aug; 479(3):245-8. PubMed ID: 20641165
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A clinical and genetic study of familial Parkinson's disease.
    Maraganore DM; Harding AE; Marsden CD
    Mov Disord; 1991; 6(3):205-11. PubMed ID: 1922124
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of the GIGYF2 gene in familial and sporadic Parkinson disease in the Spanish population.
    Samaranch L; Lorenzo E; Pastor MA; Riverol M; Luquin MR; Rodríguez-Oroz MC; Obeso JA; Pastor P
    Eur J Neurol; 2010 Feb; 17(2):321-5. PubMed ID: 19845746
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
    Gasser T; Müller-Myhsok B; Wszolek ZK; Oehlmann R; Calne DB; Bonifati V; Bereznai B; Fabrizio E; Vieregge P; Horstmann RD
    Nat Genet; 1998 Mar; 18(3):262-5. PubMed ID: 9500549
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene.
    Guella I; Pistocchi A; Asselta R; Rimoldi V; Ghilardi A; Sironi F; Trotta L; Primignani P; Zini M; Zecchinelli A; Coviello D; Pezzoli G; Del Giacco L; Duga S; Goldwurm S
    Neurobiol Aging; 2011 Nov; 32(11):1994-2005. PubMed ID: 20060621
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.
    Grimes DA; Han F; Panisset M; Racacho L; Xiao F; Zou R; Westaff K; Bulman DE
    Mov Disord; 2006 Jul; 21(7):906-9. PubMed ID: 16532445
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Study of familial Parkinson's disease in Russia, Uzbekistan, and Zambia.
    Atadzhanov M; Zumla A; Mwaba P
    Postgrad Med J; 2005 Feb; 81(952):117-21. PubMed ID: 15701745
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s disease.
    Wang L; Guo JF; Zhang WW; Xu Q; Zuo X; Shi CH; Luo LZ; Liu J; Hu L; Hu YC; Yan XX; Tang BS
    J Clin Neurosci; 2011 Dec; 18(12):1699-701. PubMed ID: 22115759
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An analysis of genetic studies of Parkinson's disease in Africa.
    Okubadejo NU
    Parkinsonism Relat Disord; 2008; 14(3):177-82. PubMed ID: 17881276
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Haplotype analysis of the PARK 11 gene, GIGYF2, in sporadic Parkinson's disease.
    Sutherland GT; Siebert GA; Newman JR; Silburn PA; Boyle RS; O'Sullivan JD; Mellick GD
    Mov Disord; 2009 Feb; 24(3):449-52. PubMed ID: 19117363
    [TBL] [Abstract][Full Text] [Related]  

  • 19. GIGYF2 Asn56Ser and Asn457Thr mutations in Parkinson disease patients.
    Guo Y; Jankovic J; Zhu S; Le W; Song Z; Xie W; Liao D; Yang H; Deng H
    Neurosci Lett; 2009 May; 454(3):209-11. PubMed ID: 19429085
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations.
    Tan EK; Lin CH; Tai CH; Tan LC; Chen ML; Li R; Lim HQ; Pavanni R; Yuen Y; Prakash KM; Zhao Y; Wu RM
    Hum Genet; 2009 Sep; 126(3):425-30. PubMed ID: 19449032
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.