These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 10965160)

  • 1. Polymorphisms of the parkin gene in sporadic Parkinson's disease among Chinese in Taiwan.
    Hu CJ; Sung SM; Liu HC; Lee CC; Tsai CH; Chang JG
    Eur Neurol; 2000; 44(2):90-3. PubMed ID: 10965160
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Polymorphism in the parkin gene in sporadic Parkinson's disease.
    Wang M; Hattori N; Matsumine H; Kobayashi T; Yoshino H; Morioka A; Kitada T; Asakawa S; Minoshima S; Shimizu N; Mizuno Y
    Ann Neurol; 1999 May; 45(5):655-8. PubMed ID: 10319889
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of codon 167 Ser/Asn heterozygosity in the parkin gene with sporadic Parkinson's disease.
    Satoh J; Kuroda Y
    Neuroreport; 1999 Sep; 10(13):2735-9. PubMed ID: 10511432
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.
    Lücking CB; Chesneau V; Lohmann E; Verpillat P; Dulac C; Bonnet AM; Gasparini F; Agid Y; Dürr A; Brice A
    Arch Neurol; 2003 Sep; 60(9):1253-6. PubMed ID: 12975291
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular genetic analysis of the alpha-synuclein and the parkin gene in Parkinson's disease in Finland.
    Autere JM; Hiltunen MJ; Mannermaa AJ; Jäkälä PA; Hartikainen PH; Majamaa K; Alafuzoff I; Soininen HS
    Eur J Neurol; 2002 Sep; 9(5):479-83. PubMed ID: 12220378
    [TBL] [Abstract][Full Text] [Related]  

  • 6. No mutation of G209A in the alpha-synuclein gene in sporadic Parkinson's disease among Taiwan Chinese.
    Hu CJ; Sung SM; Liu H; Chang JG
    Eur Neurol; 1999; 41(2):85-7. PubMed ID: 10023110
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The parkin gene is not involved in late-onset Parkinson's disease.
    Oliveri RL; Zappia M; Annesi G; Bosco D; Annesi F; Spadafora P; Pasqua AA; Tomaino C; Nicoletti G; Pirritano D; Labate A; Gambardella A; Logroscino G; Manobianca G; Epifanio A; Morgante L; Savettieri G; Quattrone A
    Neurology; 2001 Jul; 57(2):359-62. PubMed ID: 11468333
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].
    Hattori N
    Rinsho Shinkeigaku; 2004; 44(4-5):241-62. PubMed ID: 15287506
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease.
    Sinha R; Racette B; Perlmutter JS; Parsian A
    Parkinsonism Relat Disord; 2005 Sep; 11(6):341-7. PubMed ID: 16019250
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
    Abbas N; Lücking CB; Ricard S; Dürr A; Bonifati V; De Michele G; Bouley S; Vaughan JR; Gasser T; Marconi R; Broussolle E; Brefel-Courbon C; Harhangi BS; Oostra BA; Fabrizio E; Böhme GA; Pradier L; Wood NW; Filla A; Meco G; Denefle P; Agid Y; Brice A
    Hum Mol Genet; 1999 Apr; 8(4):567-74. PubMed ID: 10072423
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease.
    Madegowda RH; Kishore A; Anand A
    J Neurol Neurosurg Psychiatry; 2005 Nov; 76(11):1588-90. PubMed ID: 16227559
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Two cases of sporadic juvenile Parkinson's disease caused by homozygous deletion of Parkin gene].
    Ujike H; Yamamoto M; Yamaguchi K; Kanzaki A; Takagi M; Kuroda S
    No To Shinkei; 1999 Dec; 51(12):1061-4. PubMed ID: 10654303
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Parkin gene and its function; a key to understand nigral degeneration].
    Hattori N; Mizuno Y
    Rinsho Shinkeigaku; 1999 Dec; 39(12):1259-61. PubMed ID: 10791092
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Apolipoprotein E (APOE), PARKIN and catechol-O-methyltransferase (COMT) genes and susceptibility to sporadic Parkinson's disease in Finland.
    Eerola J; Launes J; Hellström O; Tienari PJ
    Neurosci Lett; 2002 Sep; 330(3):296-8. PubMed ID: 12270650
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Parkin mutations and susceptibility alleles in late-onset Parkinson's disease.
    Oliveira SA; Scott WK; Martin ER; Nance MA; Watts RL; Hubble JP; Koller WC; Pahwa R; Stern MB; Hiner BC; Ondo WG; Allen FH; Scott BL; Goetz CG; Small GW; Mastaglia F; Stajich JM; Zhang F; Booze MW; Winn MP; Middleton LT; Haines JL; Pericak-Vance MA; Vance JM
    Ann Neurol; 2003 May; 53(5):624-9. PubMed ID: 12730996
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of a risk haplotype of the alpha-synuclein gene in Japanese with sporadic Parkinson's disease.
    Kobayashi H; Ujike H; Hasegawa J; Yamamoto M; Kanzaki A; Sora I
    Mov Disord; 2006 Dec; 21(12):2157-64. PubMed ID: 17078049
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Single-nucleotide polymorphisms in the promoter region of the PARKIN gene and Parkinson's disease.
    Mata IF; Alvarez V; García-Moreira V; Guisasola LM; Ribacoba R; Salvador C; Blázquez M; Sarmiento RG; Lahoz CH; Menes BB; García EC
    Neurosci Lett; 2002 Aug; 329(2):149-52. PubMed ID: 12165399
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetics of Parkinson's disease.
    Gasser T
    Clin Genet; 1998 Oct; 54(4):259-65. PubMed ID: 9831335
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ubiquitination of a new form of alpha-synuclein by parkin from human brain: implications for Parkinson's disease.
    Shimura H; Schlossmacher MG; Hattori N; Frosch MP; Trockenbacher A; Schneider R; Mizuno Y; Kosik KS; Selkoe DJ
    Science; 2001 Jul; 293(5528):263-9. PubMed ID: 11431533
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lack of evidence for association of a parkin promoter polymorphism with early-onset Parkinson's disease in a Chinese population.
    Taylor JM; Wu RM; Lin CH; Delatycki MB; Lockhart PJ
    Parkinsonism Relat Disord; 2009 Feb; 15(2):149-52. PubMed ID: 18387843
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.