BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 12374768)

  • 1. Functional association of the parkin gene promoter with idiopathic Parkinson's disease.
    West AB; Maraganore D; Crook J; Lesnick T; Lockhart PJ; Wilkes KM; Kapatos G; Hardy JA; Farrer MJ
    Hum Mol Genet; 2002 Oct; 11(22):2787-92. PubMed ID: 12374768
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Parkin is linked to the ubiquitin pathway.
    Tanaka K; Suzuki T; Chiba T; Shimura H; Hattori N; Mizuno Y
    J Mol Med (Berl); 2001 Sep; 79(9):482-94. PubMed ID: 11692161
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [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]  

  • 6. 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]  

  • 7. [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]  

  • 8. Identification and characterization of the human parkin gene promoter.
    West A; Farrer M; Petrucelli L; Cookson M; Lockhart P; Hardy J
    J Neurochem; 2001 Sep; 78(5):1146-52. PubMed ID: 11553688
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Identification of a novel gene linked to parkin via a bi-directional promoter.
    West AB; Lockhart PJ; O'Farell C; Farrer MJ
    J Mol Biol; 2003 Feb; 326(1):11-9. PubMed ID: 12547187
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients.
    Shimura H; Hattori N; Kubo S; Yoshikawa M; Kitada T; Matsumine H; Asakawa S; Minoshima S; Yamamura Y; Shimizu N; Mizuno Y
    Ann Neurol; 1999 May; 45(5):668-72. PubMed ID: 10319893
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complex relationship between Parkin mutations and Parkinson disease.
    West A; Periquet M; Lincoln S; Lücking CB; Nicholl D; Bonifati V; Rawal N; Gasser T; Lohmann E; Deleuze JF; Maraganore D; Levey A; Wood N; Dürr A; Hardy J; Brice A; Farrer M;
    Am J Med Genet; 2002 Jul; 114(5):584-91. PubMed ID: 12116199
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Parkin and the molecular pathways of Parkinson's disease.
    Giasson BI; Lee VM
    Neuron; 2001 Sep; 31(6):885-8. PubMed ID: 11580890
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association study of Parkin gene polymorphisms with idiopathic Parkinson disease.
    Oliveira SA; Scott WK; Nance MA; Watts RL; Hubble JP; Koller WC; Lyons KE; Pahwa R; Stern MB; Hiner BC; Jankovic J; Ondo WG; Allen FH; Scott BL; Goetz CG; Small GW; Mastaglia FL; Stajich JM; Zhang F; Booze MW; Reaves JA; Middleton LT; Haines JL; Pericak-Vance MA; Vance JM; Martin ER
    Arch Neurol; 2003 Jul; 60(7):975-80. PubMed ID: 12873854
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Study of methylation levels of parkin gene promoter in Parkinson's disease patients.
    Cai M; Tian J; Zhao GH; Luo W; Zhang BR
    Int J Neurosci; 2011 Sep; 121(9):497-502. PubMed ID: 21663383
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Programmed cell death-2 isoform1 is ubiquitinated by parkin and increased in the substantia nigra of patients with autosomal recessive Parkinson's disease.
    Fukae J; Sato S; Shiba K; Sato K; Mori H; Sharp PA; Mizuno Y; Hattori N
    FEBS Lett; 2009 Feb; 583(3):521-5. PubMed ID: 19146857
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A novel point mutation in parkin gene was identified in an early-onset case of Parkinson's disease].
    Wang T; Liang Z; Sun S; Cao X; Peng H; Cao F; Liu H; Tong E
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):111-3. PubMed ID: 12673578
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lewy bodies and parkinsonism in families with parkin mutations.
    Farrer M; Chan P; Chen R; Tan L; Lincoln S; Hernandez D; Forno L; Gwinn-Hardy K; Petrucelli L; Hussey J; Singleton A; Tanner C; Hardy J; Langston JW
    Ann Neurol; 2001 Sep; 50(3):293-300. PubMed ID: 11558785
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers.
    Pramstaller PP; Schlossmacher MG; Jacques TS; Scaravilli F; Eskelson C; Pepivani I; Hedrich K; Adel S; Gonzales-McNeal M; Hilker R; Kramer PL; Klein C
    Ann Neurol; 2005 Sep; 58(3):411-22. PubMed ID: 16130111
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.