BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

306 related articles for article (PubMed ID: 17562432)

  • 1. The prion protein family: diversity, rivalry, and dysfunction.
    Watts JC; Westaway D
    Biochim Biophys Acta; 2007 Jun; 1772(6):654-72. PubMed ID: 17562432
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Small is not beautiful: antagonizing functions for the prion protein PrP(C) and its homologue Dpl.
    Behrens A; Aguzzi A
    Trends Neurosci; 2002 Mar; 25(3):150-4. PubMed ID: 11852147
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The prion gene complex encoding PrP(C) and Doppel: insights from mutational analysis.
    Mastrangelo P; Westaway D
    Gene; 2001 Sep; 275(1):1-18. PubMed ID: 11574147
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The CNS glycoprotein Shadoo has PrP(C)-like protective properties and displays reduced levels in prion infections.
    Watts JC; Drisaldi B; Ng V; Yang J; Strome B; Horne P; Sy MS; Yoong L; Young R; Mastrangelo P; Bergeron C; Fraser PE; Carlson GA; Mount HT; Schmitt-Ulms G; Westaway D
    EMBO J; 2007 Sep; 26(17):4038-50. PubMed ID: 17703189
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel.
    Moore RC; Lee IY; Silverman GL; Harrison PM; Strome R; Heinrich C; Karunaratne A; Pasternak SH; Chishti MA; Liang Y; Mastrangelo P; Wang K; Smit AF; Katamine S; Carlson GA; Cohen FE; Prusiner SB; Melton DW; Tremblay P; Hood LE; Westaway D
    J Mol Biol; 1999 Oct; 292(4):797-817. PubMed ID: 10525406
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Expression of doppel in the CNS of mice does not modulate transmissible spongiform encephalopathy disease.
    Tuzi NL; Gall E; Melton D; Manson JC
    J Gen Virol; 2002 Mar; 83(Pt 3):705-711. PubMed ID: 11842265
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Role of the prion protein family in the gonads.
    Allais-Bonnet A; Pailhoux E
    Front Cell Dev Biol; 2014; 2():56. PubMed ID: 25364761
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular biology of prion protein and its first homologous protein.
    Sakaguchi S
    J Med Invest; 2007 Aug; 54(3-4):211-23. PubMed ID: 17878669
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Understanding the natural variability of prion diseases.
    Geissen M; Krasemann S; Matschke J; Glatzel M
    Vaccine; 2007 Jul; 25(30):5631-6. PubMed ID: 17391814
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Absence of Strong Genetic Linkage Disequilibrium between Single Nucleotide Polymorphisms (SNPs) in the Prion Protein Gene (
    Won SY; Kim YC; Do K; Jeong BH
    Genes (Basel); 2020 May; 11(5):. PubMed ID: 32392732
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prion proteins: physiological functions and role in neurological disorders.
    Hu W; Kieseier B; Frohman E; Eagar TN; Rosenberg RN; Hartung HP; Stüve O
    J Neurol Sci; 2008 Jan; 264(1-2):1-8. PubMed ID: 17707411
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The prion's elusive reason for being.
    Aguzzi A; Baumann F; Bremer J
    Annu Rev Neurosci; 2008; 31():439-77. PubMed ID: 18558863
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Is prnt a pseudogene? Identification of ram Prt in testis and ejaculated spermatozoa.
    Pimenta J; Domingos A; Santos P; Marques CC; Cantante C; Santos A; Barbas JP; Baptista MC; Horta AE; Viegas A; Mesquita P; Gonçalves J; Fontes CA; Prates JA; Pereira RM
    PLoS One; 2012; 7(8):e42957. PubMed ID: 22937002
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular approaches to mechanisms of prion diseases.
    Bratosiewicz-Wasik J; Wasik TJ; Liberski PP
    Folia Neuropathol; 2004; 42 Suppl A():33-46. PubMed ID: 15449458
    [TBL] [Abstract][Full Text] [Related]  

  • 15. In vitro amplification of scrapie and chronic wasting disease PrP(res) using baculovirus-expressed recombinant PrP as substrate.
    Faburay B; Tark D; Kanthasamy AG; Richt JA
    Prion; 2014; 8(6):393-403. PubMed ID: 25495764
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Study on the toxic mechanism of prion protein peptide 106-126 in neuronal and non neuronal cells.
    Dupiereux I; Zorzi W; Rachidi W; Zorzi D; Pierard O; Lhereux B; Heinen E; Elmoualij B
    J Neurosci Res; 2006 Aug; 84(3):637-46. PubMed ID: 16786576
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Prions and their biology].
    Gasset M; Westaway D
    Rev Neurol; 2000 Jul 16-31; 31(2):129-32. PubMed ID: 10951668
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mammalian prion proteins: enigma, variation and vaccination.
    Westaway D; Carlson GA
    Trends Biochem Sci; 2002 Jun; 27(6):301-7. PubMed ID: 12069790
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
    Schmitz M; Lüllmann K; Zafar S; Ebert E; Wohlhage M; Oikonomou P; Schlomm M; Mitrova E; Beekes M; Zerr I
    Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polo-like kinase 3 (PLK3) mediates the clearance of the accumulated PrP mutants transiently expressed in cultured cells and pathogenic PrP(Sc) in prion infected cell line via protein interaction.
    Wang H; Tian C; Fan XY; Chen LN; Lv Y; Sun J; Zhao YJ; Zhang LB; Wang J; Shi Q; Gao C; Chen C; Shao QX; Dong XP
    Int J Biochem Cell Biol; 2015 May; 62():24-35. PubMed ID: 25724737
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.