BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

463 related articles for article (PubMed ID: 11716303)

  • 1. Biology of the prion gene complex.
    Mastrangelo P; Westaway D
    Biochem Cell Biol; 2001; 79(5):613-28. PubMed ID: 11716303
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Doppel is an N-glycosylated, glycosylphosphatidylinositol-anchored protein. Expression in testis and ectopic production in the brains of Prnp(0/0) mice predisposed to Purkinje cell loss.
    Silverman GL; Qin K; Moore RC; Yang Y; Mastrangelo P; Tremblay P; Prusiner SB; Cohen FE; Westaway D
    J Biol Chem; 2000 Sep; 275(35):26834-41. PubMed ID: 10842180
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prion encephalopathies of animals and humans.
    Prusiner SB
    Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic and infectious prion diseases.
    Prusiner SB
    Arch Neurol; 1993 Nov; 50(11):1129-53. PubMed ID: 8105771
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prion Protein Devoid of the Octapeptide Repeat Region Delays Bovine Spongiform Encephalopathy Pathogenesis in Mice.
    Hara H; Miyata H; Das NR; Chida J; Yoshimochi T; Uchiyama K; Watanabe H; Kondoh G; Yokoyama T; Sakaguchi S
    J Virol; 2018 Jan; 92(1):. PubMed ID: 29046443
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cell-autonomous PrP-Doppel interaction regulates apoptosis in PrP gene-deficient neuronal cells.
    Sakudo A; Lee DC; Nakamura I; Taniuchi Y; Saeki K; Matsumoto Y; Itohara S; Ikuta K; Onodera T
    Biochem Biophys Res Commun; 2005 Jul; 333(2):448-54. PubMed ID: 15950943
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deletion of N-terminal residues 23-88 from prion protein (PrP) abrogates the potential to rescue PrP-deficient mice from PrP-like protein/doppel-induced Neurodegeneration.
    Atarashi R; Nishida N; Shigematsu K; Goto S; Kondo T; Sakaguchi S; Katamine S
    J Biol Chem; 2003 Aug; 278(31):28944-9. PubMed ID: 12759361
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Doppel-induced cerebellar degeneration in transgenic mice.
    Moore RC; Mastrangelo P; Bouzamondo E; Heinrich C; Legname G; Prusiner SB; Hood L; Westaway D; DeArmond SJ; Tremblay P
    Proc Natl Acad Sci U S A; 2001 Dec; 98(26):15288-93. PubMed ID: 11734625
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The use of transgenic mice in the investigation of transmissible spongiform encephalopathies.
    Weissmann C; Fischer M; Raeber A; Büeler H; Sailer A; Shmerling D; Rülicke T; Brandner S; Aguzzi A
    Rev Sci Tech; 1998 Apr; 17(1):278-90. PubMed ID: 9638817
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Abnormal activation of glial cells in the brains of prion protein-deficient mice ectopically expressing prion protein-like protein, PrPLP/Dpl.
    Atarashi R; Sakaguchi S; Shigematsu K; Arima K; Okimura N; Yamaguchi N; Li A; Kopacek J; Katamine S
    Mol Med; 2001 Dec; 7(12):803-9. PubMed ID: 11844868
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Physiological and pathological functions of the prion protein homologue Dpl.
    Behrens A
    Br Med Bull; 2003; 66():35-42. PubMed ID: 14522847
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Normal neurogenesis and scrapie pathogenesis in neural grafts lacking the prion protein homologue Doppel.
    Behrens A; Brandner S; Genoud N; Aguzzi A
    EMBO Rep; 2001 Apr; 2(4):347-52. PubMed ID: 11306558
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular biology and genetics of prion diseases.
    Prusiner SB
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):447-63. PubMed ID: 7913765
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Ninth Datta Lecture. Molecular biology of transmissible spongiform encephalopathies.
    Weissmann C
    FEBS Lett; 1996 Jun; 389(1):3-11. PubMed ID: 8682199
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mouse-hamster chimeric prion protein (PrP) devoid of N-terminal residues 23-88 restores susceptibility to 22L prions, but not to RML prions in PrP-knockout mice.
    Uchiyama K; Miyata H; Yano M; Yamaguchi Y; Imamura M; Muramatsu N; Das NR; Chida J; Hara H; Sakaguchi S
    PLoS One; 2014; 9(10):e109737. PubMed ID: 25330286
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Physiopathology and molecular diagnosis for prion diseases].
    Katamine S
    Rinsho Byori; 2000 May; 48(5):437-41. PubMed ID: 10892292
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prions: pathogenesis and reverse genetics.
    Aguzzi A; Klein MA; Montrasio F; Pekarik V; Brandner S; Furukawa H; Käser P; Röckl C; Glatzel M
    Ann N Y Acad Sci; 2000; 920():140-57. PubMed ID: 11193143
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular genetics of transmissible spongiform encephalopathies: an introduction.
    Weissmann C
    J Toxicol Sci; 2002 May; 27(2):69-77. PubMed ID: 12058449
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The neuropathological phenotype in transgenic mice expressing different prion protein constructs.
    DeArmond SJ; Yang SL; Cayetano-Canlas J; Groth D; Prusiner SB
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):415-23. PubMed ID: 7913760
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.