BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 17893675)

  • 1. A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule.
    Notari S; Capellari S; Langeveld J; Giese A; Strammiello R; Gambetti P; Kretzschmar HA; Parchi P
    Lab Invest; 2007 Nov; 87(11):1103-12. PubMed ID: 17893675
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease.
    Polymenidou M; Stoeck K; Glatzel M; Vey M; Bellon A; Aguzzi A
    Lancet Neurol; 2005 Dec; 4(12):805-14. PubMed ID: 16297838
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease.
    Head MW; Northcott V; Rennison K; Ritchie D; McCardle L; Bunn TJ; McLennan NF; Ironside JW; Tullo AB; Bonshek RE
    Invest Ophthalmol Vis Sci; 2003 Jan; 44(1):342-6. PubMed ID: 12506094
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chronic wasting disease of elk and deer and Creutzfeldt-Jakob disease: comparative analysis of the scrapie prion protein.
    Xie Z; O'Rourke KI; Dong Z; Jenny AL; Langenberg JA; Belay ED; Schonberger LB; Petersen RB; Zou W; Kong Q; Gambetti P; Chen SG
    J Biol Chem; 2006 Feb; 281(7):4199-206. PubMed ID: 16338930
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes.
    Ward A; Hollister JR; McNally K; Ritchie DL; Zanusso G; Priola SA
    Acta Neuropathol Commun; 2020 Jun; 8(1):83. PubMed ID: 32517816
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Beyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob disease.
    Uro-Coste E; Cassard H; Simon S; Lugan S; Bilheude JM; Perret-Liaudet A; Ironside JW; Haik S; Basset-Leobon C; Lacroux C; Peoch' K; Streichenberger N; Langeveld J; Head MW; Grassi J; Hauw JJ; Schelcher F; Delisle MB; Andréoletti O
    PLoS Pathog; 2008 Mar; 4(3):e1000029. PubMed ID: 18389084
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics.
    Cali I; Castellani R; Alshekhlee A; Cohen Y; Blevins J; Yuan J; Langeveld JP; Parchi P; Safar JG; Zou WQ; Gambetti P
    Brain; 2009 Oct; 132(Pt 10):2643-58. PubMed ID: 19734292
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Classification of sporadic Creutzfeldt-Jakob disease revisited.
    Cali I; Castellani R; Yuan J; Al-Shekhlee A; Cohen ML; Xiao X; Moleres FJ; Parchi P; Zou WQ; Gambetti P
    Brain; 2006 Sep; 129(Pt 9):2266-77. PubMed ID: 16923954
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease.
    Notari S; Strammiello R; Capellari S; Giese A; Cescatti M; Grassi J; Ghetti B; Langeveld JP; Zou WQ; Gambetti P; Kretzschmar HA; Parchi P
    J Biol Chem; 2008 Nov; 283(45):30557-65. PubMed ID: 18753138
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of Conformational Stability of Abnormal Prion Protein Aggregates across the Spectrum of Creutzfeldt-Jakob Disease Prions.
    Cescatti M; Saverioni D; Capellari S; Tagliavini F; Kitamoto T; Ironside J; Giese A; Parchi P
    J Virol; 2016 Jul; 90(14):6244-6254. PubMed ID: 27122583
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association of an 11-12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases.
    Satoh K; Muramoto T; Tanaka T; Kitamoto N; Ironside JW; Nagashima K; Yamada M; Sato T; Mohri S; Kitamoto T
    J Gen Virol; 2003 Oct; 84(Pt 10):2885-2893. PubMed ID: 13679624
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease.
    Zou WQ; Capellari S; Parchi P; Sy MS; Gambetti P; Chen SG
    J Biol Chem; 2003 Oct; 278(42):40429-36. PubMed ID: 12917418
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular classification of sporadic Creutzfeldt-Jakob disease.
    Hill AF; Joiner S; Wadsworth JD; Sidle KC; Bell JE; Budka H; Ironside JW; Collinge J
    Brain; 2003 Jun; 126(Pt 6):1333-46. PubMed ID: 12764055
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone.
    Cali I; Miller CJ; Parisi JE; Geschwind MD; Gambetti P; Schonberger LB
    Acta Neuropathol Commun; 2015 Jun; 3():37. PubMed ID: 26108478
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients.
    Moore RA; Head MW; Ironside JW; Ritchie DL; Zanusso G; Choi YP; Priola SA
    PLoS Pathog; 2016 Feb; 12(2):e1005416. PubMed ID: 26840342
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease.
    Yull HM; Ritchie DL; Langeveld JP; van Zijderveld FG; Bruce ME; Ironside JW; Head MW
    Am J Pathol; 2006 Jan; 168(1):151-7. PubMed ID: 16400018
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Monoclonal antibody against a peptide of human prion protein discriminates between Creutzfeldt-Jacob's disease-affected and normal brain tissue.
    Curin Serbec V; Bresjanac M; Popovic M; Pretnar Hartman K; Galvani V; Rupreht R; Cernilec M; Vranac T; Hafner I; Jerala R
    J Biol Chem; 2004 Jan; 279(5):3694-8. PubMed ID: 14593100
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two-dimensional mapping of three phenotype-associated isoforms of the prion protein in sporadic Creutzfeldt-Jakob disease.
    Zanusso G; Righetti PG; Ferrari S; Terrin L; Farinazzo A; Cardone F; Pocchiari M; Rizzuto N; Monaco S
    Electrophoresis; 2002 Jan; 23(2):347-55. PubMed ID: 11840543
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature.
    Rossi M; Saverioni D; Di Bari M; Baiardi S; Lemstra AW; Pirisinu L; Capellari S; Rozemuller A; Nonno R; Parchi P
    Acta Neuropathol Commun; 2017 Nov; 5(1):87. PubMed ID: 29169405
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain.
    Puoti G; Giaccone G; Rossi G; Canciani B; Bugiani O; Tagliavini F
    Neurology; 1999 Dec; 53(9):2173-6. PubMed ID: 10599800
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.