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 *

337 related articles for article (PubMed ID: 12764055)

  • 21. 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]  

  • 22. 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]  

  • 23. Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification.
    Parchi P; Strammiello R; Notari S; Giese A; Langeveld JP; Ladogana A; Zerr I; Roncaroli F; Cras P; Ghetti B; Pocchiari M; Kretzschmar H; Capellari S
    Acta Neuropathol; 2009 Nov; 118(5):659-71. PubMed ID: 19718500
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular Subtyping of PrP
    Klug GM; Lewis V; Collins SJ
    Methods Mol Biol; 2017; 1658():347-354. PubMed ID: 28861800
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Type 1 and type 2 human PrPSc have different aggregation sizes in methionine homozygotes with sporadic, iatrogenic and variant Creutzfeldt-Jakob disease.
    Kobayashi A; Satoh S; Ironside JW; Mohri S; Kitamoto T
    J Gen Virol; 2005 Jan; 86(Pt 1):237-240. PubMed ID: 15604452
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel phenotype of sporadic Creutzfeldt-Jakob disease.
    Giaccone G; Di Fede G; Mangieri M; Limido L; Capobianco R; Suardi S; Grisoli M; Binelli S; Fociani P; Bugiani O; Tagliavini F
    J Neurol Neurosurg Psychiatry; 2007 Dec; 78(12):1379-82. PubMed ID: 18024694
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British woman.
    Mead S; Joiner S; Desbruslais M; Beck JA; O'Donoghue M; Lantos P; Wadsworth JD; Collinge J
    Arch Neurol; 2007 Dec; 64(12):1780-4. PubMed ID: 18071044
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.
    Parchi P; Cescatti M; Notari S; Schulz-Schaeffer WJ; Capellari S; Giese A; Zou WQ; Kretzschmar H; Ghetti B; Brown P
    Brain; 2010 Oct; 133(10):3030-42. PubMed ID: 20823086
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. A traceback phenomenon can reveal the origin of prion infection.
    Kobayashi A; Asano M; Mohri S; Kitamoto T
    Neuropathology; 2009 Oct; 29(5):619-24. PubMed ID: 19659941
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type.
    Cracco L; Notari S; Cali I; Sy MS; Chen SG; Cohen ML; Ghetti B; Appleby BS; Zou WQ; Caughey B; Safar JG; Gambetti P
    Sci Rep; 2017 Jan; 7():38280. PubMed ID: 28091514
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles.
    Lewis V; Hill AF; Klug GM; Boyd A; Masters CL; Collins SJ
    Neurology; 2005 Jul; 65(1):113-8. PubMed ID: 16009895
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Deciphering the pathogenesis of sporadic Creutzfeldt-Jakob disease with codon 129 M/V and type 2 abnormal prion protein.
    Kobayashi A; Iwasaki Y; Otsuka H; Yamada M; Yoshida M; Matsuura Y; Mohri S; Kitamoto T
    Acta Neuropathol Commun; 2013 Nov; 1():74. PubMed ID: 24252157
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The prion protein preference of sporadic Creutzfeldt-Jakob disease subtypes.
    Klemm HM; Welton JM; Masters CL; Klug GM; Boyd A; Hill AF; Collins SJ; Lawson VA
    J Biol Chem; 2012 Oct; 287(43):36465-72. PubMed ID: 22930754
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease.
    Ironside JW; Head MW
    Curr Top Microbiol Immunol; 2004; 284():133-59. PubMed ID: 15148991
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.
    Parchi P; Capellari S; Gambetti P
    Microsc Res Tech; 2000 Jul; 50(1):16-25. PubMed ID: 10871544
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular typing of PrPres in human sporadic CJD brain tissue.
    Lewis V; Klug GM; Hill AF; Collins SJ
    Methods Mol Biol; 2008; 459():241-7. PubMed ID: 18576159
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.