BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

251 related articles for article (PubMed ID: 25331173)

  • 21. Variably protease-sensitive prionopathy with methionine homozygosity at codon 129 in the prion protein gene.
    Clemmensen FK; Areskeviciute A; Lund EL; Roos P
    BMJ Case Rep; 2024 Feb; 17(2):. PubMed ID: 38388201
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Human prion diseases: surgical lessons learned from iatrogenic prion transmission.
    Bonda DJ; Manjila S; Mehndiratta P; Khan F; Miller BR; Onwuzulike K; Puoti G; Cohen ML; Schonberger LB; Cali I
    Neurosurg Focus; 2016 Jul; 41(1):E10. PubMed ID: 27364252
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A comparative study of abnormal prion protein isoforms between Gerstmann-Sträussler-Scheinker syndrome and Creutzfeldt-Jakob disease.
    Furukawa H; Doh-ura K; Kikuchi H; Tateishi J; Iwaki T
    J Neurol Sci; 1998 Jun; 158(1):71-5. PubMed ID: 9667781
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects.
    Jansen C; Parchi P; Capellari S; Ibrahim-Verbaas CA; Schuur M; Strammiello R; Corrado P; Bishop MT; van Gool WA; Verbeek MM; Baas F; van Saane W; Spliet WG; Jansen GH; van Duijn CM; Rozemuller AJ
    PLoS One; 2012; 7(4):e36333. PubMed ID: 22558438
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prions.
    Saverioni D; Notari S; Capellari S; Poggiolini I; Giese A; Kretzschmar HA; Parchi P
    J Biol Chem; 2013 Sep; 288(39):27972-85. PubMed ID: 23897825
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Towards authentic transgenic mouse models of heritable PrP prion diseases.
    Watts JC; Giles K; Bourkas ME; Patel S; Oehler A; Gavidia M; Bhardwaj S; Lee J; Prusiner SB
    Acta Neuropathol; 2016 Oct; 132(4):593-610. PubMed ID: 27350609
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission properties.
    Diack AB; Ritchie DL; Peden AH; Brown D; Boyle A; Morabito L; Maclennan D; Burgoyne P; Jansen C; Knight RS; Piccardo P; Ironside JW; Manson JC
    Emerg Infect Dis; 2014 Dec; 20(12):1969-79. PubMed ID: 25418327
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein.
    Zou WQ; Puoti G; Xiao X; Yuan J; Qing L; Cali I; Shimoji M; Langeveld JP; Castellani R; Notari S; Crain B; Schmidt RE; Geschwind M; Dearmond SJ; Cairns NJ; Dickson D; Honig L; Torres JM; Mastrianni J; Capellari S; Giaccone G; Belay ED; Schonberger LB; Cohen M; Perry G; Kong Q; Parchi P; Tagliavini F; Gambetti P
    Ann Neurol; 2010 Aug; 68(2):162-72. PubMed ID: 20695009
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Variably protease-sensitive prionopathy mimicking frontotemporal dementia.
    Aizpurua M; Selvackadunco S; Yull H; Kipps CM; Ironside JW; Bodi I
    Neuropathology; 2019 Apr; 39(2):135-140. PubMed ID: 30847986
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Allelic origin of protease-sensitive and protease-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease with the P102L mutation.
    Monaco S; Fiorini M; Farinazzo A; Ferrari S; Gelati M; Piccardo P; Zanusso G; Ghetti B
    PLoS One; 2012; 7(2):e32382. PubMed ID: 22384235
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Human prion diseases: from Kuru to variant Creutzfeldt-Jakob disease.
    Sikorska B; Liberski PP
    Subcell Biochem; 2012; 65():457-96. PubMed ID: 23225013
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures.
    Cassard H; Huor A; Espinosa JC; Douet JY; Lugan S; Aron N; Vilette D; Delisle MB; Marín-Moreno A; Peran P; Beringue V; Torres JM; Ironside JW; Andreoletti O
    mBio; 2020 Jun; 11(3):. PubMed ID: 32546613
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.
    Faucheux BA; Morain E; Diouron V; Brandel JP; Salomon D; Sazdovitch V; Privat N; Laplanche JL; Hauw JJ; Haïk S
    Neuropathol Appl Neurobiol; 2011 Aug; 37(5):500-12. PubMed ID: 21450052
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular pathogenesis of sporadic prion diseases in man.
    Safar JG
    Prion; 2012; 6(2):108-15. PubMed ID: 22421210
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Sporadic Creutzfeldt-Jakob disease: Real-Time Quaking Induced Conversion (RT-QuIC) assay represents a major diagnostic advance.
    Cazzaniga FA; Bistaffa E; De Luca CMG; Bufano G; Indaco A; Giaccone G; Moda F
    Eur J Histochem; 2021 Oct; 65(s1):. PubMed ID: 34657408
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.
    Schoch G; Seeger H; Bogousslavsky J; Tolnay M; Janzer RC; Aguzzi A; Glatzel M
    PLoS Med; 2006 Feb; 3(2):e14. PubMed ID: 16354106
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Variant CJD. 18 years of research and surveillance.
    Diack AB; Head MW; McCutcheon S; Boyle A; Knight R; Ironside JW; Manson JC; Will RG
    Prion; 2014; 8(4):286-95. PubMed ID: 25495404
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Variably Protease-sensitive Prionopathy in a Middle-aged Man With Rapidly Progressive Dementia.
    Huang J; Cohen M; Safar J; Auchus AP
    Cogn Behav Neurol; 2021 Sep; 34(3):220-225. PubMed ID: 34473674
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Re-assessment of PrP(Sc) distribution in sporadic and variant CJD.
    Rubenstein R; Chang B
    PLoS One; 2013; 8(7):e66352. PubMed ID: 23843953
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.