BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 26878132)

  • 41. PMCA-Based Detection of Prions in the Olfactory Mucosa of Patients With Sporadic Creutzfeldt-Jakob Disease.
    Cazzaniga FA; Bistaffa E; De Luca CMG; Portaleone SM; Catania M; Redaelli V; Tramacere I; Bufano G; Rossi M; Caroppo P; Giovagnoli AR; Tiraboschi P; Di Fede G; Eleopra R; Devigili G; Elia AE; Cilia R; Fiorini M; Bongianni M; Salzano G; Celauro L; Quarta FG; Mammana A; Legname G; Tagliavini F; Parchi P; Zanusso G; Giaccone G; Moda F
    Front Aging Neurosci; 2022; 14():848991. PubMed ID: 35401151
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Humanized knock-in mice expressing chimeric prion protein showed varied susceptibility to different human prions.
    Taguchi Y; Mohri S; Ironside JW; Muramoto T; Kitamoto T
    Am J Pathol; 2003 Dec; 163(6):2585-93. PubMed ID: 14633630
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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]  

  • 44. 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]  

  • 45. Development of an Automated Capillary Immunoassay to Detect Prion Glycotypes in Creutzfeldt-Jakob Disease.
    Myskiw J; Lamoureux L; Peterson A; Knox D; Jansen GH; Coulthart MB; Booth SA
    Lab Invest; 2023 Mar; 103(3):100029. PubMed ID: 36925197
    [TBL] [Abstract][Full Text] [Related]  

  • 46. PrP mRNA and protein expression in brain and PrP(c) in CSF in Creutzfeldt-Jakob disease MM1 and VV2.
    Llorens F; Ansoleaga B; Garcia-Esparcia P; Zafar S; Grau-Rivera O; López-González I; Blanco R; Carmona M; Yagüe J; Nos C; Del Río JA; Gelpí E; Zerr I; Ferrer I
    Prion; 2013; 7(5):383-93. PubMed ID: 24047819
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Involvement of the peripheral nervous system in human prion diseases including dural graft associated Creutzfeldt-Jakob disease.
    Ishida C; Okino S; Kitamoto T; Yamada M
    J Neurol Neurosurg Psychiatry; 2005 Mar; 76(3):325-9. PubMed ID: 15716520
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Update: Dura Mater Graft-Associated Creutzfeldt-Jakob Disease - Japan, 1975-2017.
    Ae R; Hamaguchi T; Nakamura Y; Yamada M; Tsukamoto T; Mizusawa H; Belay ED; Schonberger LB
    MMWR Morb Mortal Wkly Rep; 2018 Mar; 67(9):274-278. PubMed ID: 29518068
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Insight into the frequent occurrence of dura mater graft-associated Creutzfeldt-Jakob disease in Japan.
    Hamaguchi T; Sakai K; Noguchi-Shinohara M; Nozaki I; Takumi I; Sanjo N; Sadakane A; Nakamura Y; Kitamoto T; Saito N; Mizusawa H; Yamada M
    J Neurol Neurosurg Psychiatry; 2013 Oct; 84(10):1171-5. PubMed ID: 23595947
    [TBL] [Abstract][Full Text] [Related]  

  • 50. 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]  

  • 51. Co-existence of PrP
    Cali I; Puoti G; Smucny J; Curtiss PM; Cracco L; Kitamoto T; Occhipinti R; Cohen ML; Appleby BS; Gambetti P
    Sci Rep; 2020 Jan; 10(1):1503. PubMed ID: 32001774
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.
    Rodríguez-Martínez AB; Garrido JM; Zarranz JJ; Arteagoitia JM; de Pancorbo MM; Atarés B; Bilbao MJ; Ferrer I; Juste RA
    BMC Neurol; 2010 Oct; 10():99. PubMed ID: 20973975
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Large-scale validation of skin prion seeding activity as a biomarker for diagnosis of prion diseases.
    Zhang W; Orrú CD; Foutz A; Ding M; Yuan J; Shah SZA; Zhang J; Kotobelli K; Gerasimenko M; Gilliland T; Chen W; Tang M; Cohen M; Safar J; Xu B; Hong DJ; Cui L; Hughson AG; Schonberger LB; Tatsuoka C; Chen SG; Greenlee JJ; Wang Z; Appleby BS; Caughey B; Zou WQ
    Acta Neuropathol; 2024 Jan; 147(1):17. PubMed ID: 38231266
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Artificial strain of human prions created in vitro.
    Kim C; Xiao X; Chen S; Haldiman T; Smirnovas V; Kofskey D; Warren M; Surewicz K; Maurer NR; Kong Q; Surewicz W; Safar JG
    Nat Commun; 2018 Jun; 9(1):2166. PubMed ID: 29867164
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques.
    Bayazid R; Orru' C; Aslam R; Cohen Y; Silva-Rohwer A; Lee SK; Occhipinti R; Kong Q; Shetty S; Cohen ML; Caughey B; Schonberger LB; Appleby BS; Cali I
    Acta Neuropathol; 2023 Jul; 146(1):121-143. PubMed ID: 37156880
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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]  

  • 59. Region-specific protein misfolding cyclic amplification reproduces brain tropism of prion strains.
    Privat N; Levavasseur E; Yildirim S; Hannaoui S; Brandel JP; Laplanche JL; Béringue V; Seilhean D; Haïk S
    J Biol Chem; 2017 Oct; 292(40):16688-16696. PubMed ID: 28821618
    [TBL] [Abstract][Full Text] [Related]  

  • 60. In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP
    Wang Z; Yuan J; Shen P; Abskharon R; Lang Y; Dang J; Adornato A; Xu L; Chen J; Feng J; Moudjou M; Kitamoto T; Lee HG; Kim YS; Langeveld J; Appleby B; Ma J; Kong Q; Petersen RB; Zou WQ; Cui L
    Mol Neurobiol; 2019 Aug; 56(8):5456-5469. PubMed ID: 30612334
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.