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 *

168 related articles for article (PubMed ID: 1352391)

  • 1. Presence of prion protein in peripheral tissues of Libyan Jews with Creutzfeldt-Jakob disease.
    Meiner Z; Halimi M; Polakiewicz RD; Prusiner SB; Gabizon R
    Neurology; 1992 Jul; 42(7):1355-60. PubMed ID: 1352391
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetics and biochemistry of Creutzfeldt-Jakob disease in Libyan Jews.
    Gabizon R; Halimi M; Meiner Z
    Biomed Pharmacother; 1994; 48(8-9):385-90. PubMed ID: 7858176
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease.
    Gabizon R; Rosenman H; Meiner Z; Kahana I; Kahana E; Shugart Y; Ott J; Prusiner SB
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):385-90. PubMed ID: 7913755
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prion protein with an E200K mutation displays properties similar to those of the cellular isoform PrP(C).
    Rosenmann H; Talmor G; Halimi M; Yanai A; Gabizon R; Meiner Z
    J Neurochem; 2001 Mar; 76(6):1654-62. PubMed ID: 11259483
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews.
    Meiner Z; Gabizon R; Prusiner SB
    Medicine (Baltimore); 1997 Jul; 76(4):227-37. PubMed ID: 9279329
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease.
    Gabizon R; Telling G; Meiner Z; Halimi M; Kahana I; Prusiner SB
    Nat Med; 1996 Jan; 2(1):59-64. PubMed ID: 8564843
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).
    Gabizon R; Rosenmann H; Meiner Z; Kahana I; Kahana E; Shugart Y; Ott J; Prusiner SB
    Am J Hum Genet; 1993 Oct; 53(4):828-35. PubMed ID: 8105682
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease.
    Hsiao K; Meiner Z; Kahana E; Cass C; Kahana I; Avrahami D; Scarlato G; Abramsky O; Prusiner SB; Gabizon R
    N Engl J Med; 1991 Apr; 324(16):1091-7. PubMed ID: 2008182
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins.
    Serban D; Taraboulos A; DeArmond SJ; Prusiner SB
    Neurology; 1990 Jan; 40(1):110-7. PubMed ID: 1967489
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin.
    Korczyn AD; Chapman J; Goldfarb LG; Brown P; Gajdusek DC
    Ann N Y Acad Sci; 1991; 640():171-6. PubMed ID: 1685643
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clusterin solubility and aggregation in Creutzfeldt-Jakob disease.
    Freixes M; Puig B; Rodríguez A; Torrejón-Escribano B; Blanco R; Ferrer I
    Acta Neuropathol; 2004 Oct; 108(4):295-301. PubMed ID: 15235804
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease.
    Kitamoto T; Shin RW; Doh-ura K; Tomokane N; Miyazono M; Muramoto T; Tateishi J
    Am J Pathol; 1992 Jun; 140(6):1285-94. PubMed ID: 1351366
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular biology of prions causing infectious and genetic encephalopathies of humans as well as scrapie of sheep and BSE of cattle.
    Prusiner SB
    Dev Biol Stand; 1991; 75():55-74. PubMed ID: 1686599
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Adenosine A1 receptor protein levels and activity is increased in the cerebral cortex in Creutzfeldt-Jakob disease and in bovine spongiform encephalopathy-infected bovine-PrP mice.
    Rodríguez A; Martín M; Albasanz JL; Barrachina M; Espinosa JC; Torres JM; Ferrer I
    J Neuropathol Exp Neurol; 2006 Oct; 65(10):964-75. PubMed ID: 17021401
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inherited prion disease (PrP lysine 200) in Britain: two case reports.
    Collinge J; Palmer MS; Campbell T; Sidle KC; Carroll D; Harding A
    BMJ; 1993 Jan; 306(6873):301-2. PubMed ID: 8461647
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques.
    Ishida C; Kakishima A; Okino S; Furukawa Y; Kano M; Oda Y; Nakanishi I; Makifuchi T; Kitamoto T; Yamada M
    Neurology; 2003 Feb; 60(3):514-7. PubMed ID: 12578942
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.
    Galeno R; Di Bari MA; Nonno R; Cardone F; Sbriccoli M; Graziano S; Ingrosso L; Fiorini M; Valanzano A; Pasini G; Poleggi A; Vinci R; Ladogana A; Puopolo M; Monaco S; Agrimi U; Zanusso G; Pocchiari M
    J Virol; 2017 Jun; 91(11):. PubMed ID: 28298604
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.
    Kobayashi A; Parchi P; Yamada M; Mohri S; Kitamoto T
    Neuropathology; 2016 Jun; 36(3):305-10. PubMed ID: 26669818
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.