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.
227 related articles for article (PubMed ID: 19788047)
1. Localization of disease-related PrP in Danish patients with different subtypes of prion disease. Bergström AL; Heegaard PM; Dyrbye H; Lind P; Laursen H Clin Neuropathol; 2009; 28(5):321-32. PubMed ID: 19788047 [TBL] [Abstract][Full Text] [Related]
2. Characterisation of new monoclonal antibodies reacting with prions from both human and animal brain tissues. Cordes H; Bergström AL; Ohm J; Laursen H; Heegaard PM J Immunol Methods; 2008 Sep; 337(2):106-20. PubMed ID: 18657541 [TBL] [Abstract][Full Text] [Related]
3. The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease. Di Fede G; Giaccone G; Limido L; Mangieri M; Suardi S; Puoti G; Morbin M; Mazzoleni G; Ghetti B; Tagliavini F J Neuropathol Exp Neurol; 2007 Feb; 66(2):124-30. PubMed ID: 17278997 [TBL] [Abstract][Full Text] [Related]
4. Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease. Zanusso G; Fiorini M; Ferrari S; Meade-White K; Barbieri I; Brocchi E; Ghetti B; Monaco S J Biol Chem; 2014 Feb; 289(8):4870-81. PubMed ID: 24398683 [TBL] [Abstract][Full Text] [Related]
5. Immunohistochemical localization of 14.3.3 zeta protein in amyloid plaques in human spongiform encephalopathies. Richard M; Biacabe AG; Streichenberger N; Ironside JW; Mohr M; Kopp N; Perret-Liaudet A Acta Neuropathol; 2003 Mar; 105(3):296-302. PubMed ID: 12557018 [TBL] [Abstract][Full Text] [Related]
6. Advances in the detection of prion protein in peripheral tissues of variant Creutzfeldt-Jakob disease patients using paraffin-embedded tissue blotting. Ritchie DL; Head MW; Ironside JW Neuropathol Appl Neurobiol; 2004 Aug; 30(4):360-8. PubMed ID: 15305981 [TBL] [Abstract][Full Text] [Related]
7. [Recent advances in the research of Creutzfeldt-Jakob disease (CJD) and Gerstmann-Strüssler syndrome (GSS)]. Tateishi J Rinsho Shinkeigaku; 1991 Dec; 31(12):1306-8. PubMed ID: 1687809 [TBL] [Abstract][Full Text] [Related]
8. Creutzfeldt-Jakob disease and inclusion body myositis: abundant disease-associated prion protein in muscle. Kovacs GG; Lindeck-Pozza E; Chimelli L; Araújo AQ; Gabbai AA; Ströbel T; Glatzel M; Aguzzi A; Budka H Ann Neurol; 2004 Jan; 55(1):121-5. PubMed ID: 14705121 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. [Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Part II]. Zaborowski A Psychiatr Pol; 2004; 38(2):297-309. PubMed ID: 15307294 [TBL] [Abstract][Full Text] [Related]
12. [A trend of molecular genetics on prion diseases and prion protein]. Muramatsu Y; Shinagawa M Nihon Rinsho; 1993 Sep; 51(9):2494-502. PubMed ID: 8411733 [TBL] [Abstract][Full Text] [Related]
13. Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study. Head MW; Ritchie D; Smith N; McLoughlin V; Nailon W; Samad S; Masson S; Bishop M; McCardle L; Ironside JW Am J Pathol; 2004 Jan; 164(1):143-53. PubMed ID: 14695328 [TBL] [Abstract][Full Text] [Related]
14. The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system. Kitamoto T; Doh-ura K; Muramoto T; Miyazono M; Tateishi J Am J Pathol; 1992 Aug; 141(2):271-7. PubMed ID: 1353945 [TBL] [Abstract][Full Text] [Related]
15. The nosology of Creutzfeldt-Jakob disease and conditions related to the accumulation of PrPCJD in the nervous system. Richardson EP; Masters CL Brain Pathol; 1995 Jan; 5(1):33-41. PubMed ID: 7767489 [TBL] [Abstract][Full Text] [Related]
18. Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease. Glatzel M; Abela E; Maissen M; Aguzzi A N Engl J Med; 2003 Nov; 349(19):1812-20. PubMed ID: 14602879 [TBL] [Abstract][Full Text] [Related]
19. Pathologic prion protein spreading in the peripheral nervous system of a patient with sporadic Creutzfeldt-Jakob disease. Favereaux A; Quadrio I; Vital C; Perret-Liaudet A; Anne O; Laplanche JL; Petry KG; Vital A Arch Neurol; 2004 May; 61(5):747-50. PubMed ID: 15148153 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]