ExLibris header image
SFX Logo
Title: Prion Protein Gene Variation Among Primates
Source:

Journal of Molecular Biology [0022-2836] Schätzl, Hermann yr:1995


Collapse list of basic services Basic
Full text
Full text available via EZB-NALI5-00465 Elsevier Archive NL
GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Aguzzi, A. "The Prion's Elusive Reason for Being." Annual Review of Neuroscience 31.1 (2008): 439-77. Link to Full Text for this item Link to SFX for this item
2. Prusiner, Stanley B. "Prion Diseases and the BSE Crisis." Science 278.5336 (1997): 245-251. Link to SFX for this item
3. van Rheede, T. "Molecular evolution of the mammalian prion protein." Molecular biology and evolution 20.1 (2002): 111-21. Link to SFX for this item
4. Cohen, F E E. "Pathologic conformations of prion proteins." Annual review of biochemistry 67.1 (1998): 793-819. Link to Full Text for this item Link to SFX for this item
5. Telling, G C C. "Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity." Science 274.5295 (1997): 2079-82. Link to SFX for this item
6. Norrby, E. "Prions and protein folding diseases." Journal of internal medicine 270.1 (2011): 1-14. Link to Full Text for this item Link to SFX for this item
7. Prusiner, S B B. "Molecular biology of prion diseases." Science 252.5012: 1515-1522. Link to SFX for this item
8. Linden, R. "Physiology of the prion protein." Physiological reviews 88.2 (2008): 673-728. Link to SFX for this item
9. Prusiner, S B B. "Prions." Proceedings of the National Academy of Sciences of the United States of America 95.23: 13363-13383. Link to SFX for this item
10. Liemann, S. "Influence of Amino Acid Substitutions Related to Inherited Human Prion Diseases on the Thermodynamic Stability of the Cellular Prion Proteinâ€." Biochemistry 38.11 (1999): 3258-3267. Link to Full Text for this item Link to SFX for this item
11. Harris, D. "Copper converts the cellular prion protein into a protease-resistant species that is distinct from scrapie isoform." The Journal of biological chemistry 276.14 (2001): 11432-11438. Link to SFX for this item
12. Prusiner, Stanley B. "Prion Protein Biology-Review." Cell 93.3 (1998): 337-348. Link to SFX for this item
13. Gambetti, Pierluigi, P. "Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Clinical, pathological and molecular features." Brain pathology 5.1 (1995): 43-51. Link to SFX for this item
14. Prusiner, S B B. "Prion protein biology." Cell 93.3 (1998): 337-348. Link to SFX for this item
15. Hu, W. "Prion proteins: Physiological functions and role in neurological disorders." Journal of the Neurological Sciences 264.1-2 (2008): 1-8. Link to SFX for this item
16. Prusiner, S B B. "Shattuck lecture--neurodegenerative diseases and prions." The New England journal of medicine 344.20: 1516-1526. Link to SFX for this item
17. Collinge, J. "Prion diseases of humans and animals: their causes and molecular basis." Annual review of neuroscience 24.1: 519-550. Link to SFX for this item
18. Dobson, C M M. "Protein misfolding, evolution and disease." Trends in biochemical sciences 24.9 (1999): 329-332. Link to Full Text for this item Link to SFX for this item
19. Mead, S. "Prion disease genetics." European journal of human genetics 14.3: 273-281. Link to SFX for this item
20. Polymenidou, M. "Insights into prion strains and neurotoxicity." Nature reviews. Molecular cell biology 8.7 (2007): 552-61. Link to Full Text for this item Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced