Prion diseases
Author:
Publisher
Wiley
Subject
Genetics (clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2516.1998.440619.x/fullpdf
Reference81 articles.
1. Tracking prions: the neurografting approach;Aguzzi;Cell Mol Life Sci,1997
2. The role of PrP in the pathogenesis of experimental scrapie;Weissmann;Cold Spring Harbor Symp Quant Biol,1966
3. A ‘unified theory’ of prion propagation;Weissmann;Nature,1991
4. Autonomous and reversible folding of a soluble amino-terminally truncated segment of the mouse prion protein;Hornemann;J Mol Biol,1996
5. NMR structure of the mouse prion protein domain Prp(121-231);Riek;Nature,1996
Cited by 29 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Longitudinal microbiome investigation throughout prion disease course reveals pre- and symptomatic compositional perturbations linked to short-chain fatty acid metabolism and cognitive impairment in mice;Frontiers in Microbiology;2024-06-11
2. Cytoskeleton-dependent clustering of membrane-bound prion protein on the cell surface;Journal of Biological Chemistry;2021-01
3. Global analysis of protein degradation in prion infected cells;Scientific Reports;2020-07-01
4. Prion protein—Semisynthetic prion protein (PrP) variants with posttranslational modifications;Journal of Peptide Science;2019-10
5. Global analysis of protein degradation in prion infected cells;2019-07-23
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