Found: 15
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Atypical Scrapie Prions from Sheep and Lack of Disease in Transgenic Mice Overexpressing Human Prion Protein.
- Published in:
- Emerging Infectious Diseases, 2013, v. 19, n. 11, p. 1731, doi. 10.3201/eid1911.121341
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- Article
2.7 Å cryo-EM structure of ex vivo RML prion fibrils.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30457-7
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- Article
BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein.
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- EMBO Journal, 2002, v. 21, n. 23, p. 6358, doi. 10.1093/emboj/cdf653
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- Article
Effect of fixation on brain and lymphoreticular vCJD prions and bioassay of key positive specimens from a retrospective vCJD prevalence study.
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- Journal of Pathology, 2011, v. 223, n. 4, p. 511, doi. 10.1002/path.2821
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- Article
Isolation of Proteinase K-Sensitive Prions Using Pronase E and Phosphotungstic Acid.
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- PLoS ONE, 2010, v. 5, n. 12, p. 1, doi. 10.1371/journal.pone.0015679
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- Article
Strain-specific prion-protein conformation determined by metal ions.
- Published in:
- Nature Cell Biology, 1999, v. 1, n. 1, p. 55, doi. 10.1038/9030
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- Article
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors.
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- Brain: A Journal of Neurology, 2011, v. 134, n. 6, p. 1829, doi. 10.1093/brain/awr079
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- Article
Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.
- Published in:
- 2006
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- Publication type:
- journal article
Inherited prion disease with six octapeptide repeat insertional mutation—molecular analysis of phenotypic heterogeneity.
- Published in:
- Brain: A Journal of Neurology, 2006, v. 129, n. 9, p. 2297, doi. 10.1093/brain/awl226
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- Publication type:
- Article
Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein.
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- 2006
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- Publication type:
- journal article
Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein.
- Published in:
- Brain: A Journal of Neurology, 2006, v. 129, n. 6, p. 1557
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- Publication type:
- Article
Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.
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- PLoS Pathogens, 2015, v. 11, n. 7, p. 1, doi. 10.1371/journal.ppat.1004953
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- Article
A novel and rapid method for obtaining high titre intact prion strains from mammalian brain.
- Published in:
- Scientific Reports, 2015, p. 10062, doi. 10.1038/srep10062
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- Article
Structural features distinguishing infectious ex vivo mammalian prions from non-infectious fibrillar assemblies generated in vitro.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-36700-w
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- Publication type:
- Article
Humanized Transgenic Mice Are Resistant to Chronic Wasting Disease Prions From Norwegian Reindeer and Moose.
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- 2022
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- Publication type:
- journal article