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Scrapie
Known as:
Rida
, Scrapie [Disease/Finding]
A fatal disease of the nervous system in sheep and goats, characterized by pruritus, debility, and locomotor incoordination. It is caused by…
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National Institutes of Health
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Related topics
Related topics
10 relations
In Blood
Microbiological
PrPSc Proteins
Prion Diseases
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Broader (1)
Spongiform encephalopathy
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2003
Highly Cited
2003
A quantitative, highly sensitive cell-based infectivity assay for mouse scrapie prions
P. Klöhn
,
L. Stoltze
,
E. Flechsig
,
M. Enari
,
Charles Weissmann
Proceedings of the National Academy of Sciences…
2003
Corpus ID: 32584218
Prions are usually quantified by bioassays based on intracerebral inoculation of mice that are slow, imprecise, and costly. We…
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Highly Cited
1999
Highly Cited
1999
Scrapie replication in lymphoid tissues depends on prion protein-expressing follicular dendritic cells
Karen Brown
,
K. Stewart
,
+5 authors
Moira E. Bruce
Nature Network Boston
1999
Corpus ID: 1714679
The immune system is central in the pathogenesis of scrapie and other transmissible spongiform encephalopathies (TSEs) or 'prion…
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Highly Cited
1997
Highly Cited
1997
Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform.
T. L. James
,
He Liu
,
+8 authors
F. Cohen
Proceedings of the National Academy of Sciences…
1997
Corpus ID: 22767202
The scrapie prion protein (PrPSc) is the major, and possibly the only, component of the infectious prion; it is generated from…
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Highly Cited
1993
Highly Cited
1993
Sulfated polyanion inhibition of scrapie-associated PrP accumulation in cultured cells
B. Caughey
,
G. J. Raymond
Journal of Virology
1993
Corpus ID: 41887520
The accumulation of an abnormal, protease-resistant form of the protein PrP (PrP-res) in hosts with scrapie and related…
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Highly Cited
1993
Highly Cited
1993
Conformational transitions, dissociation, and unfolding of scrapie amyloid (prion) protein.
Jiri SafarSj
,
Peter P. Rollern
,
Carleton GajdusekS
,
C. Gibbs
Journal of Biological Chemistry
1993
Corpus ID: 10644351
The infectious form of the scrapie amyloid (prion) precursor, PrPSc, is a host-derived protein and a component of the infectious…
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Highly Cited
1993
Highly Cited
1993
Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes
Michael H. Scott
,
D. Groth
,
+4 authors
S. Prusiner
Cell
1993
Corpus ID: 45519398
Highly Cited
1992
Highly Cited
1992
Nearly ubiquitous tissue distribution of the scrapie agent precursor protein
P. Bendheim
,
H. Brown
,
+6 authors
D. C. Bolton
Neurology
1992
Corpus ID: 35776094
The “modified host protein” model of scrapie proposes that the transmissible agent is composed of the degradation-resistant…
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Highly Cited
1991
Highly Cited
1991
Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy.
B. Caughey
,
A. Dong
,
K. Bhat
,
D. Ernst
,
S. F. Hayes
,
W. Caughey
Biochemistry
1991
Corpus ID: 6101261
A protease-resistant form of the protein PrP (PrP-res) accumulates in tissues of mammals infected with scrapie, Creutzfeldt-Jakob…
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Highly Cited
1989
Highly Cited
1989
Diversity of oligosaccharide structures linked to asparagines of the scrapie prion protein.
T. Endo
,
D. Groth
,
S. Prusiner
,
A. Kobata
Biochemistry
1989
Corpus ID: 37971290
Prion proteins from humans and rodents contain two consensus sites for asparagine-linked glycosylation near their C-termini. The…
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Highly Cited
1982
Highly Cited
1982
Measurement of the scrapie agent using an incubation time interval assay
S. Prusiner
,
S. P. Cochran
,
D. Groth
,
D. Downey
,
K. Bowman
,
Hugo M. Martinez
Annals of Neurology
1982
Corpus ID: 28998012
The titer of the scrapie agent was determined by measurements of time intervals from inoculation to onset of illness and from…
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