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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
2007
Highly Cited
2007
Role of galectin-3 in prion infections of the CNS.
S. Mok
,
C. Riemer
,
+5 authors
M. Baier
Biochemical and Biophysical Research…
2007
Corpus ID: 20364212
Highly Cited
2006
Highly Cited
2006
Polymorphism and ultrastructural organization of prion protein amyloid fibrils: an insight from high resolution atomic force microscopy.
M. Anderson
,
O. Bocharova
,
N. Makarava
,
L. Breydo
,
V. Salnikov
,
I. Baskakov
Journal of Molecular Biology
2006
Corpus ID: 21592844
Highly Cited
2002
Highly Cited
2002
Subclinical scrapie infection in a resistant species: persistence, replication, and adaptation of infectivity during four passages.
R. Race
,
Kimberly Meade-White
,
Anne Raines
,
G. J. Raymond
,
B. Caughey
,
B. Chesebro
Journal of Infectious Diseases
2002
Corpus ID: 10191935
Cross-species infection with transmissible spongiform encephalopathy agents may lead to subclinical infection and to adaptation…
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Highly Cited
1996
Highly Cited
1996
Strain specific and common pathogenic events in murine models of scrapie and bovine spongiform encephalopathy.
C. Lasmézas
,
J. Deslys
,
R. Demaimay
,
K. Adjou
,
J. Hauw
,
D. Dormont
Journal of General Virology
1996
Corpus ID: 41921723
The development of transmissible spongiform encephalopathies in experimental models depends on two major factors: the…
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Highly Cited
1993
Highly Cited
1993
Scrapie prions alter receptor‐mediated calcium responses in cultured cells
K. Kristensson
,
B. Feuerstein
,
A. Taraboulos
,
W. Hyun
,
S. B. Prusiner
,
S. DeArmond
Neurology
1993
Corpus ID: 21026835
The molecular basis of neurologic dysfunction in prion diseases is unknown. Spongiform degeneration of neurons is the most…
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Highly Cited
1986
Highly Cited
1986
Detection of scrapie-associated fibril (SAF) proteins using anti-SAF antibody in non-purified tissue preparations.
R. Rubenstein
,
R. Kascsak
,
+4 authors
H. Wiśniewski
Journal of General Virology
1986
Corpus ID: 9776548
Antisera raised to scrapie-associated fibril (SAF) proteins were used to detect scrapie-specific polypeptides in three different…
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Highly Cited
1985
Highly Cited
1985
Specific proteins associated with Creutzfeldt-Jakob disease and scrapie share antigenic and carbohydrate determinants.
L. Manuelidis
,
S. Valley
,
E. E. Manuelidis
Proceedings of the National Academy of Sciences…
1985
Corpus ID: 24861423
Small amounts of brain tissue (2 g) infected with Creutzfeldt-Jakob disease (CJD) can be fractionated by using a simple 1-day…
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Highly Cited
1984
Highly Cited
1984
Preclinical changes in weight of scrapie-infected mice as a function of scrapie agent-mouse strain combination.
R. Carp
,
S. M. Callahan
,
E. Sersen
,
R. Moretz
Intervirology
1984
Corpus ID: 46767015
Several inbred strains of mice were injected with different scrapie agents and their total body weight was monitored throughout…
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Review
1984
Review
1984
Prions: novel infectious pathogens.
S. B. Prusiner
Advances in Virus Research
1984
Corpus ID: 30106071
Highly Cited
1978
Highly Cited
1978
The scrapie agent: evidence against its dependence for replication on intrinsic nucleic acid.
T. Alper
,
D. Haig
,
M. Clarke
Journal of General Virology
1978
Corpus ID: 25286133
Exposure of the scrapie agent to u.v. light at various wavelengths has shown that light of 237 nm is 4 to 5 times as effective in…
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