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Prions

Known as: prion proteins, prion protein, Prions [Chemical/Ingredient] 
Small proteinaceous infectious particles which resist inactivation by procedures that modify NUCLEIC ACIDS and contain an abnormal isoform of a… Expand
National Institutes of Health

Papers overview

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Review
2019
Review
2019
TAR DNA binding protein 43 (TDP-43) is a versatile RNA/DNA binding protein involved in RNA-related metabolism. Hyper… Expand
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Review
2019
Review
2019
The central nervous system can respond to threat via the induction of an inflammatory response. Under normal circumstances this… Expand
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Review
2007
Review
2007
Prions are lethal mammalian pathogens composed of aggregated conformational isomers of a host-encoded glycoprotein and which… Expand
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Highly Cited
2005
Highly Cited
2005
Prions are unconventional infectious agents responsible for transmissible spongiform encephalopathy (TSE) diseases. They are… Expand
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Highly Cited
2005
Highly Cited
2005
Neurodegenerative diseases such as Alzheimer's, Parkinson's and the transmissible spongiform encephalopathies (TSEs) are… Expand
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Highly Cited
2004
Highly Cited
2004
Recombinant mouse prion protein (recMoPrP) produced in Escherichia coli was polymerized into amyloid fibrils that represent a… Expand
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Highly Cited
2004
Highly Cited
2004
Prion diseases are infectious neurodegenerative disorders linked to the accumulation in the central nervous system of the… Expand
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Review
2001
Review
2001
  • J Collinge
  • Annual review of neuroscience
  • 2001
  • Corpus ID: 18915904
Prion diseases are transmissible neurodegenerative conditions that include Creutzfeldt-Jakob disease (CJD) in humans and bovine… Expand
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Highly Cited
1997
Highly Cited
1997
Epidemiological and clinicopathological studies, allied with pathological prion protein (PrPSc) analysis, strongly support the… Expand
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Review
1991
Review
1991
Prions cause transmissible and genetic neurodegenerative diseases, including scrapie and bovine spongiform encephalopathy of… Expand
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