Prion protein PrP nucleic acid binding and mobilization implicates retroelements as the replicative component of transmissible spongiform encephalopathy
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1432-8798
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Prion protein PrP nucleic acid binding and mobilization implicates retroelements as the replicative component of transmissible spongiform encephalopathy ; volume:165 ; number:3 ; day:5 ; month:2 ; year:2020 ; pages:535-556 ; date:3.2020
Archives of virology ; 165, Heft 3 (5.2.2020), 535-556, 3.2020
- Creator
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s00705-020-04529-2
- URN
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urn:nbn:de:101:1-2020051319405407107557
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:01 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Lathe, Richard
- Darlix, Jean-Luc
- SpringerLink (Online service)
Other Objects (12)
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Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein
Peroxiredoxin 6 promotes upregulation of the prion protein (PrP) in neuronal cells of prion-infected mice
Generierung von transgenen Mäusen, die das bovine Prion-Protein (PrP) überexprimieren
PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions
Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathy
Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions
In vitro prion protein conversion suggests risk of bighorn sheep (Ovis canadensis) to transmissible spongiform encephalopathies
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Expression und Charakterisierung von Insertionsmutanten des Prion-Proteins (PrP)
Infectious prion strain directed conformational conversion of recombinant PrP
Infectious Prion Strain Directed Conformational Conversion of Recombinant PrP
Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein
Peroxiredoxin 6 promotes upregulation of the prion protein (PrP) in neuronal cells of prion-infected mice
Generierung von transgenen Mäusen, die das bovine Prion-Protein (PrP) überexprimieren
PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions
Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathy
Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions
In vitro prion protein conversion suggests risk of bighorn sheep (Ovis canadensis) to transmissible spongiform encephalopathies
Prions prions prions
Transmissible Spongiforme Enzephalopathien (TSE)
Expression und Charakterisierung von Insertionsmutanten des Prion-Proteins (PrP)
Infectious prion strain directed conformational conversion of recombinant PrP
Infectious Prion Strain Directed Conformational Conversion of Recombinant PrP
Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein
Peroxiredoxin 6 promotes upregulation of the prion protein (PrP) in neuronal cells of prion-infected mice
Generierung von transgenen Mäusen, die das bovine Prion-Protein (PrP) überexprimieren
PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions
Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathy
Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions
In vitro prion protein conversion suggests risk of bighorn sheep (Ovis canadensis) to transmissible spongiform encephalopathies
Prions prions prions