PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1432-0533
- 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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PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions ; day:4 ; month:7 ; year:2016 ; pages:1-14
Acta neuropathologica ; (4.7.2016), 1-14
- Creator
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Barron, Rona M.
- Contributor
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King, Declan
Jeffrey, Martin
McGovern, Gillian
Agarwal, Sonya
Gill, Andrew C.
Piccardo, Pedro
SpringerLink (Online service)
- DOI
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10.1007/s00401-016-1594-5
- URN
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urn:nbn:de:1111-201607055193
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:54 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Barron, Rona M.
- King, Declan
- Jeffrey, Martin
- McGovern, Gillian
- Agarwal, Sonya
- Gill, Andrew C.
- Piccardo, Pedro
- SpringerLink (Online service)
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Predicting the consequences of selecting on PrP genotypes on PrP frequencies, performance and inbreeding in commercial meat sheep populations
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Impact of the hydrophobic core on PrP function and conversion
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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
Generierung von transgenen Mäusen, die das bovine Prion-Protein (PrP) überexprimieren
A Fluorescent Oligothiophene-Bis-Triazine ligand interacts with PrP fibrils and detects SDS-resistant oligomers in human prion diseases
Peroxiredoxin 6 promotes upregulation of the prion protein (PrP) in neuronal cells of prion-infected mice
Predicting the consequences of selecting on PrP genotypes on PrP frequencies, performance and inbreeding in commercial meat sheep populations
Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions
High Prion and PrPSc Levels but Delayed Onset of Disease in Scrapie-Inoculated Mice Heterozygous for a Disrupted PrP Gene
Impact of the hydrophobic core on PrP function and conversion
Protecting effect of PrP codons M142 and K222 in goats orally challenged with bovine spongiform encephalopathy prions
Prion protein PrP nucleic acid binding and mobilization implicates retroelements as the replicative component of transmissible spongiform encephalopathy
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
Generierung von transgenen Mäusen, die das bovine Prion-Protein (PrP) überexprimieren
A Fluorescent Oligothiophene-Bis-Triazine ligand interacts with PrP fibrils and detects SDS-resistant oligomers in human prion diseases
Peroxiredoxin 6 promotes upregulation of the prion protein (PrP) in neuronal cells of prion-infected mice
Predicting the consequences of selecting on PrP genotypes on PrP frequencies, performance and inbreeding in commercial meat sheep populations
Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions
High Prion and PrPSc Levels but Delayed Onset of Disease in Scrapie-Inoculated Mice Heterozygous for a Disrupted PrP Gene
Impact of the hydrophobic core on PrP function and conversion
Protecting effect of PrP codons M142 and K222 in goats orally challenged with bovine spongiform encephalopathy prions