Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathy
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathy ; volume:12 ; number:1 ; day:13 ; month:10 ; year:2022 ; pages:1-9 ; date:12.2022
Scientific reports ; 12, Heft 1 (13.10.2022), 1-9, 12.2022
- Urheber
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Jackson, Graham S.
Linehan, Jacqueline
Brandner, Sebastian
Asante, Emmanuel A.
Wadsworth, Jonathan D. F.
Collinge, John
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1038/s41598-022-21608-3
- URN
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urn:nbn:de:101:1-2022123021064070873364
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:30 MESZ
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Beteiligte
- Jackson, Graham S.
- Linehan, Jacqueline
- Brandner, Sebastian
- Asante, Emmanuel A.
- Wadsworth, Jonathan D. F.
- Collinge, John
- SpringerLink (Online service)
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Prion protein PrP nucleic acid binding and mobilization implicates retroelements as the replicative component of transmissible spongiform encephalopathy
Investigation of scrapie associated prion protein PrP27-30 and strain differentiation of transmissible spongiform encephalopathy by Fourier transform infrared spectroscopy techniques
Biodegradation of bovine spongiform encephalopathy prions in compost
Microdissection: A method developed to investigate mechanisms involved in transmissible spongiform encephalopathy pathogenesis
Co-occurrence of chronic traumatic encephalopathy and prion disease
Differential expression of interferon responsive genes in rodent models of transmissible spongiform encephalopathy disease
Transgenic overexpression of furin increases epileptic susceptibility
In vitro prion protein conversion suggests risk of bighorn sheep (Ovis canadensis) to transmissible spongiform encephalopathies
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Unusual cerebral vascular prion protein amyloid distribution in scrapie-infected transgenic mice expressing anchorless prion protein
Overexpression of chemokine ligand 7 is associated with the progression of canine transmissible venereal tumor
Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein
Prion protein PrP nucleic acid binding and mobilization implicates retroelements as the replicative component of transmissible spongiform encephalopathy
Investigation of scrapie associated prion protein PrP27-30 and strain differentiation of transmissible spongiform encephalopathy by Fourier transform infrared spectroscopy techniques
Biodegradation of bovine spongiform encephalopathy prions in compost
Microdissection: A method developed to investigate mechanisms involved in transmissible spongiform encephalopathy pathogenesis
Co-occurrence of chronic traumatic encephalopathy and prion disease
Differential expression of interferon responsive genes in rodent models of transmissible spongiform encephalopathy disease
Transgenic overexpression of furin increases epileptic susceptibility
In vitro prion protein conversion suggests risk of bighorn sheep (Ovis canadensis) to transmissible spongiform encephalopathies
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Unusual cerebral vascular prion protein amyloid distribution in scrapie-infected transgenic mice expressing anchorless prion protein