Inflammatory response of microglia to prions is controlled by sialylation of PrPSc
- 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
-
online resource.
- Erschienen in
-
Inflammatory response of microglia to prions is controlled by sialylation of PrPSc ; volume:8 ; number:1 ; day:27 ; month:7 ; year:2018 ; pages:1-15 ; date:12.2018
Scientific reports ; 8, Heft 1 (27.7.2018), 1-15, 12.2018
- Klassifikation
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Biowissenschaften, Biologie
- Urheber
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Srivastava, Saurabh
- Beteiligte Personen und Organisationen
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Katorcha, Elizaveta
Makarava, Natallia
Barrett, James P.
Loane, David J.
Baskakov, Ilia V.
SpringerLink (Online service)
- DOI
-
10.1038/s41598-018-29720-z
- URN
-
urn:nbn:de:101:1-2018092521422463206515
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:22 MESZ
Datenpartner
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Beteiligte
- Srivastava, Saurabh
- Katorcha, Elizaveta
- Makarava, Natallia
- Barrett, James P.
- Loane, David J.
- Baskakov, Ilia V.
- SpringerLink (Online service)
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PrPSc spreading patterns in the brain of sheep linked to different prion types
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Propagation of PrPSc in mice reveals impact of aggregate composition on prion disease pathogenesis
Cellular trafficking of the pathogenic prion protein PrPSc and phenotypic characterisation of deletion mutants in the hydrophobic domain of the normal prion protein PrPC
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Microglia are not required for prion-induced retinal photoreceptor degeneration
Retrograde Transport by Clathrin-Coated Vesicles is Involved in Intracellular Transport of PrPSc in Persistently Prion-Infected Cells
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Microglia Increase Inflammatory Responses in iPSC-Derived Human BrainSpheres
Prion protein amino acid sequence influences formation of authentic synthetic PrPSc
PrPSc spreading patterns in the brain of sheep linked to different prion types
iPSC-derived PSEN2 (N141I) astrocytes and microglia exhibit a primed inflammatory phenotype
Propagation of PrPSc in mice reveals impact of aggregate composition on prion disease pathogenesis
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High Prion and PrPSc Levels but Delayed Onset of Disease in Scrapie-Inoculated Mice Heterozygous for a Disrupted PrP Gene
Microglia are not required for prion-induced retinal photoreceptor degeneration
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