Mutant huntingtin confers cell-autonomous phenotypes on Huntington’s disease iPSC-derived microglia
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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Mutant huntingtin confers cell-autonomous phenotypes on Huntington’s disease iPSC-derived microglia ; volume:13 ; number:1 ; day:22 ; month:11 ; year:2023 ; pages:1-15 ; date:12.2023
Scientific reports ; 13, Heft 1 (22.11.2023), 1-15, 12.2023
- Urheber
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Stöberl, Nina
Donaldson, Jasmine
Binda, Caroline S.
McAllister, Branduff
Hall-Roberts, Hazel
Jones, Lesley
Massey, Thomas H.
Allen, Nicholas D.
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1038/s41598-023-46852-z
- URN
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urn:nbn:de:101:1-2024021211121017448893
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:37 MESZ
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Beteiligte
- Stöberl, Nina
- Donaldson, Jasmine
- Binda, Caroline S.
- McAllister, Branduff
- Hall-Roberts, Hazel
- Jones, Lesley
- Massey, Thomas H.
- Allen, Nicholas D.
- SpringerLink (Online service)
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Salivary levels of total huntingtin are elevated in Huntington’s disease patients
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Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients
Analysis of mutant and total huntingtin expression in Huntington’s disease murine models
Mutant huntingtin induces iron overload via up-regulating IRP1 in Huntington’s disease
Analysis of mutant huntingtin aggregation and toxicity in Drosophila models of Huntington’s disease
Siah-1-interacting protein regulates mutated huntingtin protein aggregation in Huntington’s disease models
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Salivary levels of total huntingtin are elevated in Huntington’s disease patients
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