Mutant huntingtin confers cell-autonomous phenotypes on Huntington’s disease iPSC-derived microglia
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
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
- Creator
-
Stöberl, Nina
Donaldson, Jasmine
Binda, Caroline S.
McAllister, Branduff
Hall-Roberts, Hazel
Jones, Lesley
Massey, Thomas H.
Allen, Nicholas D.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41598-023-46852-z
- URN
-
urn:nbn:de:101:1-2024021211121017448893
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:37 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
- Stöberl, Nina
- Donaldson, Jasmine
- Binda, Caroline S.
- McAllister, Branduff
- Hall-Roberts, Hazel
- Jones, Lesley
- Massey, Thomas H.
- Allen, Nicholas D.
- SpringerLink (Online service)
Other Objects (12)
Soluble mutant huntingtin drives early human pathogenesis in Huntington’s disease
Polyglutamine expansion affects huntingtin conformation in multiple Huntington’s disease models
HAP40 modulates mutant Huntingtin aggregation and toxicity in Huntington’s disease mice
Salivary levels of total huntingtin are elevated in Huntington’s disease patients
Genistein induces degradation of mutant huntingtin in fibroblasts from Huntington’s disease patients
Analysis of mutant and total huntingtin expression in Huntington’s disease murine models
Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients
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
The emerging role of the first 17 amino acids of huntingtin in Huntington’s disease
Making (anti-) sense out of huntingtin levels in Huntington disease
Soluble mutant huntingtin drives early human pathogenesis in Huntington’s disease
Polyglutamine expansion affects huntingtin conformation in multiple Huntington’s disease models
HAP40 modulates mutant Huntingtin aggregation and toxicity in Huntington’s disease mice
Salivary levels of total huntingtin are elevated in Huntington’s disease patients
Genistein induces degradation of mutant huntingtin in fibroblasts from Huntington’s disease patients
Analysis of mutant and total huntingtin expression in Huntington’s disease murine models
Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients
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
The emerging role of the first 17 amino acids of huntingtin in Huntington’s disease
Making (anti-) sense out of huntingtin levels in Huntington disease
Soluble mutant huntingtin drives early human pathogenesis in Huntington’s disease
Polyglutamine expansion affects huntingtin conformation in multiple Huntington’s disease models
HAP40 modulates mutant Huntingtin aggregation and toxicity in Huntington’s disease mice
Salivary levels of total huntingtin are elevated in Huntington’s disease patients
Genistein induces degradation of mutant huntingtin in fibroblasts from Huntington’s disease patients
Analysis of mutant and total huntingtin expression in Huntington’s disease murine models
Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients
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
The emerging role of the first 17 amino acids of huntingtin in Huntington’s disease