The distribution and density of Huntingtin inclusions across the Huntington disease neocortex: regional correlations with Huntingtin repeat expansion independent of pathologic grade
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2051-5960
- 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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The distribution and density of Huntingtin inclusions across the Huntington disease neocortex: regional correlations with Huntingtin repeat expansion independent of pathologic grade ; volume:10 ; number:1 ; day:19 ; month:4 ; year:2022 ; pages:1-12 ; date:12.2022
Acta Neuropathologica Communications ; 10, Heft 1 (19.4.2022), 1-12, 12.2022
- Creator
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Hickman, Richard A.
Faust, Phyllis L.
Marder, Karen
Yamamoto, Ai
Vonsattel, Jean-Paul
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s40478-022-01364-1
- URN
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urn:nbn:de:101:1-2022070220451295453833
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:30 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
- Hickman, Richard A.
- Faust, Phyllis L.
- Marder, Karen
- Yamamoto, Ai
- Vonsattel, Jean-Paul
- SpringerLink (Online service)
Other Objects (12)
Huntingtin assoziierte Proteine
Huntingtin Lowering Strategies
Soluble mutant huntingtin drives early human pathogenesis in Huntington’s disease
Polyglutamine expansion affects huntingtin conformation in multiple Huntington’s disease models
Making (anti-) sense out of huntingtin levels in Huntington disease
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
The evolution of the huntingtin‑associated protein 40 (HAP40) in conjunction with huntingtin
Huntingtin assoziierte Proteine
Huntingtin Lowering Strategies
Soluble mutant huntingtin drives early human pathogenesis in Huntington’s disease
Polyglutamine expansion affects huntingtin conformation in multiple Huntington’s disease models
Making (anti-) sense out of huntingtin levels in Huntington disease
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
The evolution of the huntingtin‑associated protein 40 (HAP40) in conjunction with huntingtin
Huntingtin assoziierte Proteine
Huntingtin Lowering Strategies
Soluble mutant huntingtin drives early human pathogenesis in Huntington’s disease
Polyglutamine expansion affects huntingtin conformation in multiple Huntington’s disease models
Making (anti-) sense out of huntingtin levels in Huntington disease
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