Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients
- 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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Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients ; volume:10 ; number:1 ; day:20 ; month:11 ; year:2020 ; pages:1-14 ; date:12.2020
Scientific reports ; 10, Heft 1 (20.11.2020), 1-14, 12.2020
- Urheber
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Lee, C. Y. Daniel
Wang, Nan
Shen, Koning
Stricos, Matthew
Langfelder, Peter
Cheon, Kristina H.
Cortés, Etty P.
Vinters, Harry V.
Vonsattel, Jean Paul
Wexler, Nancy S.
Damoiseaux, Robert
Frydman, Judith
Yang, X. William
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1038/s41598-020-77164-1
- URN
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urn:nbn:de:101:1-2020122721002640711619
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:35 MESZ
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Beteiligte
- Lee, C. Y. Daniel
- Wang, Nan
- Shen, Koning
- Stricos, Matthew
- Langfelder, Peter
- Cheon, Kristina H.
- Cortés, Etty P.
- Vinters, Harry V.
- Vonsattel, Jean Paul
- Wexler, Nancy S.
- Damoiseaux, Robert
- Frydman, Judith
- Yang, X. William
- SpringerLink (Online service)
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Discovery of an autophagy inducer J3 to lower mutant huntingtin and alleviate Huntington’s disease-related phenotype
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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
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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Making (anti-) sense out of huntingtin levels in Huntington disease
Discovery of an autophagy inducer J3 to lower mutant huntingtin and alleviate Huntington’s disease-related phenotype
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
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
Mutant huntingtin confers cell-autonomous phenotypes on Huntington’s disease iPSC-derived microglia