Salivary levels of total huntingtin are elevated in 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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Salivary levels of total huntingtin are elevated in Huntington’s disease patients ; volume:8 ; number:1 ; day:9 ; month:5 ; year:2018 ; pages:1-9 ; date:12.2018
Scientific reports ; 8, Heft 1 (9.5.2018), 1-9, 12.2018
- Urheber
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Corey-Bloom, Jody
- Beteiligte Personen und Organisationen
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Haque, Ameera S.
Park, Sungmee
Nathan, Ajay S.
Baker, Robert W.
Thomas, Elizabeth A.
SpringerLink (Online service)
- DOI
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10.1038/s41598-018-25095-3
- URN
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urn:nbn:de:101:1-2018070621374874103089
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:22 MESZ
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Beteiligte
- Corey-Bloom, Jody
- Haque, Ameera S.
- Park, Sungmee
- Nathan, Ajay S.
- Baker, Robert W.
- Thomas, Elizabeth A.
- SpringerLink (Online service)
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Making (anti-) sense out of huntingtin levels in Huntington disease
Analysis of mutant and total huntingtin expression in Huntington’s disease murine models
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
Genistein induces degradation of mutant huntingtin in fibroblasts from Huntington’s disease patients
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
Mutant huntingtin confers cell-autonomous phenotypes on Huntington’s disease iPSC-derived microglia
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
Analysis of mutant and total huntingtin expression in Huntington’s disease murine models
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
Genistein induces degradation of mutant huntingtin in fibroblasts from Huntington’s disease patients
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
Mutant huntingtin confers cell-autonomous phenotypes on Huntington’s disease iPSC-derived microglia
The emerging role of the first 17 amino acids of huntingtin in Huntington’s disease