Mutant huntingtin induces iron overload via up-regulating IRP1 in Huntington’s disease
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-3701
- 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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Mutant huntingtin induces iron overload via up-regulating IRP1 in Huntington’s disease ; volume:8 ; number:1 ; day:4 ; month:7 ; year:2018 ; pages:1-12 ; date:12.2018
Cell & bioscience ; 8, Heft 1 (4.7.2018), 1-12, 12.2018
- Urheber
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Niu, Li
- Beteiligte Personen und Organisationen
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Ye, Cuifang
Sun, Yun
Peng, Ting
Yang, Shiming
Wang, Weixi
Li, He
SpringerLink (Online service)
- DOI
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10.1186/s13578-018-0239-x
- URN
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urn:nbn:de:101:1-2018091213063701727505
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:33 MESZ
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Beteiligte
- Niu, Li
- Ye, Cuifang
- Sun, Yun
- Peng, Ting
- Yang, Shiming
- Wang, Weixi
- Li, He
- SpringerLink (Online service)
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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
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
Facilitating Charge Reactions in Al‐S Batteries with Redox Mediators
APC/C independent function of the spindle assembly checkpoint
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
Disruption of zinc transporter ZnT3 transcriptional activity and synaptic vesicular zinc in the brain of Huntington’s disease transgenic mouse
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
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
Facilitating Charge Reactions in Al‐S Batteries with Redox Mediators
APC/C independent function of the spindle assembly checkpoint
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
Disruption of zinc transporter ZnT3 transcriptional activity and synaptic vesicular zinc in the brain of Huntington’s disease transgenic mouse
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
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
Facilitating Charge Reactions in Al‐S Batteries with Redox Mediators
APC/C independent function of the spindle assembly checkpoint
Analysis of mutant huntingtin aggregation and toxicity in Drosophila models of Huntington’s disease