Discovery of an autophagy inducer J3 to lower mutant huntingtin and alleviate Huntington’s disease-related phenotype
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-3701
- 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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Discovery of an autophagy inducer J3 to lower mutant huntingtin and alleviate Huntington’s disease-related phenotype ; volume:12 ; number:1 ; day:8 ; month:10 ; year:2022 ; pages:1-16 ; date:12.2022
Cell & bioscience ; 12, Heft 1 (8.10.2022), 1-16, 12.2022
- Creator
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Long, Jiahui
Luo, Xia
Fang, Dongmei
Song, Haikun
Fang, Weibin
Shan, Hao
Liu, Peiqing
Lu, Boxun
Yin, Xiao-Ming
Hong, Liang
Li, Min
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13578-022-00906-3
- URN
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urn:nbn:de:101:1-2022122621075793280297
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:38 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Long, Jiahui
- Luo, Xia
- Fang, Dongmei
- Song, Haikun
- Fang, Weibin
- Shan, Hao
- Liu, Peiqing
- Lu, Boxun
- Yin, Xiao-Ming
- Hong, Liang
- Li, Min
- SpringerLink (Online service)
Other Objects (12)
Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients
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
The emerging role of the first 17 amino acids of huntingtin in Huntington’s disease
Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients
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
The emerging role of the first 17 amino acids of huntingtin in Huntington’s disease
Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients
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