Quantifying mutant huntingtin protein in human cerebrospinal fluid to support the development of huntingtin-lowering therapies
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource, 1 online resource.
- Language
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Englisch
- Bibliographic citation
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Quantifying mutant huntingtin protein in human cerebrospinal fluid to support the development of huntingtin-lowering therapies ; volume:13 ; number:1 ; day:1 ; month:4 ; year:2023 ; pages:1-17 ; date:12.2023
Scientific reports ; 13, Heft 1 (1.4.2023), 1-17, 12.2023
- Creator
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Vauleon, Stephanie
Schutz, Katharina
Massonnet, Benoit
Gruben, Nanda
Manchester, Marianne
Buehler, Alessandra
Schick, Eginhard
Boak, Lauren
Hawellek, David J.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41598-023-32630-4
- URN
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urn:nbn:de:101:1-2023081721025171354092
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:53 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
- Vauleon, Stephanie
- Schutz, Katharina
- Massonnet, Benoit
- Gruben, Nanda
- Manchester, Marianne
- Buehler, Alessandra
- Schick, Eginhard
- Boak, Lauren
- Hawellek, David J.
- SpringerLink (Online service)
Other Objects (12)
Huntingtin Lowering Strategies
Huntingtin assoziierte Proteine
The evolution of the huntingtin‑associated protein 40 (HAP40) in conjunction with huntingtin
The evolution of the huntingtin-associated protein 40 (HAP40) in conjunction with huntingtin
Endogenous mutant Huntingtin alters the corticogenesis via lowering Golgi recruiting ARF1 in cortical organoid
Apoptotic regulation by the huntingtin protein
Apoptotic regulation by the Huntingtin protein
Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form
Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients
Elucidating a normal function of huntingtin by functional and microarray analysis of huntingtin-null mouse embryonic fibroblasts
Lineare Ubiquitinierung schützt vor Huntingtin-induzierter Toxizität
Essential sequence of the N-terminal cytoplasmic localization-related domain of huntingtin and its effect on huntingtin aggregates
Huntingtin Lowering Strategies
Huntingtin assoziierte Proteine
The evolution of the huntingtin‑associated protein 40 (HAP40) in conjunction with huntingtin
The evolution of the huntingtin-associated protein 40 (HAP40) in conjunction with huntingtin
Endogenous mutant Huntingtin alters the corticogenesis via lowering Golgi recruiting ARF1 in cortical organoid
Apoptotic regulation by the huntingtin protein
Apoptotic regulation by the Huntingtin protein
Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form
Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients
Elucidating a normal function of huntingtin by functional and microarray analysis of huntingtin-null mouse embryonic fibroblasts
Lineare Ubiquitinierung schützt vor Huntingtin-induzierter Toxizität
Essential sequence of the N-terminal cytoplasmic localization-related domain of huntingtin and its effect on huntingtin aggregates
Huntingtin Lowering Strategies
Huntingtin assoziierte Proteine
The evolution of the huntingtin‑associated protein 40 (HAP40) in conjunction with huntingtin
The evolution of the huntingtin-associated protein 40 (HAP40) in conjunction with huntingtin
Endogenous mutant Huntingtin alters the corticogenesis via lowering Golgi recruiting ARF1 in cortical organoid
Apoptotic regulation by the huntingtin protein
Apoptotic regulation by the Huntingtin protein
Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form
Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients
Elucidating a normal function of huntingtin by functional and microarray analysis of huntingtin-null mouse embryonic fibroblasts
Lineare Ubiquitinierung schützt vor Huntingtin-induzierter Toxizität