Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: 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

Creator: 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

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-020-77164-1

URN: urn:nbn:de:101:1-2020122721002640711619

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:35 AM CEST

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Associated

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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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

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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

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

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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

Making (anti-) sense out of huntingtin levels in Huntington disease

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Disease-related Huntingtin seeding activities in cerebrospinal fluids of Huntington’s disease patients

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Other Objects (12)

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

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

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

Making (anti-) sense out of huntingtin levels in Huntington disease

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