Reprogrammed human lateral ganglionic eminence precursors generate striatal neurons and restore motor function in a rat model of Huntington’s disease
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
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Reprogrammed human lateral ganglionic eminence precursors generate striatal neurons and restore motor function in a rat model of Huntington’s disease ; volume:15 ; number:1 ; day:22 ; month:11 ; year:2024 ; pages:1-17 ; date:12.2024
Stem cell research & therapy ; 15, Heft 1 (22.11.2024), 1-17, 12.2024
- Classification
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Biowissenschaften, Biologie
- Creator
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McCaughey-Chapman, Amy
Burgers, Anne Lieke
Combrinck, Catharina
Marriott, Laura
Gordon, David
Connor, Bronwen
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13287-024-04057-9
- URN
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urn:nbn:de:101:1-2502082231457.863195070000
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
- 15.08.2025, 7:35 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
- McCaughey-Chapman, Amy
- Burgers, Anne Lieke
- Combrinck, Catharina
- Marriott, Laura
- Gordon, David
- Connor, Bronwen
- SpringerLink (Online service)
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Motor skill learning modulates striatal extracellular vesicles’ content in a mouse model of Huntington’s disease
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Functional connectivity modeling of consistent cortico-striatal degeneration in Huntington's disease
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Striatal Interneurons in Transgenic Nonhuman Primate Model of Huntington’s Disease
Cortical and striatal neurone number in Huntington's disease
3D imaging of striatal transplants in a small animal model of Huntington’s disease
Deficits in coordinated neuronal activity and network topology are striatal hallmarks in Huntington’s disease
Motor skill learning modulates striatal extracellular vesicles’ content in a mouse model of Huntington’s disease
Investigating longitudinal changes to frontal cortico-striatal tracts in Huntington’s disease: the IMAGE-HD study
Fibroblast Growth Factor 9 Suppresses Striatal Cell Death Dominantly Through ERK Signaling in Huntington’s Disease
Huntington
The potential therapeutic role of Lisinopril in augmenting the striatal neuroplasticity via the striatal ACE2/Ang1-7/MAS receptor axis in 3-nitropropionic acid-induced Huntington’s disease in rats: shifting paradigms in Huntington’s disease treatment
Functional connectivity modeling of consistent cortico-striatal degeneration in Huntington's disease
Huntington's chorea
Chorea Huntington
Striatal Interneurons in Transgenic Nonhuman Primate Model of Huntington’s Disease
Cortical and striatal neurone number in Huntington's disease
3D imaging of striatal transplants in a small animal model of Huntington’s disease
Deficits in coordinated neuronal activity and network topology are striatal hallmarks in Huntington’s disease
Motor skill learning modulates striatal extracellular vesicles’ content in a mouse model of Huntington’s disease
Investigating longitudinal changes to frontal cortico-striatal tracts in Huntington’s disease: the IMAGE-HD study
Fibroblast Growth Factor 9 Suppresses Striatal Cell Death Dominantly Through ERK Signaling in Huntington’s Disease
Huntington
The potential therapeutic role of Lisinopril in augmenting the striatal neuroplasticity via the striatal ACE2/Ang1-7/MAS receptor axis in 3-nitropropionic acid-induced Huntington’s disease in rats: shifting paradigms in Huntington’s disease treatment
Functional connectivity modeling of consistent cortico-striatal degeneration in Huntington's disease
Huntington's chorea