Mutated LRRK2 induces a reactive phenotype and alters migration in human iPSC-derived pericyte-like cells
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Mutated LRRK2 induces a reactive phenotype and alters migration in human iPSC-derived pericyte-like cells ; volume:21 ; number:1 ; day:18 ; month:11 ; year:2024 ; pages:1-12 ; date:12.2024
Fluids and barriers of the CNS ; 21, Heft 1 (18.11.2024), 1-12, 12.2024
- Creator
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Peltonen, Sanni
Sonninen, Tuuli-Maria
Niskanen, Jonna
Koistinaho, Jari
Ruponen, Marika
Lehtonen, Šárka
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12987-024-00592-y
- URN
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urn:nbn:de:101:1-2502040903237.599113675285
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:24 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
- Peltonen, Sanni
- Sonninen, Tuuli-Maria
- Niskanen, Jonna
- Koistinaho, Jari
- Ruponen, Marika
- Lehtonen, Šárka
- SpringerLink (Online service)
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Human iPSC-derived microglia carrying the LRRK2-G2019S mutation show a Parkinson’s disease related transcriptional profile and function
Establishment of an in vitro model for analyzing mitochondrial ultrastructure in PRKN-mutated patient iPSC-derived dopaminergic neurons
Generation of human iPSC-derived 3D bile duct within liver organoid by incorporating human iPSC-derived blood vessel
LRRK2 G2019S induces axonal dysfunction in human iPSC-derived neurons that can be linked to α-synuclein, Tau and clinical severity
Role of iPSC-derived pericytes on barrier function of iPSC-derived brain microvascular endothelial cells in 2D and 3D
Establishment of autologous iPSC-derived hair follicle models
iPSC-derived lung and lung cancer organoid model to evaluate cisplatin encapsulated autologous iPSC-derived mesenchymal stromal cell-isolated extracellular vesicles
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ACTN2 Mutant Causes Proteopathy in Human iPSC-Derived Cardiomyocytes
Modeling LRRK2 mutant-associated cellular alterations in iPSC-derived mesencephalic dopamine neurons
Mutations in LRRK2 impair NF-κB pathway in iPSC-derived neurons
Human iPSC-derived pericyte-like cells carrying APP Swedish mutation overproduce beta-amyloid and induce cerebral amyloid angiopathy-like changes
Human iPSC-derived microglia carrying the LRRK2-G2019S mutation show a Parkinson’s disease related transcriptional profile and function
Establishment of an in vitro model for analyzing mitochondrial ultrastructure in PRKN-mutated patient iPSC-derived dopaminergic neurons
Generation of human iPSC-derived 3D bile duct within liver organoid by incorporating human iPSC-derived blood vessel
LRRK2 G2019S induces axonal dysfunction in human iPSC-derived neurons that can be linked to α-synuclein, Tau and clinical severity
Role of iPSC-derived pericytes on barrier function of iPSC-derived brain microvascular endothelial cells in 2D and 3D
Establishment of autologous iPSC-derived hair follicle models
iPSC-derived lung and lung cancer organoid model to evaluate cisplatin encapsulated autologous iPSC-derived mesenchymal stromal cell-isolated extracellular vesicles
Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors