Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2045-2322
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations ; volume:9 ; number:1 ; day:14 ; month:1 ; year:2019 ; pages:1-11 ; date:12.2019
Scientific reports ; 9, Heft 1 (14.1.2019), 1-11, 12.2019
- Classification
-
Naturwissenschaften
- Creator
-
Gouder, Laura
Vitrac, Aline
Goubran-Botros, Hany
Danckaert, Anne
Tinevez, Jean-Yves
André-Leroux, Gwenaëlle
Atanasova, Ekaterina
Lemière, Nathalie
Biton, Anne
Leblond, Claire S.
Poulet, Aurélie
Boland, Anne
Deleuze, Jean-François
Benchoua, Alexandra
Delorme, Richard
Bourgeron, Thomas
Cloëz-Tayarani, Isabelle
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41598-018-36993-x
- URN
-
urn:nbn:de:101:1-2019021202055870970978
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:01 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
- Gouder, Laura
- Vitrac, Aline
- Goubran-Botros, Hany
- Danckaert, Anne
- Tinevez, Jean-Yves
- André-Leroux, Gwenaëlle
- Atanasova, Ekaterina
- Lemière, Nathalie
- Biton, Anne
- Leblond, Claire S.
- Poulet, Aurélie
- Boland, Anne
- Deleuze, Jean-François
- Benchoua, Alexandra
- Delorme, Richard
- Bourgeron, Thomas
- Cloëz-Tayarani, Isabelle
- SpringerLink (Online service)
Other Objects (12)
SHANK3 deficiency leads to myelin dysregulation in a Shank3∆11(-/-) mouse model and human iPSC-derived cerebral organoids
Generation of human iPSC-derived 3D bile duct within liver organoid by incorporating human iPSC-derived blood vessel
Mutations in DNAJC19 cause altered mitochondrial structure and increased mitochondrial respiration in human iPSC-derived cardiomyocytes
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
Human iPSC-derived microglia carrying the LRRK2-G2019S mutation show a Parkinson’s disease related transcriptional profile and function
Human iPSC-derived pericyte-like cells carrying APP Swedish mutation overproduce beta-amyloid and induce cerebral amyloid angiopathy-like changes
Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors
ACTN2 Mutant Causes Proteopathy in Human iPSC-Derived Cardiomyocytes
How is Excitotoxicity Being Modelled in iPSC-Derived Neurons?
Novel CDKL5 targets identified in human iPSC-derived neurons
SHANK3 deficiency leads to myelin dysregulation in a Shank3∆11(-/-) mouse model and human iPSC-derived cerebral organoids
Generation of human iPSC-derived 3D bile duct within liver organoid by incorporating human iPSC-derived blood vessel
Mutations in DNAJC19 cause altered mitochondrial structure and increased mitochondrial respiration in human iPSC-derived cardiomyocytes
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
Human iPSC-derived microglia carrying the LRRK2-G2019S mutation show a Parkinson’s disease related transcriptional profile and function
Human iPSC-derived pericyte-like cells carrying APP Swedish mutation overproduce beta-amyloid and induce cerebral amyloid angiopathy-like changes
Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors
ACTN2 Mutant Causes Proteopathy in Human iPSC-Derived Cardiomyocytes
How is Excitotoxicity Being Modelled in iPSC-Derived Neurons?
Novel CDKL5 targets identified in human iPSC-derived neurons
SHANK3 deficiency leads to myelin dysregulation in a Shank3∆11(-/-) mouse model and human iPSC-derived cerebral organoids
Generation of human iPSC-derived 3D bile duct within liver organoid by incorporating human iPSC-derived blood vessel
Mutations in DNAJC19 cause altered mitochondrial structure and increased mitochondrial respiration in human iPSC-derived cardiomyocytes
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
Human iPSC-derived microglia carrying the LRRK2-G2019S mutation show a Parkinson’s disease related transcriptional profile and function
Human iPSC-derived pericyte-like cells carrying APP Swedish mutation overproduce beta-amyloid and induce cerebral amyloid angiopathy-like changes
Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors
ACTN2 Mutant Causes Proteopathy in Human iPSC-Derived Cardiomyocytes
How is Excitotoxicity Being Modelled in iPSC-Derived Neurons?