Pluripotent stem cell-induced skeletal muscle progenitor cells with givinostat promote myoangiogenesis and restore dystrophin in injured Duchenne dystrophic muscle
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1757-6512
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Pluripotent stem cell-induced skeletal muscle progenitor cells with givinostat promote myoangiogenesis and restore dystrophin in injured Duchenne dystrophic muscle ; volume:12 ; number:1 ; day:12 ; month:2 ; year:2021 ; pages:1-15 ; date:12.2021
Stem cell research & therapy ; 12, Heft 1 (12.2.2021), 1-15, 12.2021
- Creator
-
Xuan, Wanling
Khan, Mahmood
Ashraf, Muhammad
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13287-021-02174-3
- URN
-
urn:nbn:de:101:1-2021040313163106614851
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:58 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
- Xuan, Wanling
- Khan, Mahmood
- Ashraf, Muhammad
- SpringerLink (Online service)
Other Objects (12)
Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function
The role of the dystrophin glycoprotein complex in muscle cell mechanotransduction
Quantitative immuno-mass spectrometry imaging of skeletal muscle dystrophin
Dystrophic Muscle Affects Motoneuron Axon Outgrowth and NMJ Assembly
Wnt7a is required for regeneration of dystrophic skeletal muscle
A case of dystrophic calcification in the masseter muscle
Single nuclei transcriptomics of muscle reveals intra-muscular cell dynamics linked to dystrophin loss and rescue
Targeted expression of heme oxygenase-1 in satellite cells improves skeletal muscle pathology in dystrophic mice
Dystrophin deficiency exacerbates skeletal muscle pathology in dysferlin-null mice
DRP-1-mediated apoptosis induces muscle degeneration in dystrophin mutants
Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle
Mll4 in skeletal muscle fibers maintains muscle stem cells
Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function
The role of the dystrophin glycoprotein complex in muscle cell mechanotransduction
Quantitative immuno-mass spectrometry imaging of skeletal muscle dystrophin
Dystrophic Muscle Affects Motoneuron Axon Outgrowth and NMJ Assembly
Wnt7a is required for regeneration of dystrophic skeletal muscle
A case of dystrophic calcification in the masseter muscle
Single nuclei transcriptomics of muscle reveals intra-muscular cell dynamics linked to dystrophin loss and rescue
Targeted expression of heme oxygenase-1 in satellite cells improves skeletal muscle pathology in dystrophic mice
Dystrophin deficiency exacerbates skeletal muscle pathology in dysferlin-null mice
DRP-1-mediated apoptosis induces muscle degeneration in dystrophin mutants
Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle
Mll4 in skeletal muscle fibers maintains muscle stem cells
Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function
The role of the dystrophin glycoprotein complex in muscle cell mechanotransduction
Quantitative immuno-mass spectrometry imaging of skeletal muscle dystrophin
Dystrophic Muscle Affects Motoneuron Axon Outgrowth and NMJ Assembly
Wnt7a is required for regeneration of dystrophic skeletal muscle
A case of dystrophic calcification in the masseter muscle
Single nuclei transcriptomics of muscle reveals intra-muscular cell dynamics linked to dystrophin loss and rescue
Targeted expression of heme oxygenase-1 in satellite cells improves skeletal muscle pathology in dystrophic mice
Dystrophin deficiency exacerbates skeletal muscle pathology in dysferlin-null mice
DRP-1-mediated apoptosis induces muscle degeneration in dystrophin mutants
Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle