Genome Editing and Muscle Stem Cells as a Therapeutic Tool for Muscular Dystrophies
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2198-7866
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Genome Editing and Muscle Stem Cells as a Therapeutic Tool for Muscular Dystrophies ; day:24 ; month:4 ; year:2017 ; pages:1-12
Current stem cell reports ; (24.4.2017), 1-12
- Creator
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Pini, Veronica
- Contributor
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Morgan, Jennifer E.
Muntoni, Francesco
O’Neill, Helen C.
SpringerLink (Online service)
- DOI
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10.1007/s40778-017-0076-6
- URN
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urn:nbn:de:1111-201705066068
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:54 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
- Pini, Veronica
- Morgan, Jennifer E.
- Muntoni, Francesco
- O’Neill, Helen C.
- SpringerLink (Online service)
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Timed immersion expiration measures in patients with muscular dystrophies
Therapy development for spinal muscular atrophy: perspectives for muscular dystrophies and neurodegenerative disorders
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Human iPSC Models to Study Orphan Diseases: Muscular Dystrophies
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Systemic cell therapy for muscular dystrophies : The ultimate transplantable muscle progenitor cell and current challenges for clinical efficacy
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Comparison of splicing and nuclear envelope alterations in three muscular dystrophies
A human skeletal muscle interactome centered on proteins involved in muscular dystrophies: LGMD interactome
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Calpain 3 is important for muscle regeneration: Evidence from patients with limb girdle muscular dystrophies
Timed immersion expiration measures in patients with muscular dystrophies
Therapy development for spinal muscular atrophy: perspectives for muscular dystrophies and neurodegenerative disorders
Muscle Stem/Progenitor Cells and Mesenchymal Stem Cells of Bone Marrow Origin for Skeletal Muscle Regeneration in Muscular Dystrophies
Human iPSC Models to Study Orphan Diseases: Muscular Dystrophies
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