Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model ; volume:9 ; number:1 ; day:7 ; month:2 ; year:2019 ; pages:1-12 ; date:12.2019
Scientific reports ; 9, Heft 1 (7.2.2019), 1-12, 12.2019
- Creator
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Fongy, Anaïs
Falcone, Sestina
Lainé, Jeanne
Prudhon, Bernard
Martins-Bach, Aurea
Bitoun, Marc
- Contributor
-
SpringerLink (Online service)
- DOI
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10.1038/s41598-018-38184-0
- URN
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urn:nbn:de:101:1-2019030822530419740834
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:56 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
- Fongy, Anaïs
- Falcone, Sestina
- Lainé, Jeanne
- Prudhon, Bernard
- Martins-Bach, Aurea
- Bitoun, Marc
- SpringerLink (Online service)
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Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy
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Differential impact of ubiquitous and muscle dynamin 2 isoforms in muscle physiology and centronuclear myopathy
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Cell stress molecules in the skeletal muscle of GNE myopathy
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy
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Age-dependent loss of Crls1 causes myopathy and skeletal muscle regeneration failure
Function of a mutant ryanodine receptor (T4709M) linked to congenital myopathy
Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy
Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy
Kalirin12 interacts with dynamin
Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy
Defects of Vps15 in skeletal muscles lead to autophagic vacuolar myopathy and lysosomal disease
Differential impact of ubiquitous and muscle dynamin 2 isoforms in muscle physiology and centronuclear myopathy
Shell Dynamin
Cell stress molecules in the skeletal muscle of GNE myopathy
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy
Skeletal myopathy in Pompe disease: a failure of satellite cell activation?
Age-dependent loss of Crls1 causes myopathy and skeletal muscle regeneration failure
Function of a mutant ryanodine receptor (T4709M) linked to congenital myopathy
Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy
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