Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2044-5040

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function ; volume:10 ; number:1 ; day:27 ; month:11 ; year:2020 ; pages:1-16 ; date:12.2020
Skeletal muscle ; 10, Heft 1 (27.11.2020), 1-16, 12.2020

Creator: Hall, Arielle
Fontelonga, Tatiana
Wright, Alec
Bugda Gwilt, Katlynn
Widrick, Jeffrey
Pasut, Alessandra
Villa, Francesco
Miranti, Cynthia K.
Gibbs, Devin
Jiang, Evan
Meng, Hui
Lawlor, Michael W.
Gussoni, Emanuela

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13395-020-00252-3

URN: urn:nbn:de:101:1-2021010718301484334091

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:38 AM CEST

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Associated

Hall, Arielle
Fontelonga, Tatiana
Wright, Alec
Bugda Gwilt, Katlynn
Widrick, Jeffrey
Pasut, Alessandra
Villa, Francesco
Miranti, Cynthia K.
Gibbs, Devin
Jiang, Evan
Meng, Hui
Lawlor, Michael W.
Gussoni, Emanuela
SpringerLink (Online service)

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Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function

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Other Objects (12)

Stem cell activation in skeletal muscle regeneration

Pluripotent stem cell-induced skeletal muscle progenitor cells with givinostat promote myoangiogenesis and restore dystrophin in injured Duchenne dystrophic muscle

Dystrophic Muscle Affects Motoneuron Axon Outgrowth and NMJ Assembly

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A case of dystrophic calcification in the masseter muscle

Combinatorial activation of the WNT ‐dependent fibrogenic program by distinct complement subunits in dystrophic muscle

A muscle model for hybrid muscle activation

Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle

Relative persistence of AAV serotype 1 vector genomes in dystrophic muscle

Mll4 in skeletal muscle fibers maintains muscle stem cells

Preoperative muscle thickness influences muscle activation after arthroscopic knee surgery

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Stem cell activation in skeletal muscle regeneration

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Dystrophic Muscle Affects Motoneuron Axon Outgrowth and NMJ Assembly

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A case of dystrophic calcification in the masseter muscle

Combinatorial activation of the WNT ‐dependent fibrogenic program by distinct complement subunits in dystrophic muscle

A muscle model for hybrid muscle activation

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Stem cell activation in skeletal muscle regeneration

Pluripotent stem cell-induced skeletal muscle progenitor cells with givinostat promote myoangiogenesis and restore dystrophin in injured Duchenne dystrophic muscle

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

Combinatorial activation of the WNT ‐dependent fibrogenic program by distinct complement subunits in dystrophic muscle

A muscle model for hybrid muscle activation

Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle

Relative persistence of AAV serotype 1 vector genomes in dystrophic muscle

Mll4 in skeletal muscle fibers maintains muscle stem cells

Preoperative muscle thickness influences muscle activation after arthroscopic knee surgery

Hoxa9 activation by epigenetic alterations in aging muscle stem cells induces developmental signals impairing regeneration of aging muscle

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