Satellite cells deficiency and defective regeneration in dynamin 2-related centronuclear myopathy.
GTPase
congenital
injury
muscle
stem cell
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
ISSN: 1530-6860
Titre abrégé: FASEB J
Pays: United States
ID NLM: 8804484
Informations de publication
Date de publication:
04 2021
04 2021
Historique:
revised:
23
11
2020
received:
27
05
2020
accepted:
21
12
2020
entrez:
14
3
2021
pubmed:
15
3
2021
medline:
22
7
2021
Statut:
ppublish
Résumé
Dynamin 2 (DNM2) is a ubiquitously expressed protein involved in many functions related to trafficking and remodeling of membranes and cytoskeleton dynamics. Mutations in the DNM2 gene cause the autosomal dominant centronuclear myopathy (AD-CNM), characterized mainly by muscle weakness and central nuclei. Several defects have been identified in the KI-Dnm2
Identifiants
pubmed: 33715228
doi: 10.1096/fj.202001313RRR
doi:
Substances chimiques
Myogenic Regulatory Factors
0
DNM2 protein, mouse
EC 3.6.5.5
Dynamin II
EC 3.6.5.5
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e21346Informations de copyright
© 2021 Federation of American Societies for Experimental Biology.
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