Differential impact of ubiquitous and muscle dynamin 2 isoforms in muscle physiology and centronuclear myopathy
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2041-1723
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Differential impact of ubiquitous and muscle dynamin 2 isoforms in muscle physiology and centronuclear myopathy ; volume:13 ; number:1 ; day:11 ; month:11 ; year:2022 ; pages:1-20 ; date:12.2022
Nature Communications ; 13, Heft 1 (11.11.2022), 1-20, 12.2022
- Urheber
-
Gómez-Oca, Raquel
Edelweiss, Evelina
Djeddi, Sarah
Gerbier, Mathias
Massana-Muñoz, Xènia
Oulad-Abdelghani, Mustapha
Crucifix, Corinne
Spiegelhalter, Coralie
Messaddeq, Nadia
Poussin-Courmontagne, Pierre
Koebel, Pascale
Cowling, Belinda S.
Laporte, Jocelyn
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-022-34490-4
- URN
-
urn:nbn:de:101:1-2023012521195974871996
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:36 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Gómez-Oca, Raquel
- Edelweiss, Evelina
- Djeddi, Sarah
- Gerbier, Mathias
- Massana-Muñoz, Xènia
- Oulad-Abdelghani, Mustapha
- Crucifix, Corinne
- Spiegelhalter, Coralie
- Messaddeq, Nadia
- Poussin-Courmontagne, Pierre
- Koebel, Pascale
- Cowling, Belinda S.
- Laporte, Jocelyn
- SpringerLink (Online service)
Ähnliche Objekte (12)
Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model
Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy
Cyclo His‐Pro Attenuates Muscle Degeneration in Murine Myopathy Models
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy
Cell stress molecules in the skeletal muscle of GNE myopathy
Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy
Ultrasound-guided muscle biopsy: a practical alternative for investigation of myopathy
Muscle-fiber transdifferentiation in an experimental model of respiratory chain myopathy
Nemaline myopathy in Brazilian patients: clinical, muscle imaging and molecular characterization
GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice
Muscle fiber transdifferentiation in an experimental model of respiratory chain myopathy
GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice
Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model
Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy
Cyclo His‐Pro Attenuates Muscle Degeneration in Murine Myopathy Models
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy
Cell stress molecules in the skeletal muscle of GNE myopathy
Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy
Ultrasound-guided muscle biopsy: a practical alternative for investigation of myopathy
Muscle-fiber transdifferentiation in an experimental model of respiratory chain myopathy
Nemaline myopathy in Brazilian patients: clinical, muscle imaging and molecular characterization
GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice
Muscle fiber transdifferentiation in an experimental model of respiratory chain myopathy
GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice
Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model
Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy
Cyclo His‐Pro Attenuates Muscle Degeneration in Murine Myopathy Models
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy
Cell stress molecules in the skeletal muscle of GNE myopathy
Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy
Ultrasound-guided muscle biopsy: a practical alternative for investigation of myopathy
Muscle-fiber transdifferentiation in an experimental model of respiratory chain myopathy
Nemaline myopathy in Brazilian patients: clinical, muscle imaging and molecular characterization
GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice
Muscle fiber transdifferentiation in an experimental model of respiratory chain myopathy