Decrease of myofiber branching via muscle-specific expression of the olfactory receptor mOR23 in dystrophic muscle leads to protection against mechanical stress

Abnormal branched myofibers within skeletal muscles are commonly found in diverse animal models of muscular dystrophy as well as in patients. Branched myofibers from dystrophic mice are more susceptible to break than unbranched myofibers suggesting that muscles containing a high percentage of these...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Skeletal muscle 2016-01, Vol.6 (2), p.2-2, Article 2
Hauptverfasser:	Pichavant, Christophe, Burkholder, Thomas J, Pavlath, Grace K
Format:	Artikel
Sprache:	eng
Schlagworte:	Age Factors Animals Barium Compounds - toxicity Cell Membrane - metabolism Cell Membrane - pathology Chlorides - toxicity Disease Models, Animal Female G proteins Hybridization, Genetic Male Membrane proteins Mice, Inbred mdx Mice, Transgenic Muscle Contraction Muscle, Skeletal - drug effects Muscle, Skeletal - metabolism Muscle, Skeletal - pathology Muscle, Skeletal - physiopathology Muscles Muscular Dystrophy, Duchenne - genetics Muscular Dystrophy, Duchenne - metabolism Muscular Dystrophy, Duchenne - pathology Muscular Dystrophy, Duchenne - physiopathology Myofibrils - drug effects Myofibrils - metabolism Myofibrils - pathology Receptors, Odorant - genetics Receptors, Odorant - metabolism Regeneration Stress, Mechanical Up-Regulation
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!