Results 1 to 10 of about 25,961 (162)

FGF6 in myogenesis

open access: yesBiochimica Et Biophysica Acta - Molecular Cell Research, 2006
Important functions in myogenesis have been proposed for FGF6, a member of the fibroblast growth factor family accumulating almost exclusively in the myogenic lineage. However, the analyses of Fgf6 (-/-) mutant mice gave contradictory results and the role of FGF6 during myogenesis remained largely unclear.
Christophe Chanoine
exaly   +5 more sources

Coupling between Myogenesis and Angiogenesis during Skeletal Muscle Regeneration Is Stimulated by Restorative Macrophages

open access: yesStem Cell Reports, 2017
Summary: In skeletal muscle, new functions for vessels have recently emerged beyond oxygen and nutrient supply, through the interactions that vascular cells establish with muscle stem cells. Here, we demonstrate in human and mouse that endothelial cells (
Claire Latroche   +2 more
exaly   +3 more sources

Wnt signaling in myogenesis [PDF]

open access: yesTrends in Cell Biology, 2012
The formation of skeletal muscle is a tightly regulated process that is critically modulated by Wnt signaling. Myogenesis is dependent on the precise and dynamic integration of multiple Wnt signals allowing self-renewal and progression of muscle precursors in the myogenic lineage.
Julia Von Maltzahn   +2 more
exaly   +3 more sources

Non-regenerative myogenesis in adult skeletal muscles: myofiber death-independent muscle satellite cell expansion [PDF]

open access: yesSkeletal Muscle
Muscle regeneration processes triggered by injuries following myofiber death have been extensively investigated owing to the availability of suitable in vivo animal models, including disease models.
So-ichiro Fukada   +3 more
doaj   +2 more sources

The Role of Oxidative Stress in Skeletal Muscle Myogenesis and Muscle Disease

open access: yesAntioxidants, 2022
The contractile activity, high oxygen consumption and metabolic rate of skeletal muscle cause it to continuously produce moderate levels of oxidant species, such as reactive oxygen species (ROS) and reactive nitrogen species (RNS).
Di Lian, Mingming Chen, Hanyu Wu
exaly   +3 more sources

Pitx2 Differentially Regulates the Distinct Phases of Myogenic Program and Delineates Satellite Cell Lineages During Muscle Development

open access: yesFrontiers in Cell and Developmental Biology, 2022
The knowledge of the molecular mechanisms that regulate embryonic myogenesis from early myogenic progenitors to myoblasts, as well as the emergence of adult satellite stem cells (SCs) during development, are key concepts to understanding the genesis and ...
Felícitas Ramírez de Acuña   +16 more
doaj   +1 more source

miR-106b is a novel target to promote muscle regeneration and restore satellite stem cell function in injured Duchenne dystrophic muscle

open access: yesMolecular Therapy: Nucleic Acids, 2022
Satellite cells (SCs), muscle stem cells, display functional heterogeneity, and dramatic changes linked to their regenerative capabilities are associated with muscle-wasting diseases.
Lara Rodriguez-Outeiriño   +11 more
doaj   +1 more source

Mitochondrial Oxidative Stress and Mitophagy Activation Contribute to TNF-Dependent Impairment of Myogenesis

open access: yesAntioxidants, 2023
Many muscular pathologies are associated with oxidative stress and elevated levels of the tumor necrosis factor (TNF) that cause muscle protein catabolism and impair myogenesis.
Daniil A. Chernyavskij   +7 more
doaj   +1 more source

TNF Signaling Acts Downstream of MiR-322/-503 in Regulating DM1 Myogenesis

open access: yesFrontiers in Endocrinology, 2022
Myotonic dystrophy type 1 (DM1) is caused by the expanded CUG repeats and usually displays defective myogenesis. Although we previously reported that ectopic miR-322/-503 expression improved myogenesis in DM1 by targeting the toxic RNA, the underlying ...
Meng Li   +18 more
doaj   +1 more source

Inhibition of Postn Rescues Myogenesis Defects in Myotonic Dystrophy Type 1 Myoblast Model

open access: yesFrontiers in Cell and Developmental Biology, 2021
Myotonic dystrophy type 1 (DM1) is an inherited neuromuscular disease caused by expanded CTG repeats in the 3′ untranslated region (3′UTR) of the DMPK gene.
Xiaopeng Shen   +27 more
doaj   +1 more source

Home - About - Disclaimer - Privacy