Upon submission, in your cover letter, please include the names of at least five potential reviewers, in the relevant field of research, to review your manuscript. In light of this, please ensure that there are no conflicts of interest.
Call for Papers: Cellular microenvironments in skeletal muscle homeostasis, regeneration, and disease
Skeletal Muscle is calling for submissions to our new Collection on Cellular microenvironments in skeletal muscle homeostasis, regeneration, and disease. This Collection focuses on signaling interactions, changes during muscle regeneration, perturbations in aging and disease, and the biomechanical cues involved in muscle homeostasis and repair.
Call for Papers: Skeletal Muscle Fiber Heterogeneity
Skeletal Muscle is calling for submissions to our new Collection on Skeletal Muscle Fiber Heterogeneity. This Collection aims to explore the diverse facets of muscle fiber heterogeneity.
Call for Papers: In Vitro Models of Skeletal Muscle
Skeletal Muscle is calling for submissions to our new Collection on In Vitro Models of Skeletal Muscle. This Collection aims to showcase advancements in in vitro modeling of skeletal muscle physiology and pathology.
Featured Article: Zebrafish and cellular models of SELENON-Congenital myopathy exhibit novel embryonic and metabolic phenotypes
SELENON-Congenital Myopathy (SELENON-CM) is a rare congenital myopathy caused by mutations of the SELENON gene characterized by axial muscle weakness and progressive respiratory insufficiency. Muscle histopathology may be non-specific, but commonly includes multiminicores or a dystrophic pattern. The SELENON gene encodes selenoprotein N (SelN), a selenocysteine-containing redox enzyme located in the endo/sarcoplasmic reticulum membrane where it colocalizes with mitochondria-associated membranes. However, the molecular mechanism(s) by which SelN deficiency cause SELENON-CM remain poorly understood. A hurdle is the lack of cellular and animal models that show easily assayable phenotypes.
Authors: Pamela Barraza-Flores, Behzad Moghadaszadeh, Won Lee, Biju Isaac, Liang Sun, Emily T. Hickey, Shira Rockowitz, Piotr Sliz & Alan H. Beggs
Published: 15 March 2025
Additional Cover Letter Guidelines
Articles
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Forskolin treatment enhances muscle regeneration and shows therapeutic potential with limitations in Duchenne muscular dystrophy
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Pharmacology and macrophage modulation of HPGDS inhibitor PK007 demonstrate reduced disease severity in DMD-affected muscles of the mdx mouse model
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Endurance exercise with reduced muscle glycogen content influences substrate utilization and attenuates acute mTORC1- and autophagic signaling in human type I and type II muscle fibers
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Generation of a novel mouse model of nemaline myopathy due to recurrent NEB exon 55 deletion
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The endogenous molecular clock orchestrates the temporal separation of substrate metabolism in skeletal muscle
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Aberrant repair and fibrosis development in skeletal muscle
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Regulation of skeletal muscle growth by the IGF1-Akt/PKB pathway: insights from genetic models
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Idiopathic inflammatory myopathies: pathogenic mechanisms of muscle weakness
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T-tubule biogenesis and triad formation in skeletal muscle and implication in human diseases
Aims and scope
Skeletal Muscle is a peer-reviewed, open access, online journal that publishes articles investigating molecular mechanisms underlying the biology of skeletal muscle. A wide range of skeletal muscle biology is included: development, metabolism, the regulation of mass and function, aging, degeneration, dystrophy and regeneration. The emphasis is on understanding adult skeletal muscle, its maintenance, and its interactions with non-muscle cell types and regulatory modulators.
Editor quotes
Carmen Birchmeier, co-Editor- in-Chief
"Skeletal muscle provides a platform for work on basic mechanisms used during muscle development, regeneration disease and aging. I find the similarities and differences between developing and adult muscle stem cells particularly fascinating."
Markus A Rüegg, co-Editor-in-Chief
"Skeletal Muscle publishes influential mechanistic and methodological papers in the field and has become an important journal for my own research. I hope to further strengthen the journal´s coverage of mechanisms involved in the pathology of neuromuscular diseases."
David Glass, Founding Editor-in-Chief
"The goal of the journal is to understand how the skeletal muscle relevant cellular systems work, so that one might be able to improve human health and combat disease.”
Annual Journal Metrics
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Citation Impact 2023
Journal Impact Factor: 5.3
5-year Journal Impact Factor: 5.0
Source Normalized Impact per Paper (SNIP): 1.140
SCImago Journal Rank (SJR): 1.856Speed 2024
Submission to first editorial decision (median days): 8
Submission to acceptance (median days): 126Usage 2024
Downloads: 440,684
Altmetric mentions: 211