Skeletal Muscle

Papers
(The median citation count of Skeletal Muscle is 4. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-05-01 to 2026-05-01.)
ArticleCitations
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy62
The paradox of hnRNPK: both absence and excess impair skeletal muscle function in mice58
Metabolic signatures and potential biomarkers of sarcopenia in suburb-dwelling older Chinese: based on untargeted GC–MS and LC–MS53
Non-regenerative myogenesis in adult skeletal muscles: myofiber death-independent muscle satellite cell expansion41
Abnormalities in the genioglossus muscle and its neuromuscular synapse in leptin-deficient male mice40
Pirfenidone treatment improves ischemic muscle function in mice with chronic kidney disease30
Golodirsen restores DMD transcript imbalance in Duchenne Muscular Dystrophy patient muscle cells26
Pilot investigations into the mechanistic basis for adverse effects of glucocorticoids in dysferlinopathy25
Zebrafish and cellular models of SELENON-Congenital myopathy exhibit novel embryonic and metabolic phenotypes23
SIX transcription factors are necessary for the activation of DUX4 expression in facioscapulohumeral muscular dystrophy22
ASM is a therapeutic target in dermatomyositis by regulating the differentiation of naive CD4 + T cells into Th17 and Treg subsets21
A knock down strategy for rapid, generic, and versatile modelling of muscular dystrophies in 3D-tissue-engineered-skeletal muscle20
Fibro-adipogenic progenitor cells in skeletal muscle unloading: metabolic and functional impairments18
Spiny mice are primed but fail to regenerate volumetric skeletal muscle loss injuries17
Comparative lipidomic and metabolomic profiling of mdx and severe mdx-apolipoprotein e-null mice16
AAV-NRIP gene therapy ameliorates motor neuron degeneration and muscle atrophy in ALS model mice15
Integrin αVβ5 regulates myoblast proliferation and differentiation in sarcopenia mice treated with FNDC5 gene delivery15
New tools for the investigation of muscle fiber-type spatial distributions across histological sections15
Extensive striated muscle damage in a rat model of Duchenne muscular dystrophy with Dmd exons 10–17 duplication14
Functional and structural pathologies in skeletal muscle of a rat model of Duchenne muscular dystrophy14
The contribution of skeletal muscle interstitial cells to myogenesis14
High-throughput muscle fiber typing from RNA sequencing data14
Necessity of Notch3 signaling in myofiber maturation in a pluripotent stem cell transplant model13
Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice12
Expression of Myomaker and Myomerger in myofibers causes muscle pathology12
Macroglossia and less advanced dystrophic change in the tongue muscle of the Duchenne muscular dystrophy rat11
Generation of a novel mouse model of nemaline myopathy due to recurrent NEB exon 55 deletion11
Decreased number of satellite cells-derived myonuclei in both fast- and slow-twitch muscles in HeyL-KO mice during voluntary running exercise10
The Myotube Analyzer: how to assess myogenic features in muscle stem cells10
Wnt7a is required for regeneration of dystrophic skeletal muscle10
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 fibers10
Fusion of myofibre branches is a physiological feature of healthy human skeletal muscle regeneration10
A 3D skeletal muscle system for disease modelling and secretome profiling of Duchenne muscular dystrophy10
Mll4 in skeletal muscle fibers maintains muscle stem cells9
Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1G93A amyotrophic lateral sclerosis (ALS) mouse model9
Role and mechanism of myonectin in severe acute pancreatitis: a crosstalk between skeletal muscle and pancreas9
Fighting for every beat: cardiac therapies in Duchenne muscular dystrophy9
IL-33-ST2 signaling in fibro-adipogenic progenitors alleviates immobilization-induced muscle atrophy in mice9
Spatiotemporal analysis of dystrophin expression during muscle repair8
CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I8
Eldecalcitol prevents muscle loss and osteoporosis in disuse muscle atrophy via NF-κB signaling in mice8
The metabolic role of corticotropin-releasing hormone receptor 2 and its UCN peptides: emerging therapeutic potential8
Multiple cis-regulatory modules ensure robust tup/islet1 function in dorsal muscle identity specification8
Angiogenesis precedes myogenesis during regeneration following biopsy injury of skeletal muscle8
Prolonged FOS activity disrupts a global myogenic transcriptional program by altering 3D chromatin architecture in primary muscle progenitor cells8
N-acetylglucosamine facilitates coordinated flow-like movement of myoblasts, forming a foundation for efficient myogenesis8
CtBP1 sustains activity-dependent muscle properties and dampens synaptic, contractile and metabolic changes triggered by denervation7
Electrical impedance myography detects dystrophin-related muscle changes in mdx mice7
TET exhibits enzymatic-independent and-dependent functions during Drosophila flight muscle development and aging7
Intramuscular fatty infiltration and its correlation with muscle composition and function in hip osteoarthritis7
FLASH: innovative integrated enzymatic-fluorescent labeling for automated muscle fiber typing, metabolic and morphometric analysis7
Contrasting Becker and Duchenne muscular dystrophy serum biomarker candidates by using data independent acquisition LC-MS/MS7
Metabolic pathways for removing reactive aldehydes are diminished in the skeletal muscle during heart failure7
TRPV1 manipulating polarization of M1/M2 macrophages to promote skeletal muscle regeneration7
Regulation of injury-induced skeletal myofiber regeneration by glucose transporter 4 (GLUT4)6
The double homeodomain protein DUX4c is associated with regenerating muscle fibers and RNA-binding proteins5
Sarcopenia: investigation of metabolic changes and its associated mechanisms5
Age-related gene expression signatures from limb skeletal muscles and the diaphragm in mice and rats reveal common and species-specific changes5
Displaced myonuclei are attributable to both resident myonuclear migration and stem cell fusion during mechanical loading in adult skeletal muscle5
Absence of the Z-disc protein α-actinin-3 impairs the mechanical stability of Actn3KO mouse fast-twitch muscle fibres without altering their contractile properties or twitch kinetics5
Pharmacology and macrophage modulation of HPGDS inhibitor PK007 demonstrate reduced disease severity in DMD-affected muscles of the mdx mouse model5
Extracellular vesicle distribution and localization in skeletal muscle at rest and following disuse atrophy5
Humidity impacts volatile anesthetic and heat responses of malignant hyperthermia susceptible mice4
Biomarkers for Duchenne muscular dystrophy progression: impact of age in the mdx tongue spared muscle4
Growth differentiation factor 10 inhibits fat infiltration in tongue muscles of mice with high-fat diet4
Aminoguanidine hemisulfate improves mitochondrial autophagy, oxidative stress, and muscle force in Duchenne muscular dystrophy via the AKT/FOXO1 pathway in mdx mice4
The prevalence of low muscle mass associated with obesity in the USA4
Identifying kinematic biomarkers of the dystrophic phenotype in a zebrafish model of Duchenne muscular dystrophy4
Cellular and molecular alterations to muscles and neuromuscular synapses in a mouse model of MEGF10-related myopathy4
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