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 2021-09-01 to 2025-09-01.)
ArticleCitations
Abnormalities in the genioglossus muscle and its neuromuscular synapse in leptin-deficient male mice126
Metabolic signatures and potential biomarkers of sarcopenia in suburb-dwelling older Chinese: based on untargeted GC–MS and LC–MS92
The paradox of hnRNPK: both absence and excess impair skeletal muscle function in mice84
The SarcoEndoplasmic Reticulum Calcium ATPase (SERCA) pump: a potential target for intervention in aging and skeletal muscle pathologies40
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy40
Golodirsen restores DMD transcript imbalance in Duchenne Muscular Dystrophy patient muscle cells38
ASM is a therapeutic target in dermatomyositis by regulating the differentiation of naive CD4 + T cells into Th17 and Treg subsets28
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 phenotypes24
Fibro-adipogenic progenitor cells in skeletal muscle unloading: metabolic and functional impairments23
SIX transcription factors are necessary for the activation of DUX4 expression in facioscapulohumeral muscular dystrophy22
Comparative lipidomic and metabolomic profiling of mdx and severe mdx-apolipoprotein e-null mice19
A knock down strategy for rapid, generic, and versatile modelling of muscular dystrophies in 3D-tissue-engineered-skeletal muscle19
Spiny mice are primed but fail to regenerate volumetric skeletal muscle loss injuries17
AAV-NRIP gene therapy ameliorates motor neuron degeneration and muscle atrophy in ALS model mice15
Effect of chronic intermittent hypoxia (CIH) on neuromuscular junctions and mitochondria in slow- and fast-twitch skeletal muscles of mice—the role of iNOS14
High-throughput muscle fiber typing from RNA sequencing data13
New tools for the investigation of muscle fiber-type spatial distributions across histological sections13
Improved CRISPR/Cas9 gene editing in primary human myoblasts using low confluency cultures on Matrigel13
Extensive striated muscle damage in a rat model of Duchenne muscular dystrophy with Dmd exons 10–17 duplication13
Decreased number of satellite cells-derived myonuclei in both fast- and slow-twitch muscles in HeyL-KO mice during voluntary running exercise12
Generation of a novel mouse model of nemaline myopathy due to recurrent NEB exon 55 deletion12
Expression of Myomaker and Myomerger in myofibers causes muscle pathology12
Metabolomic signatures for the longitudinal reduction of muscle strength over 10 years12
Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice11
Fusion of myofibre branches is a physiological feature of healthy human skeletal muscle regeneration11
Macroglossia and less advanced dystrophic change in the tongue muscle of the Duchenne muscular dystrophy rat11
Wnt7a is required for regeneration of dystrophic skeletal muscle11
The Myotube Analyzer: how to assess myogenic features in muscle stem cells10
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
IL-33-ST2 signaling in fibro-adipogenic progenitors alleviates immobilization-induced muscle atrophy in mice9
Role and mechanism of myonectin in severe acute pancreatitis: a crosstalk between skeletal muscle and pancreas9
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
Mll4 in skeletal muscle fibers maintains muscle stem cells9
Prolonged FOS activity disrupts a global myogenic transcriptional program by altering 3D chromatin architecture in primary muscle progenitor cells8
Eldecalcitol prevents muscle loss and osteoporosis in disuse muscle atrophy via NF-κB signaling in mice8
Electrical impedance myography detects dystrophin-related muscle changes in mdx mice7
Intramuscular fatty infiltration and its correlation with muscle composition and function in hip osteoarthritis7
Multiple cis-regulatory modules ensure robust tup/islet1 function in dorsal muscle identity specification7
Novel γ-sarcoglycan interactors in murine muscle membranes7
Angiogenesis precedes myogenesis during regeneration following biopsy injury of skeletal muscle7
CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I7
Metabolic pathways for removing reactive aldehydes are diminished in the skeletal muscle during heart failure7
Muscle stem cell adaptations to cellular and environmental stress7
Contrasting Becker and Duchenne muscular dystrophy serum biomarker candidates by using data independent acquisition LC-MS/MS6
Sarcopenia: investigation of metabolic changes and its associated mechanisms6
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 kinetics6
Pharmacology and macrophage modulation of HPGDS inhibitor PK007 demonstrate reduced disease severity in DMD-affected muscles of the mdx mouse model6
Functional replacement of myostatin with GDF-11 in the germline of mice6
Age-related gene expression signatures from limb skeletal muscles and the diaphragm in mice and rats reveal common and species-specific changes6
Identifying kinematic biomarkers of the dystrophic phenotype in a zebrafish model of Duchenne muscular dystrophy6
Regulation of injury-induced skeletal myofiber regeneration by glucose transporter 4 (GLUT4)6
Extracellular vesicle distribution and localization in skeletal muscle at rest and following disuse atrophy6
Growth differentiation factor 10 inhibits fat infiltration in tongue muscles of mice with high-fat diet6
Cellular and molecular alterations to muscles and neuromuscular synapses in a mouse model of MEGF10-related myopathy5
Dysregulated ATX-LPA and YAP/TAZ signaling in dystrophic Sgcd−/− mice with early fibrosis and inflammation5
Aminoguanidine hemisulfate improves mitochondrial autophagy, oxidative stress, and muscle force in Duchenne muscular dystrophy via the AKT/FOXO1 pathway in mdx mice5
The double homeodomain protein DUX4c is associated with regenerating muscle fibers and RNA-binding proteins5
DUX4 at 25: how it emerged from “junk DNA” to become the cause of facioscapulohumeral muscular dystrophy4
The prevalence of low muscle mass associated with obesity in the USA4
Age-related differences in the loss and recovery of serial sarcomere number following disuse atrophy in rats4
Biomarkers for Duchenne muscular dystrophy progression: impact of age in the mdx tongue spared muscle4
David J. Glass elected to the U.S. National Academy of Sciences4
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