OOIR: Observatory of International Research

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 2022-08-01 to 2026-08-01.)

Article	Citations
Enhancers integrate microenvironmental signals in muscle stem cells during regeneration in health, disease, and aging	62
iPSC-derived skeletal muscle spheroids for Duchenne Muscular Dystrophy modeling	41
Abnormalities in the genioglossus muscle and its neuromuscular synapse in leptin-deficient male mice	33
Caloric restriction reprograms skeletal muscle molecular pathways in non-human primates: potential relevance to human aging biology	31
The paradox of hnRNPK: both absence and excess impair skeletal muscle function in mice	30
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy	28
Metabolic signatures and potential biomarkers of sarcopenia in suburb-dwelling older Chinese: based on untargeted GC–MS and LC–MS	26
Non-regenerative myogenesis in adult skeletal muscles: myofiber death-independent muscle satellite cell expansion	25
Targeting muscle fibrosis using non-specific collagenase injections destabilizes the basal lamina and induces matrix remodeling	22
Pirfenidone treatment improves ischemic muscle function in mice with chronic kidney disease	20
Golodirsen restores DMD transcript imbalance in Duchenne Muscular Dystrophy patient muscle cells	19
Pilot investigations into the mechanistic basis for adverse effects of glucocorticoids in dysferlinopathy	18
Zebrafish and cellular models of SELENON-Congenital myopathy exhibit novel embryonic and metabolic phenotypes	17
A knock down strategy for rapid, generic, and versatile modelling of muscular dystrophies in 3D-tissue-engineered-skeletal muscle	16
ASM is a therapeutic target in dermatomyositis by regulating the differentiation of naive CD4 + T cells into Th17 and Treg subsets	16
SIX transcription factors are necessary for the activation of DUX4 expression in facioscapulohumeral muscular dystrophy	15
Fibro-adipogenic progenitor cells in skeletal muscle unloading: metabolic and functional impairments	15
Duchenne muscular dystrophy: from gene to gene-ius therapies	15
Comparative lipidomic and metabolomic profiling of mdx and severe mdx-apolipoprotein e-null mice	14
Spiny mice are primed but fail to regenerate volumetric skeletal muscle loss injuries	13
AAV-NRIP gene therapy ameliorates motor neuron degeneration and muscle atrophy in ALS model mice	13
Integrin αVβ5 regulates myoblast proliferation and differentiation in sarcopenia mice treated with FNDC5 gene delivery	12
Extensive striated muscle damage in a rat model of Duchenne muscular dystrophy with Dmd exons 10–17 duplication	12
New tools for the investigation of muscle fiber-type spatial distributions across histological sections	12
Functional and structural pathologies in skeletal muscle of a rat model of Duchenne muscular dystrophy	11

The contribution of skeletal muscle interstitial cells to myogenesis	11
Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice	11
Necessity of Notch3 signaling in myofiber maturation in a pluripotent stem cell transplant model	11
Expression of Myomaker and Myomerger in myofibers causes muscle pathology	11
Elizabeth Chen is elected to the U.S. National Academy of Sciences	11
Generation of a novel mouse model of nemaline myopathy due to recurrent NEB exon 55 deletion	10
Decreased number of satellite cells-derived myonuclei in both fast- and slow-twitch muscles in HeyL-KO mice during voluntary running exercise	10
Wnt7a is required for regeneration of dystrophic skeletal muscle	9
A 3D skeletal muscle system for disease modelling and secretome profiling of Duchenne muscular dystrophy	9
Eldecalcitol prevents muscle loss and osteoporosis in disuse muscle atrophy via NF-κB signaling in mice	9
Fusion of myofibre branches is a physiological feature of healthy human skeletal muscle regeneration	9
Macroglossia and less advanced dystrophic change in the tongue muscle of the Duchenne muscular dystrophy rat	9
Fighting for every beat: cardiac therapies in Duchenne muscular dystrophy	9
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	9
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 model	9
Spatiotemporal analysis of dystrophin expression during muscle repair	8
Angiogenesis precedes myogenesis during regeneration following biopsy injury of skeletal muscle	8
IL-33-ST2 signaling in fibro-adipogenic progenitors alleviates immobilization-induced muscle atrophy in mice	8
Prolonged FOS activity disrupts a global myogenic transcriptional program by altering 3D chromatin architecture in primary muscle progenitor cells	8
Role and mechanism of myonectin in severe acute pancreatitis: a crosstalk between skeletal muscle and pancreas	8
Mll4 in skeletal muscle fibers maintains muscle stem cells	8
N-acetylglucosamine facilitates coordinated flow-like movement of myoblasts, forming a foundation for efficient myogenesis	7
CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I	7
Metabolic pathways for removing reactive aldehydes are diminished in the skeletal muscle during heart failure	7
The metabolic role of corticotropin-releasing hormone receptor 2 and its UCN peptides: emerging therapeutic potential	7
Intramuscular fatty infiltration and its correlation with muscle composition and function in hip osteoarthritis	7
Multiple cis-regulatory modules ensure robust tup/islet1 function in dorsal muscle identity specification	7
FLASH: innovative integrated enzymatic-fluorescent labeling for automated muscle fiber typing, metabolic and morphometric analysis	6
Contrasting Becker and Duchenne muscular dystrophy serum biomarker candidates by using data independent acquisition LC-MS/MS	6
CtBP1 sustains activity-dependent muscle properties and dampens synaptic, contractile and metabolic changes triggered by denervation	6
Electrical impedance myography detects dystrophin-related muscle changes in mdx mice	6
TRPV1 manipulating polarization of M1/M2 macrophages to promote skeletal muscle regeneration	6
Sarcopenia: investigation of metabolic changes and its associated mechanisms	5
Regulation of injury-induced skeletal myofiber regeneration by glucose transporter 4 (GLUT4)	5
TET exhibits enzymatic-independent and-dependent functions during Drosophila flight muscle development and aging	5
Displaced myonuclei are attributable to both resident myonuclear migration and stem cell fusion during mechanical loading in adult skeletal muscle	5
Extracellular vesicle distribution and localization in skeletal muscle at rest and following disuse atrophy	5
Combatting ventilator induced diaphragm dysfunction with human bone marrow mesenchymal stromal cell-derived extracellular vesicles	4
NSAIDs trigger drug-specific response to exercise: a multi-omics systems biology analysis of a randomized crossover trial	4
Humidity impacts volatile anesthetic and heat responses of malignant hyperthermia susceptible mice	4
Identifying kinematic biomarkers of the dystrophic phenotype in a zebrafish model of Duchenne muscular dystrophy	4
Pharmacology and macrophage modulation of HPGDS inhibitor PK007 demonstrate reduced disease severity in DMD-affected muscles of the mdx mouse model	4
Growth differentiation factor 10 inhibits fat infiltration in tongue muscles of mice with high-fat diet	4
Biomarkers for Duchenne muscular dystrophy progression: impact of age in the mdx tongue spared muscle	4
Age-related gene expression signatures from limb skeletal muscles and the diaphragm in mice and rats reveal common and species-specific changes	4
The double homeodomain protein DUX4c is associated with regenerating muscle fibers and RNA-binding proteins	4
DUX4 at 25: how it emerged from “junk DNA” to become the cause of facioscapulohumeral muscular dystrophy	4