Skeletal Muscle

Papers
(The TQCC of Skeletal Muscle is 10. 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
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy40
The SarcoEndoplasmic Reticulum Calcium ATPase (SERCA) pump: a potential target for intervention in aging and skeletal muscle pathologies40
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
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
High-throughput muscle fiber typing from RNA sequencing data13
New tools for the investigation of muscle fiber-type spatial distributions across histological sections13
Metabolomic signatures for the longitudinal reduction of muscle strength over 10 years12
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
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
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
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
The Myotube Analyzer: how to assess myogenic features in muscle stem cells10
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