Skeletal Muscle

Papers
(The median citation count of Skeletal Muscle is 6. 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 2020-03-01 to 2024-03-01.)
ArticleCitations
A reference single-cell transcriptomic atlas of human skeletal muscle tissue reveals bifurcated muscle stem cell populations113
Protein profile of fiber types in human skeletal muscle: a single-fiber proteomics study60
Origins, potency, and heterogeneity of skeletal muscle fibro-adipogenic progenitors—time for new definitions55
Exercise promotes satellite cell contribution to myofibers in a load-dependent manner50
Muscle spindle function in healthy and diseased muscle47
Ryanodine receptor 1-related disorders: an historical perspective and proposal for a unified nomenclature44
Epigenetic regulation of satellite cell fate during skeletal muscle regeneration40
The Notch signaling network in muscle stem cells during development, homeostasis, and disease37
Transgenic mice expressing tunable levels of DUX4 develop characteristic facioscapulohumeral muscular dystrophy-like pathophysiology ranging in severity36
The SarcoEndoplasmic Reticulum Calcium ATPase (SERCA) pump: a potential target for intervention in aging and skeletal muscle pathologies32
Optimized method for extraction of exosomes from human primary muscle cells30
Functional effects of muscle PGC-1alpha in aged animals28
Exercise enhances mitochondrial fission and mitophagy to improve myopathy following critical limb ischemia in elderly mice via the PGC1a/FNDC5/irisin pathway27
MyoSight—semi-automated image analysis of skeletal muscle cross sections26
High-throughput proteomics fiber typing (ProFiT) for comprehensive characterization of single skeletal muscle fibers26
Acute conversion of patient-derived Duchenne muscular dystrophy iPSC into myotubes reveals constitutive and inducible over-activation of TGFβ-dependent pro-fibrotic signaling25
Amiloride ameliorates muscle wasting in cancer cachexia through inhibiting tumor-derived exosome release24
A novel chemical-combination screen in zebrafish identifies epigenetic small molecule candidates for the treatment of Duchenne muscular dystrophy19
The influence of age, sex, and exercise on autophagy, mitophagy, and lysosome biogenesis in skeletal muscle19
Expression of MuRF1 or MuRF2 is essential for the induction of skeletal muscle atrophy and dysfunction in a murine pulmonary hypertension model19
The role of Nrf2 in acute and chronic muscle injury18
The pan HDAC inhibitor Givinostat improves muscle function and histological parameters in two Duchenne muscular dystrophy murine models expressing different haplotypes of the LTBP4 gene17
Differences in muscle satellite cell dynamics during muscle hypertrophy and regeneration17
The ties that bind: functional clusters in limb-girdle muscular dystrophy16
Severe acute myopathy following SARS-CoV-2 infection: a case report and review of recent literature15
Complementary NAD+ replacement strategies fail to functionally protect dystrophin-deficient muscle14
MiR-1290 promotes myoblast differentiation and protects against myotube atrophy via Akt/p70/FoxO3 pathway regulation14
Preservation of satellite cell number and regenerative potential with age reveals locomotory muscle bias14
Simvastatin does not alleviate muscle pathology in a mouse model of Duchenne muscular dystrophy13
X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterisation12
Efficient engraftment of pluripotent stem cell-derived myogenic progenitors in a novel immunodeficient mouse model of limb girdle muscular dystrophy 2I12
Meeting report: the 2021 FSHD International Research Congress11
A novel approach for the isolation and long-term expansion of pure satellite cells based on ice-cold treatment11
The prevalence of low muscle mass associated with obesity in the USA10
Analysis of human satellite cell dynamics on cultured adult skeletal muscle myofibers10
SMN-deficiency disrupts SERCA2 expression and intracellular Ca2+ signaling in cardiomyocytes from SMA mice and patient-derived iPSCs9
Dynamics of myogenic differentiation using a novel Myogenin knock-in reporter mouse9
Angiotensin-converting-enzyme inhibitor prevents skeletal muscle fibrosis in myocardial infarction mice9
Exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue9
Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function9
ViaFuse: Fiji macros to calculate skeletal muscle cell viability and fusion index9
Sarcoglycan A mutation in miniature dachshund dogs causes limb-girdle muscular dystrophy 2D8
Multi-omics reveals age-related differences in the diaphragm response to mechanical ventilation: a pilot study8
Nanopattern surface improves cultured human myotube maturation8
A novel transplantable model of lung cancer-associated tissue loss and disrupted muscle regeneration8
The Myotube Analyzer: how to assess myogenic features in muscle stem cells8
Muscle atrophy induced by overexpression of ALAS2 is related to muscle mitochondrial dysfunction7
Effect of chronic intermittent hypoxia (CIH) on neuromuscular junctions and mitochondria in slow- and fast-twitch skeletal muscles of mice—the role of iNOS7
Extracellular vesicle distribution and localization in skeletal muscle at rest and following disuse atrophy7
Pro-myogenic small molecules revealed by a chemical screen on primary muscle stem cells7
Transcription factor signal transducer and activator of transcription 6 (STAT6) is an inhibitory factor for adult myogenesis6
Investigating the correlation of muscle function tests and sarcomere organization in C. elegans6
Mouse models of SMA show divergent patterns of neuronal vulnerability and resilience6
Functional replacement of myostatin with GDF-11 in the germline of mice6
Angiogenesis precedes myogenesis during regeneration following biopsy injury of skeletal muscle6
Growth differentiation factor 11 induces skeletal muscle atrophy via a STAT3-dependent mechanism in pulmonary arterial hypertension6
Prolonged FOS activity disrupts a global myogenic transcriptional program by altering 3D chromatin architecture in primary muscle progenitor cells6
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