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• Adult onset tubulo-interstitial nephropathy in MT-ND5-related phenotypes
• Advances in the understanding of nuclear pore complexes in human diseases
• Advancing Tissue Damage Repair in Geriatric Diseases: Prospects of Combining Stem Cell-Derived Exosomes with Hydrogels
• Altered brown adipose tissue mitochondrial function in newborn fragile X syndrome mice
• Altered mitochondrial metabolism in peripheral blood cells from patients with inborn errors of β-oxidation
• Altered muscle mitochondrial, inflammatory and trophic markers, and reduced exercise training adaptations in type 1 diabetes
• ASC-1 Is a Cell Cycle Regulator Associated with Severe and Mild Forms of Myopathy
• Association of fingerprint bodies with rods in a case with mutations in the LMOD3 gene
• Autophagy Defects in Skeletal Myopathies
• Barth syndrome cardiomyopathy: targeting the mitochondria with elamipretide
• Beta-hydroxy beta-methyl butyrate decreases muscle protein degradation via increased Akt/FoxO3a signaling and mitochondrial biogenesis in weanling piglets after lipopolysaccharide challenge
• Case Report: PNPLA2 Gene Complex Heterozygous Mutation Leading to Neutral Lipid Storage Disease With Myopathy
• Chaperones in sporadic inclusion body myositis-Validation of proteomic data
• Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation
• Curcumin alleviates arsenic-induced injury in duck skeletal muscle via regulating the PINK1/Parkin pathway and protecting mitochondrial function
• CYLD dysregulation in pathogenesis of sporadic inclusion body myositis
• Cytotoxic immune cells do not affect TDP-43 and p62 sarcoplasmic aggregation but influence TDP-43 localisation
• Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy
• Diagnosis and Clinical Development of Sporadic Inclusion Body Myositis and Polymyositis With Mitochondrial Pathology: A Single-Center Retrospective Analysis
• Diet-induced vitamin D deficiency reduces skeletal muscle mitochondrial respiration
• Distal myopathy and thrombocytopenia due to a novel GNE mutation
• DLK Activation Synergizes with Mitochondrial Dysfunction to Downregulate Axon Survival Factors and Promote SARM1-Dependent Axon Degeneration
• Early detection of skeletal muscle bioenergetic deficit by magnetic resonance spectroscopy in cigarette smoke-exposed mice
• Effects of Triheptanoin on Mitochondrial Respiration and Glycolysis in Cultured Fibroblasts from Neutral Lipid Storage Disease Type M (NLSD-M) Patients
• Essential amino acid formulations to prevent mitochondrial dysfunction and oxidative stress
• Expressing a Z-disk nebulin fragment in nebulin-deficient mouse muscle: effects on muscle structure and function
• Expression of huntingtin-associated protein 1 in adult mouse dorsal root ganglia and its neurochemical characterization in reference to sensory neuron subpopulations
• Feeder-supported in vitro exercise model using human satellite cells from patients with sporadic inclusion body myositis
• Golgi Outposts Nucleate Microtubules in Cells with Specialized Shapes
• Granulomatous myopathy: Sarcoidosis and beyond
• Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy
• High-dose atorvastatin therapy progressively decreases skeletal muscle mitochondrial respiratory capacity in humans
• High-fat diet affects skeletal muscle mitochondria comparable to pressure overload-induced heart failure
• Histology, Cell
• Histology, Cell
• Impact of sex, age at onset, and anti-cN1A antibodies on sporadic inclusion body myositis
• Impacts of exercise interventions on different diseases and organ functions in mice
• Increased intra-mitochondrial lipofuscin aggregates with spherical dense body formation in mitochondrial myopathy
• Increased mitochondrial Ca(2+) contributes to health decline with age and Duchene muscular dystrophy in C. elegans
• Increased mitochondrial Ca²⁺ contributes to health decline with age and Duchene muscular dystrophy in C. elegans
• Linkage between growth retardation and pituitary cell morphology in a dystrophin-deficient pig model of Duchenne muscular dystrophy
• Loss of TDP-43 function and rimmed vacuoles persist after T cell depletion in a xenograft model of sporadic inclusion body myositis
• Mechanisms and therapeutic prospects of mesenchymal stem cells-derived exosomes for tendinopathy
• Mesenchymal stromal cells ameliorate diabetes-induced muscle atrophy through exosomes by enhancing AMPK/ULK1-mediated autophagy
• Mitochondria and Critical Illness
• Mitochondrial augmentation of hematopoietic stem cells in children with single large-scale mitochondrial DNA deletion syndromes
• Mitochondrial Bioenergetics and Turnover during Chronic Muscle Disuse
• Mitochondrial creatine sensitivity is lost in the D2.<em>mdx</em> model of Duchenne muscular dystrophy and rescued by the mitochondrial-enhancing compound Olesoxime
• Mitochondrial creatine sensitivity is lost in the D2.mdx model of Duchenne muscular dystrophy and rescued by the mitochondrial-enhancing compound Olesoxime
• Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing
• Mitochondrial dysfunction and skeletal muscle atrophy: Causes, mechanisms, and treatment strategies
• Mitochondrial dysfunction underlying sporadic inclusion body myositis is ameliorated by the mitochondrial homing drug MA-5
• Mitochondrial transfer and implications for muscle function in idiopathic inflammatory myopathies
• Muscle weakness and mitochondrial stress occur before severe metastasis in a novel mouse model of ovarian cancer cachexia
• Muscular phenotype description of abnormal THOC2 splicing
• Myosin XVIII
• N2A Titin: Signaling Hub and Mechanical Switch in Skeletal Muscle
• Novel variants, muscle imaging, and myopathological changes in Chinese patients with VCP-related multisystem proteinopathy
• Nuclear pore pathology underlying multisystem proteinopathy type 3-related inclusion body myopathy
• Obesity worsens mitochondrial quality control and does not protect against skeletal muscle wasting in murine cancer cachexia
• Oxidative stress, mitochondrial dysfunction, and respiratory chain enzyme defects in inflammatory myopathies
• Parallel enlargement of Marinesco bodies and nuclei and progressive deposition of p62 in pigmented neurons of the substantia nigra
• Parkin Overexpression Attenuates Sepsis-Induced Muscle Wasting
• Passive exercise is an effective alternative to HRT for restoring OVX induced mitochondrial dysfunction in skeletal muscle
• Pathogenic variants of Valosin-containing protein induce lysosomal damage and transcriptional activation of autophagy regulators in neuronal cells
• Pathological mechanisms of vacuolar aggregate myopathy arising from a Casq1 mutation
• Polyglutamine-Expanded Androgen Receptor Alteration of Skeletal Muscle Homeostasis and Myonuclear Aggregation Are Affected by Sex, Age and Muscle Metabolism
• Primrose syndrome: Characterization of the phenotype in 42 patients
• Progerin in muscle leads to thermogenic and metabolic defects via impaired calcium homeostasis
• Pros and cons of different ways to address dysfunctional autophagy in Pompe disease
• Relevance of Mitochondrial Dysfunction in the Reserpine-Induced Experimental Fibromyalgia Model
• Review: Cytoplasmic dynein motors in photoreceptors
• Sarcomeric deficits underlie MYBPC1-associated myopathy with myogenic tremor
• Seeding competent TDP-43 persists in human patient and mouse muscle
• Segmental Arterial Mediolysis: A Multiguised Vasospastic Arteriopathy with Collateral Mesangial Cell Hyperplasia and Cardiac Toxicity Generated by Norepinephrine and Hyperdense Adrenoceptors Alone or by Crosstalk with Other Pressor Agents
• Skeletal muscle mitochondrial function and whole-body metabolic energetics in the +/G610C mouse model of osteogenesis imperfecta
• Skeletal muscle-specific DJ-1 ablation-induced atrogenes expression and mitochondrial dysfunction contributing to muscular atrophy
• Sporadic Inclusion Body Myositis
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• Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance: Report of four patients
• SVIP is a molecular determinant of lysosomal dynamic stability, neurodegeneration and lifespan
• The 2022 Lady Estelle Wolfson lectureship on neurofilaments
• The Ca(2+) Sensor STIM in Human Diseases
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• The effect of cardiolipin side chain composition on cytochrome c protein conformation and peroxidase activity
• The FLNC Ala1186Val Variant Linked to Cytoplasmic Body Myopathy and Cardiomyopathy Causes Protein Instability
• The interferon in idiopathic inflammatory myopathies: Different signatures and new therapeutic perspectives. A literature review
• The role of fibrosis in the pathophysiology of muscular dystrophy
• The role of protein aggregation in the pathogenesis of inclusion body myositis
• The spectrum of neurodevelopmental, neuromuscular and neurodegenerative disorders due to defective autophagy
• Transcriptional derepression of CHD4/NuRD-regulated genes in the muscle of patients with dermatomyositis and anti-Mi2 autoantibodies
• Two Weeks of Smoking Cessation Reverse Cigarette Smoke-Induced Skeletal Muscle Atrophy and Mitochondrial Dysfunction in Mice
• Value of insoluble PABPN1 accumulation in the diagnosis of oculopharyngeal muscular dystrophy
• VCP activator reverses nuclear proteostasis defects and enhances TDP-43 aggregate clearance in multisystem proteinopathy models
• VK2 regulates slow-twitch muscle fibers expression and mitochondrial function via SIRT1/SIRT3 signaling