Rescue of dystrophic skeletal muscle by PGC-1α involves a fast to slow fiber type shift in the mdx mouse - Wikidata - wikimedia - TriplyDB

Rescue of dystrophic skeletal muscle by PGC-1α involves a fast to slow fiber type shift in the mdx mouse

Rescue of dystrophic skeletal muscle by PGC-1α involves a fast to slow fiber type shift in the mdx mouse

http://www.wikidata.org/entity/Q27310125

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Resveratrol and Myopathy SIRT1: A Novel Target for the Treatment of Muscular Dystrophies Metabogenic and Nutriceutical Approaches to Address Energy Dysregulation and Skeletal Muscle Wasting in Duchenne Muscular Dystrophy Pre-clinical drug tests in the mdx mouse as a model of dystrophinopathies: an overview New insights into PGC-1 coactivators: redefining their role in the regulation of mitochondrial function and beyond Muscle-specific SIRT1 gain-of-function increases slow-twitch fibers and ameliorates pathophysiology in a mouse model of duchenne muscular dystrophy Effects of resveratrol on the recovery of muscle mass following disuse in the plantaris muscle of aged rats Nutraceuticals and Their Potential to Treat Duchenne Muscular Dystrophy: Separating the Credible from the Conjecture Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy Metformin protects skeletal muscle from cardiotoxin induced degeneration Long-Term Quercetin Dietary Enrichment Partially Protects Dystrophic Skeletal Muscle TWEAK/Fn14, a pathway and novel therapeutic target in myotonic dystrophy.Muscle structure influences utrophin expression in mdx mice.Resveratrol induces expression of the slow, oxidative phenotype in mdx mouse muscle together with enhanced activity of the SIRT1-PGC-1α axis.Oxidative damage in the gastrocnemius of patients with peripheral artery disease is myofiber type selective.Systemic down-regulation of delta-9 desaturase promotes muscle oxidative metabolism and accelerates muscle function recovery following nerve injury.Porcine models of muscular dystrophy Metabolic remodeling agents show beneficial effects in the dystrophin-deficient mdx mouse model Effect of genetic background on the dystrophic phenotype in mdx mice.Perm1 enhances mitochondrial biogenesis, oxidative capacity, and fatigue resistance in adult skeletal muscle.Defects in mitochondrial localization and ATP synthesis in the mdx mouse model of Duchenne muscular dystrophy are not alleviated by PDE5 inhibition Loss of cIAP1 attenuates soleus muscle pathology and improves diaphragm function in mdx mice.Muscle-Specific Myosin Heavy Chain Shifts in Response to a Long-Term High Fat/High Sugar Diet and Resveratrol Treatment in Nonhuman Primates.Abnormally Small Neuromuscular Junctions in the Extraocular Muscles From Subjects With Idiopathic Nystagmus and Nystagmus Associated With Albinism.Trip12, a HECT domain E3 ubiquitin ligase, targets Sox6 for proteasomal degradation and affects fiber type-specific gene expression in muscle cells.Prospect of gene therapy for cardiomyopathy in hereditary muscular dystrophy.Distribution of myosin heavy chain isoforms in muscular dystrophy: insights into disease pathology.Long-term wheel running compromises diaphragm function but improves cardiac and plantarflexor function in the mdx mouse Comparative Genomics of X-linked Muscular Dystrophies: The Golden Retriever Model Blunted angiogenesis and hypertrophy are associated with increased fatigue resistance and unchanged aerobic capacity in old overloaded mouse muscle.Coupling of mitochondrial function and skeletal muscle fiber type by a miR-499/Fnip1/AMPK circuit.PGC-1α modulates necrosis, inflammatory response, and fibrotic tissue formation in injured skeletal muscle.Molecular mechanism of sphingosine-1-phosphate action in Duchenne muscular dystrophy.Mitochondria mediate cell membrane repair and contribute to Duchenne muscular dystrophy.Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice.Turn up the power - pharmacological activation of mitochondrial biogenesis in mouse models.Increased AMP-activated protein kinase in skeletal muscles of Murphy Roth Large mice and its potential role in altered metabolism.Role of PGC-1α signaling in skeletal muscle health and disease.Duchenne muscular dystrophy drug discovery - the application of utrophin promoter activation screening.Mechanisms for fiber-type specificity of skeletal muscle atrophy.

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Rescue of dystrophic skeletal muscle by PGC-1α involves a fast to slow fiber type shift in the mdx mouse

http://www.wikidata.org/entity/Q27310125

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Rescue of dystrophic skeletal ...... er type shift in the mdx mouse

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Rescue of dystrophic skeletal ...... er type shift in the mdx mouse

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Rescue of dystrophic skeletal ...... er type shift in the mdx mouse

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Rescue of dystrophic skeletal ...... er type shift in the mdx mouse

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Rescue of dystrophic skeletal ...... er type shift in the mdx mouse

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Rescue of dystrophic skeletal ...... er type shift in the mdx mouse

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Rescue of dystrophic skeletal ...... er type shift in the mdx mouse

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Elisabeth R Barton

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H Lee Sweeney

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Joshua T Selsby

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Kevin J Morine

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Klara Pendrak

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Novel adeno-associated viruses from rhesus monkeys as vectors for human gene therapy

Erralpha and Gabpa/b specify PGC-1alpha-dependent oxidative phosphorylation gene expression that is altered in diabetic muscle

Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes

Transducer of regulated CREB-binding proteins (TORCs) induce PGC-1alpha transcription and mitochondrial biogenesis in muscle cells

Resveratrol improves health and survival of mice on a high-calorie diet

Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1

Nutrient control of glucose homeostasis through a complex of PGC-1alpha and SIRT1

Mechanism of human SIRT1 activation by resveratrol

Resveratrol improves mitochondrial function and protects against metabolic disease by activating SIRT1 and PGC-1alpha

Expression of utrophin A mRNA correlates with the oxidative capacity of skeletal muscle fiber types and is regulated by calcineurin/NFAT signaling

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