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Introduction Skeletal muscle is a tissue mainly composed of muscle fibers, which form multinucleated contractile cells. It accounts for approximately 30% of women's body weight and 40% of men's body weight and is essential for locomotion
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Pompe disease, morbidity and mortality are mainly caused by progressive skeletal muscle weakness and wasting ( 2 ). Even though treatment with recombinant acid alpha-glucosidase improves walking distance and lung function, and slows down disease
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Department of Health & Life Sciences, Charles R. Drew University of Medicine and Science, Los Angeles, California, USA
Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, USA
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Department of Health & Life Sciences, Charles R. Drew University of Medicine and Science, Los Angeles, California, USA
Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California, USA
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level there is also evidence of VDR expression and direct effects of vitamin D on human skeletal muscle precursor cells ( 7 ), which provides a rationale for a direct role of vitamin D in muscle function. Furthermore, mice lacking VDR show an abnormal
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Division of Endocrinology and Metabolism, Diabetes Center, Kurume Medical Center, Kokubu-machi, Kurume-city, Fukuoka, Japan
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Division of Endocrinology and Metabolism, Diabetes Center, Kurume Medical Center, Kokubu-machi, Kurume-city, Fukuoka, Japan
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early morning after an 8-h fast. The urinary glucose levels were examined along with the urinary volume of the day and calculated as the excreted amount per day. The amounts of skeletal muscle and body fat and their distributions were analyzed before and
University of Helsinki, Department of Medicine, and Abdominal Center, Endocrinology, Helsinki University Central Hospital, Helsinki, Finland
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University of Helsinki, Department of Medicine, and Abdominal Center, Endocrinology, Helsinki University Central Hospital, Helsinki, Finland
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University of Helsinki, Department of Medicine, and Abdominal Center, Endocrinology, Helsinki University Central Hospital, Helsinki, Finland
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University of Helsinki, Department of Medicine, and Abdominal Center, Endocrinology, Helsinki University Central Hospital, Helsinki, Finland
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Introduction Excess dietary fat and sedentary lifestyle predispose to insulin resistance and type 2 diabetes. As skeletal muscle accounts for 80% of glucose disposal under insulin-stimulated conditions ( 1 , 2 ), it is an important target
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-IUGR, characterized by nutrition insults in early life. However, currently, the role of LRP6-mediated Wnt signaling in the insulin resistance of CG-IUGR is unknown. Under normal circumstances, skeletal muscle is one of the most critical organs for maintaining
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into a new type of adipocytes, beige adipocytes ( 2 , 3 ), which have a similar thermogenic function to that of BAT. Increased thermogenesis in skeletal muscle caused by exercise is related to peroxisome proliferator-activated receptor-gamma co
Monash Centre for Health Research and Implementation, Monash University, Clayton, Victoria, Australia
Australian Institute for Musculoskeletal Science, Victoria University, Melbourne, Victoria, Australia
Medicine-Western Health, Faculty of Medicine, Dentistry and Health Science, Melbourne University, Melbourne, Victoria, Australia
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Australian Institute for Musculoskeletal Science, Victoria University, Melbourne, Victoria, Australia
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Division of Diabetes, Endocrinology & Gastroenterology, School of Medical Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK
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Diabetes and Endocrine Units, Monash Health, Clayton, Victoria, Australia
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(extrinsic insulin resistance ( 9 , 10 , 13 )). Intrinsic insulin resistance in PCOS is likely due to a dysfunctional response to insulin in metabolically active peripheral tissues including adipose tissue and skeletal muscle ( 8 , 13 ). As skeletal muscle
Department of Medicine, University of Helsinki, Helsinki University Central Hospital, Helsinki, Finland
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Department of Medicine, University of Helsinki, Helsinki University Central Hospital, Helsinki, Finland
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Department of Medicine, University of Helsinki, Helsinki University Central Hospital, Helsinki, Finland
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Department of Medicine, University of Helsinki, Helsinki University Central Hospital, Helsinki, Finland
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Department of Medicine, University of Helsinki, Helsinki University Central Hospital, Helsinki, Finland
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, which enables these to diffuse non-selectively into non-hepatic tissues such as skeletal muscle ( 11 ). This idea is supported by the PRIMO-study, which showed hydrophilic statins, such as pravastatin, causing less myalgia, whereas highly lipophilic
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, rats develop polyarthritis together with a marked loss of white adipose tissue (WAT) and skeletal muscle mass and cachexia (3, 4) . Skeletal muscle wasting is not secondary to the decrease in food intake in arthritic rats, as it was not observed in