Search Results
Search for other papers by Gabriela Capllonch-Amer in
Google Scholar
PubMed
Search for other papers by Miquel Sbert-Roig in
Google Scholar
PubMed
Search for other papers by Bel M Galmés-Pascual in
Google Scholar
PubMed
Grup Metabolisme Energètic i Nutrició, Centro de Investigación Biomédica en Red Fisiopatología de la Obesidad y la Nutrición (CIBERobn, Departament de Biologia Fonamental i Ciències de la Salut, Institut Universitari d'Investigació en Ciències de la Salut (IUNICS), Universitat de les Illes Balears, Ctra. Valldemossa, km 7,5. E-07122 Palma de Mallorca, Illes Balears, Spain
Search for other papers by Ana M Proenza in
Google Scholar
PubMed
Grup Metabolisme Energètic i Nutrició, Centro de Investigación Biomédica en Red Fisiopatología de la Obesidad y la Nutrición (CIBERobn, Departament de Biologia Fonamental i Ciències de la Salut, Institut Universitari d'Investigació en Ciències de la Salut (IUNICS), Universitat de les Illes Balears, Ctra. Valldemossa, km 7,5. E-07122 Palma de Mallorca, Illes Balears, Spain
Search for other papers by Isabel Lladó in
Google Scholar
PubMed
Grup Metabolisme Energètic i Nutrició, Centro de Investigación Biomédica en Red Fisiopatología de la Obesidad y la Nutrición (CIBERobn, Departament de Biologia Fonamental i Ciències de la Salut, Institut Universitari d'Investigació en Ciències de la Salut (IUNICS), Universitat de les Illes Balears, Ctra. Valldemossa, km 7,5. E-07122 Palma de Mallorca, Illes Balears, Spain
Search for other papers by Magdalena Gianotti in
Google Scholar
PubMed
Grup Metabolisme Energètic i Nutrició, Centro de Investigación Biomédica en Red Fisiopatología de la Obesidad y la Nutrición (CIBERobn, Departament de Biologia Fonamental i Ciències de la Salut, Institut Universitari d'Investigació en Ciències de la Salut (IUNICS), Universitat de les Illes Balears, Ctra. Valldemossa, km 7,5. E-07122 Palma de Mallorca, Illes Balears, Spain
Search for other papers by Francisco J García-Palmer in
Google Scholar
PubMed
Introduction Sexual dimorphism in mitochondrial functionality has been described in many rat tissues such as liver, adipose tissue, brain, and skeletal muscle ( Colom et al . 2007 a , b , Valle et al . 2007 a , b , Gómez-Pérez et al . 2008
MRC-Versus Arthritis Centre for Musculoskeletal Ageing Research, Clinical, Metabolic and Molecular Physiology, University of Nottingham, Royal Derby Hospital Centre, Derby, UK
Mitochondrial Metabolism and Ageing Laboratory, Garvan Institute of Medical Research, Sydney, New South Wales, Australia
Search for other papers by Stephen P Ashcroft in
Google Scholar
PubMed
Search for other papers by Gareth Fletcher in
Google Scholar
PubMed
St Vincent’s Clinical School, UNSW Medicine, UNSW Sydney, New South Wales, Australia
Search for other papers by Ashleigh M Philp in
Google Scholar
PubMed
ANZAC Research Institute, University of Sydney, Sydney, New South Wales, Australia
Search for other papers by Carl Jenkinson in
Google Scholar
PubMed
UTS Centenary Centre for Inflammation, University Technology Sydney, New South Wales, Australia
Search for other papers by Shatarupa Das in
Google Scholar
PubMed
UTS Centenary Centre for Inflammation, University Technology Sydney, New South Wales, Australia
Search for other papers by Philip M Hansbro in
Google Scholar
PubMed
Search for other papers by Philip J Atherton in
Google Scholar
PubMed
St Vincent’s Clinical School, UNSW Medicine, UNSW Sydney, New South Wales, Australia
Search for other papers by Andrew Philp in
Google Scholar
PubMed
of skeletal muscle function ( Girgis et al. 2013 ). Within human populations, multiple observational studies have reported a positive association between serum 25(OH)D, skeletal muscle strength and lower extremity function in older individuals
Search for other papers by Yuriko Kitajima in
Google Scholar
PubMed
Search for other papers by Yusuke Ono in
Google Scholar
PubMed
. 2015 ). Thus, understanding the regulation of satellite cells is critical to elucidate the mechanisms in skeletal muscle maintenance. Several studies have reported that estrogens appear to favor muscle regeneration after injury ( Diel 2014 ). Estrogens
Search for other papers by Juthamard Surapongchai in
Google Scholar
PubMed
Search for other papers by Mujalin Prasannarong in
Google Scholar
PubMed
Search for other papers by Tepmanas Bupha-Intr in
Google Scholar
PubMed
Search for other papers by Vitoon Saengsirisuwan in
Google Scholar
PubMed
Introduction Insulin resistance of skeletal muscle represents a major defect in the maintenance of euglycemia and is often accompanied by a variety of metabolic and cardiovascular abnormalities, including glucose intolerance, hyperinsulinemia
Search for other papers by Kok Lim Kua in
Google Scholar
PubMed
Search for other papers by Shanming Hu in
Google Scholar
PubMed
Search for other papers by Chunlin Wang in
Google Scholar
PubMed
Search for other papers by Jianrong Yao in
Google Scholar
PubMed
Search for other papers by Diana Dang in
Google Scholar
PubMed
Search for other papers by Alexander B Sawatzke in
Google Scholar
PubMed
Search for other papers by Jeffrey L Segar in
Google Scholar
PubMed
Search for other papers by Kai Wang in
Google Scholar
PubMed
Department of Biochemistry, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA
Fraternal Order of Eagles Diabetes Research Center, University of Iowa, Iowa City, Iowa, USA
Search for other papers by Andrew W Norris in
Google Scholar
PubMed
hyperglycemia rapidly developed skeletal muscle insulin resistance while still in utero . The insulin signaling defects persisted through postnatal life, localized to skeletal muscle. Uteroplacental insufficiency and fetal hyperinsulinism did not have these
Search for other papers by J Kwakkel in
Google Scholar
PubMed
Search for other papers by H C van Beeren in
Google Scholar
PubMed
Search for other papers by M T Ackermans in
Google Scholar
PubMed
Search for other papers by M C Platvoet-ter Schiphorst in
Google Scholar
PubMed
Search for other papers by E Fliers in
Google Scholar
PubMed
Search for other papers by W M Wiersinga in
Google Scholar
PubMed
Search for other papers by A Boelen in
Google Scholar
PubMed
prohormone thyroxine (T 4 ) into the active hormone T 3 by outer-ring deiodination. D2 is expressed in brain, pituitary, skeletal muscle, brown adipose tissue, and placenta and is present as an active dimer in the endoplasmic reticulum ( Kohrle 2000
Search for other papers by John-Paul Fuller-Jackson in
Google Scholar
PubMed
Search for other papers by Belinda A Henry in
Google Scholar
PubMed
energy expenditure is reduced adaptive thermogenesis ( Rosenbaum et al . 2008 , Camps et al . 2015 , Henry et al . 2017 ), which occurs in both skeletal muscle and brown adipose tissue (BAT). To investigate the specific metabolic adaptations that
Search for other papers by Ishita Bakshi in
Google Scholar
PubMed
Search for other papers by Eurwin Suryana in
Google Scholar
PubMed
Search for other papers by Lewin Small in
Google Scholar
PubMed
Search for other papers by Lake-Ee Quek in
Google Scholar
PubMed
Sydney Medical School, Charles Perkins Centre, University of Sydney, Sydney, New South Wales, Australia
Search for other papers by Amanda E Brandon in
Google Scholar
PubMed
Search for other papers by Nigel Turner in
Google Scholar
PubMed
Sydney Medical School, Charles Perkins Centre, University of Sydney, Sydney, New South Wales, Australia
Search for other papers by Gregory J Cooney in
Google Scholar
PubMed
Introduction Reduced levels of glycolysis and glycogen synthesis are a well characterised feature of skeletal muscle in type 2 diabetes ( Bouche et al . 2004 , Abdul-Ghani & DeFronzo 2010 ). In general, the flux through glycolysis is
Search for other papers by Nele Cielen in
Google Scholar
PubMed
Search for other papers by Nele Heulens in
Google Scholar
PubMed
Search for other papers by Karen Maes in
Google Scholar
PubMed
Search for other papers by Geert Carmeliet in
Google Scholar
PubMed
Search for other papers by Chantal Mathieu in
Google Scholar
PubMed
Search for other papers by Wim Janssens in
Google Scholar
PubMed
Search for other papers by Ghislaine Gayan-Ramirez in
Google Scholar
PubMed
Introduction Chronic obstructive pulmonary disease (COPD) is not only a lung disease, but also associates with several comorbidities. Among them, skeletal muscle dysfunction is of major concern, as it contributes, independently of lung
Search for other papers by Jonathan M Mudry in
Google Scholar
PubMed
Search for other papers by Julie Massart in
Google Scholar
PubMed
Search for other papers by Ferenc L M Szekeres in
Google Scholar
PubMed
Section for Integrative Physiology, Section for Integrative Physiology, Department of Molecular Medicine and Surgery
Search for other papers by Anna Krook in
Google Scholar
PubMed
investigated gene. TWIST proteins play important roles in tissue differentiation. In skeletal muscle, TWIST1 blocks myogenesis via inhibition of MYOD transactivation ( Hamamori et al . 1997 ), which may lead to myotube dedifferentiation ( Hjiantoniou et al