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Wellcome Trust Sanger Institute, Metabolic Research Laboratories, Wellcome Trust Genome Campus, Hinxton, UK
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Wellcome Trust Sanger Institute, Metabolic Research Laboratories, Wellcome Trust Genome Campus, Hinxton, UK
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cellular models based on hES and IPS cell technology for BAT differentiation/activation to be used in functional studies, -omics based analyses and validation of therapeutic approaches. A matter of adipocyte colours: brown, white, and beige/brite Until
Reproductive Science Research Program, Morehouse School of Medicine, Atlanta, Georgia, USA
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Department of Physiology, Morehouse School of Medicine, Atlanta, Georgia, USA
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Introduction Mammalian granulosa cells (GCs) are multilayered somatic cells residing within the ovarian follicle that support oogenesis through proliferation, differentiation, and interactive communications. These events are under the control
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splicing of exons 5 gives rise to a unique E domain of MGF (MGF E peptide) ( Dai et al . 2010 ). It is reported that MGF E peptide activated myoblasts C2C12 and myocardial cells H9C2 proliferation, while delaying the differentiation of C2C12 ( Yang
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papillary thyroid carcinoma (PTC), follicular thyroid carcinoma (FTC), anaplastic thyroid carcinoma (ATC), and medullary thyroid carcinoma. FTC and PTC are also defined as differentiated thyroid carcinoma (DTC), accounting for 90% of thyroid malignancies
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stem cells ( Chew et al. 2005 ). The expression of these pluripotency genes gradually decreases during cell differentiation ( Miyamoto et al. 2015 ). Mature osteoblasts are the primary component in the bone formation process, which includes matrix
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allow for the proper levels of biologically active retinoids to be achieved in specific cell types in the body. Since RA regulates stem cell differentiation and is active at nanomolar concentrations in cells, levels of this signaling molecule must be
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with condensation of mesenchymal cells with their subsequent differentiation into chondrocytes ( Hall & Miyake 1995 ). The chondrocytes proliferate thereby increasing the size of the primary skeletal element. The cells in the center of the element stop
Nanchang Joint Programme, Queen Mary, University of London, London, UK
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Department of Pharmacology, School of Pharmacy, Nanchang University, Nanchang, Jiangxi Province, People’s Republic of China
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Nanchang Joint Programme, Queen Mary, University of London, London, UK
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Department of Pharmacology, School of Pharmacy, Nanchang University, Nanchang, Jiangxi Province, People’s Republic of China
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FOXO1, FOXO3, FOXO4 and FOXO6 ( Ogg et al. 1997 , Tzivion et al. 2011 ). FOXO1 is one of the downstream targets of AKT ( Fig. 1 ) and takes part in cell cycle control, apoptosis, metabolism and adipocyte differentiation ( Dowell et al. 2003
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Dipartimento di Patologia Generale, Dipartimento di Patologia e Microbiologia Sperimentale, University of Southern Denmark, Dipartimento di Studi Farmaceutici, Department of Cancer Biology, Università degli Studi di Milano, CNR-IGB, Seconda Università di Napoli, 80138 Napoli, Italy
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Dipartimento di Patologia Generale, Dipartimento di Patologia e Microbiologia Sperimentale, University of Southern Denmark, Dipartimento di Studi Farmaceutici, Department of Cancer Biology, Università degli Studi di Milano, CNR-IGB, Seconda Università di Napoli, 80138 Napoli, Italy
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Dipartimento di Patologia Generale, Dipartimento di Patologia e Microbiologia Sperimentale, University of Southern Denmark, Dipartimento di Studi Farmaceutici, Department of Cancer Biology, Università degli Studi di Milano, CNR-IGB, Seconda Università di Napoli, 80138 Napoli, Italy
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the regulation of differentiation, such as myogenesis ( Lu et al . 2000 ), neuronal differentiation ( Chawla et al . 2003 ), and osteogenesis ( Hug 2004 ). Mechanistically, class IIa members may compete with the histone acetyltransferase p300 for
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represents an interesting challenge ( Cypess et al . 2009 , Vitali et al . 2012 , Berry & Rodeheffer 2013 , Lidell et al . 2014 ). The differentiation of beige adipocytes from precursor cells and WAT beiging transdifferentiation from white adipocytes is