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Department of Clinical Research, University of Basel, Basel, Switzerland
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Department of Clinical Research, University of Basel, Basel, Switzerland
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Department of Clinical Research, University of Basel, Basel, Switzerland
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Department of Clinical Research, University of Basel, Basel, Switzerland
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Central Laboratory, University Hospital Würzburg, Würzburg, Germany
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Leipzig University Medical Center, IFB Adiposity Diseases, Leipzig, Germany
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Department of Clinical Research, University of Basel, Basel, Switzerland
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obesity, metabolic syndrome, and nonalcoholic fatty liver in children: a longitudinal analysis . Journal of Clinical Endocrinology and Metabolism 2012 97 2143 – 2150 . (doi:10.1210/jc.2012-1221) 10 Nakanishi K Nishida M Harada M Ohama T Kawada N
Department of Clinical Research, University of Basel and University Hospital Basel, Basel, Switzerland
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Department of Clinical Research, University of Basel and University Hospital Basel, Basel, Switzerland
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Department of Clinical Research, University of Basel and University Hospital Basel, Basel, Switzerland
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Department of Biomedicine, University of Basel, Basel, Switzerland
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Department of Clinical Research, University of Basel and University Hospital Basel, Basel, Switzerland
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.2015-2362 ) 23 Barchetta I Enhörning S Cimini FA Capoccia D Chiappetta C Cristofano C Di Silecchia G Leonetti F Melander O Cavallo MG . Elevated plasma copeptin levels identify the presence and severity of non-alcoholic fatty
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had dyslipidemia, and 4 (3.9%) subjects had hyperlipidemia. In total, 17 (16.7%) were found to have nonalcoholic fatty liver disease (NAFLD). The results of further laboratory tests are shown in Table 2 . Table 2 Laboratory results presented as
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a relatively higher PRL level was associated with lower risk of diabetes, nonalcoholic fatty liver disease and metabolic syndrome ( 12 , 13 , 14 , 15 ). The previous study showed that obese patients had different PRL levels compared to non
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-regulation in nonalcoholic fatty liver disease . Biochimica et Biophysica Acta 2013 1831 803 – 818 . ( https://doi.org/10.1016/j.bbalip.2012.12.014 ) 27 Liu Y Zhang Y Yin J Ruan Z Wu X & Yin Y . Uridine dynamic administration affects circadian
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: insulin resistance, fatty liver and non-alcoholic fatty pancreas disease (NAFPD) in C57BL/6 mice fed a high fat diet. Journal of Clinical Biochemistry and Nutrition 2010 46 212 – 223 . ( https://doi.org/10.3164/jcbn.09-83 ) 20490316 10.3164/jcbn.09
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Deutsches Herzzentrum München, Technische Universität München, DZHK (German Centre for Cardiovascular Research), Partner Site Munich Heart Alliance, Munich, Germany
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Lehrstuhl für Experimentelle Genetik, Technische Universität München, Freising-Weihenstephan, Germany
Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore
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German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Germany
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German Centre for Cardiovascular Research (DZHK), Partner Site Munich, Munich, Germany
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nonalcoholic fatty liver disease: a systematic review and meta-analysis . Annals of Hepatology 2017 16 382 – 394 . ( https://doi.org/10.5604/16652681.1235481 ) 47 Burger HG . Androgen production in women . Fertility and Sterility 2002 77
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Center for Healthy Aging Research, Oregon State University, Corvallis, Oregon, USA
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Center for Healthy Aging Research, Oregon State University, Corvallis, Oregon, USA
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41 Giles DA Moreno-Fernandez ME Stankiewicz TE Graspeuntner S Cappelletti M Wu D Mukherjee R Chan CC Lawson MJ Klarquist J , et al . Thermoneutral housing exacerbates nonalcoholic fatty liver disease in mice and allows for sex
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, cancer, neurodegenerative diseases, metabolic diseases, ischemia–reperfusion injury (IRI), and damage to the liver, kidneys, and many more ( Fig. 2 ). Recently, a large number of studies have documented the vital impact of ferroptosis on the development
Department of Diabetes and Endocrinology, Blacktown Hospital, Blacktown, New South Wales, Australia
Department of Diabetes and Endocrinology, Westmead Hospital, Westmead, New South Wales, Australia
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Department of Diabetes and Endocrinology, Blacktown Hospital, Blacktown, New South Wales, Australia
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Crown Princess Mary Cancer Centre, Westmead Hospital, Westmead, New South Wales, Australia
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Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia
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Department of Diabetes and Endocrinology, Blacktown Hospital, Blacktown, New South Wales, Australia
School of Medicine, UNSW Sydney, Sydney, New South Wales, Australia
Translational Health Research Institute, Penrith, New South Wales, Australia
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Department of Diabetes and Endocrinology, Blacktown Hospital, Blacktown, New South Wales, Australia
Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia
School of Medicine, UNSW Sydney, Sydney, New South Wales, Australia
Translational Health Research Institute, Penrith, New South Wales, Australia
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367 965 – 967 . ( https://doi.org/10.1056/NEJMcibr1203160 ) 10.1056/NEJMcibr1203160 37 Eagon PK Elm MS Stafford EA Porter LE . Androgen receptor in human liver: characterization and quantitation in normal and diseased liver . Hepatology 1994