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, Offenburg, Germany). Insulin was analyzed with sandwich immunoassay technique (ELISA) using double MABs against insulin (Mercodia, Uppsala, Sweden). Glucagon was measured by RIA (Millipore, Billerica, MA, USA). Levels of intact GLP1 were determined by
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Chemical Gmbh, Germany). Insulin and catecholamines were measured at rest and after exercise with enzyme-linked immunosorbent assays (Insulin ELISA kit, Dako, Glostrup, Denmark, and 2-CAT plasma ELISA kit, Labor Diagnostica Nord GmbH & Co) and a Modulus II
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Department of Cell Biology and Anatomy, Department of Medicine, Turku PET Centre, Department of Radiology, Medical Imaging Centre of Southwest Finland, Department of Endocrinology, Abdominal Center: Endocrinology, Minerva Foundation Institute for Medical Research, Institute of Biomedicine, University of Turku, FI-20520 Turku, Finland
Department of Cell Biology and Anatomy, Department of Medicine, Turku PET Centre, Department of Radiology, Medical Imaging Centre of Southwest Finland, Department of Endocrinology, Abdominal Center: Endocrinology, Minerva Foundation Institute for Medical Research, Institute of Biomedicine, University of Turku, FI-20520 Turku, Finland
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Department of Cell Biology and Anatomy, Department of Medicine, Turku PET Centre, Department of Radiology, Medical Imaging Centre of Southwest Finland, Department of Endocrinology, Abdominal Center: Endocrinology, Minerva Foundation Institute for Medical Research, Institute of Biomedicine, University of Turku, FI-20520 Turku, Finland
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Department of Cell Biology and Anatomy, Department of Medicine, Turku PET Centre, Department of Radiology, Medical Imaging Centre of Southwest Finland, Department of Endocrinology, Abdominal Center: Endocrinology, Minerva Foundation Institute for Medical Research, Institute of Biomedicine, University of Turku, FI-20520 Turku, Finland
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telopeptides of type I collagen (CTX) and tartrate-resistant acid phosphatase 5b (TRAcP5b) using serum IDS-iSYS CTX-I (CrossLaps) ELISA and BoneTRAP (TRAcP 5b) ELISA (both from IDS Ltd, Boldon, Tyne and Wear, UK). Bone formation was assessed by measuring serum
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the final weighted mean AR CAG repeat length was the average of these two determinations. Antinuclear antibody assay Levels of ANAs were measured in serum samples using the ELISA technique (Inova Diagnostics, San Diego, CA, USA). A positive result in
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after restoration of thyroid function. Thyrotropin receptor antibodies (TRAbs) were assessed in the hyperthyroid group before the onset of therapy and when the euthyroidism was anticipated. ELISA Assay Kit from Phoenix Pharmaceuticals was used to assess
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Faculty of Life Sciences and Medicine, Kings College London, London, UK
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Department of Clinical Biochemistry, King’s College Hospital NHS Foundation Trust, Denmark Hill, London, UK
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Neuroendocrine Tumour Unit, Kings Health Partners ENETS Centre of Excellence, Denmark Hill, London, UK
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Barts and the London School of Medicine, Centre for Endocrinology, William Harvey Institute, London, UK
Neuroendocrine Tumour Unit, Royal Free Hospital, London, UK
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Faculty of Life Sciences and Medicine, Kings College London, London, UK
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Faculty of Life Sciences and Medicine, School of Life Course Sciences, Obesity Immunometabolism and Diabetes Group, King’s College London, London, UK
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developed in the late 1980s ( 8 ). In the early 2000s, there was a movement to fluorescent and chemiluminescent tests, which were more accurate. Enzyme-linked immunoassay (ELISA) technique was used, but an issue with ELISA was heterophilic antibody
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was determined with UltraSensitive Mouse Insulin ELISA Kit (EMINS, Thermo Fisher Scientific). A top-loading balance (Fisher Scientific) was used to measure body weight. Liver dissection Six pregnant mice were sacrificed on GD 20, and blood and
Department of Urology, Foundation IRCCS Ca’ Granda – Ospedale Maggiore Policlinico, University of Milan, Milan, Italy
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University Vita-Salute San Raffaele, Milan, Italy
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University Vita-Salute San Raffaele, Milan, Italy
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University Vita-Salute San Raffaele, Milan, Italy
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University Vita-Salute San Raffaele, Milan, Italy
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University Vita-Salute San Raffaele, Milan, Italy
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University Vita-Salute San Raffaele, Milan, Italy
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University Vita-Salute San Raffaele, Milan, Italy
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-stimulating hormone (FSH) and luteinizing hormone (LH) were measured using a heterogeneous competitive magnetic separation assay (Bayer Immuno 1 System, Bayer Corp.). Inhibin B (InhB) was measured by an ELISA (Beckman Coulter AMH Gen II ELISA). Total testosterone was
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incubated with a fresh KRB buffer with different glucose concentrations for 1 h at 37°C. The cumulative insulin release over 1 h was quantified in duplicate using commercial ELISA kit (Cat No. EZRMI-13K, Merck Millipore). Immunohistochemistry and
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insulin, lipids and high-sensitivity C-reactive protein (hsCRP) were measured as described previously ( 23 ). Total serum chemerin was measured with an ELISA kit (Biovendor, Brno, Czech Republic) with a sensitivity of 0.1 ng/mL and with intra-assay and