Federica Saponaro
Federica Saponaro
Department of Surgical, Medical, Molecular and Critical Area Pathology, Laboratory of Biochemistry, University of Pisa, Pisa, Italy
Endocrinology Unit 2, University of Pisa, Pisa, Italy
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Endocrinology Unit 2, University of Pisa, Pisa, Italy
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Alessandro Saba
Alessandro Saba
Department of Surgical, Medical, Molecular and Critical Area Pathology, Laboratory of Biochemistry, University of Pisa, Pisa, Italy
Laboratory of Clinical Pathology, University Hospital of Pisa, Pisa, Italy
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Laboratory of Clinical Pathology, University Hospital of Pisa, Pisa, Italy
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Sabina Frascarelli
Sabina Frascarelli
Department of Surgical, Medical, Molecular and Critical Area Pathology, Laboratory of Biochemistry, University of Pisa, Pisa, Italy
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Concetta Prontera
Concetta Prontera
Fondazione Toscana Gabriele Monasterio, Pisa, Italy
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Aldo Clerico
Aldo Clerico
Fondazione Toscana Gabriele Monasterio, Pisa, Italy
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Marco Scalese
Marco Scalese
Institute of Clinical Physiology, National Council of Research, Pisa, Italy
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Maria Rita Sessa
Maria Rita Sessa
Laboratory of Endocrinology, University Hospital of Pisa, Pisa, Italy
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Filomena Cetani
Filomena Cetani
Endocrinology Unit 2, University of Pisa, Pisa, Italy
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Simona Borsari
Simona Borsari
Endocrinology Unit 2, University of Pisa, Pisa, Italy
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Elena Pardi
Elena Pardi
Endocrinology Unit 2, University of Pisa, Pisa, Italy
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Antonella Marvelli
Antonella Marvelli
Department of Translational Research and of New Surgical and Medical Technologies, University of Pisa, Pisa, Italy
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Claudio Marcocci
Claudio Marcocci
Endocrinology Unit 2, University of Pisa, Pisa, Italy
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Claudio Passino
Claudio Passino
Fondazione Toscana Gabriele Monasterio, Pisa, Italy
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Riccardo Zucchi
Riccardo Zucchi
Department of Surgical, Medical, Molecular and Critical Area Pathology, Laboratory of Biochemistry, University of Pisa, Pisa, Italy
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measurement. To achieve a good performance, laboratories are required to have 75% of assessable results within ±25% of the true values from DEQAS. The accurate measurement of 25 hydroxyvitamin D3 (25OHD3) status was carried out by isotope dilution mass
Maria Luisa Brandi
Maria Luisa Brandi
Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy
Fondazione Italiana Ricerca sulle Malattie dell’Osso (FIRMO Onlus), Florence, Italy
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Fondazione Italiana Ricerca sulle Malattie dell’Osso (FIRMO Onlus), Florence, Italy
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Stefania Bandinelli
Stefania Bandinelli
Geriatric Unit, Azienda Sanitaria Toscana Centro, Florence, Italy
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Teresa Iantomasi
Teresa Iantomasi
Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy
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Francesca Giusti
Francesca Giusti
Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy
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Eleonora Talluri
Eleonora Talluri
Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy
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Giovanna Sini
Giovanna Sini
Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy
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Fabrizio Nannipieri
Fabrizio Nannipieri
Clinical Research, Abiogen Pharma, Pisa, Italy
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Santina Battaglia
Santina Battaglia
Clinical Research, Abiogen Pharma, Pisa, Italy
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Riccardo Giusti
Riccardo Giusti
Clinical Research, Abiogen Pharma, Pisa, Italy
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Colin Gerard Egan
Colin Gerard Egan
CE Medical Writing SRLS, Pisa, Italy
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Luigi Ferrucci
Luigi Ferrucci
Longitudinal Study Section, Translation Gerontology Branch, National Institute on Aging, Baltimore, Maryland, USA
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to a reference procedure (isotope dilution mass spectrometry) and automatized on a Cobas 8000. Serum VDBP was measured by enzyme-linked immuno assay method (R&D Systems). BPA analysis was performed on urine samples using the HPLC/mass spectrometry by
Vickie Braithwaite
Vickie Braithwaite
Medical Research Council (MRC) Human Nutrition Research, MRC Keneba, Elsie Widdowson Laboratories, Fulbourn Road, Cambridge CB1 9NL, UK
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Kerry S Jones
Kerry S Jones
Medical Research Council (MRC) Human Nutrition Research, MRC Keneba, Elsie Widdowson Laboratories, Fulbourn Road, Cambridge CB1 9NL, UK
Medical Research Council (MRC) Human Nutrition Research, MRC Keneba, Elsie Widdowson Laboratories, Fulbourn Road, Cambridge CB1 9NL, UK
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Medical Research Council (MRC) Human Nutrition Research, MRC Keneba, Elsie Widdowson Laboratories, Fulbourn Road, Cambridge CB1 9NL, UK
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Shima Assar
Shima Assar
Medical Research Council (MRC) Human Nutrition Research, MRC Keneba, Elsie Widdowson Laboratories, Fulbourn Road, Cambridge CB1 9NL, UK
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Inez Schoenmakers
Inez Schoenmakers
Medical Research Council (MRC) Human Nutrition Research, MRC Keneba, Elsie Widdowson Laboratories, Fulbourn Road, Cambridge CB1 9NL, UK
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Ann Prentice
Ann Prentice
Medical Research Council (MRC) Human Nutrition Research, MRC Keneba, Elsie Widdowson Laboratories, Fulbourn Road, Cambridge CB1 9NL, UK
Medical Research Council (MRC) Human Nutrition Research, MRC Keneba, Elsie Widdowson Laboratories, Fulbourn Road, Cambridge CB1 9NL, UK
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Medical Research Council (MRC) Human Nutrition Research, MRC Keneba, Elsie Widdowson Laboratories, Fulbourn Road, Cambridge CB1 9NL, UK
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status and intestinal integrity Two-day weighed dietary assessment was conducted using Gambian food composition tables (26) in the same way as described previously (13) . H. pylori infection was determined using a non-invasive stable isotope urea
L Johnsen
L Johnsen
Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
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N B Lyckegaard
N B Lyckegaard
Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
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P Khanal
P Khanal
Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
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B Quistorff
B Quistorff
Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
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K Raun
K Raun
Diabetes and Obesity Pharmacology, Novo Nordisk A/S, Måløv, Denmark
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M O Nielsen
M O Nielsen
Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
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used for free ranging animals ( 29 , 30 , 31 , 32 ). The breath samples were used for measurement of the 13 C: 12 C isotope ratios (δ 13 C, ‰) using an IRIS (infrared isotope analyzer system, 13 C Wagner Analysen Technik GmbH, Bremen, Germany
Ingeborg Brønstad
Ingeborg Brønstad
Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
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Lars Breivik
Lars Breivik
Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
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Paal Methlie
Paal Methlie
Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
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Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
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Anette S B Wolff
Anette S B Wolff
Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
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Eirik Bratland
Eirik Bratland
Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
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Ingrid Nermoen
Ingrid Nermoen
Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
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Kristian Løvås
Kristian Løvås
Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
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Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
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Eystein S Husebye
Eystein S Husebye
Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
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Department of Clinical Science, Department of Medicine, Division of Medicine, University of Bergen, 5021 Bergen, Norway
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molecular weight of wt 21OH (56 kDa) were cut out for trypsin treatment. Stable isotope-labelled synthetic peptides (N-terminal replacement of lysine ( 13 C 6 , 15 N 2 ) or arginine ( 13 C 6 , 15 N 4 ) respectively) were added in constant amount before
Jesper Krogh
Jesper Krogh
Department of Endocrinology & Metabolism, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
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Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
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Peter Plomgaard
Peter Plomgaard
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
Department of Clinical Biochemistry, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark
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Department of Clinical Biochemistry, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark
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Ruth Frikke-Schmidt
Ruth Frikke-Schmidt
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
Department of Clinical Biochemistry, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark
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Department of Clinical Biochemistry, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark
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Sten Velschow
Sten Velschow
Fluisense ApS, Lillerød, Denmark
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Jesper Johannesen
Jesper Johannesen
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
Department of Pediatrics, Copenhagen University Hospital - Herlev & Gentofte, Copenhagen, Denmark
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Department of Pediatrics, Copenhagen University Hospital - Herlev & Gentofte, Copenhagen, Denmark
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Linda Maria Hilsted
Linda Maria Hilsted
Department of Clinical Biochemistry, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark
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Malene Schrøder
Malene Schrøder
Fluisense ApS, Lillerød, Denmark
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Ulla Feldt-Rasmussen
Ulla Feldt-Rasmussen
Department of Endocrinology & Metabolism, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
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Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
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-0564) using a Wallac DBS Puncher (PerkinElme). Cortisol was extracted from the DBS with 200 μL extraction solvent (acetonitrile/water: 80:20) containing the stable isotopically labeled cortisol-( 13 C3) internal standard (30 nmol/L) by vigorously mixing
Kathrin R Frey
Kathrin R Frey
Department of Medicine I, Endocrine and Diabetes Unit, University Hospital, University of Würzburg, Würzburg, Germany
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Tina Kienitz
Tina Kienitz
Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany
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Julia Schulz
Julia Schulz
Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany
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Manfred Ventz
Manfred Ventz
Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany
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Kathrin Zopf
Kathrin Zopf
Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany
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Marcus Quinkler
Marcus Quinkler
Endocrinology in Charlottenburg, Berlin, Germany
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Winterer JC Loriaux DL . Daily cortisol production rate in man determuned by stable isotope dilution/mass spectrometry . Journal of Clinical Endocrinology and Metabolism 1991 72 39 – 45 . ( https://doi.org/10.1210/jcem-72-1-39 ) 10.1210/jcem-72
Kjell Oberg
Kjell Oberg
Uppsala University, Uppsala, Sweden
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Eric Krenning
Eric Krenning
Erasmus Medical Center, Rotterdam, Netherlands
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Anders Sundin
Anders Sundin
Uppsala University, Uppsala, Sweden
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Lisa Bodei
Lisa Bodei
Memorial Sloan Kettering Cancer Center, New York, New York, USA
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Mark Kidd
Mark Kidd
Wren Laboratories, Branford, Connecticut, USA
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Margot Tesselaar
Margot Tesselaar
Netherlands Cancer Institute, Amsterdam, Netherlands
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Valentina Ambrosini
Valentina Ambrosini
University of Bologna, Bologna, Italy
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Richard P Baum
Richard P Baum
Zentralklinik Bad Berka, Bad Berka, Germany
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Matthew Kulke
Matthew Kulke
Dana Farber Cancer Institute, Boston, Massachusetts, USA
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Marianne Pavel
Marianne Pavel
Charite Hospital, Berlin, Germany
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Jaroslaw Cwikla
Jaroslaw Cwikla
University of Warmia and Mazury, Olsztyn, Poland
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Ignat Drozdov
Ignat Drozdov
Wren Laboratories, Branford, Connecticut, USA
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Massimo Falconi
Massimo Falconi
Ospedale San Raffaele, Milan, Italy
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Nicola Fazio
Nicola Fazio
IEO (European Institute of Oncology), Milan, Italy
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Andrea Frilling
Andrea Frilling
Imperial College London, London, UK
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Robert Jensen
Robert Jensen
National Institutes of Health, Bethesda, Maryland, USA
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Klaus Koopmans
Klaus Koopmans
Martini Ziekenhuis, Groningen, Netherlands
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Tiny Korse
Tiny Korse
Netherlands Cancer Institute, Amsterdam, Netherlands
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Dik Kwekkeboom
Dik Kwekkeboom
Erasmus Medical Center, Rotterdam, Netherlands
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Helmut Maecke
Helmut Maecke
University Hospital Freiburg, Freiburg, Germany
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Giovanni Paganelli
Giovanni Paganelli
Instituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori, Meldola, Italy
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Ramon Salazar
Ramon Salazar
Instituto Catala d’Oncologia, Barcelona, Spain
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Stefano Severi
Stefano Severi
Instituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori, Meldola, Italy
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Jonathan Strosberg
Jonathan Strosberg
H. Lee Moffitt Cancer Center, Tampa, Florida, USA
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Vikas Prasad
Vikas Prasad
Charite Hospital, Berlin, Germany
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Aldo Scarpa
Aldo Scarpa
University of Verona, Verona, Italy
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Ashley Grossman
Ashley Grossman
Univeristy of Oxford, Oxford, UK
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Annemeik Walenkamp
Annemeik Walenkamp
University of Groningen, Groningen, Netherlands
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Mauro Cives
Mauro Cives
H. Lee Moffitt Cancer Center, Tampa, Florida, USA
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Irene Virgolini
Irene Virgolini
Medical University Innsbruck, Innsbruck, Austria
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Andreas Kjaer
Andreas Kjaer
Copenhagen University, Copenhagen, Denmark
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Irvin M Modlin
Irvin M Modlin
Yale University, New Haven, Connecticut, USA
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-specific symptoms, as well as knowledge regarding the patient’s overall condition. However, they also decided that clinical knowledge alone was inadequate for predicting whether a NEN would be progressive or exhibit a stable disease. Although a wait-and-see strategy
Kristian Almstrup
Kristian Almstrup
Department of Growth and Reproduction, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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Hanne Frederiksen
Hanne Frederiksen
Department of Growth and Reproduction, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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Anna-Maria Andersson
Anna-Maria Andersson
Department of Growth and Reproduction, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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Anders Juul
Anders Juul
Department of Growth and Reproduction, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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to inclusion of more samples when using the mean of yearly dichotomized values, but it could also reflect a more general exposure and hence a more stable effect on the epigenome in contrast to same-day levels. Our study population was peri
Lesley A Hill
Lesley A Hill
Departments of Cellular and Physiological Sciences and Obstetrics and Gynaecology, The University of British Columbia, Vancouver, British Columbia, Canada
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Zeynep Sumer-Bayraktar
Zeynep Sumer-Bayraktar
School of Life and Environmental Science, Charles Perkins Centre, The University of Sydney, Sydney, New South Wales, Australia
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John G Lewis
John G Lewis
Canterbury Health Laboratories, Christchurch, New Zealand
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Eva Morava
Eva Morava
Mayo Clinic, Department of Clinical Genomics, CIM, Rochester, Minnesota, USA
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Morten Thaysen-Andersen
Morten Thaysen-Andersen
Department of Molecular Sciences, Macquarie University, Sydney, New South Wales, Australia
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Geoffrey L Hammond
Geoffrey L Hammond
Departments of Cellular and Physiological Sciences and Obstetrics and Gynaecology, The University of British Columbia, Vancouver, British Columbia, Canada
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lines, Lec1 (ATCC CRL-1735) or Lec2 (ATCC CRL-1736), for recombinant protein expression ( 12 ). As previously observed ( 24 ), variability in the expression of CBG constructs in CHO cell lines is likely due to differences in the proportion of stably
