U
Ulla G. Sidelmann
Researcher at Novo Nordisk
Publications - 26
Citations - 1843
Ulla G. Sidelmann is an academic researcher from Novo Nordisk. The author has contributed to research in topics: Glucuronide & Metabolite. The author has an hindex of 22, co-authored 26 publications receiving 1791 citations. Previous affiliations of Ulla G. Sidelmann include Birkbeck, University of London.
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Journal ArticleDOI
Contemporary issues in toxicology the role of metabonomics in toxicology and its evaluation by the COMET project.
John C. Lindon,Jeremy K. Nicholson,Elaine Holmes,Henrik Antti,Mary E. Bollard,Hector C. Keun,Olaf Beckonert,Timothy M. D. Ebbels,Michael D. Reily,Donald G. Robertson,Gregory J. Stevens,Peter Luke,Alan P. Breau,Glenn H. Cantor,Roy H. Bible,Urs Niederhauser,Hans Senn,Goetz Schlotterbeck,Ulla G. Sidelmann,Steen Møller Laursen,Adrienne A. Tymiak,Bruce D. Car,Lois D. Lehman-McKeeman,Jean-Marie Colet,Ali Loukaci,Craig E. Thomas +25 more
TL;DR: The role that metabonomics has in the evaluation of xenobiotic toxicity studies is presented here and an evaluation of intersite NMR analytical reproducibility has revealed a high degree of robustness.
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Small-molecule agonists for the glucagon-like peptide 1 receptor
Lotte Bjerre Knudsen,Dan Kiel,Min Teng,Carsten Behrens,Dilip Bhumralkar,János Tibor Kodra,Jens J. Holst,Claus Bekker Jeppesen,Michael D. L. Johnson,Johannes Cornelis De Jong,Anker Steen Jorgensen,Tim Kercher,Jarek Kostrowicki,Peter Madsen,Preben H. Olesen,Jacob S. Petersen,Fritz Poulsen,Ulla G. Sidelmann,Jeppe Sturis,Larry Kenneth Truesdale,John F. May,Jesper Lau +21 more
TL;DR: A series of small molecules known as ago-allosteric modulators selective for the human GLP-1 receptor are discovered, which act as both allosteric activators of the receptor and independent agonists.
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CYP2C8 and CYP3A4 are the principal enzymes involved in the human in vitro biotransformation of the insulin secretagogue repaglinide.
Tanja Busk Bidstrup,Inga Bjørnsdottir,Ulla G. Sidelmann,Mikael S. Thomsen,Kristian Tage Hansen +4 more
TL;DR: An important role for both CYP3A4 and CYP2C8 in the human in vitro biotransformation of repaglinide is confirmed, which may have consequences for the clinical pharmacokinetics and drug-drug interactions involving repaglinside if one CYP pathway has sufficient capacity to compensate if the other is inhibited.
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Direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models
Marc-Emmanuel Dumas,Steven P. Wilder,Marie-Thérèse Bihoreau,Richard H. Barton,Jane F. Fearnside,Karène Argoud,Lisa D'Amato,Robert H. Wallis,Christine Blancher,Hector C. Keun,Dorrit Baunsgaard,James Scott,Ulla G. Sidelmann,Jeremy K. Nicholson,Dominique Gauguier +14 more
TL;DR: Mapping metabotypic QTLs provides a practical approach to understanding genome-phenotype relationships in mammals and may uncover deeper biological complexity, as extended genome perturbations that affect disease processes through transgenomic effects may influence QTL detection.
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Directly Coupled HPLC-NMR and Its Application to Drug Metabolism
TL;DR: Directly coupled HPLC-NMR and its application to drug metabolism was discussed in this paper, where the authors present a comparison of the two types of NMR-based methods.