Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jan Ungewiss"'
Autor:
Maria Lucey, Philip Pickford, Stavroula Bitsi, James Minnion, Jan Ungewiss, Katja Schoeneberg, Guy A. Rutter, Stephen R. Bloom, Alejandra Tomas, Ben Jones
Publikováno v:
Molecular Metabolism, Vol 37, Iss , Pp 100991- (2020)
Objective: The objective of this study was to determine how pharmacokinetically advantageous acylation impacts on glucagon-like peptide-1 receptor (GLP-1R) signal bias, trafficking, anti-hyperglycaemic efficacy, and appetite suppression. Methods: In
Externí odkaz:
https://doaj.org/article/6622263a11a0409ea4a255d09f36f3b7
Autor:
Dirk Zboralski, Frank Osterkamp, Esben Christensen, Anne Bredenbeck, Anne Schumann, Aileen Hoehne, Eberhard Schneider, Matthias Paschke, Jan Ungewiss, Christian Haase, Liliane Robillard, Andrew D. Simmons, Thomas C. Harding, Minh Nguyen
Publikováno v:
European Journal of Nuclear Medicine and Molecular Imaging.
Purpose FAP is a membrane-bound protease under investigation as a pan-cancer target, given its high levels in tumors but limited expression in normal tissues. FAP-2286 is a radiopharmaceutical in clinical development for solid tumors that consists of
Autor:
Dirk Zboralski, Aileen Hoehne, Anne Bredenbeck, Anne Schumann, Minh Nguyen, Eberhard Schneider, Jan Ungewiss, Matthias Paschke, Christian Haase, Jan L. von Hacht, Tanya Kwan, Kevin K. Lin, Jan Lenore, Thomas C. Harding, Jim Xiao, Andrew D. Simmons, Ajay-Mohan Mohan, Nicola Beindorff, Ulrich Reineke, Christiane Smerling, Frank Osterkamp
Publikováno v:
European Journal of Nuclear Medicine and Molecular Imaging. 49:3651-3667
Purpose Fibroblast activation protein (FAP) is a membrane-bound protease that has limited expression in normal adult tissues but is highly expressed in the tumor microenvironment of many solid cancers. FAP-2286 is a FAP-binding peptide coupled to a r
Autor:
James Minnion, Alejandra Tomas, Philip Pickford, Ben Jones, Guy A. Rutter, Jan Ungewiss, Katja Schoeneberg, Stephen R. Bloom, Maria Lucey
Publikováno v:
bioRxiv
ObjectiveTo determine how pharmacokinetically advantageous acylation impacts on glucagon-like peptide-1 receptor (GLP-1R) signal bias, trafficking, anti-hyperglycaemic efficacy and appetite suppression.MethodsIn vitro signalling responses were measur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fedd1c716a085ce9f42a303cde8d8708
https://doi.org/10.1101/855874
https://doi.org/10.1101/855874
Autor:
Philip Pickford, Guy A. Rutter, Alejandra Tomas, Stephen R. Bloom, James Minnion, Ben Jones, Katja Schoeneberg, Stavroula Bitsi, Jan Ungewiss, Maria Lucey
Publikováno v:
Molecular Metabolism
Molecular Metabolism, Vol 37, Iss, Pp 100991-(2020)
Molecular Metabolism, Vol 37, Iss, Pp 100991-(2020)
Objective The objective of this study was to determine how pharmacokinetically advantageous acylation impacts on glucagon-like peptide-1 receptor (GLP-1R) signal bias, trafficking, anti-hyperglycaemic efficacy, and appetite suppression. Methods In vi
Publikováno v:
Journal of pharmaceutical sciences. 108(3)
The plasma protein binding capability of drug substances represents an important assay parameter in drug discovery and development. For very strong plasma protein binding molecules, however, the free fraction in plasma f
Autor:
Hermann Fromme, Ludwig Gruber, Martin Schlummer, Sigrun Böhmer, Jan Ungewiss, Gerd Wolz, Angela Möller, Wolfgang Dekant, D Twardella, Richard Mayer, Bernhard Liebl
Publikováno v:
Environmental Science & Technology. 41:7928-7933
Because dietary intake is supposed to be an important route of human exposure we quantified the dietary intake of perfluorooctane sulfonate (PFOS), perfluorooctanoate (PFOA), perfluorohexane sulfonate (PFHxS), perfluorohexanoate (PFHxA), and perfluor
Autor:
Klaus-Peter Wittern, Claudius Rapp, Reiner Salzer, Hartmut Dr. Schmidt-Lewerkühne, Jan Ungewiß, Jens-Peter Vietzke
Publikováno v:
Analytical and Bioanalytical Chemistry. 381:1401-1407
Cationic polysaccharides containing N-hydroxypropyl-N,N,N-trimethylammonium substituents are widely used as conditioning agents for hair-care products. A sensitive method has been developed for the quantitation of these polymers. After acidic extract
Autor:
Simon Michaelis, Anna K. Schrey, Olivia Y. Graebner, Hubert Koester, Anne Diehl, Jenny J. Fischer, Sabine Horzowski, Mirko Glinski, Mathias Dreger, Friedrich Kroll, Jan Ungewiss
Publikováno v:
Proteomics. 11(20)
Suberoylanilide hydroxamic acid (SAHA) is a potent histone deacetylase (HDAC) inhibitor. Inhibitors of HDACs are used in cancer therapy based on the role HDACs play in transcription by regulating chromatin compaction and non-histone proteins such as
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