Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Jacob A. Olsen"'
Autor:
Dieter Schmoll, Nicole Ziegler, Benoit Viollet, Marc Foretz, Patrick C. Even, Dalila Azzout‐Marniche, Andreas Nygaard Madsen, Martin Illemann, Karen Mandrup, Michael Feigh, Jörg Czech, Heiner Glombik, Jacob A. Olsen, Wolfgang Hennerici, Klaus Steinmeyer, Ralf Elvert, Tamara R. Castañeda, Aimo Kannt
Publikováno v:
Hepatology Communications, Vol 4, Iss 7, Pp 1056-1072 (2020)
The worldwide obesity and type 2 diabetes epidemics have led to an increase in nonalcoholic fatty liver disease (NAFLD). NAFLD covers a spectrum of hepatic pathologies ranging from simple steatosis to nonalcoholic steatohepatitis, characterized by fi
Externí odkaz:
https://doaj.org/article/9426e7d8200a4cacaf75487e613184ae
Autor:
Jacob C. Olsen, Robert A. Bettinger
Publikováno v:
AIAA SCITECH 2022 Forum.
Publikováno v:
Hydrology, Vol 5, Iss 3, p 45 (2018)
Atmospheric nutrient loading through wet and dry deposition is one of the least understood, yet can be one of the most important, pathways of nutrient transport into lakes and reservoirs. Nutrients, specifically phosphorus and nitrogen, are essential
Externí odkaz:
https://doaj.org/article/69939230aa7940f3a21ef1acb611082f
Autor:
Jacob Valdbjørn Olsen, Morten Meldal, Morten Petersen, Frederik Præstholm Jørgensen, Daniel H. Madsen, Mikael Bols, Jeppe Granhøj
Publikováno v:
Journal of Medicinal Chemistry. 62:5191-5216
A series of 35 analogues of Shld with modifications in the A-residue and the C-residues were prepared and investigated for binding to FKBP and GFP accumulation in transgenic plants. The modifications investigated explored variations that were suppose
Autor:
Martin Illemann, Ralf Elvert, Dieter Schmoll, Nicole Ziegler, Andreas Nygaard Madsen, Patrick C. Even, Jacob A Olsen, Marc Foretz, Heiner Glombik, Benoit Viollet, Dalila Azzout-Marniche, Klaus Steinmeyer, Wolfgang Hennerici, Michael Feigh, Aimo Kannt, Karen Mandrup, Jörg Czech, Tamara R. Castañeda
Publikováno v:
International Hepatology Communications
International Hepatology Communications, Elsevier, 2020, 4 (7), pp.1056-1072. ⟨10.1002/hep4.1508⟩
Hepatology Communications, Vol 4, Iss 7, Pp 1056-1072 (2020)
Hepatology Communications
International Hepatology Communications, 2020, 4 (7), pp.1056-1072. ⟨10.1002/hep4.1508⟩
International Hepatology Communications, Elsevier, 2020, 4 (7), pp.1056-1072. ⟨10.1002/hep4.1508⟩
Hepatology Communications, Vol 4, Iss 7, Pp 1056-1072 (2020)
Hepatology Communications
International Hepatology Communications, 2020, 4 (7), pp.1056-1072. ⟨10.1002/hep4.1508⟩
The worldwide obesity and type 2 diabetes epidemics have led to an increase in nonalcoholic fatty liver disease (NAFLD). NAFLD covers a spectrum of hepatic pathologies ranging from simple steatosis to nonalcoholic steatohepatitis, characterized by fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03d47db58e3758ae0ac431a232885e99
https://www.hal.inserm.fr/inserm-02886252
https://www.hal.inserm.fr/inserm-02886252
Publikováno v:
Wang, B, Olsen, J I, Laursen, B W, Poulsen, J C N & Bols, M 2017, ' Determination of protonation states of iminosugar-enzyme complexes using photoinduced electron transfer ', Chemical Science, vol. 8, no. 11, pp. 7383-7393 . https://doi.org/10.1039/c7sc01540b
A series of N-alkylated analogues of 1-deoxynojirimycin containing a fluorescent 10-chloro-9-anthracene group in the N-alkyl substituent were prepared. The anthracene group acted as a reporting group for protonation at the nitrogen in the iminosugar
Autor:
Óscar López, José G. Fernández-Bolaños, Jacob Ingemar Olsen, Mikael Bols, José M. Padrón, Gabriela B. Plata
Publikováno v:
European Journal of Medicinal Chemistry. 123:155-160
Herein we report the synthesis of N-alkylated deoxynojirimycin derivatives decorated with a selenoureido motif at the hydrocarbon tether as an example of unprecedented multitarget agents. Title compounds were designed as dual drugs for tackling simul
Publikováno v:
Tetrahedron Letters. 57:35-38
Novel thiomannosyl donors with a 2,3-(phenyl-1,2-ethylidine) tethering group were designed so that the phenyl group would act as a molecular lever and force the pyranoside into its most reactive conformation. It was demonstrated that this type of mol
Publikováno v:
Organic & Biomolecular Chemistry. 13:3116-3121
Four substituted cis and trans-4,5-dihydroxyhexahydropyridazines that were expected to undergo pH induced conformational switching were synthesized and carefully investigated by NMR analyses and calculations. For two of the compounds a large differen
Autor:
Lars Olsen, Liwei Han, Jacob Ingemar Olsen, Ulf Madsen, Niklas Sköld, Tommy N. Johansen, Birgitte Nielsen, Darryl S. Pickering, Jesper L. Kristensen
Publikováno v:
Bioorganic & Medicinal Chemistry. 22:5368-5377
In order to identify compounds selective for the GluK1 and GluK3 subtypes of kainate receptors we have designed and synthesized a series of (S)-2-amino-3-((2-carboxyethyl)phenyl)propanoic acid analogs with hydrogen bond donating and accepting substit