Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Moret, Ed E."'
Publikováno v:
In BBA - Proteins and Proteomics February 2013 1834(2):524-535
Akademický článek
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Autor:
van Scherpenzeel, Monique, Conte, Federica, Büll, Christian, Ashikov, Angel, Hermans, Esther, Willems, Anke, van Tol, Walinka, Kragt, Else, Moret, Ed E., Heise, Torben, Langereis, Jeroen D., Rossing, Emiel, Zimmermann, Michael, Rubio-Gozalbo, M. Estela, de Jonge, Marien I., Adema, Gosse J., Zamboni, Nicola, Boltje, Thomas, Lefeber, Dirk J.
Publikováno v:
bioRxiv
Synthetic sugar analogs are widely applied in metabolic oligosaccharide engineering (MOE) and as novel drugs to interfere with glycoconjugate biosynthesis. However, mechanistic insights on their exact metabolism in the cell and over time are mostly l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42d1e0fe604f01f226ea67540ddcfb2a
https://hdl.handle.net/20.500.11850/525491
https://hdl.handle.net/20.500.11850/525491
The role of peptide loops of the Bordetella pertussis protein P.69 pertactin in antibody recognition
Autor:
Hijnen, Marcel, de Voer, Richarda, Mooi, Frits R., Schepp, Rutger, Moret, Ed E., van Gageldonk, Pieter, Smits, Gaby, Berbers, Guy A.M.
Publikováno v:
In Vaccine 2007 25(31):5902-5914
Autor:
Scherpenzeel, Monique van, Conte, Federica, Büll, Christian, Ashikov, Angel, Hermans, Esther, Willems, Anke, Tol, Walinka van, Kragt, Else, Noga, Marek, Moret, Ed E, Heise, Torben, Langereis, Jeroen D, Rossing, Emiel, Zimmermann, Michael, Rubio-Gozalbo, M Estela, Jonge, Marien I de, Adema, Gosse J, Zamboni, Nicola, Boltje, Thomas, Lefeber, Dirk J
Publikováno v:
Glycobiology; Mar2022, Vol. 39 Issue 3, p239-250, 12p
Autor:
van Haren, Matthijs J, Taig, Rebecca, Kuppens, Jilles, Sastre Toraño, Javier, Moret, Ed E, Parsons, Richard B, Sartini, Davide, Emanuelli, Monica, Martin, Nathaniel I, Chemical Biology and Drug Discovery, Afd Chemical Biology and Drug Discovery
Publikováno v:
Van Haren, M J, Taig, R, Kuppens, J, Sastre Toraño, J, Moret, E E, Parsons, R B, Sartini, D, Emanuelli, M & Martin, N I 2017, ' Inhibitors of nicotinamide : N-methyltransferase designed to mimic the methylation reaction transition state ', ORGANIC AND BIOMOLECULAR CHEMISTRY, vol. 15, no. 31, pp. 6656-6667 . https://doi.org/10.1039/c7ob01357d
Organic and Biomolecular Chemistry, 15(31), 6656. Royal Society of Chemistry
Organic and Biomolecular Chemistry, 15(31), 6656. Royal Society of Chemistry
Nicotinamide N-methyltransferase (NNMT) is an enzyme that catalyses the methylation of nicotinamide to form N′-methylnicotinamide. Both NNMT and its methylated product have recently been linked to a variety of diseases, suggesting a role for the en
Autor:
Gao, Yongzhi, Van Haren, Matthijs J., Moret, Ed E., Rood, Johannes J.M., Sartini, Davide, Salvucci, Alessia, Emanuelli, Monica, Craveur, Pierrick, Babault, Nicolas, Jin, Jian, Martin, Nathaniel I., Afd Chemical Biology and Drug Discovery, Afd Pharmacoepi & Clinical Pharmacology, Chemical Biology and Drug Discovery, Pharmacoepidemiology and Clinical Pharmacology
Publikováno v:
Journal of Medicinal Chemistry, 62(14), 6597-6614
Journal of Medicinal Chemistry, 62(14), 6597. American Chemical Society : Division of Carbohydrate Chemistry
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry, 62(14), 6597. American Chemical Society : Division of Carbohydrate Chemistry
Journal of Medicinal Chemistry
Nicotinamide N-methyltransferase (NNMT) catalyzes the methylation of nicotinamide to form N-methylnicotinamide. Overexpression of NNMT is associated with a variety of diseases, including a number of cancers and metabolic disorders, suggesting a role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f90dcd09358f06fca023908bee46e10d
http://hdl.handle.net/1887/82062
http://hdl.handle.net/1887/82062
Autor:
de Haan, Ellen C, Wauben, Marca H.M, Grosfeld-Stulemeyer, Mayken C, Kruijtzer, John A.W, Liskamp, Rob M.J, Moret, Ed E
Publikováno v:
In Bioorganic & Medicinal Chemistry 2002 10(6):1939-1945
Autor:
Sevsek, Alen, Šrot, Luka, Rihter, Jakob, Čelan, Maša, van Ufford, Linda Quarles, Moret, Ed E, Martin, Nathaniel I, Pieters, Roland J
A series of lipidated guanidino and urea derivatives of 1,5-dideoxy-1,5-imino-d-xylitol were prepared from d-xylose using a concise synthetic protocol. Inhibition assays with a panel of glycosidases revealed that the guanidino analogues display poten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______101::44e975779488813cbbfed4c8a8716068
https://dspace.library.uu.nl/handle/1874/350689
https://dspace.library.uu.nl/handle/1874/350689
Akademický článek
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