Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Jesper Villadsen"'
Publikováno v:
Rocznik Andragogiczny, Vol 21, Iss 0, Pp 423-434 (2015)
This article was prepared by a team of authors from the Den Frie Lærerskole (English name: The Independent Academy for Free School Teaching) in Ollerup – Danish independent institution of higher education that prepares teaching staff for free scho
Externí odkaz:
https://doaj.org/article/2ce2f4dcf80d452d86a1db52e78e950d
Publikováno v:
Diabetes. 71
ZP8396, currently in phase 1, is a long-acting, amylin analogue designed to improve solubility and stability and allow for co-formulation with other peptides at physiological pH. Here we present in-vivo efficacy and formulation design space of ZP8396
Autor:
Casper Rønn Hoeck, Christian A. Olsen, Pernille Harris, Tina Friis, Niels Johan Christensen, Alex Maolanon, Jesper Villadsen, Charlotte Held Gotfredsen, Peter Fristrup
Publikováno v:
Journal of Medicinal Chemistry. 57:9644-9657
Natural, nonribosomal cyclotetrapeptides have traditionally been a rich source of inspiration for design of potent histone deacetylase (HDAC) inhibitors. We recently disclosed the total synthesis and full HDAC profiling of the naturally occurring azu
Publikováno v:
Villadsen, J, Stephansen, H M, Maolanon, A, Harris, P & Olsen, C A 2013, ' Total Synthesis and Full Histone Deacetylase Inhibitory Profiling of Azumamides A–E as Well as β2-epi-Azumamide E and β3-epi-Azumamide E ', Open Journal of Medicinal Chemistry, vol. 56, no. 16, pp. 206512-6520 . https://doi.org/10.1021/jm4008449
Cyclic tetrapeptide and depsipeptide natural products have proven useful as biological probes and drug candidates due to their potent activities as histone deacetylase (HDAC) inhibitors. Here, we present the syntheses of a class of cyclic tetrapeptid
Autor:
Betül Kitir, Jesper Villadsen, Tina Friis, Christian A. Olsen, Andreas Stahl Madsen, Kathrine Wich
Publikováno v:
Villadsen, J, Kitir, B, Wich, K, Friis, T, Madsen, A S & Olsen, C A 2014, ' An azumamide C analogue without the zinc-binding functionality ', MedChemComm, vol. 5, pp. 1849-1855 . https://doi.org/10.1039/C4MD00252K
Histone deacetylase (HDAC) inhibitors have attracted considerable attention due to their promise as therapeutic agents. Most HDAC inhibitors adhere to a general “ cap-linker-Zn 2+ -binding group ” architecture but recent studies have indicated th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04808be18ea5e0c6cb1d1b9b15962c0e
https://orbit.dtu.dk/en/publications/7b44e82b-f3d2-4094-96f8-6d810fd8dd25
https://orbit.dtu.dk/en/publications/7b44e82b-f3d2-4094-96f8-6d810fd8dd25
Autor:
Jesper Villadsen, George A. Elliott
Publikováno v:
Canadian Journal of Mathematics. 52:1164-1191
A simple C*-algebra is constructed for which theMurray-von Neumann equivalence classes of projections, with the usual addition—induced by addition of orthogonal projections—form the additive semigroup{0, 2, 3, . . .}.(This is a particularly simpl
Autor:
Jesper Villadsen, Mikael Rø
Publikováno v:
K-Theory. 15:307-322
Autor:
Jesper Villadsen
Publikováno v:
K-Theory. 15:1-12
Autor:
Jesper Villadsen
Publikováno v:
Journal of Functional Analysis. 154:110-116
Simple C*-algebras are constructed for which the ordered K 0 -group is not weakly unperforated. The algebras are approximately homogeneous and do not have slow dimension growth.
Autor:
Maike Bublitz, Poul Nissen, Ditte F. Bonde, Ingrid Dach, Eleonora Tenori, Jesper V. Møller, Henriette Elisabeth Autzen, S. Brøgger Christensen, Pankaj Sehgal, Mette Alstrup Lie, Jesper Villadsen, Eleonora S. Paulsen, Claus Olesen, Birgit Schiøtt, Huizhen Liu
Publikováno v:
Paulsen, E S, Villadsen, J, Tenori, E, Liu, H, Bonde, D F, Lie, M A, Bublitz, M, Olesen, C, Autzen, H E, Dach, I, Sehgal, P, Nissen, P, Møller, J V, Schiøtt, B & Christensen, SB 2013, ' Water-mediated interactions influence the binding of thapsigargin to sarco/endoplasmic reticulum calcium adenosinetriphosphatase ', Journal of Medicinal Chemistry, vol. 56, no. 9, pp. 3609-3619 . https://doi.org/10.1021/jm4001083
A crystal structure suggests four water molecules are present in the binding cavity of thapsigargin in sarco/endoplasmic reticulum calcium ATPase (SERCA). Computational chemistry indicates that three of these water molecules mediate an extensive hydr