Zobrazeno 1 - 10
of 377
pro vyhledávání: '"Klaus, Mohr"'
Autor:
Matthias Irmen, Janine Holze, Michael Kauk, Marcel Bermudez, Marco De Amici, Clelia Dallanoce, Klaus Mohr, Theresa Bödefeld, Gabriele M. König, Andreas Bock, Eva Marie Pfeil, Carsten Hoffmann, Gerhard Wolber, Carlo Matera, Ulrike Holzgrabe, Evi Kostenis, Ramona Schrage, Christian Tränkle
Publikováno v:
ACS Pharmacol Transl Sci
[Image: see text] Allosteric coupling describes a reciprocal process whereby G-protein-coupled receptors (GPCRs) relay ligand-induced conformational changes from the extracellular binding pocket to the intracellular signaling surface. Therefore, GPCR
Publikováno v:
Naunyn-Schmiedeberg's Archives of Pharmacology. 391:1295-1299
Muscarinic M2 and M4 receptors resemble each other in brain distribution, function, and Gi/o protein signaling. However, there is evidence from human recombinant receptors that the M4 receptor also couples to Gs protein whereas such an alternative si
Autor:
Fabian Krebs, Klaus Mohr, Martin J. Lohse, Marcel Bermudez, Ulrike Holzgrabe, Andreas Bock, Gerhard Wolber
Publikováno v:
ACS Chemical Biology. 12:1743-1748
G protein-coupled receptors transmit extracellular signals across cell membranes via different G protein classes and β-arrestins. Some pathways may be therapeutically beneficial, whereas others may be detrimental under certain pathophysiological con
Autor:
Klaus Mohr, Evi Kostenis, Mathias Muth, Ramona Schrage, Jessica Kloeckner, Janine Holze, Anna De Min, Carlo Matera, Ulrike Holzgrabe, Terry P. Kenakin, Clelia Dallanoce, Andreas Bock, Marco De Amici, Christian Traenkle
Publikováno v:
Molecular Pharmacology. 91:348-356
Protean agonists are of great pharmacological interest as their behavior may change in magnitude and direction depending on the constitutive activity of a receptor. Yet, this intriguing phenomenon has been poorly described and understood, due to the
Autor:
Janine Holze, Dina Manetti, Christian Tränkle, Klaus Mohr, Elisabetta Teodori, Maria Vittoria Martino, Cristina Bellucci, Maria Novella Romanelli, Giulio Vistoli, Jessica Welzel, Silvia Dei, Angelica Mazzolari, Marta Nesi, Ulrike Bartz, Rosanna Matucci
Publikováno v:
European journal of pharmacology. 883
Although agonists and antagonists of muscarinic receptors have been known for long time, there is renewed interest in compounds (such as allosteric or bitopic ligands, or biased agonists) able to differently and selectively modulate these receptors.
Publikováno v:
Naunyn-Schmiedeberg's archives of pharmacology. 391(11)
Muscarinic M
Publikováno v:
British Journal of Pharmacology. 173:3018-3027
Ligands targeting GPCRs can be categorized according to their intrinsic efficacy to trigger a specific, receptor-mediated response. A ligand endowed with the same level of efficacy as the endogenous agonist can be classified as a full agonist, wherea
Autor:
Evi Kostenis, Jesus Gomeza, Theresa Bödefeld, Anne-Gaelle Letombe, Michel Gillard, Ramona Schrage, Qing Richard Lu, Liguo Zhang, Julia Fischer, Nicole Merten, Klaus Mohr, Ralf Schröder, Katharina Simon, Celine Vermeiren, Oliver Brüstle, Lucas Peters, Stephanie Hennen
Publikováno v:
Cell chemical biology. 25(6)
Identification of additional uses for existing drugs is a hot topic in drug discovery and a viable alternative to de novo drug development. HAMI3379 is known as an antagonist of the cysteinyl-leukotriene CysLT(2) receptor, and was initially developed
Autor:
Marcel, Bermudez, Andreas, Bock, Fabian, Krebs, Ulrike, Holzgrabe, Klaus, Mohr, Martin J, Lohse, Gerhard, Wolber
Publikováno v:
ACS chemical biology. 12(7)
G protein-coupled receptors transmit extracellular signals across cell membranes via different G protein classes and β-arrestins. Some pathways may be therapeutically beneficial, whereas others may be detrimental under certain pathophysiological con
Autor:
Klaus Mohr, Marcel Bermudez, Ramona Schrage, Ulrike Holzgrabe, Jens Schmitz, Gerhard Wolber, Dorina van der Mey, Christian Tränkle, Evi Kostenis, Jessica Klöckner
Publikováno v:
Journal of Medicinal Chemistry. 57:6739-6750
Bivalent ligands of G protein-coupled receptors have been shown to simultaneously either bind to two adjacent receptors or to bridge different parts of one receptor protein. Recently, we found that bivalent agonists of muscarinic receptors can simult