Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Andreas Rinne"'
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
Externí odkaz:
https://doaj.org/article/030e116712aa4a96ba9ee9c5b6ade6fe
Autor:
Lutz Pott, Evi Kostenis, Gabriele M. König, Anne Niemeyer, Andreas Rinne, Marie-Cécile Kienitz
Publikováno v:
Journal of Molecular and Cellular Cardiology. 130:107-121
Ca2+-sensing receptors (CaSRs) belong to the class C of G protein-coupled receptors and are activated by extracellular Ca2+. CaSRs display biased G protein signaling by coupling to different classes of heterotrimeric G proteins depending on agonist a
Publikováno v:
Cellular Signalling. 42:114-126
Muscarinic receptors (M-Rs) for acetylcholine (ACh) belong to the class A of G protein-coupled receptors. M-Rs are activated by orthosteric agonists that bind to a specific site buried in the M-R transmembrane helix bundle. In the active conformation
Publikováno v:
Journal of Biological Chemistry. 291:26410-26426
Activation of Gq protein-coupled receptors (GqPCRs) might induce divergent cellular responses, related to receptor-specific activation of different branches of the Gq signaling pathway. Receptor-specific desensitization provides a mechanism of effect
Publikováno v:
Cellular signalling. 64
G Protein-activated K
Autor:
Marie-Cecile, Kienitz, Anne, Niemeyer, Gabriele M, König, Evi, Kostenis, Lutz, Pott, Andreas, Rinne
Publikováno v:
Journal of molecular and cellular cardiology. 130
Ca
Publikováno v:
Biochemical Journal. 454:515-523
Many physiological and pathophysiological processes are regulated by cAMP. Different therapies directly or indirectly influence the cellular concentration of this second messenger. A wide variety of receptors either activates or inhibits adenylate cy
Publikováno v:
Neuromethods ISBN: 9781493928576
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84af23aba5a36486f27add530277e7c0
https://doi.org/10.1007/978-1-4939-2858-3_8
https://doi.org/10.1007/978-1-4939-2858-3_8
Publikováno v:
Science signaling. 8(401)
Signaling by many heterotrimeric guanine nucleotide-binding protein (G protein)-coupled receptors (GPCRs) is either enhanced or attenuated by changes in plasma membrane potential. To identify structural correlates of the voltage sensitivity of GPCR s
Publikováno v:
Biophysical Journal. 112:170a-171a
G-protein coupled receptors (GPCRs) encompass the largest group of membrane proteins in eukaryotes and regulate numerous intracellular pathways. Class A GPCRs are activated by binding of specific agonists to an orthosteric binding site, which is form