Structural basis of M3 muscarinic receptor dimer/oligomer formation
about
Activation and allosteric modulation of a muscarinic acetylcholine receptorOligomer size of the serotonin 5-hydroxytryptamine 2C (5-HT2C) receptor revealed by fluorescence correlation spectroscopy with photon counting histogram analysis: evidence for homodimers without monomers or tetramersA G Protein-Coupled Receptor Dimerization Interface in Human Cone OpsinsApelin receptor homodimer-oligomers revealed by single-molecule imaging and novel G protein-dependent signaling.Fluorescence correlation spectroscopy analysis of serotonin, adrenergic, muscarinic, and dopamine receptor dimerization: the oligomer number puzzleM3 muscarinic receptor interaction with phospholipase C β3 determines its signaling efficiency.Dynamic Regulation of Quaternary Organization of the M1 Muscarinic Receptor by Subtype-selective Antagonist Drugs.Regulation of oligomeric organization of the serotonin 5-hydroxytryptamine 2C (5-HT2C) receptor observed by spatial intensity distribution analysisStructural aspects of M₃ muscarinic acetylcholine receptor dimer formation and activationDistinct Agonist Regulation of Muscarinic Acetylcholine M2-M3 Heteromers and Their Corresponding Homomers.Mapping human protease-activated receptor 4 (PAR4) homodimer interface to transmembrane helix 4From atomic structures to neuronal functions of g protein-coupled receptorsSpinophilin as a novel regulator of M3 muscarinic receptor-mediated insulin release in vitro and in vivo.Disruption of Rhodopsin Dimerization with Synthetic Peptides Targeting an Interaction InterfaceDesign and functional characterization of a novel, arrestin-biased designer G protein-coupled receptor.A G Protein-biased Designer G Protein-coupled Receptor Useful for Studying the Physiological Relevance of Gq/11-dependent Signaling Pathways.Muscarinic receptors as model targets and antitargets for structure-based ligand discovery.Novel insights on thyroid-stimulating hormone receptor signal transduction.Protease-activated receptor 1 (PAR1) and PAR4 heterodimers are required for PAR1-enhanced cleavage of PAR4 by α-thrombin.Novel structural and functional insights into M3 muscarinic receptor dimer/oligomer formation.Revealing G-protein-coupled receptor oligomerization at the single-molecule level through a nanoscopic lens: methods, dynamics and biological function.Muscarinic drugs regulate the PKG-II-dependent phosphorylation of M3 muscarinic acetylcholine receptors at plasma membranes from airway smooth muscle.Cyclic GMP regulates M₃AChR activity at plasma membranes from airway smooth muscle.Muscarinic receptor oligomerization.Spatial Intensity Distribution Analysis: Studies of G Protein-Coupled Receptor Oligomerisation.
P2860
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P2860
Structural basis of M3 muscarinic receptor dimer/oligomer formation
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Structural basis of M3 muscarinic receptor dimer/oligomer formation
@ast
Structural basis of M3 muscarinic receptor dimer/oligomer formation
@en
type
label
Structural basis of M3 muscarinic receptor dimer/oligomer formation
@ast
Structural basis of M3 muscarinic receptor dimer/oligomer formation
@en
prefLabel
Structural basis of M3 muscarinic receptor dimer/oligomer formation
@ast
Structural basis of M3 muscarinic receptor dimer/oligomer formation
@en
P2093
P2860
P356
P1476
Structural basis of M3 muscarinic receptor dimer/oligomer formation
@en
P2093
Jürgen Wess
Moritz Heusel
Sara M McMillin
Stefano Costanzi
P2860
P304
28584-28598
P356
10.1074/JBC.M111.259788
P407
P577
2011-06-17T00:00:00Z