A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer.
about
Biosynthesis and actions of 5-oxoeicosatetraenoic acid (5-oxo-ETE) on feline granulocytesComputational approaches in target identification and drug discoveryThe Role of Chemokines in Shaping the Balance Between CD4(+) T Cell Subsets and Its Therapeutic Implications in Autoimmune and Cancer DiseasesCardiac cAMP: production, hydrolysis, modulation and detectionActivators of G protein signaling exhibit broad functionality and define a distinct core signaling triadQuaternary structure of a G-protein-coupled receptor heterotetramer in complex with Gi and Gs.Biosynthesis, biological effects, and receptors of hydroxyeicosatetraenoic acids (HETEs) and oxoeicosatetraenoic acids (oxo-ETEs) derived from arachidonic acidThe eosinophil chemoattractant 5-oxo-ETE and the OXE receptorUpdate on leukotriene, lipoxin and oxoeicosanoid receptors: IUPHAR Review 7Relation between sequence and structure in membrane proteins.Testosterone stimulates Duox1 activity through GPRC6A in skin keratinocytesHeteromerization of GPR55 and cannabinoid CB2 receptors modulates signalling3,1-Benzothiazines, 1,4-Benzodioxines and 1,4-Benzoxazines as Inhibitors of Matriptase-2: Outcome of a Focused Screening Approach.New paradigms in GPCR drug discovery.Recent molecular approaches to understanding astrocyte function in vivo.CXCL11-dependent induction of FOXP3-negative regulatory T cells suppresses autoimmune encephalomyelitis.Approaches for probing allosteric interactions at 7 transmembrane spanning receptors.Molecular targeting of Gα and Gβγ subunits: a potential approach for cancer therapeutics.Recent developments in biased agonism.Biased signaling pathways via CXCR3 control the development and function of CD4+ T cell subsets.Holistic Methods for the Analysis of cNMP Effects.Functional Selectivity of CB2 Cannabinoid Receptor Ligands at a Canonical and Noncanonical Pathway.Label-Free Dynamic Mass Redistribution and Bio-Impedance Methods for Drug Discovery.β2-Adrenoceptor-mediated regulation of glucose uptake in skeletal muscle--ligand-directed signalling or a reflection of system complexity?Design, characterization and cellular uptake studies of fluorescence-labeled prototypic cathepsin inhibitors.
P2860
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P2860
A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
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2012年论文
@zh-cn
name
A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer.
@en
A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer.
@nl
type
label
A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer.
@en
A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer.
@nl
prefLabel
A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer.
@en
A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer.
@nl
P2093
P2860
P50
P356
P1476
A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer
@en
P2093
C David Weaver
Evi Kostenis
Jürgen Gäb
Klaus Mohr
Lucas Peters
Michael Gütschow
Petra Luschnig
Philipp Aaron Ottersbach
Rahul Tyagi
Ralf Schröder
P2860
P2888
P304
P356
10.1038/NCHEMBIO.962
P577
2012-05-27T00:00:00Z