Three classes of ligands each bind to distinct sites on the orphan G protein-coupled receptor GPR84
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Three classes of ligands each bind to distinct sites on the orphan G protein-coupled receptor GPR84 ; volume:7 ; number:1 ; day:20 ; month:12 ; year:2017 ; pages:1-15 ; date:12.2017
Scientific reports ; 7, Heft 1 (20.12.2017), 1-15, 12.2017
- Classification
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Biowissenschaften, Biologie
- Creator
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Mahmud, Zobaer Al
- Contributor
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Jenkins, Laura
Ulven, Trond
Labéguère, Frédéric
Gosmini, Romain
De Vos, Steve
Hudson, Brian D.
Tikhonova, Irina G.
Milligan, Graeme
SpringerLink (Online service)
- DOI
-
10.1038/s41598-017-18159-3
- URN
-
urn:nbn:de:101:1-2018091710512913051264
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:36 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Mahmud, Zobaer Al
- Jenkins, Laura
- Ulven, Trond
- Labéguère, Frédéric
- Gosmini, Romain
- De Vos, Steve
- Hudson, Brian D.
- Tikhonova, Irina G.
- Milligan, Graeme
- SpringerLink (Online service)
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Design, synthesis and optimization of receptor ligands: tools for studying purine-activated and related orphan G protein-coupled receptors
Synthesis and biological evaluation of novel ligands for the cannabinoid-like orphan G protein-coupled receptors GPR18 and GPR55
The physiological relevance of the orphan G protein-coupled receptor GPR82
Chromen-4-ones as novel potent and selective ligands for purinoceptor-related class A delta-branch orphan G protein-coupled receptors
HATRIC-based identification of receptors for orphan ligands
Computational studies on δ-branch G protein-coupled P2Y and related orphan receptors
Synthesis, optimization, and characterization of chromen-4-one and 1,7-phenanthroline derivatives as ligands for the orphan G protein-coupled receptors 35 and 84
Structural and functional characterization of G protein-coupled adenosine receptors and the orphan receptor GPR143
The oligodendrocyte-enriched orphan G protein-coupled receptor Gpr62 is dispensable for central nervous system myelination
Development of new in silico methods to identify ligands for orphan GPCR
The orphan G protein-coupled receptor GPR17: its pharmacology and function in recombinant and primary cell expression systems
Development of tools and ligands for the uracil nucleotide-activated G protein-coupled P2Y receptors
Design, synthesis and optimization of receptor ligands: tools for studying purine-activated and related orphan G protein-coupled receptors
Synthesis and biological evaluation of novel ligands for the cannabinoid-like orphan G protein-coupled receptors GPR18 and GPR55
The physiological relevance of the orphan G protein-coupled receptor GPR82
Chromen-4-ones as novel potent and selective ligands for purinoceptor-related class A delta-branch orphan G protein-coupled receptors
HATRIC-based identification of receptors for orphan ligands
Computational studies on δ-branch G protein-coupled P2Y and related orphan receptors
Synthesis, optimization, and characterization of chromen-4-one and 1,7-phenanthroline derivatives as ligands for the orphan G protein-coupled receptors 35 and 84
Structural and functional characterization of G protein-coupled adenosine receptors and the orphan receptor GPR143
The oligodendrocyte-enriched orphan G protein-coupled receptor Gpr62 is dispensable for central nervous system myelination
Development of new in silico methods to identify ligands for orphan GPCR
The orphan G protein-coupled receptor GPR17: its pharmacology and function in recombinant and primary cell expression systems