Basic Pharmacological and Structural Evidence for Class A G-Protein-Coupled Receptor Heteromerization-Reference-Cited by-同舟云学术

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Basic Pharmacological and Structural Evidence for Class A G-Protein-Coupled Receptor Heteromerization

Published:2016-03-31 Issue: Volume:7 Page:
ISSN:1663-9812
Container-title:Frontiers in Pharmacology
language:
Short-container-title:Front. Pharmacol.

Author:

Franco Rafael,Martínez-Pinilla Eva,Lanciego José L.,Navarro Gemma

Funder

Ministerio de EconomÃ-a y Competitividad

FundaciÓ la MaratÓ de TV3

Publisher

Frontiers Media SA

Subject

Pharmacology (medical),Pharmacology

Reference92 articles.

1. Ligands that interact with putative MOR-mGluR5 heteromer in mice with inflammatory pain produce potent antinociception.;Akgün;Proc. Natl. Acad. Sci. U.S.A.,2013

2. Time-resolved FRET between GPCR ligands reveals oligomers in native tissues.;Albizu;Nat. Chem. Biol.,2010

3. Heteromerization of GPR55 and cannabinoid CB2 receptors modulates signaling.;Balenga;Br. J. Pharmacol.,2014

4. Integrated methods for the construction of three-dimensional models and computational probing of structure-function relations in G protein-coupled receptors.;Ballesteros;Methods Neurosci.,1995

5. Structure-based analysis of GPCR function: evidence for a novel pentameric assembly between the dimeric leukotriene B4 receptor BLT1 and the G-protein.;Banères;J. Mol. Biol.,2003

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