Evidence map›Paper›PMID 25956432›Full record

ReviewMolecular pharmacology2015

Adhesion G Protein-Coupled Receptors: From In Vitro Pharmacology to In Vivo Mechanisms.

Kelly R Monk, Jörg Hamann, Tobias Langenhan, Saskia Nijmeijer, Torsten Schöneberg, Ines Liebscher

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 59 citations in OpenAlex.

  1. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
    Review
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  12. Emerging roles of adhesion G protein-coupled receptors.Biochemical Society transactions · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 3 countries.

Kelly R MonkDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri (K.R.M.); Department of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands (J.H.); Department of Neurophysiology, Institute of Physiology, University of Würzburg, Würzburg, Germany (T.L.); Department of Medicinal Chemistry/Amsterdam Institute for Molecules, Medicines and Systems, VU University, Amsterdam, The Netherlands (S.N.); and Institute of Biochemistry, Molecular Biochemistry, Medical Faculty, University of Leipzig, Leipzig, Germany (T.S., I.L.).
Jörg HamannDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri (K.R.M.); Department of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands (J.H.); Department of Neurophysiology, Institute of Physiology, University of Würzburg, Würzburg, Germany (T.L.); Department of Medicinal Chemistry/Amsterdam Institute for Molecules, Medicines and Systems, VU University, Amsterdam, The Netherlands (S.N.); and Institute of Biochemistry, Molecular Biochemistry, Medical Faculty, University of Leipzig, Leipzig, Germany (T.S., I.L.).
Tobias LangenhanDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri (K.R.M.); Department of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands (J.H.); Department of Neurophysiology, Institute of Physiology, University of Würzburg, Würzburg, Germany (T.L.); Department of Medicinal Chemistry/Amsterdam Institute for Molecules, Medicines and Systems, VU University, Amsterdam, The Netherlands (S.N.); and Institute of Biochemistry, Molecular Biochemistry, Medical Faculty, University of Leipzig, Leipzig, Germany (T.S., I.L.).
Saskia NijmeijerDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri (K.R.M.); Department of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands (J.H.); Department of Neurophysiology, Institute of Physiology, University of Würzburg, Würzburg, Germany (T.L.); Department of Medicinal Chemistry/Amsterdam Institute for Molecules, Medicines and Systems, VU University, Amsterdam, The Netherlands (S.N.); and Institute of Biochemistry, Molecular Biochemistry, Medical Faculty, University of Leipzig, Leipzig, Germany (T.S., I.L.).
Torsten SchönebergDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri (K.R.M.); Department of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands (J.H.); Department of Neurophysiology, Institute of Physiology, University of Würzburg, Würzburg, Germany (T.L.); Department of Medicinal Chemistry/Amsterdam Institute for Molecules, Medicines and Systems, VU University, Amsterdam, The Netherlands (S.N.); and Institute of Biochemistry, Molecular Biochemistry, Medical Faculty, University of Leipzig, Leipzig, Germany (T.S., I.L.).
Ines LiebscherDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri (K.R.M.); Department of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands (J.H.); Department of Neurophysiology, Institute of Physiology, University of Würzburg, Würzburg, Germany (T.L.); Department of Medicinal Chemistry/Amsterdam Institute for Molecules, Medicines and Systems, VU University, Amsterdam, The Netherlands (S.N.); and Institute of Biochemistry, Molecular Biochemistry, Medical Faculty, University of Leipzig, Leipzig, Germany (T.S., I.L.) ines.liebscher@medizin.uni-leipzig.de.
Leipzig University · DEUniversity of Amsterdam · NLVrije Universiteit Amsterdam · NLWashington University in St. Louis · US

Funding

MOLECULAR AND GENETIC ANALYSIS OF GPR126 IN PERIPHERAL NERVE.R01NS079445 · NINDS · WASHINGTON UNIVERSITY · PI MONK, KELLY R · 2012 to 2020
$3.1M
Chemical and genetic screens for modulators of nervous system development and myelinationR01HD080601 · NICHD · WASHINGTON UNIVERSITY · PI MONK, KELLY R · 2014 to 2018
$1.6M
NICHD NIH HHS R01 HD080601NICHD NIH HHS R01-HD080601NINDS NIH HHS R01 NS079445NINDS NIH HHS R01-NS079445
6 · The paper itself

Abstract

The adhesion family of G protein-coupled receptors (aGPCRs) comprises 33 members in humans. aGPCRs are characterized by their enormous size and complex modular structures. While the physiologic importance of many aGPCRs has been clearly demonstrated in recent years, the underlying molecular functions have only recently begun to be elucidated. In this minireview, we present an overview of our current knowledge on aGPCR activation and signal transduction with a focus on the latest findings regarding the interplay between ligand binding, mechanical force, and the tethered agonistic Stachel sequence, as well as implications on translational approaches that may derive from understanding aGPCR pharmacology.

Indexed as

Cell AdhesionAnimalsHumansProtein BindingReceptors, G-Protein-CoupledReceptors, PeptideSignal TransductionReceptors, G-Protein-CoupledReceptors, Peptide

Identifiers

PMID25956432
PMCPMC4551055
OpenAlexW2413335515

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.