Evidence map›Paper›PMID 30271982›Full record

ArticleCommunications biology2018

Expression map of 78 brain-expressed mouse orphan GPCRs provides a translational resource for neuropsychiatric research.

Aliza T Ehrlich, Grégoire Maroteaux, Anne Robe, Lydie Venteo, Md Taufiq Nasseef, Leon C van Kempen, Naguib Mechawar, Gustavo Turecki, Emmanuel Darcq, Brigitte L Kieffer

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 66 citations in OpenAlex.

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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

10 authors at 4 institutions in 3 countries.

Aliza T EhrlichIGBMC, Institut Génétique Biologie Moléculaire Cellulaire, Illkirch, France.
Grégoire MaroteauxDouglas Mental Health University Institute and McGill University, Department of Psychiatry, Montreal, Canada.
Anne RobeIGBMC, Institut Génétique Biologie Moléculaire Cellulaire, Illkirch, France.
Lydie VenteoLabel Histologie, 51100, Reims, France.
Md Taufiq NasseefDouglas Mental Health University Institute and McGill University, Department of Psychiatry, Montreal, Canada.
Leon C van KempenLady Davis Institute for Medical Research, Jewish General Hospital and McGill University, Department of Pathology, Montreal, Canada.
Naguib MechawarDouglas Mental Health University Institute and McGill University, Department of Psychiatry, Montreal, Canada.
Gustavo TureckiDouglas Mental Health University Institute and McGill University, Department of Psychiatry, Montreal, Canada.
Emmanuel DarcqDouglas Mental Health University Institute and McGill University, Department of Psychiatry, Montreal, Canada.
Brigitte L KiefferIGBMC, Institut Génétique Biologie Moléculaire Cellulaire, Illkirch, France. brigitte.kieffer@douglas.mcgill.ca.ORCID http://orcid.org/0000-0002-8809-8334
Douglas Mental Health University Institute · CAInserm · FRInstitut de génétique et de biologie moléculaire et cellulaire · FRUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Orphan G-protein-coupled receptors (oGPCRs) possess untapped potential for drug discovery. In the brain, oGPCRs are generally expressed at low abundance and their function is understudied. Expression profiling is an essential step to position oGPCRs in brain function and disease, however public databases provide only partial information. Here, we fine-map expression of 78 brain-oGPCRs in the mouse, using customized probes in both standard and supersensitive in situ hybridization. Images are available at http://ogpcr-neuromap.douglas.qc.ca. This searchable database contains over 8000 coronal brain sections across 1350 slides, providing the first public mapping resource dedicated to oGPCRs. Analysis with public mouse (60 oGPCRs) and human (56 oGPCRs) genome-wide datasets identifies 25 oGPCRs with potential to address emotional and/or cognitive dimensions of psychiatric conditions. We probe their expression in postmortem human brains using nanoString, and included data in the resource. Correlating human with mouse datasets reveals excellent suitability of mouse models for oGPCRs in neuropsychiatric research.

Identifiers

PMID30271982
PMCPMC6123746
OpenAlexW2886037034

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.