Evidence map›Paper›PMID 34484125›Full record

ArticleFrontiers in endocrinology2021

Biased Coupling to β-Arrestin of Two Common Variants of the CB

Gábor Turu, Eszter Soltész-Katona, András Dávid Tóth, Cintia Juhász, Miklós Cserző, Ádám Misák, András Balla, Marc G Caron, László Hunyady

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 19 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

9 authors at 3 institutions in 2 countries.

Gábor TuruDepartment of Physiology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Eszter Soltész-KatonaDepartment of Physiology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
András Dávid TóthDepartment of Physiology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Cintia JuhászDepartment of Physiology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Miklós CserzőDepartment of Physiology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Ádám MisákDepartment of Physiology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
András BallaDepartment of Physiology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Marc G CaronDepartment of Cell Biology, Duke University Medical Center, Duke University School of Medicine, Durham, NC, United States.
László HunyadyDepartment of Physiology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Semmelweis University · HUHungarian Academy of Sciences · HUDuke University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

β-arrestins are partners of the G protein-coupled receptors (GPCRs), regulating their intracellular trafficking and signaling. Development of biased GPCR agonists, selectively targeting either G protein or β-arrestin pathways, are in the focus of interest due to their therapeutic potential in different pathological conditions. The CB

Indexed as

Mutation, Missensebeta-ArrestinsHEK293 CellsHumansProtein BindingProtein TransportReceptor, Cannabinoid, CB2beta-ArrestinsReceptor, Cannabinoid, CB2biasedCB2 cannabinoid receptorCB2RL133IpolymorphismsQ63Rsignalingβ-arrestin2

Identifiers

PMID34484125
PMCPMC8415483
OpenAlexW3196068385

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.