Evidence map›Paper›PMID 35955656›Full record

ArticleInternational journal of molecular sciences2022

Examination of Intracellular GPCR-Mediated Signaling with High Temporal Resolution.

Nadine Gruteser, Arnd Baumann

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

2 authors at 1 institution in 1 country.

Nadine GruteserInstitute of Biological Information Processing, IBI-1, Research Center Jülich, 52428 Jülich, Germany.
Arnd BaumannInstitute of Biological Information Processing, IBI-1, Research Center Jülich, 52428 Jülich, Germany.ORCID 0000-0001-9456-7275
Forschungszentrum Jülich · DE

Funding

Deutsche Forschungsgemeinschaft 491111487Federal Ministry of Education and Research FKZ 031A095A
6 · The paper itself

Abstract

The GTP-binding protein-coupled receptors (GPCRs) play important roles in physiology and neuronal signaling. More than a thousand genes, excluding the olfactory receptors, have been identified that encode these integral membrane proteins. Their pharmacological and functional properties make them fascinating targets for drug development, since various disease states can be treated and overcome by pharmacologically addressing these receptors and/or their downstream interacting partners. The activation of the GPCRs typically causes transient changes in the intracellular second messenger concentrations as well as in membrane conductance. In contrast to ion channel-mediated electrical signaling which results in spontaneous cellular responses, the GPCR-mediated metabotropic signals operate at a different time scale. Here we have studied the kinetics of two common GPCR-induced signaling pathways: (a) Ca

Indexed as

Cyclic AMPOlfactory Receptor NeuronsCalciumCyclic Nucleotide-Gated Cation ChannelsGTP-Binding ProteinsSecond Messenger SystemsSignal TransductionCalciumCyclic AMPCyclic Nucleotide-Gated Cation ChannelsGTP-Binding Proteinsbiogenic aminesCa2+ imagingcaged compoundscell-based functional assayscyclic adenosine monophosphatestopped-flow measurements

Identifiers

PMID35955656
PMCPMC9369311
OpenAlexW4289174136

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.