Evidence map›Paper›PMID 39149480›Full record

ArticleResearch square2024

Mechanism of human α3β GlyR modulation in inflammatory pain and 2, 6-DTBP interaction.

Weiwei Wang, Xiaofen Liu

Abstract readPreprint
In one paragraph

Article in Research square, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Weiwei WangUniversity of Texas Southwestern Medical Center.ORCID 0000-0002-0215-9467
Xiaofen LiuUniversity of Texas Southwestern Medical Center.ORCID 0000-0003-3560-0850

Funding

Understanding higher-order glycine receptor assemblies in neurotransmissionR35GM146860 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Weiwei Wang · 2022 to 2026
$2.0M
NIGMS NIH HHS R35 GM146860
6 · The paper itself

Abstract

α3β glycine receptor (GlyR) is a subtype of the GlyRs that belongs to the Cys-loop receptor superfamily. It is a target for non-psychoactive pain control drug development due to its high expression in the spinal dorsal horn and indispensable roles in pain sensation. α3β GlyR activity is inhibited by a phosphorylation in the large internal M3/M4 loop of α3 through the prostaglandin E2 (PGE

Identifiers

PMID39149480
PMCPMC11326354

What OpenQuestion holds

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Registered trials

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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.