Evidence map›Paper›PMID 37202821›Full record

ReviewCell division2023

Molecular mechanisms involved in regulating protein activity and biological function of MST3.

Jing Qiu, Junzhi Xiong, Lu Jiang, Xinmin Wang, Kebin Zhang, Hua Yu

Open access · goldAbstract readReview
In one paragraph

Review in Cell division, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

6 authors at 2 institutions in 1 country.

Jing QiuDepartment of Pharmacy, Xinqiao Hospital, Army Medical University, Chongqing, China.
Junzhi XiongClinical Medical Research Center, Xinqiao Hospital, Army Medical University, Chongqing, China.
Lu JiangClinical Medical Research Center, Xinqiao Hospital, Army Medical University, Chongqing, China.
Xinmin WangClinical Medical Research Center, Xinqiao Hospital, Army Medical University, Chongqing, China.
Kebin ZhangClinical Medical Research Center, Xinqiao Hospital, Army Medical University, Chongqing, China.
Hua YuClinical Medical Research Center, Xinqiao Hospital, Army Medical University, Chongqing, China. peter.pan210@163.com.
Army Medical University · CNXinqiao Hospital · CN

Funding

National Natural Science Foundation of China 31872634
6 · The paper itself

Abstract

Mammalian sterile 20-like (Ste20-like) protein kinase 3 (MST3) or serine/threonine-protein kinase 24 (STK24) is a serine/threonine protein kinase that belongs to the mammalian STE20-like protein kinase family. MST3 is a pleiotropic protein that plays a critical role in regulating a variety of events, including apoptosis, immune response, metabolism, hypertension, tumor progression, and development of the central nervous system. The MST3-mediated regulation is intricately related to protein activity, post-translational modification, and subcellular location. Here, we review the recent progress on the regulatory mechanisms against MST3 and its-mediated control of disease progression.

Indexed as

Biological functionDisease progressionMST3Post-translational modificationProtein activity

Identifiers

PMID37202821
PMCPMC10193606
OpenAlexW4377094074

What Socratic 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 Socratic graph.