Evidence map›Paper›PMID 34603394›Full record

ReviewFrontiers in genetics2021

The Role of m6A Ribonucleic Acid Modification in the Occurrence of Atherosclerosis.

Jie Fu, Xinghui Cui, Xiaoyun Zhang, Min Cheng, Xiaoxia Li, Zhiliang Guo, Xiaodong Cui

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Peli1, regulated by mCommunications biology · 2025
    Article
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  6. Article
  7. Article
  8. NAging and disease · 2024
    Review
  9. Article
  10. Article
  11. Transcriptome-wide NBMC genomics · 2023
    Article
  12. Article
  13. Article
  14. NHeliyon · 2023
    Article
  15. Article
  16. Review
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

7 authors at 2 institutions in 1 country.

Jie FuSchool of Clinical Medicine, Weifang Medical University, Weifang, China.
Xinghui CuiSchool of Clinical Medicine, Weifang Medical University, Weifang, China.
Xiaoyun ZhangSchool of Clinical Medicine, Weifang Medical University, Weifang, China.
Min ChengSchool of Clinical Medicine, Weifang Medical University, Weifang, China.
Xiaoxia LiInstitute of Stem Cell and Regenerative Medicine, Department of Basic Medicine, Qingdao University Medical College, Qingdao, China.
Zhiliang GuoThe 80th Group Army Hospital of Chinese People' Liberation Army, Weifang, China.
Xiaodong CuiSchool of Basic Medicine Sciences, Weifang Medical University, Weifang, China.
Weifang Medical University · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The N6-methyladenosine (m6A) modification is the most abundant epitranscriptomic modification in eukaryotic messenger RNA (mRNA). The m6A modification process is jointly regulated by various enzymes and proteins, such as methyltransferases, demethylases and related m6A-binding proteins. The process is dynamic and reversible, and it plays an essential role in mRNA metabolism and various biological activities. Recently, an increasing number of researchers have confirmed that the onset and development of many diseases are closely associated with the molecular biological mechanism of m6A RNA methylation. This study focuses on the relationship between m6A RNA modification and atherosclerosis (AS). It thoroughly summarizes the mechanisms and processes of m6A RNA modification in AS-related cells and the relationships between m6A RNA modification and AS risk factors, and it provides a reference for exploring new targets for the early diagnosis and treatment of AS.

Indexed as

atherosclerosiserasers-demethylasesmethyltransferaseN6methyladenosine (m6A) modificationvascular endothelial cells

Identifiers

PMID34603394
PMCPMC8481608
OpenAlexW3200264607

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.