Evidence map›Paper›PMID 41417662›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Mettl3-Mediated m6A Modification Represents a Novel Therapeutic Target for FSGS.

Fubin Zhu, Hongzhi Li, Xiang Li, Chunxiu Du, Ting Wang, Xuling Zhou, Xiaobei Xie, Yunxia Shao, Yingzhi Huang, Yanling Hu and 5 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Mettl3-Mediated m6A Modification Represents a Novel Therapeutic Target for FSGS.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    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

15 authors.

Fubin ZhuNephrosis Precision Medicine Innovation Center, School of Basic Medicine, Beihua University, Jilin, 132011, China.
Hongzhi LiNephrosis Precision Medicine Innovation Center, School of Basic Medicine, Beihua University, Jilin, 132011, China.
Xiang LiNephrosis Precision Medicine Innovation Center, School of Basic Medicine, Beihua University, Jilin, 132011, China.
Chunxiu DuHealth Science Center, East China Normal University, Shanghai, 200241, China.
Ting WangNephrosis Precision Medicine Innovation Center, School of Basic Medicine, Beihua University, Jilin, 132011, China.
Xuling ZhouNephrosis Precision Medicine Innovation Center, School of Basic Medicine, Beihua University, Jilin, 132011, China.
Xiaobei XieNephrosis Precision Medicine Innovation Center, School of Basic Medicine, Beihua University, Jilin, 132011, China.
Yunxia ShaoDepartment of Nephrology, Wuhu Hospital, East China Normal University, Wuhu, China.
Yingzhi HuangHealth Science Center, East China Normal University, Shanghai, 200241, China.
Yanling HuNephrosis Precision Medicine Innovation Center, School of Basic Medicine, Beihua University, Jilin, 132011, China.
Xinxin GuoNephrosis Precision Medicine Innovation Center, School of Basic Medicine, Beihua University, Jilin, 132011, China.
Bin ZhuDepartment of Nephrology, Zhejiang Provincial People's Hospital, the Affiliated People's Hospital, School of Basic Medicine, Hangzhou Medical College, Hangzhou, Zhejiang, 311399, China.
Shanshan YuNephrosis Precision Medicine Innovation Center, School of Basic Medicine, Beihua University, Jilin, 132011, China.
Xiaoyan ZhangHealth Science Center, East China Normal University, Shanghai, 200241, China.
Binghai ZhaoNephrosis Precision Medicine Innovation Center, School of Basic Medicine, Beihua University, Jilin, 132011, China.ORCID https://orcid.org/0000-0002-5037-6423

Funding

National Natural Science Foundation of China 82270703National Natural Science Foundation of China 82270753National Natural Science Foundation of China 82470742National Natural Science Foundation of China 82570839The Jilin Province science and technology innovation platform construction project YDZJ202502CXJD054The Jilin Provincial Natural Science Foundation YDZJ202301ZYTS132
6 · The paper itself

Abstract

Focal segmental glomerulosclerosis (FSGS) is a common glomerular lesion that manifests as a primary podocyte injury. Multiple genetic risk factors have been reported to be associated with the development of FSGS. However, whether epigenetic factors, especially N6-methyladenosine (m6A) modifications, are involved in the pathogenesis of FSGS remains unclear. By generating a mouse line with a specific deletion of N6-adenosine-methyltransferase-like 3 (Mettl3) in podocytes (Mettl3

Indexed as

AdenosineGlomerulosclerosis, Focal SegmentalMethyltransferasesAnimalsDisease Models, AnimalHumansMiceMice, KnockoutPodocytesAdenosineMethyltransferasesMETTL3 protein, humanMettl3 protein, mouseN-methyladenosineEpegeneticsFSGSm6AMettl3Tight Junction

Identifiers

PMID41417662
PMCPMC12915192

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.