Evidence map›Paper›PMID 42878183›Full record

ArticleAging cell2026

METTL14-Mediated m

Shixiao Wang, Jie Zhang, Ying Ao, Dan Rao, Cong Yu, Chenzhong Xu, Ming Wang, Mingying Li, Xin Huang, Jianfei Zhang and 8 more

Abstract read
In one paragraph

Article in Aging cell, 2026. 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

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

18 authors.

Shixiao WangShenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.
Jie ZhangNational Health Commission Key Laboratory of Bone Aging, Shenzhen University Medical School, Shenzhen, China.ORCID https://orcid.org/0009-0006-4449-872X
Ying AoNational Health Commission Key Laboratory of Bone Aging, Shenzhen University Medical School, Shenzhen, China.ORCID https://orcid.org/0009-0004-4091-6088
Dan RaoShenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.ORCID https://orcid.org/0009-0006-9150-0415
Cong YuShenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.
Chenzhong XuShenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.
Ming WangSchool of Basic Medical Sciences, Wannan Medical University, Wuhu, China.ORCID https://orcid.org/0000-0002-7000-1063
Mingying LiShenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.
Xin HuangShenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.
Jianfei ZhangShenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.
Rui MeiShenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.
Zhen ZhangShenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.ORCID https://orcid.org/0009-0007-6115-0968
Jie SunShenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.
Juanli DuanDepartment of Hepatobiliary Surgery, Xi-Jing Hospital, Fourth Military Medical University, Xi'an, China.
Ying SunJiangsu Key Laboratory of Geriatric Precision Medicine and Aging Intervention, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Zimei WangNational Health Commission Key Laboratory of Bone Aging, Shenzhen University Medical School, Shenzhen, China.ORCID https://orcid.org/0000-0002-7288-3821
Wen SuNational Health Commission Key Laboratory of Bone Aging, Shenzhen University Medical School, Shenzhen, China.ORCID https://orcid.org/0000-0001-5576-1286
Baohua LiuShenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.ORCID https://orcid.org/0000-0002-1599-8059

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hutchinson-Gilford progeria syndrome (HGPS) is a rare premature aging disorder most commonly caused by a de novo synonymous mutation (c.1824C>T) in the LMNA gene. This mutation activates aberrant splicing of prelamin A, leading to the production and accumulation of progerin, which drives accelerated aging, with patients predominantly succumbing to cardiovascular disease. However, while cardiac pathologies are well documented, the cell-autonomous contribution of cardiomyocytes to HGPS-associated cardiac remodeling remains poorly understood. Here, we generated a cardiomyocyte-specific progerin-expressing mouse model (Myh6-Cre; Lmna

Indexed as

AdenosineMethyltransferasesMyocytes, CardiacProgeriaVentricular RemodelingAnimalsHomeostasisHumansMethylationMiceRNA MethylationAdenosineMethyltransferasesN-methyladenosinecardiac agingcardiac hypertrophyHGPSMETTL14METTL3

Identifiers

PMID42878183
PMCPMC13670420

What OpenQuestion holds

Textmetadata
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.