Evidence map›Paper›PMID 42638938›Full record

ArticleJournal of analytical methods in chemistry2026

Development and Validation of an UPLC-MS/MS Method for Remodelin Quantification in Mouse Plasma and Tissues: Application to Biodistribution and Ultrastructural Assessment.

Litao Wang, Quanyu Liu, Cheng Yu, Yu Zhong, Minxia Wu, Xi Lin, Yan Hu

Abstract read
In one paragraph

Article in Journal of analytical methods in chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Litao WangThe Graduate School of Fujian Medical University, Fuzhou 350004, China, fjmu.edu.cn.
Quanyu LiuDepartment of Pharmacy, Fujian Health College, Fuzhou 350101, China, fjwx.com.cn.
Cheng YuDepartment of Cardiology, Fujian Medical Center for Cardiovascular Diseases, Fujian Institute of Coronary Heart Disease, Fujian Medical University Union Hospital, Fuzhou 350000, China, fjmu.edu.cn.ORCID https://orcid.org/0000-0001-8335-9403
Yu ZhongThe School of Pharmacy, Fujian Medical University, Fuzhou 350004, China, fjmu.edu.cn.
Minxia WuPublic Technology Service Center, Fujian Medical University, Fuzhou 350004, China, fjmu.edu.cn.
Xi LinPublic Technology Service Center, Fujian Medical University, Fuzhou 350004, China, fjmu.edu.cn.
Yan HuPublic Technology Service Center, Fujian Medical University, Fuzhou 350004, China, fjmu.edu.cn.ORCID https://orcid.org/0009-0008-8413-4159

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Remodelin, a selective N-acetyltransferase 10 (NAT10) inhibitor, has emerged as a promising therapeutic candidate for degenerative diseases with nuclear abnormalities and acetylation dysregulation. However, its pharmacological development has been hindered by the lack of a sufficiently sensitive bioanalytical method. To address this limitation, a simple, sensitive, and reliable ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC-MS/MS) method was established and fully validated. This method achieved accurate quantification of remodelin at low pg/mL levels, representing a significant improvement in sensitivity and excellent linearity (

Indexed as

bioanalytical validationbiodistributioncell ultrastructureremodelinUPLC–MS/MS

Identifiers

PMID42638938
PMCPMC13501163

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.