Evidence map›Paper›PMID 41796262›Full record

ArticleScience China. Life sciences2026

WTAP mediated m

Kuanxiang Sun, Lin Zhang, Wenjing Liu, Can Chen, Jiajie He, Jinrui Cai, Xiaoyan Jiang, Yeming Yang, Zhenglin Yang, Xianjun Zhu

Abstract read
PubMed Publisher
In one paragraph

Article in Science China. Life sciences, 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

10 authors.

Kuanxiang Sun *The Sichuan Provincial Key Laboratory for Genetic Diseases and Center for Medical Genetics, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610072, China.
Lin Zhang *The Sichuan Provincial Key Laboratory for Genetic Diseases and Center for Medical Genetics, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610072, China.
Wenjing Liu *The Sichuan Provincial Key Laboratory for Genetic Diseases and Center for Medical Genetics, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610072, China.
Can Chen *The Sichuan Provincial Key Laboratory for Genetic Diseases and Center for Medical Genetics, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610072, China.
Jiajie HeThe Sichuan Provincial Key Laboratory for Genetic Diseases and Center for Medical Genetics, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610072, China.
Jinrui CaiThe Sichuan Provincial Key Laboratory for Genetic Diseases and Center for Medical Genetics, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610072, China.
Xiaoyan JiangThe Sichuan Provincial Key Laboratory for Genetic Diseases and Center for Medical Genetics, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610072, China.
Yeming YangThe Sichuan Provincial Key Laboratory for Genetic Diseases and Center for Medical Genetics, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610072, China. nickyym@uestc.edu.cn.
Zhenglin YangThe Sichuan Provincial Key Laboratory for Genetic Diseases and Center for Medical Genetics, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610072, China. yangzhenglin@cashq.ac.cn.
Xianjun ZhuThe Sichuan Provincial Key Laboratory for Genetic Diseases and Center for Medical Genetics, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610072, China. xjzhu@uestc.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited retinal dystrophies (IRDs) are a leading cause of visual impairment and irreversible blindness worldwide, yet their precise molecular and genetic mechanisms remain unclear. N

Indexed as

Alcohol OxidoreductasesCyclic Nucleotide Phosphodiesterases, Type 6Eye ProteinsPhotoreceptor Cells, VertebrateAnimalsEpitranscriptomeMiceMice, Inbred C57BLMice, KnockoutRetinaRetinal DegenerationRNA MethylationAlcohol OxidoreductasesCyclic Nucleotide Phosphodiesterases, Type 6Eye ProteinsPde6b protein, mousegene therapyIRDsN 6-methyladenosinephotoreceptor degenerationWTAP

Identifiers

PMID41796262

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.