Evidence map›Paper›PMID 38816193›Full record

ArticleJournal of medical genetics2024

ZFYVE19 deficiency: a ciliopathy involving failure of cell division, with cell death.

Jing Yang, Ya-Nan Zhang, Ren-Xue Wang, Chen-Zhi Hao, Yiling Qiu, Hao Chi, Wei-Sha Luan, HongYi Tang, Xiu-Juan Zhang, XuXu Sun and 4 more

Abstract read
In one paragraph

Article in Journal of medical genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

14 authors.

Jing YangDepartment of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, China.ORCID 0000-0001-6739-951X
Ya-Nan ZhangDepartment of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, China.
Ren-Xue WangBC Cancer Agency, Vancouver, British Columbia, Canada.
Chen-Zhi HaoThe Center for Liver Diseases, Children's Hospital of Fudan University, Shanghai, China.
Yiling QiuDepartment of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, China.ORCID 0000-0002-7296-9115
Hao ChiDepartment of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, China.
Wei-Sha LuanDepartment of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, China.ORCID 0000-0002-2130-6426
HongYi TangDepartment of Biochemistry and Molecular Cell Biology, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Xiu-Juan ZhangDepartment of Pathophysiology, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
XuXu SunDepartment of Biochemistry and Molecular Cell Biology, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Jonathan A ShepsBC Cancer Agency, Vancouver, British Columbia, Canada.
Victor LingBC Cancer Agency, Vancouver, British Columbia, Canada jshwang@shmu.edu.cn muqingcao@sjtu.edu.cn vling@bccrc.ca.ORCID 0000-0003-0823-586X
Muqing CaoDepartment of Pathophysiology, Shanghai Jiao Tong University School of Medicine, Shanghai, China jshwang@shmu.edu.cn muqingcao@sjtu.edu.cn vling@bccrc.ca.ORCID 0000-0002-0352-6548
Jian-She WangThe Center for Liver Diseases, Children's Hospital of Fudan University, Shanghai, China jshwang@shmu.edu.cn muqingcao@sjtu.edu.cn vling@bccrc.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsVariants in

methods

resultsThe

conclusionsOur findings demonstrated that ZFYVE19 deficiency is a ciliopathy with novel histological features. Failure of cell division with ciliary abnormalities and cell death activates macrophages and may thus lead to biliary fibrosis via TGF-β pathway in the disease.

Indexed as

Cell DeathCiliopathiesMice, KnockoutAnimalsCell DivisionCiliaDisease Models, AnimalHumansLiverMiceOncogene ProteinsSignal TransductionOncogene ProteinsZFYVE19 protein, humanCell DivisionCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesGenetic Diseases, InbornLiver Diseases

Identifiers

PMID38816193
PMCPMC11287636

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.