Evidence map›Paper›PMID 38301267›Full record

ArticleAmerican journal of respiratory cell and molecular biology2024

Ddx5 Targeted Epigenetic Modification of Pericytes in Pulmonary Hypertension After Intrauterine Growth Restriction.

Chengcheng Hang, Lu Zu, Xiaofei Luo, Yu Wang, Lingling Yan, Ziming Zhang, Kaixing Le, Yajie Huang, Lixia Ye, Yuhan Ying and 4 more

Abstract read
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In one paragraph

Article in American journal of respiratory cell and molecular biology, 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
1.3field-weighted citation impact, top 22% of its field
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, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. When a DEAD-Box Protein Is the Key: A Novel Role for DDX5 in Lung Pericyte Dysfunction.American journal of respiratory cell and molecular biology · 2024
    Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 1 country.

Chengcheng HangDepartment of Neonatology and.ORCID 0000-0001-5758-7541
Lu ZuDepartment of Neonatology and.
Xiaofei LuoDepartment of Pediatrics, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, People's Republic of China; and.ORCID 0000-0003-1667-5048
Yu WangDepartment of Neonatology and.
Lingling YanDepartment of Pediatrics, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, People's Republic of China; and.
Ziming ZhangDepartment of Neonatology and.
Kaixing LeAcademy of Pediatrics, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, People's Republic of China.
Yajie HuangDepartment of Neonatology and.
Lixia YeDepartment of Neonatology and.
Yuhan YingDepartment of Neonatology and.
Kewei ChenDepartment of Neonatology and.
Xuefeng XuDepartment of Rheumatology, Immunology, and Allergy, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang Province, People's Republic of China.
Qiannan LvDepartment of Neonatology and.
Lizhong DuDepartment of Neonatology and.
First Affiliated Hospital Zhejiang University · CNChildren's Hospital of Zhejiang University · CNZhejiang Academy of Social Sciences · CN

Funding

National Natural Science Foundation of China 81630037
6 · The paper itself

Abstract

Newborns with intrauterine growth restriction (IUGR) have a higher likelihood of developing pulmonary arterial hypertension (PAH) in adulthood. Although there is increasing evidence suggesting that pericytes play a role in regulating myofibroblast transdifferentiation and angiogenesis in malignant and cardiovascular diseases, their involvement in the pathogenesis of IUGR-related pulmonary hypertension and the underlying mechanisms remain incompletely understood. To address this issue, a study was conducted using a Sprague-Dawley rat model of IUGR-related pulmonary hypertension. Our investigation revealed increased proliferation and migration of pulmonary microvascular pericytes in IUGR-related pulmonary hypertension, accompanied by weakened endothelial-pericyte interactions. Through whole-transcriptome sequencing,

Indexed as

Cell ProliferationDEAD-box RNA HelicasesEpigenesis, GeneticFetal Growth RetardationGlycogen Synthase Kinase 3 betaHypertension, PulmonaryMicroRNAsPericytesRats, Sprague-DawleyAnimalsbeta CateninCell MovementFemaleHumansMaleRatsbeta CateninDdx5 protein, humanDdx5 protein, ratDEAD-box RNA HelicasesGlycogen Synthase Kinase 3 betaMicroRNAsDEAD-box protein 5intrauterine growth restrictionmicroRNA-205pericytespulmonary hypertension

Identifiers

PMID38301267
OpenAlexW4391425585

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.