Evidence map›Paper›PMID 29143549›Full record

ArticleCell cycle (Georgetown, Tex.)2018

Negative impact of hyperglycaemia on mouse alveolar development.

Mei-Yao He, Guang Wang, Sha-Sha Han, Ke Li, Ya Jin, Meng Liu, Zhen-Peng Si, Ju Wang, Guo-Sheng Liu, Xuesong Yang

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

10 authors at 2 institutions in 2 countries.

Mei-Yao Hea Department of Pediatrics and Neonatology , Institute of Fetal-Preterm Labor Medicine ; The First Affiliated Hospital , Jinan University , Guangzhou 510630 , China.
Guang Wangb Division of Histology & Embryology , Key Laboratory for Regenerative Medicine of the Ministry of Education , Medical College , Jinan University , Guangzhou 510632 , China.
Sha-Sha Hana Department of Pediatrics and Neonatology , Institute of Fetal-Preterm Labor Medicine ; The First Affiliated Hospital , Jinan University , Guangzhou 510630 , China.
Ke Lib Division of Histology & Embryology , Key Laboratory for Regenerative Medicine of the Ministry of Education , Medical College , Jinan University , Guangzhou 510632 , China.
Ya Jina Department of Pediatrics and Neonatology , Institute of Fetal-Preterm Labor Medicine ; The First Affiliated Hospital , Jinan University , Guangzhou 510630 , China.
Meng Liub Division of Histology & Embryology , Key Laboratory for Regenerative Medicine of the Ministry of Education , Medical College , Jinan University , Guangzhou 510632 , China.
Zhen-Peng Sia Department of Pediatrics and Neonatology , Institute of Fetal-Preterm Labor Medicine ; The First Affiliated Hospital , Jinan University , Guangzhou 510630 , China.
Ju Wangc Institute of Biomedicine , National Engineering Research Center of Genetic Medicine , Jinan University , Guangzhou 510632 , China.
Guo-Sheng Liua Department of Pediatrics and Neonatology , Institute of Fetal-Preterm Labor Medicine ; The First Affiliated Hospital , Jinan University , Guangzhou 510630 , China.
Xuesong Yangb Division of Histology & Embryology , Key Laboratory for Regenerative Medicine of the Ministry of Education , Medical College , Jinan University , Guangzhou 510632 , China.
Human Growth Foundation · USJinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetes mellitus in pregnancy has been known to affect the embryonic development of various systems, including cardiovascular and nervous systems. However, whether this disease could have a negative impact on embryonic respiratory system remains controversial. In this study, we demonstrated that pregestational diabetes mellitus (PGDM)-induced defects in lung development in mice are mainly characterized by the changes in the morphological structure of the lung. Immunostaining and Western blotting showed that proliferation increased and apoptosis decreased in PGDM. Hyperglycaemia caused pulmonary tissue fibrationas manifested by an increase in Masson staining and decorin expression in PGDM lungs, and the immunofluorescent pro-SPC

Indexed as

AnimalsBiomarkersCell DifferentiationCell LineCell ProliferationEpithelial CellsFemaleFibroblast Growth FactorsGATA6 Transcription FactorHyperglycemiaMiceModels, BiologicalPulmonary AlveoliWnt Signaling PathwayBiomarkersFibroblast Growth FactorsGATA6 Transcription FactorEMTFgf signallingGATA6PGDMWnt signalling

Identifiers

PMID29143549
PMCPMC5815430
OpenAlexW2770617840

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.