Evidence map›Paper›PMID 30181691›Full record

ArticleExperimental neurobiology2018

Spatiotemporal Protein Atlas of Cell Death-Related Molecules in the Rat MCAO Stroke Model.

Jeong Seon Yoon, Darong Jo, Hye-Sun Lee, Seung-Wan Yoo, Tae-Young Lee, Woo Sup Hwang, Jung-Mi Choi, Eunhee Kim, Sung-Soo Kim, Haeyoung Suh-Kim

Abstract read
In one paragraph

Article in Experimental neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. [Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2025
    Article
  5. Article
  6. The role and mechanisms of microvascular damage in the ischemic myocardium.Cellular and molecular life sciences : CMLS · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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.

Jeong Seon YoonDepartment of Anatomy, Ajou University School of Medicine, Suwon 16499, Korea.
Darong JoDepartment of Biomedical Sciences, Ajou Graduate School, Suwon 16499, Korea.
Hye-Sun LeeDepartment of Anatomy, Ajou University School of Medicine, Suwon 16499, Korea.
Seung-Wan YooDepartment of Anatomy, Ajou University School of Medicine, Suwon 16499, Korea.
Tae-Young LeeDepartment of Biomedical Sciences, Ajou Graduate School, Suwon 16499, Korea.
Woo Sup HwangDepartment of Anatomy, Ajou University School of Medicine, Suwon 16499, Korea.
Jung-Mi ChoiDepartment of Anatomy, Ajou University School of Medicine, Suwon 16499, Korea.
Eunhee KimDepartment of Biological Sciences and Graduate School of New Drug Discovery and Development, Chungnam National University, Daejeon 34134, Korea.
Sung-Soo KimDepartment of Anatomy, Ajou University School of Medicine, Suwon 16499, Korea.
Haeyoung Suh-KimDepartment of Anatomy, Ajou University School of Medicine, Suwon 16499, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ischemic stroke and cerebral infarction triggered by the blockage of blood supply can cause damage to the brain via a complex series of pathological changes. Recently, diverse therapies have emerged as promising candidates for the treatment of stroke. These treatments exert therapeutic effects by acting on diverse target molecules and cells in different time windows from the acute to chronic phases. Here, using immunohistochemistry, we show pathophysiological changes in the brain microenvironment at the hyperacute (within 6 h), acute (1~3 days), subacute (7 days), and chronic (1 month) phases following ischemic injury. Ischemic injury in rats was induced by occluding the middle cerebral artery and was validated by magnetic resonance imaging. The progression of damage to the brain was evaluated by immunohistochemistry for NeuN

Indexed as

Antibody stainingBrain ischemiaCell deathChronic strokeStem cell therapy

Identifiers

PMID30181691
PMCPMC6120968

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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.