Evidence map›Paper›PMID 29232931›Full record

ReviewInternational journal of molecular sciences2017

Molecular Mechanisms and Management of a Cutaneous Inflammatory Disorder: Psoriasis.

Yu Ri Woo, Dae Ho Cho, Hyun Jeong Park

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 110 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Antioxidants (Basel, Switzerland) · 2024
    Article
  9. Article
  10. Review
  11. Role of TNFPain research & management · 2024
    Review
  12. Article
  13. Review
  14. In Vitro and In Vivo Anti-Psoriasis Activity ofLife (Basel, Switzerland) · 2023
    Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. 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

3 authors at 2 institutions in 1 country.

Yu Ri WooDepartment of Dermatology, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 07345, Korea. w1206@naver.com.ORCID 0000-0003-2903-9534
Dae Ho ChoDepartment of Life Science, Sookmyung Women's University, Seoul 04310, Korea. cdhkor@sookmyung.ac.kr.
Hyun Jeong ParkDepartment of Dermatology, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 07345, Korea. hjpark@catholic.ac.kr.
The Catholic University of Korea Yeouido St. Mary's Hospital · KRSookmyung Women's University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psoriasis is a complex chronic inflammatory cutaneous disorder. To date, robust molecular mechanisms of psoriasis have been reported. Among diverse aberrant immunopathogenetic mechanisms, the current model emphasizes the role of Th1 and the IL-23/Th17 axis, skin-resident immune cells and major signal transduction pathways involved in psoriasis. The multiple genetic risk loci for psoriasis have been rapidly revealed with the advent of a novel technology. Moreover, identifying epigenetic modifications could bridge the gap between genetic and environmental risk factors in psoriasis. This review will provide a better understanding of the pathogenesis of psoriasis by unraveling the complicated interplay among immunological abnormalities, genetic risk foci, epigenetic modification and environmental factors of psoriasis. With advances in molecular biology, diverse new targets are under investigation to manage psoriasis. The recent advances in treatment modalities for psoriasis based on targeted molecules are also discussed.

Indexed as

Biological ProductsClinical Trials as TopicEpigenesis, GeneticGenetic Predisposition to DiseaseHumansInterleukin-17PsoriasisSignal TransductionSmall Molecule LibrariesTh17 CellsTh1 CellsBiological ProductsInterleukin-17Small Molecule Librariesbiologicsepigeneticsgeneticsinterleukin-23psoriasissignaling pathwaysmall moleculesT helper 17 cells

Identifiers

PMID29232931
PMCPMC5751286
OpenAlexW2773298891

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.