Evidence map›Paper›PMID 35054504›Full record

ArticleLife (Basel, Switzerland)2022

Transcriptional Analysis-Based Alterations Affecting Neuritogenesis of the Peripheral Nervous System in Psoriasis.

Dóra Romhányi, Kornélia Szabó, Lajos Kemény, Endre Sebestyén, Gergely Groma

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Psoriasis, Is It a Microdamage of Our "Sixth Sense"? A Neurocentric View.International journal of molecular sciences · 2022
    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

5 authors at 2 institutions in 1 country.

Dóra RomhányiDepartment of Dermatology and Allergology, University of Szeged, H-6720 Szeged, Hungary.
Kornélia SzabóDepartment of Dermatology and Allergology, University of Szeged, H-6720 Szeged, Hungary.
Lajos KeményDepartment of Dermatology and Allergology, University of Szeged, H-6720 Szeged, Hungary.ORCID 0000-0002-2119-9501
Endre Sebestyén1st Department of Pathology and Experimental Cancer Research, Semmelweis University, H-1085 Budapest, Hungary.
Gergely GromaDepartment of Dermatology and Allergology, University of Szeged, H-6720 Szeged, Hungary.ORCID 0000-0001-8487-0465
University of Szeged · HUSemmelweis University · HU

Funding

NKFI, Széchenyi 2020 GINOP-2.2.1-15-2016-00007Supported by SZTE ÁOK-KKA Hetényi Géza 2021-5S 269 (A202)
6 · The paper itself

Abstract

An increasing amount of evidence indicates the critical role of the cutaneous nervous system in the initiation and maintenance of psoriatic skin lesions by neurogenic inflammation. However, molecular mechanisms affecting cutaneous neurons are largely uncharacterized. Therefore, we reanalyzed a psoriatic RNA sequencing dataset from published transcriptome experiments of nearly 300 individuals. Using the Ingenuity Pathway Analysis software, we associated several hundreds of differentially expressed transcripts (DETs) to nervous system development and functions. Since neuronal projections were previously reported to be affected in psoriasis, we performed an in-depth analysis of neurite formation-related process. Our

Indexed as

axon developmentcutaneous nervous systemmyelinationpsoriasis

Identifiers

PMID35054504
PMCPMC8778302
OpenAlexW4225670289

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.