Evidence map›Paper›PMID 25545474›Full record

ArticlePloS one2014

Melanocytes in the skin--comparative whole transcriptome analysis of main skin cell types.

Paula Reemann, Ene Reimann, Sten Ilmjärv, Orm Porosaar, Helgi Silm, Viljar Jaks, Eero Vasar, Külli Kingo, Sulev Kõks

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
1.4field-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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 1 country.

Paula ReemannDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Ene ReimannCore Facility of Clinical Genomics, Department of Pathophysiology, Department of Biomedicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia; The Institute of Veterinary Medicine and Animal Sciences of the Estonian University of Life Sciences, Competence Centre on Reproductive Medicine and Biology, Tartu, Estonia.
Sten IlmjärvDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu and Quretec Ltd (private limited company), Tartu, Estonia.
Orm PorosaarDepartment of Pediatric Surgery, Tallinn Children's Hospital, Tallinn, Estonia.
Helgi SilmClinic of Dermatology, Tartu University Hospital, Department of Dermatology, University of Tartu, Tartu, Estonia.
Viljar JaksInstitute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
Eero VasarDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu and Centre of Translational Medicine, University of Tartu, Tartu, Estonia.
Külli KingoClinic of Dermatology, Tartu University Hospital, Department of Dermatology, University of Tartu, Tartu, Estonia.
Sulev KõksThe Institute of Veterinary Medicine and Animal Sciences of the Estonian University of Life Sciences, Competence Centre on Reproductive Medicine and Biology, Tartu, Estonia; Department of Pathophysiology, Institute of Biomedicine and Translational Medicine, University of Tartu and Centre of Translational Medicine, University of Tartu, Tartu, Estonia.
University of Tartu · EECompetence Centre on Health Technologies (Estonia) · EEQuretec (Estonia) · EETallinn Health Care College · EETartu University Hospital · EE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanocytes possess several functions besides a role in pigment synthesis, but detailed characteristics of the cells are still unclear. We used whole transcriptome sequencing (RNA-Seq) to assess differential gene expression of cultivated normal human melanocytes with respect to keratinocytes, fibroblasts and whole skin. The present results reveal cultivated melanocytes as highly proliferative cells with possible stem cell-like properties. The enhanced readiness to regenerate makes melanocytes the most vulnerable cells in the skin and explains their high risk of developing into malignant melanoma.

Indexed as

AdolescentCarcinogenesisCells, CulturedChildChild, PreschoolFibroblastsGene Expression ProfilingHistonesHumansInfantInflammationKeratinocytesMelanocytesProtein IsoformsSequence Analysis, RNASkinHistonesProtein Isoforms

Identifiers

PMID25545474
PMCPMC4278762
OpenAlexW2018416085

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.