Evidence map›Paper›PMID 31121896›Full record

ReviewCells2019

3D-Organotypic Cultures to Unravel Molecular and Cellular Abnormalities in Atopic Dermatitis and Ichthyosis Vulgaris.

Géraldine Leman, Verena Moosbrugger-Martinz, Stefan Blunder, Petra Pavel, Sandrine Dubrac

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2019. 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
2.9field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Current research landscape and future prospects of in silico modeling approaches for atopic dermatitis.JID innovations : skin science from molecules to population health · 2026
    Review
  2. 3D human epithelial models: a promising platform for studyingFrontiers in cellular and infection microbiology · 2025
    Article
  3. Review
  4. Ichthyosis vulgaris: An updated review.Skin health and disease · 2023
    Review
  5. Revisiting the Roles of Filaggrin in Atopic Dermatitis.International journal of molecular sciences · 2022
    Review
  6. Atopic Dermatitis: The Fate of the Fat.International journal of molecular sciences · 2022
    Review
  7. Review
  8. Article
  9. Peroxisomal Fatty Acid Oxidation and Glycolysis Are Triggered in Mouse Models of Lesional Atopic Dermatitis.JID innovations : skin science from molecules to population health · 2021
    Article
  10. Review
  11. Article
  12. Xenobiotic Receptors and Their Mates in Atopic Dermatitis.International journal of molecular sciences · 2019
    Review
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 1 institution in 1 country.

Géraldine LemanEpidermal Biology Laboratory, Department of Dermatology, Venereology and Allergology, Medical University of Innsbruck, 6020 Innsbruck, Austria. geraldine.leman@i-med.ac.at.
Verena Moosbrugger-MartinzEpidermal Biology Laboratory, Department of Dermatology, Venereology and Allergology, Medical University of Innsbruck, 6020 Innsbruck, Austria. Verena.Martinz@i-med.ac.at.
Stefan BlunderEpidermal Biology Laboratory, Department of Dermatology, Venereology and Allergology, Medical University of Innsbruck, 6020 Innsbruck, Austria. stefan.blunder@i-med.ac.at.
Petra PavelEpidermal Biology Laboratory, Department of Dermatology, Venereology and Allergology, Medical University of Innsbruck, 6020 Innsbruck, Austria. petra.pavel@i-med.ac.at.
Sandrine DubracEpidermal Biology Laboratory, Department of Dermatology, Venereology and Allergology, Medical University of Innsbruck, 6020 Innsbruck, Austria. sandrine.dubrac@i-med.ac.at.ORCID 0000-0002-2936-8488
Innsbruck Medical University · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atopic dermatitis (AD) is characterized by dry and itchy skin evolving into disseminated skin lesions. AD is believed to result from a primary acquired or a genetically-induced epidermal barrier defect leading to immune hyper-responsiveness. Filaggrin (FLG) is a protein found in the cornified envelope of fully differentiated keratinocytes, referred to as corneocytes. Although

Indexed as

Cells, CulturedDermatitis, AtopicFilaggrin ProteinsHumansHypersensitivityIchthyosis VulgarisInflammationIntermediate Filament ProteinsModels, BiologicalMutationSkinFilaggrin ProteinsFLG protein, humanIntermediate Filament Proteinsatopic dermatitisepidermal equivalentfilaggrinichthyosisorganotypic cultureskin equivalent

Identifiers

PMID31121896
PMCPMC6562513
OpenAlexW2946687872

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.