Evidence map›Paper›PMID 33652877›Full record

ReviewBiomedicines2021

Experimental Models for the Study of Hereditary Cornification Defects.

Dragan Copic, Maria Laggner, Polina Kalinina, Katharina Klas, Erwin Tschachler, Michael Mildner

Abstract readReview
In one paragraph

Review in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Dragan CopicLaboratory for Cardiac and Thoracic Diagnosis, Regeneration and Applied Immunology, Department of Surgery, Research Laboratories, Medical University of Vienna, 1090 Vienna, Austria.
Maria LaggnerLaboratory for Cardiac and Thoracic Diagnosis, Regeneration and Applied Immunology, Department of Surgery, Research Laboratories, Medical University of Vienna, 1090 Vienna, Austria.
Polina KalininaDepartment of Dermatology, Medical University of Vienna, 1090 Vienna, Austria.
Katharina KlasLaboratory for Cardiac and Thoracic Diagnosis, Regeneration and Applied Immunology, Department of Surgery, Research Laboratories, Medical University of Vienna, 1090 Vienna, Austria.
Erwin TschachlerDepartment of Dermatology, Medical University of Vienna, 1090 Vienna, Austria.
Michael MildnerDepartment of Dermatology, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-6892-925X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ichthyoses comprise a broad spectrum of keratinization disorders due to hereditary defects of cornification. Until now, mutations in more than 50 genes, mostly coding for structural proteins involved in epidermal barrier formation, have been identified as causes for different types of these keratinization disorders. However, due to the high heterogeneity and difficulties in the establishment of valid experimental models, research in this field remains challenging and translation of novel findings to clinical practice is difficult. In this review, we provide an overview of existing models to study hereditary cornification defects with focus on ichthyoses and palmoplantar keratodermas.

Indexed as

cornification defectgene knockdownichthyosisorganotypic skin model

Identifiers

PMID33652877
PMCPMC7996736

What OpenQuestion holds

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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.