Evidence map›Paper›PMID 34199056›Full record

ArticleInternational journal of molecular sciences2021

Post Zygotic, Somatic, Deletion in KERATIN 1 V1 Domain Generates Structural Alteration of the K1/K10 Dimer, Producing a Monolateral Palmar Epidermolytic Nevus.

Sabrina Caporali, Biagio Didona, Mauro Paradisi, Alessandro Mauriello, Elena Campione, Mattia Falconi, Federico Iacovelli, Marilena Minieri, Massimo Pieri, Sergio Bernardini and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
  2. Review
  3. 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

11 authors at 1 institution in 1 country.

Sabrina CaporaliDepartment of Industrial Engineering, University of Rome Tor Vergata, 00133 Rome, Italy.
Biagio DidonaFondazione Luigi Maria Monti, IDI-IRCCS, 00167 Rome, Italy.
Mauro ParadisiDepartment of Experimental Medicine, University of Tor Vergata, 00133 Rome, Italy.
Alessandro MaurielloDepartment of Experimental Medicine, University of Tor Vergata, 00133 Rome, Italy.ORCID 0000-0002-7351-5676
Elena CampioneDepartment of Systems Medicine, University of Tor Vergata, 00133 Rome, Italy.
Mattia FalconiDepartment of Biology, University of Rome Tor Vergata, Via della Ricerca Scientifica, 00133 Rome, Italy.ORCID 0000-0002-3990-4758
Federico IacovelliDepartment of Biology, University of Rome Tor Vergata, Via della Ricerca Scientifica, 00133 Rome, Italy.ORCID 0000-0001-7511-6575
Marilena MinieriDepartment of Experimental Medicine, University of Tor Vergata, 00133 Rome, Italy.ORCID 0000-0002-2512-4793
Massimo PieriDepartment of Experimental Medicine, University of Tor Vergata, 00133 Rome, Italy.
Sergio BernardiniDepartment of Experimental Medicine, University of Tor Vergata, 00133 Rome, Italy.
Alessandro TerrinoniDepartment of Experimental Medicine, University of Tor Vergata, 00133 Rome, Italy.ORCID 0000-0002-7442-2252
University of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Palmoplantar keratodermas (PPKs) are characterized by thickness of stratum corneum and epidermal hyperkeratosis localized in palms and soles. PPKs can be epidermolytic (EPPK) or non epidermolytic (NEPPK). Specific mutations of keratin 16 (K16) and keratin 1 (K1) have been associated to EPPK, and NEPPK. Cases of mosaicism in PPKs due to somatic keratin mutations have also been described in scientific literature. We evaluated a patient presenting hyperkeratosis localized monolaterally in the right palmar area, characterized by linear yellowish hyperkeratotic lesions following the Blaschko lines. No other relatives of the patient showed any dermatological disease. Light and confocal histological analysis confirmed the presence of epidermolityic hyperkeratosis. Genetic analysis performed demonstrates the heterozygous deletion NM_006121.4:r.274_472del for a total of 198 nucleotides, in

Indexed as

Protein Interaction Domains and MotifsSequence DeletionAmino Acid SequenceBase SequenceBiopsyDNA Mutational AnalysisFluorescent Antibody TechniqueHumansImmunohistochemistryKeratin-1Keratin-10Models, MolecularNevusProtein ConformationProtein MultimerizationSkin NeoplasmsKeratin-1Keratin-10KRT10 protein, humanKRT1 protein, humanEPPKgenodermatosiskeratinskeratin structureKIFmosaicNEPPK

Identifiers

PMID34199056
PMCPMC8269197
OpenAlexW3173300716

What OpenQuestion holds

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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.