Evidence map›Paper›PMID 36374931›Full record

ArticlePloS one2022

Witch Nails (Krt90whnl): A spontaneous mouse mutation affecting nail growth and development.

John P Sundberg, Hannah Galantino-Homer, Heather Fairfield, Patricia F Ward-Bailey, Belinda S Harris, Melissa Berry, C Herbert Pratt, Nicholas E Gott, Lesley S Bechtold, Pauline R Kaplan and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 46% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. The development of hair follicles and nail.Developmental biology · 2024
    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

13 authors at 4 institutions in 1 country.

John P SundbergThe Jackson Laboratory, Bar Harbor, ME, United States of America.
Hannah Galantino-HomerNew Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Kennett Square, PA, United States of America.ORCID 0000-0002-1435-100X
Heather FairfieldMaine Medical Center Research Institute, Scarborough, ME, United States of America.
Patricia F Ward-BaileyThe Jackson Laboratory, Bar Harbor, ME, United States of America.
Belinda S HarrisThe Jackson Laboratory, Bar Harbor, ME, United States of America.
Melissa BerryThe Jackson Laboratory, Bar Harbor, ME, United States of America.
C Herbert PrattThe Jackson Laboratory, Bar Harbor, ME, United States of America.
Nicholas E GottThe Jackson Laboratory, Bar Harbor, ME, United States of America.
Lesley S BechtoldThe Jackson Laboratory, Bar Harbor, ME, United States of America.
Pauline R KaplanDepartment of Environmental Toxicology, University of California, Davis, CA, United States of America.
Blythe P Durbin-JohnsonDepartment of Applied Biosciences, University of California, Davis, CA, United States of America.
David M RockeDepartment of Applied Biosciences, University of California, Davis, CA, United States of America.
Robert H RiceDepartment of Environmental Toxicology, University of California, Davis, CA, United States of America.ORCID 0000-0003-2058-4405
Jackson Laboratory · USUniversity of California, Davis · USMaine Medical Center · USUniversity of Pennsylvania · US

Funding

UC Davis Clinical and Translational Science CenterUL1TR001860 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KENYON, NICHOLAS J., LYLES, COURTNEY REES · 2016 to 2025
$47.3M
NCATS NIH HHS UL1 TR001860
6 · The paper itself

Abstract

Numerous single gene mutations identified in humans and mice result in nail deformities with many similarities between the species. A spontaneous, autosomal, recessive mutation called witch nails (whnl) is described here where the distal nail matrix and nail bed undergo degenerative changes resulting in formation of an abnormal nail plate causing mice to develop long, curved nails. This mutation arose spontaneously in a colony of MRL/MpJ-Faslpr/J at The Jackson Laboratory. Homozygous mutant mice are recognizable by 8 weeks of age by their long, curved nails. The whnl mutation, mapped on Chromosome 15, is due to a 7-bp insertion identified in the 3' region of exon 9 in the Krt90 gene (formerly Riken cDNA 4732456N10Rik), and is predicted to result in a frameshift that changes serine 476 to arginine and subsequently introduces 36 novel amino acids into the protein before a premature stop codon (p. Ser476ArgfsTer36). By immunohistochemistry the normal KRT90 protein is expressed in the nail matrix and nail bed in control mice where lesions are located in mutant mice. Immunoreactivity toward equine KRT124, the ortholog of mouse KRT90, is restricted to the hoof lamellae (equine hoof wall and lamellae are homologous to the mouse nail plate and nail bed) and the mouse nail bed. Equine laminitis lesions are similar to those observed in this mutant mouse suggesting that the latter may be a useful model for hoof and nail diseases. This first spontaneous mouse mutation affecting the novel Krt90 gene provides new insight into the normal regulation of the molecular pathways of nail development.

Indexed as

Nail DiseasesNails, MalformedAnimalsGrowth and DevelopmentHorsesMiceMutationNails

Identifiers

PMID36374931
PMCPMC9662738
OpenAlexW4308965204

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.