Evidence map›Paper›PMID 11489919›Full record

ArticleThe Journal of cell biology2001

Discovery of a novel murine keratin 6 (K6) isoform explains the absence of hair and nail defects in mice deficient for K6a and K6b.

S M Wojcik, M A Longley, D R Roop

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.8field-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

33 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Article
  3. Keratin isoform shifts modulate motility signals during wound healing.bioRxiv : the preprint server for biology · 2024
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Gene expression profiling in pachyonychia congenita skin.Journal of dermatological science · 2015
    Article
  12. Article
  13. Article
  14. Comparative anatomy of mouse and human nail units.Anatomical record (Hoboken, N.J. : 2007) · 2013
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Novel molecular therapies for heritable skin disorders.The Journal of investigative dermatology · 2012
    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

3 authors at 1 institution in 1 country.

S M WojcikDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA.
M A Longley
D R Roop
Baylor College of Medicine · US

Funding

REGULATION AND FUNCTION OF KERATINS IN THE EPIDERMISR01HD025479 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI ROOP, DENNIS · 1989 to 2003
$1.2M
NICHD NIH HHS HD25479
6 · The paper itself

Abstract

The murine genome is known to have two keratin 6 (K6) genes, mouse K6 (MK6)a and MK6b. These genes display a complex expression pattern with constitutive expression in the epithelia of oral mucosa, hair follicles, and nail beds. We generated mice deficient for both genes through embryonic stem cell technology. The majority of MK6a/b-/- mice die of starvation within the first two weeks of life. This is due to a localized disintegration of the dorsal tongue epithelium, which results in the build up of a plaque of cell debris that severely impairs feeding. However, approximately 25% of MK6a/b-/- mice survive to adulthood. Remarkably, the surviving MK6a/b-/- mice have normal hair and nails. To our surprise, we discovered MK6 staining both in the hair follicle and the nail bed of MK6a/b-/- mice, indicating the presence of a third MK6 gene. We cloned this previously unknown murine keratin gene and found it to be highly homologous to human K6hf, which is expressed in hair follicles. We therefore termed this gene MK6 hair follicle (MK6hf). The presence of MK6hf in the MK6a/b-/- follicles and nails offers an explanation for the absence of hair and nail defects in MK6a/b-/- animals.

Indexed as

AnimalsEpithelial CellsGene DeletionHair DiseasesHyperplasiaIsomerismKeratinsMiceMice, KnockoutMicroscopy, ElectronMolecular Sequence DataMouth DiseasesNail DiseasesPhenotypeSequence Homology, Amino AcidSkinKeratins

Identifiers

PMID11489919
PMCPMC2196416
OpenAlexW2107248656

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.