Evidence map›Paper›PMID 17143583›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2006

Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71rco12 and Krt71rco13.

Fabian Runkel, Matthias Klaften, Kerstin Koch, Volker Böhnert, Heinrich Büssow, Helmut Fuchs, Thomas Franz, Martin Hrabé de Angelis

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In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 46 citations in OpenAlex.

  1. Polymorphism of Keratin GeneAnimals : an open access journal from MDPI · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. AGenes · 2021
    Article
  7. Article
  8. The bald and the beautiful: hairlessness in domestic dog breeds.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017
    Article
  9. Article
  10. CtBP1 overexpression in keratinocytes perturbs skin homeostasis.The Journal of investigative dermatology · 2014
    Article
  11. Insights into morphology and disease from the dog genome project.Annual review of cell and developmental biology · 2014
    Review
  12. Article
  13. Article
  14. Article
  15. The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71.Mammalian genome : official journal of the International Mammalian Genome Society · 2010
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

8 authors at 3 institutions in 1 country.

Fabian RunkelAnatomisches Institut, Rheinische Friedrich-Wilhelms-Universität Bonn, Nussallee 10, D-53115 Bonn, Germany.
Matthias Klaften
Kerstin Koch
Volker Böhnert
Heinrich Büssow
Helmut Fuchs
Thomas Franz
Martin Hrabé de Angelis
University of Bonn · DEInstitute of Groundwater Ecology · DEInstitute for Biodiversity · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have analyzed two novel mouse mutant strains, Rco12 and Rco13, displaying a wavy pelage and curly vibrissae that have been identified in an ENU screen for dominant mutations affecting the pelage. The mutations were mapped to mouse Chromosome 15 and identified as missense point mutations in the first exon of the Krt71 (formerly called Krt2-6g) gene causing alterations of amino acid residue 143 from alanine to glycine (Rco12) and residue 146 from isoleucine to phenylalanine. The morphologic analyses demonstrated that both mutations cause identical phenotypes leading to the formation of filamentous aggregates in Henle's and Huxley's layers of the inner root sheath (IRS) of the hair follicle that leads to the bending of the hair shaft. Both novel mutations are located in the immediate vicinity of previously identified mutations in murine Krt71 that cause similar phenotypes and alter the helix initiation motif of the keratin. The characterization of these mutants demonstrates the importance of this Krt71 domain for the formation of linear IRS intermediate filaments.

Indexed as

Mutation, MissensePoint MutationAlkylating AgentsAnimalsChromosome MappingChromosomes, MammalianEthylnitrosoureaFemaleHair FollicleKeratin-6MaleMiceMice, Inbred C3HMice, Inbred C57BLMice, KnockoutPhenotypeAlkylating AgentsEthylnitrosoureaKeratin-6Krt71 protein, mouse

Identifiers

PMID17143583
OpenAlexW2026310172

What OpenQuestion holds

Textmetadata
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.