Evidence map›Paper›PMID 15020428›Full record

ArticleGenetics2004

Velvet, a dominant Egfr mutation that causes wavy hair and defective eyelid development in mice.

Xin Du, Koichi Tabeta, Kasper Hoebe, Haiquan Liu, Navjiwan Mann, Suzanne Mudd, Karine Crozat, Sosathya Sovath, Xiaohua Gong, Bruce Beutler

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

36 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Discovery of an Experimental Model of Unicuspid Aortic Valve.Journal of the American Heart Association · 2018
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. IL-33 promotes an innate immune pathway of intestinal tissue protection dependent on amphiregulin-EGFR interactions.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  13. Article
  14. Article
  15. Review
  16. ADAM17 transactivates EGFR signaling during embryonic eyelid closure.Investigative ophthalmology & visual science · 2013
    Article
  17. Review
  18. Article
  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

10 authors at 2 institutions in 1 country.

Xin DuDepartment of Immunology, Scripps Research Institute, La Jolla, California 92037, USA.
Koichi Tabeta
Kasper Hoebe
Haiquan Liu
Navjiwan Mann
Suzanne Mudd
Karine Crozat
Sosathya Sovath
Xiaohua Gong
Bruce Beutler
Scripps Research Institute · USUniversity of California, Berkeley · US

Funding

Mutagenetic analysis of LPS responsesR37GM067759 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI BEUTLER, BRUCE A · 2007 to 2016
$8.6M
OPTIMIZATION OF DNA HARDWARE FOR ALLERGEN GENE VACCINATIONP01AI040682 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RAZ, EYAL · 1997 to 2006
$8.4M
TLR4 AS AN LPS SENSOR AND SUSCEPTIBILITY LOCUSR01GM060031 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI BEUTLER, BRUCE A · 2000 to 2007
$4.5M
Mutagenic analysis of LPS responsesR01GM067759 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI BEUTLER, BRUCE A · 2003 to 2006
$1.8M
NIAID NIH HHS 2P01-AI40682NIGMS NIH HHS GM067759NIGMS NIH HHS GM60031PHS HHS U54A154523
6 · The paper itself

Abstract

In the course of a large-scale program of ENU mutagenesis, we isolated a dominant mutation, called Velvet. The mutation was found to be uniformly lethal to homozygotes, which do not survive E13.5. Mice heterozygous for the Velvet mutation are born with eyelids open and demonstrate a wavy coat and curly vibrissae. The mutation was mapped to the proximal end of chromosome 11 by genome-wide linkage analysis. On 249 meioses, the locus was confined to a 2.7-Mb region, which included the epidermal growth factor receptor gene (Egfr). An A --> G transition in the Egfr coding region of Velvet mice was identified, causing the amino acid substitution D833G. This substitution alters an essential triad of amino acids (DFG --> GFG) that is normally required for coordination of the ATP substrate. As such, kinase activity is at least mostly abolished, but quaternary structure of the receptor is presumably maintained, accounting for the dominant effect. Velvet is the first known dominant representative of the Egfr allelic series that is fully viable, a fact that makes it particularly useful for developmental studies.

Indexed as

Genes, erbB-1MutationAnimalsBase SequenceChromosome MappingDNA, ComplementaryErbB ReceptorsEyelidsFemaleGenes, DominantHairHeterozygoteHomozygoteMaleMiceMice, Inbred C3HDNA, ComplementaryErbB Receptors

Identifiers

PMID15020428
PMCPMC1470694
OpenAlexW2143369970

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.