Evidence map›Paper›PMID 9166583›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society1997

The mouse Cat4 locus maps to chromosome 8 and mutants express lens-corneal adhesion.

J Favor, P Grimes, A Neuhäuser-Klaus, W Pretsch, D Stambolian

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 28 citations in OpenAlex.

  1. Microphthalmia, parkinsonism, and enhanced nociception in Pitx3 ( 416insG ) mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2010
    Article
  2. Mouse models of cataract.Journal of genetics · 2009
    Review
  3. Article
  4. Article
  5. Article
  6. Cell autonomous roles for AP-2alpha in lens vesicle separation and maintenance of the lens epithelial cell phenotype.Developmental dynamics : an official publication of the American Association of Anatomists · 2008
    Article
  7. Ocular defects associated with a null mutation in the mouse arylamine N-acetyltransferase 2 gene.Mammalian genome : official journal of the International Mammalian Genome Society · 2007
    Article
  8. Article
  9. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

J FavorInstitute of Mammalian Genetics, GSF-National Research Center for Environment and Health, Ingolstädter Landstr. 1, D-85764 Neuherberg, Germany.
P Grimes
A Neuhäuser-Klaus
W Pretsch
D Stambolian
Institute of Groundwater Ecology · DEUniversity of Pennsylvania · US

Funding

GENETIC STUDIES OF AUTOSOMAL DOMINANT CATARACTSR01EY010321 · NEI · UNIVERSITY OF PENNSYLVANIA · PI STAMBOLIAN, DWIGHT EDWARD · 1994 to 2003
$1.4M
NEI NIH HHS R01EY10321
6 · The paper itself

Abstract

Cat4 is the second largest allelism group in the collection of mouse dominant eye mutations recovered in Neuherberg and carriers express anterior polar cataract, central corneal opacity, and lens-corneal adhesions. We have mapped the Cat4 locus of the mouse to central Chromosome (Chr) 8 at position cM 31. Histological characterization of Cat4(a) heterozygotes and homozygotes indicates failure of separation of the lens vesicle from the surface ectoderm. Human anterior segment ocular dysgenesis (ASOD) is autosomal dominant, carriers express an eye phenotype similar to that of Cat4(a) carriers, and it has been mapped to a region of 4q homologous to mouse central Chr 8. Thus, on the basis of phenotype and map position, Cat4 may be a mouse model of human ASOD. The genes Junb, Jund1, Mel, and Zfp42 are discussed as possible candidates for Cat4.

Indexed as

Chromosome MappingMutationAnimalsAnterior Eye SegmentCorneaCorneal DiseasesCorneal OpacityCrosses, GeneticEyeEye AbnormalitiesGamma RaysGenetic LinkageGenetic MarkersHeterozygoteHomozygoteHumansGenetic Markers

Identifiers

PMID9166583
OpenAlexW2069772961

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.