Evidence map›Paper›PMID 23349879›Full record

ArticlePloS one2013

Requirement for Dlgh-1 in planar cell polarity and skeletogenesis during vertebrate development.

Charlene Rivera, Sara J S Simonson, Idella F Yamben, Shalini Shatadal, Minh M Nguyen, Maryline Beurg, Paul F Lambert, Anne E Griep

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Discs large 1 controls daughter-cell polarity after cytokinesis in vertebrate morphogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Eyelid closure in embryogenesis is required for ocular adnexa development.Investigative ophthalmology & visual science · 2014
    Article
  11. Article
  12. Article
  13. Review
  14. Spindle orientation and epidermal morphogenesis.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2013
    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

8 authors at 2 institutions in 2 countries.

Charlene RiveraDepartment of Cell and Regenerative Biology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Sara J S Simonson
Idella F Yamben
Shalini Shatadal
Minh M Nguyen
Maryline Beurg
Paul F Lambert
Anne E Griep
University of Wisconsin–Madison · USHôpital Pellegrin · FR

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AMY TRENTHAM-DIETZ · 1985 to 2026
$142.6M
Regulation of Ocular Lens Development by PDZ ProteinsR01EY009091 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI GRIEP, ANNE E · 1992 to 2011
$5.3M
NCI NIH HHS CA908428NCI NIH HHS P30 CA014520NCI NIH HHS P30 CA14520NEI NIH HHS EY09091NEI NIH HHS R01 EY009091
6 · The paper itself

Abstract

The development of specialized organs is tightly linked to the regulation of cell growth, orientation, migration and adhesion during embryogenesis. In addition, the directed movements of cells and their orientation within the plane of a tissue, termed planar cell polarity (PCP), appear to be crucial for the proper formation of the body plan. In Drosophila embryogenesis, Discs large (dlg) plays a critical role in apical-basal cell polarity, cell adhesion and cell proliferation. Craniofacial defects in mice carrying an insertional mutation in Dlgh-1 suggest that Dlgh-1 is required for vertebrate development. To determine what roles Dlgh-1 plays in vertebrate development, we generated mice carrying a null mutation in Dlgh-1. We found that deletion of Dlgh-1 caused open eyelids, open neural tube, and misorientation of cochlear hair cell stereociliary bundles, indicative of defects in planar cell polarity (PCP). Deletion of Dlgh-1 also caused skeletal defects throughout the embryo. These findings identify novel roles for Dlgh-1 in vertebrates that differ from its well-characterized roles in invertebrates and suggest that the Dlgh-1 null mouse may be a useful animal model to study certain human congenital birth defects.

Indexed as

AnimalsBone and BonesCell AdhesionCell PolarityCell ProliferationDiscs Large Homolog 1 ProteinEmbryonic DevelopmentEyelidsGerm-Line MutationGuanylate KinasesHumansMembrane ProteinsMiceMice, KnockoutMutationNeural TubeDiscs Large Homolog 1 ProteinDlg1 protein, mouseGuanylate KinasesMembrane Proteins

Identifiers

PMID23349879
PMCPMC3551758
OpenAlexW2014543214

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.