Evidence map›Paper›PMID 33871356›Full record

ArticleeLife2021

DCC regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation.

Laura Morcom, Ilan Gobius, Ashley Pl Marsh, Rodrigo Suárez, Jonathan Wc Lim, Caitlin Bridges, Yunan Ye, Laura R Fenlon, Yvrick Zagar, Amelia M Douglass and 12 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Netrin-1 Is an Important Mediator in Microglia Migration.International journal of molecular sciences · 2024
    Article
  7. Article
  8. Review
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  10. Article
  11. 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

22 authors at 4 institutions in 3 countries.

Laura MorcomThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.ORCID 0000-0001-6683-4356
Ilan GobiusThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.
Ashley Pl MarshBruce Lefroy Centre for Genetic Health Research, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Australia.ORCID 0000-0001-6049-6931
Rodrigo SuárezThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.ORCID 0000-0001-5153-5652
Jonathan Wc LimThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.ORCID 0000-0002-5074-6359
Caitlin BridgesThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.
Yunan YeThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.ORCID 0000-0001-9084-6314
Laura R FenlonThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.ORCID 0000-0002-5132-2419
Yvrick ZagarSorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
Amelia M DouglassThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.ORCID 0000-0001-5398-6473
Amber-Lee S DonahooThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.
Thomas FothergillThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.
Samreen ShaikhThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.
Peter KozulinThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.ORCID 0000-0002-7872-9884
Timothy J EdwardsThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.
Helen M CooperThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.ORCID 0000-0001-9838-5743
IRC5 ConsortiumMembers and Affiliates of the International Research Consortium for the Corpus Callosum and Cerebral Connectivity (IRC5), Los Angeles, United States.
Elliott H SherrDepartments of Neurology and Pediatrics, Institute of Human Genetics and Weill Institute of Neurosciences, University of California, San Francisco, San Francisco, United States.ORCID 0000-0002-4118-5385
Alain ChédotalSorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.ORCID 0000-0001-7577-3794
Richard J LeventerDepartment of Paediatrics, University of Melbourne, Parkville, Australia.
Paul J LockhartBruce Lefroy Centre for Genetic Health Research, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Australia.ORCID 0000-0003-2531-8413
Linda J RichardsThe University of Queensland, Queensland Brain Institute, Brisbane, Australia.ORCID 0000-0002-7590-7390
The University of Queensland · AURoyal Children's Hospital · AUCentre National de la Recherche Scientifique · FRUniversity of California, San Francisco · US

Funding

De novo copy number variation and gene discovery in human brain malformationsR01NS058721 · NINDS · UNIVERSITY OF CHICAGO · PI ARGILLI, EMANUELA · 2008 to 2025
$10.9M
NINDS NIH HHS R01 NS058721
6 · The paper itself

Abstract

The forebrain hemispheres are predominantly separated during embryogenesis by the interhemispheric fissure (IHF). Radial astroglia remodel the IHF to form a continuous substrate between the hemispheres for midline crossing of the corpus callosum (CC) and hippocampal commissure (HC). Deleted in colorectal carcinoma (DCC) and netrin 1 (NTN1) are molecules that have an evolutionarily conserved function in commissural axon guidance. The CC and HC are absent in

Indexed as

Agenesis of Corpus CallosumAnimalsAstrocytesCell Line, TumorCell MovementCell ShapeChlorocebus aethiopsCorpus CallosumCOS CellsDCC ReceptorGene Expression Regulation, DevelopmentalGenotypeGestational AgeHEK293 CellsHumansMiceDCC protein, humanDcc protein, mouseDCC ReceptorNetrin-1Ntn1 protein, mouseagenesis of the corpusastrocyte morphologycallosumdeleted in colorectal cancerdevelopmental biologyhumaninterhemispheric fissure remodellingmidline zipper gliamouseneurosciencetelencephalic development

Identifiers

PMID33871356
PMCPMC8116049
OpenAlexW3152899381

What OpenQuestion holds

Textmetadata
LicenceCC0
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.