Evidence map›Paper›PMID 29590636›Full record

ArticleDisease models & mechanisms2018

Vangl2 disruption alters the biomechanics of late spinal neurulation leading to spina bifida in mouse embryos.

Gabriel L Galea, Oleksandr Nychyk, Matteo A Mole, Dale Moulding, Dawn Savery, Evanthia Nikolopoulou, Deborah J Henderson, Nicholas D E Greene, Andrew J Copp

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Hindbrain neuropore tissue geometry determines asymmetric cell-mediated closure dynamics in mouse embryos.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  18. Intrinsic Mechanical Cues and Their Impact on Stem Cells and Embryogenesis.Frontiers in cell and developmental biology · 2021
    Review
  19. Article
  20. 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

9 authors at 2 institutions in 1 country.

Gabriel L GaleaDevelopmental Biology of Birth Defects, UCL GOS Institute of Child Health, London, WC1N 1EH, UK g.galea@ucl.ac.uk.ORCID 0000-0003-2515-1342
Oleksandr NychykDevelopmental Biology of Birth Defects, UCL GOS Institute of Child Health, London, WC1N 1EH, UK.
Matteo A MoleDevelopmental Biology of Birth Defects, UCL GOS Institute of Child Health, London, WC1N 1EH, UK.
Dale MouldingDevelopmental Biology of Birth Defects, UCL GOS Institute of Child Health, London, WC1N 1EH, UK.
Dawn SaveryDevelopmental Biology of Birth Defects, UCL GOS Institute of Child Health, London, WC1N 1EH, UK.
Evanthia NikolopoulouDevelopmental Biology of Birth Defects, UCL GOS Institute of Child Health, London, WC1N 1EH, UK.
Deborah J HendersonCardiovascular Research Centre, Institute of Genetic Medicine, Newcastle University, Central Parkway, Newcastle upon Tyne, NE1 3BZ, UK.
Nicholas D E GreeneDevelopmental Biology of Birth Defects, UCL GOS Institute of Child Health, London, WC1N 1EH, UK.ORCID 0000-0002-4170-5248
Andrew J CoppDevelopmental Biology of Birth Defects, UCL GOS Institute of Child Health, London, WC1N 1EH, UK.ORCID 0000-0002-2544-9117
University College London · GBCentre for Life · GB

Funding

British Heart Foundation PG/11/76/29108Medical Research Council G0801124Medical Research Council J003794Medical Research Council K022741Medical Research Council MR/J003794/1Wellcome TrustWellcome Trust 087525Wellcome Trust 107474/Z/15/Z
6 · The paper itself

Abstract

Human mutations in the planar cell polarity component VANGL2 are associated with the neural tube defect spina bifida. Homozygous Vangl2 mutation in mice prevents initiation of neural tube closure, precluding analysis of its subsequent roles in neurulation. Spinal neurulation involves rostral-to-caudal 'zippering' until completion of closure is imminent, when a caudal-to-rostral closure point, 'Closure 5', arises at the caudal-most extremity of the posterior neuropore (PNP). Here, we used

Indexed as

Gene DeletionNeurulationActinsAnimalsBiomechanical PhenomenaCell BodyCell DivisionCell PolarityDNA-Binding ProteinsEctodermEmbryo, MammalianEpitheliumIntracellular Signaling Peptides and ProteinsMembrane ProteinsMice, Inbred C57BLNerve Tissue ProteinsActinsDNA-Binding ProteinsGrhl3 protein, mouseIntracellular Signaling Peptides and ProteinsLtap protein, mouseMembrane ProteinsNerve Tissue ProteinsTranscription FactorsVANGL2 protein, humanBiomechanicsEmbryoF-actinMouseNeural tubeVangl2

Identifiers

PMID29590636
PMCPMC5897727
OpenAlexW2793962270

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.