Evidence map›Paper›PMID 28835474›Full record

ArticleDevelopment (Cambridge, England)2017

Multi-scale quantification of tissue behavior during amniote embryo axis elongation.

Bertrand Bénazéraf, Mathias Beaupeux, Martin Tchernookov, Allison Wallingford, Tasha Salisbury, Amelia Shirtz, Andrew Shirtz, David Huss, Olivier Pourquié, Paul François and 1 more

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
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

37 citing papers in PubMed.

  1. Article
  2. Article
  3. Differential sensitivity of midline development to mitosis during and after primitive streak extension.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
  4. Article
  5. Article
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  9. Mechanically guided cell fate determination in early development.Cellular and molecular life sciences : CMLS · 2024
    Review
  10. Article
  11. Conserved physical mechanisms of cell and tissue elongation.Development (Cambridge, England) · 2024
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  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

11 authors.

Bertrand BénazérafDepartment of Development and Stem cells, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), CNRS (UMR 7104), Inserm U964, Université de Strasbourg, 67400 Illkirch Graffenstaden, France bertrand.benazeraf@univ-tlse3.fr pourquie@genetics.med.harvard.edu paulf@physics.mcgill.ca rustylansford@gmail.com.
Mathias BeaupeuxDepartment of Physics, Ernest Rutherford Physics Building, McGill University, 3600 rue University, Montréal, QC, H3A 2T8, Canada.
Martin TchernookovDepartment of Physics, Ernest Rutherford Physics Building, McGill University, 3600 rue University, Montréal, QC, H3A 2T8, Canada.
Allison WallingfordDepartment of Radiology and Developmental Neuroscience Program, Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, CA 90027, USA.
Tasha SalisburyDepartment of Radiology and Developmental Neuroscience Program, Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, CA 90027, USA.ORCID 0000-0001-6012-0264
Amelia ShirtzDepartment of Radiology and Developmental Neuroscience Program, Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, CA 90027, USA.ORCID 0000-0001-5628-395X
Andrew ShirtzNorthern Michigan University, Computer Science and Mathematics Department, Marquette, MI 49855, USA.
David HussDepartment of Radiology and Developmental Neuroscience Program, Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, CA 90027, USA.ORCID 0000-0002-3239-8477
Olivier PourquiéDepartment of Development and Stem cells, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), CNRS (UMR 7104), Inserm U964, Université de Strasbourg, 67400 Illkirch Graffenstaden, France bertrand.benazeraf@univ-tlse3.fr pourquie@genetics.med.harvard.edu paulf@physics.mcgill.ca rustylansford@gmail.com.
Paul FrançoisDepartment of Physics, Ernest Rutherford Physics Building, McGill University, 3600 rue University, Montréal, QC, H3A 2T8, Canada bertrand.benazeraf@univ-tlse3.fr pourquie@genetics.med.harvard.edu paulf@physics.mcgill.ca rustylansford@gmail.com.
Rusty LansfordDepartment of Radiology and Developmental Neuroscience Program, Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, CA 90027, USA bertrand.benazeraf@univ-tlse3.fr pourquie@genetics.med.harvard.edu paulf@physics.mcgill.ca rustylansford@gmail.com.ORCID 0000-0002-2159-3699

Funding

Dynamic Imaging of Embryogenesis Using Transgenic QuailR21HD047347 · NICHD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI LANSFORD, RUSTY D · 2006 to 2007
$347k
NICHD NIH HHS R21 HD047347
6 · The paper itself

Abstract

Embryonic axis elongation is a complex multi-tissue morphogenetic process responsible for the formation of the posterior part of the amniote body. How movements and growth are coordinated between the different posterior tissues (e.g. neural tube, axial and paraxial mesoderm, lateral plate, ectoderm, endoderm) to drive axis morphogenesis remain largely unknown. Here, we use quail embryos to quantify cell behavior and tissue movements during elongation. We quantify the tissue-specific contribution to axis elongation using 3D volumetric techniques, then quantify tissue-specific parameters such as cell density and proliferation. To study cell behavior at a multi-tissue scale, we used high-resolution 4D imaging of transgenic quail embryos expressing fluorescent proteins. We developed specific tracking and image analysis techniques to analyze cell motion and compute tissue deformations in 4D. This analysis reveals extensive sliding between tissues during axis extension. Further quantification of tissue tectonics showed patterns of rotations, contractions and expansions, which are consistent with the multi-tissue behavior observed previously. Our approach defines a quantitative and multi-scale method to analyze the coordination between tissue behaviors during early vertebrate embryo morphogenetic events.

Indexed as

AnimalsAnimals, Genetically ModifiedApoptosisBiomechanical PhenomenaBody PatterningCell CountCell MovementCell ProliferationCell SizeCoturnixImaging, Three-DimensionalLuminescent ProteinsMorphogenesisLuminescent ProteinsAxis elongationConfocal microscopyLive imagingMorphogenesisMulti-tissueProliferationPSMQuail embryoTissue deformations

Identifiers

PMID28835474
PMCPMC13471720

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.