Evidence map›Paper›PMID 28414273›Full record

ArticleeLife2017

Oriented clonal cell dynamics enables accurate growth and shaping of vertebrate cartilage.

Marketa Kaucka, Tomas Zikmund, Marketa Tesarova, Daniel Gyllborg, Andreas Hellander, Josef Jaros, Jozef Kaiser, Julian Petersen, Bara Szarowska, Phillip T Newton and 19 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

46 citing papers in PubMed, 62 citations in OpenAlex.

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  16. Evolutionary mechanisms modulating the mammalian skull development.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Review
  17. Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Review
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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

29 authors at 12 institutions in 7 countries.

Marketa KauckaDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-8781-9769
Tomas ZikmundCentral European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
Marketa TesarovaCentral European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
Daniel GyllborgUnit of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Andreas HellanderDepartment of Information Technology, Uppsala University, Uppsala, Sweden.
Josef JarosDepartment of Histology and Embryology, Medical Faculty, Masaryk University, Brno, Czech Republic.
Jozef KaiserCentral European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
Julian PetersenCenter for Brain Research, Medical University Vienna, Vienna, Austria.
Bara SzarowskaCenter for Brain Research, Medical University Vienna, Vienna, Austria.
Phillip T NewtonDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Vyacheslav DyachukDepartment of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Lei LiDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Hong QianDepartment of Medicine, Karolinska Institutet, Stockholm, Sweden.
Anne-Sofie JohanssonDepartment of Medicine, Karolinska Institutet, Stockholm, Sweden.
Yuji MishinaDepartment of Biologic and Materials Sciences, University of Michigan School of Dentistry, Ann Arbor, United States.
Joshua D CurrieCenter for Regenerative Therapies, Technische Universität Dresden, Dresden, Germany.
Elly M TanakaCenter for Regenerative Therapies, Technische Universität Dresden, Dresden, Germany.
Alek EricksonDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, United States.
Andrew DudleyDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, United States.
Hjalmar BrismarScience for Life Laboratory, Royal Institute of Technology, Solna, Sweden.ORCID 0000-0003-0578-4003
Paul SouthamJohn Innes Centre, Norwich, United Kingdom.
Enrico CoenJohn Innes Centre, Norwich, United Kingdom.ORCID 0000-0001-8454-8767
Min ChenNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, United States.
Lee S WeinsteinNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, United States.
Ales HamplDepartment of Histology and Embryology, Medical Faculty, Masaryk University, Brno, Czech Republic.
Ernest ArenasUnit of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Andrei S ChaginDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-2696-5850
Kaj FriedDepartment of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Igor AdameykoDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-5471-0356
Karolinska Institutet · SECentral European Institute of Technology · CZJohn Innes Centre · GBMasaryk University · CZMedical University of Vienna · ATNational Institutes of Health · USTechnische Universität Dresden · DEUniversity of Nebraska Medical Center · USScience for Life Laboratory · SESechenov University · RUUniversity of Michigan · USUppsala University · SE

Funding

Role of the Gnas Gene in Metabolic RegulationZIADK043313 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI WEINSTEIN, LEE · 2009 to 2025
$4.9M
StochSS: A Next-Generation Toolkit for Simulation-Driven Biological DiscoveryR01EB014877 · NIBIB · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI PETZOLD, LINDA R. · 2012 to 2022
$3.9M
Biotechnology and Biological Sciences Research Council BBS/E/J/00000152NIBIB NIH HHS R01 EB014877
6 · The paper itself

Abstract

Cartilaginous structures are at the core of embryo growth and shaping before the bone forms. Here we report a novel principle of vertebrate cartilage growth that is based on introducing transversally-oriented clones into pre-existing cartilage. This mechanism of growth uncouples the lateral expansion of curved cartilaginous sheets from the control of cartilage thickness, a process which might be the evolutionary mechanism underlying adaptations of facial shape. In rod-shaped cartilage structures (Meckel, ribs and skeletal elements in developing limbs), the transverse integration of clonal columns determines the well-defined diameter and resulting rod-like morphology. We were able to alter cartilage shape by experimentally manipulating clonal geometries. Using in silico modeling, we discovered that anisotropic proliferation might explain cartilage bending and groove formation at the macro-scale.

Indexed as

AnimalsCartilageComputer SimulationMiceModels, BiologicalVertebratesBMPchondrocraniumdevelopmental biologyfacial cartilage growthGSalphamathematical and material modellingmousemouse mutantsscaling and shapingstem cellsWnt/PCP

Identifiers

PMID28414273
PMCPMC5417851
OpenAlexW2606442180

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.