Evidence map›Paper›PMID 30028292›Full record

ArticleeLife2018

Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity.

Tim Davies, Han X Kim, Natalia Romano Spica, Benjamin J Lesea-Pringle, Julien Dumont, Mimi Shirasu-Hiza, Julie C Canman

Open access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Cleavage-furrow formation without F-actin inProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Tim DaviesDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, United States.ORCID 0000-0003-2247-9449
Han X KimDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, United States.
Natalia Romano SpicaDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, United States.
Benjamin J Lesea-PringleDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, United States.
Julien DumontInstitut Jacques Monod, CNRS UMR 7592, Université Paris Diderot, Paris, France.
Mimi Shirasu-HizaDepartment of Genetics and Development, Columbia University Medical Center, New York, United States.
Julie C CanmanDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, United States.ORCID 0000-0001-8135-2072
Columbia University Irving Medical Center · USCentre National de la Recherche Scientifique · FR

Funding

Circadian-Regulated Aging PhysiologiesR01AG045842 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Michele M Shirasu-Hiza · 2013 to 2026
$5.1M
Circadian regulation of physiological functionsR35GM127049 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Michele M Shirasu-Hiza · 2018 to 2026
$3.9M
Cell type-variation of cytokinesisR01GM117407 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CANMAN, JULIE C · 2016 to 2023
$2.9M
IR-LAMP: Optigenetic technology to spatially manipulate protein function in vivoDP2OD008773 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CANMAN, JULIE C · 2011 to 2011
$2.4M
Circadian regulation of phagocytosisR01GM105775 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SHIRASU-HIZA, MICHELE M · 2013 to 2017
$1.6M
Agence Nationale de la Recherche ANR-16-CE13-0020-01Charles H. Revson Foundation Charles H. Revson Senior Fellowship in Biomedical ScienceFondation pour la Recherche Médicale FRM DEQ20160334869NIA NIH HHS R01 AG045842NIGMS NIH HHS R01 GM105775NIGMS NIH HHS R01 GM117407NIGMS NIH HHS R35 GM127049NIH HHS DP2 OD008773NIH HHS NIH DP2OD008773NIH HHS NIH R01AG045842NIH HHS NIH R01GM105775NIH HHS NIH R01GM117407
6 · The paper itself

Abstract

Cytokinesis, the physical division of one cell into two, is powered by constriction of an actomyosin contractile ring. It has long been assumed that all animal cells divide by a similar molecular mechanism, but growing evidence suggests that cytokinetic regulation in individual cell types has more variation than previously realized. In the four-cell

Indexed as

Cell LineageCytokinesisActin CytoskeletonAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsEmbryonic DevelopmentEmbryo, NonmammalianSignal Transductionsrc-Family KinasesCaenorhabditis elegans Proteinscyk-1 protein, C eleganssrc-Family KinasesactomyosinC. eleganscell biologycell extrinsiccell intrinsiccytokinesisdevelopmental biologySrc kinase

Identifiers

PMID30028292
PMCPMC6054530
OpenAlexW2884443433

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.