Evidence map›Paper›PMID 21761474›Full record

ReviewDevelopmental dynamics : an official publication of the American Association of Anatomists2011

Cell biological regulation of division fate in vertebrate neuroepithelial cells.

Minde I Willardsen, Brian A Link

Open access · bronzeAbstract readReview
In one paragraph

Review in Developmental dynamics : an official publication of the American Association of Anatomists, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Design principles and developmental mechanisms underlying retinal mosaics.Biological reviews of the Cambridge Philosophical Society · 2015
    Review
  11. Article
  12. Review
  13. A novel function for Foxm1 in interkinetic nuclear migration in the developing telencephalon and anxiety-related behavior.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
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

2 authors at 1 institution in 1 country.

Minde I WillardsenDepartment of Cell Biology, Neurobiology, and Anatomy, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA. mwillardsen@mcw.edu
Brian A Link
Medical College of Wisconsin · US

Funding

Integrative Analysis of Vertebrate Retinal LaminationR01EY014167 · NEI · MEDICAL COLLEGE OF WISCONSIN · PI LINK, BRIAN A · 2003 to 2017
$4.6M
Development of an Improved Digital Glare Testing DeviceR44EY014767 · NEI · INTERSCIENCE, INC. · PI SIMKULET, MICHELLE D · 2004 to 2005
$765k
Development of an Improved Digital Glare Testing DeviceR43EY014767 · NEI · INTERSCIENCE, INC. · PI SIMKULET, MICHELLE D · 2003 to 2003
$97k
NEI NIH HHS R01 EY014167NEI NIH HHS R01EY014767NEI NIH HHS R43 EY014767NEI NIH HHS R44 EY014767
6 · The paper itself

Abstract

The developing nervous system derives from neuroepithelial progenitor cells that divide to generate all of the mature neuronal types. For the proper complement of cell types to form, the progenitors must produce postmitotic cells, yet also replenish the progenitor pool. Progenitor divisions can be classified into three general types: symmetric proliferative (producing two progenitors), asymmetric neurogenic (producing one progenitor and one postmitotic cell), and symmetric neurogenic (producing two postmitotic cells). The appropriate ratios for these modes of cell division require intrinsic polarity, which is one of the characteristics that define neuroepithelial progenitor cells. The type of division an individual progenitor undergoes can be influenced by cellular features, or behaviors, which are heterogeneous within the population of progenitors. Here we review three key cellular parameters, asymmetric inheritance, cell cycle kinetics, and interkinetic nuclear migration, and the possible mechanisms for how these features influence progenitor fates.

Indexed as

VertebratesAnimalsCell DifferentiationCell DivisionCell LineageCell NucleusCell PolarityCell ProliferationNeuroepithelial CellsNeurogenesisSignal TransductionStem Cells

Identifiers

PMID21761474
PMCPMC3140019
OpenAlexW2025784189

What OpenQuestion holds

Textmetadata
LicenceTDM
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.