Evidence map›Paper›PMID 24550288›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Predicting the spatiotemporal dynamics of hair follicle patterns in the developing mouse.

Chi Wa Cheng, Ben Niu, Mya Warren, Larysa Halyna Pevny, Robin Lovell-Badge, Terence Hwa, Kathryn S E Cheah

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Chemotactic self-organization captures the dynamics of mammalian hair follicle patterning.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Patterning of theFrontiers in cell and developmental biology · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Systems for intricate patterning of the vertebrate anatomy.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Frontiers in cell and developmental biology · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Dentin on the nanoscale: Hierarchical organization, mechanical behavior and bioinspired engineering.Dental materials : official publication of the Academy of Dental Materials · 2017
    Review
  19. 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

7 authors.

Chi Wa ChengDepartment of Biochemistry, Li Ka Shing Faculty of Medicine, University of Hong Kong, Pokfulam, Hong Kong SAR, China.
Ben Niu
Mya Warren
Larysa Halyna Pevny
Robin Lovell-Badge
Terence Hwa
Kathryn S E Cheah

Funding

Medical Research Council U117512772
6 · The paper itself

Abstract

Reaction-diffusion models have been used as a paradigm for describing the de novo emergence of biological patterns such as stripes and spots. In many organisms, these initial patterns are typically refined and elaborated over the subsequent course of development. Here we study the formation of secondary hair follicle patterns in the skin of developing mouse embryos. We used the expression of sex-determining region Y box 2 to identify and distinguish the primary and secondary hair follicles and to infer the spatiotemporal dynamics of the follicle formation process. Quantitative analysis of the specific follicle patterns observed reveals a simple geometrical rule governing the formation of secondary follicles, and motivates an expansion-induction (EI) model in which new follicle formation is driven by the physical growth of the embryo. The EI model requires only one diffusible morphogen and provides quantitative, accurate predictions on the relative positions and timing of secondary follicle formation, using only the observed configuration of primary follicles as input. The same model accurately describes the positions of additional follicles that emerge from skin explants treated with an activator. Thus, the EI model provides a simple and robust mechanism for predicting secondary space-filling patterns in growing embryos.

Indexed as

Models, BiologicalAnimalsBasic Helix-Loop-Helix ProteinsBody PatterningCarrier ProteinsComputer SimulationGalactosidesHair FollicleHistological TechniquesIndolesMiceMorphogenesisNoggin Protein5-bromo-4-chloro-3-indolyl beta-galactosideAtoh1 protein, mouseBasic Helix-Loop-Helix ProteinsCarrier ProteinsGalactosidesIndolesNoggin Proteingrowth and patternsinhibitory morphogenTuring patternVoronoi analysis

Identifiers

PMID24550288
PMCPMC3932898

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.