Evidence map›Paper›PMID 25285079›Full record

ArticleFrontiers in physiology2014

Comparative studies between mice molars and incisors are required to draw an overview of enamel structural complexity.

Michel Goldberg, O Kellermann, S Dimitrova-Nakov, Y Harichane, A Baudry

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Genes · 2025
    Review
  4. Article
  5. Article
  6. Challenges of Studying Amelogenesis in Gene-Targeted Mouse Models.International journal of molecular sciences · 2025
    Review
  7. Article
  8. Review
  9. Article
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  12. Article
  13. Article
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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

5 authors at 3 institutions in 1 country.

Michel GoldbergINSERM UMR-S 1124, Cellules Souches, Signalisation et Prions Paris, France ; Université Paris Descartes, Sorbonne Paris Cité, UMR-S 1124 Paris, France.
O KellermannINSERM UMR-S 1124, Cellules Souches, Signalisation et Prions Paris, France ; Université Paris Descartes, Sorbonne Paris Cité, UMR-S 1124 Paris, France.
S Dimitrova-NakovINSERM UMR-S 1124, Cellules Souches, Signalisation et Prions Paris, France ; Université Paris Descartes, Sorbonne Paris Cité, UMR-S 1124 Paris, France.
Y HarichaneINSERM UMR-S 1124, Cellules Souches, Signalisation et Prions Paris, France ; Université Paris Descartes, Sorbonne Paris Cité, UMR-S 1124 Paris, France.
A BaudryINSERM UMR-S 1124, Cellules Souches, Signalisation et Prions Paris, France ; Université Paris Descartes, Sorbonne Paris Cité, UMR-S 1124 Paris, France.
Université Paris Cité · FRDélégation Paris 5 · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the field of dentistry, the murine incisor has long been considered as an outstanding model to study amelogenesis. However, it clearly appears that enamel from wild type mouse incisors and molars presents several structural differences. In incisor, exclusively radial enamel is observed. In molars, enamel displays a high level of complexity since the inner part is lamellar whereas the outer enamel shows radial and tangential structures. Recently, the serotonin 2B receptor (5-HT2BR) was shown to be involved in ameloblast function and enamel mineralization. The incisors from 5HT2BR knockout (KO) mice exhibit mineralization defects mostly in the outer maturation zone and porous matrix network in the inner zone. In the molars, the mutation affects both secretory and maturation stages of amelogenesis since pronounced alterations concern overall enamel structures. Molars from 5HT2BR KO mice display reduction in enamel thickness, alterations of inner enamel architecture including defects in Hunter-Schreger Bands arrangements, and altered maturation of the outer radial enamel. Differences of enamel structure were also observed between incisor and molar from other KO mice depleted for genes encoding enamel extracellular matrix proteins. Thus, upon mutation, enamel analysis based exclusively on incisor defects would be biased. In view of the functional relationship between enamel structure and tooth morphogenesis, identification of molecular actors involved in amelogenesis requires comparative studies between mice molars and incisors.

Indexed as

gene deletionHunter-Schreger bandsincisormaturationmolarserotonin receptor

Identifiers

PMID25285079
PMCPMC4168675
OpenAlexW1989963589

What OpenQuestion holds

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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.