Evidence map›Paper›PMID 40379916›Full record

ArticleBulletin of mathematical biology2025

Modelling Population-Level Hes1 Dynamics: Insights from a Multi-framework Approach.

Gesina Menz, Stefan Engblom

Abstract read
In one paragraph

Article in Bulletin of mathematical biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Gesina MenzDivision of Scientific Computing, Department of Information Technology, Uppsala University, 751 05, Uppsala, Sweden.ORCID http://orcid.org/0000-0002-3589-9824
Stefan EngblomDivision of Scientific Computing, Department of Information Technology, Uppsala University, 751 05, Uppsala, Sweden. stefane@it.uu.se.ORCID http://orcid.org/0000-0002-3614-1732

Funding

Vetenskapsrådet 2019-03471
6 · The paper itself

Abstract

Mathematical models of living cells have been successively refined with advancements in experimental techniques. A main concern is striking a balance between modelling power and the tractability of the associated mathematical analysis. In this work we model the dynamics for the transcription factor Hairy and enhancer of split-1 (Hes1), whose expression oscillates during neural development, and which critically enables stable fate decision in the embryonic brain. We design, parametrise, and analyse a detailed spatial model using ordinary differential equations (ODEs) over a grid capturing both transient oscillatory behaviour and fate decision on a population-level. We also investigate the relationship between this ODE model and a more realistic grid-based model involving intrinsic noise using mostly directly biologically motivated parameters. While we focus specifically on Hes1 in neural development, the approach of linking deterministic and stochastic grid-based models shows promise in modelling various biological processes taking place in a cell population. In this context, our work stresses the importance of the interpretability of complex computational models into a framework which is amenable to mathematical analysis.

Indexed as

Basic Helix-Loop-Helix ProteinsModels, BiologicalModels, NeurologicalTranscription Factor HES-1AnimalsBrainComputer SimulationGene Expression Regulation, DevelopmentalHumansMathematical ConceptsMiceNeurogenesisStochastic ProcessesBasic Helix-Loop-Helix ProteinsTranscription Factor HES-1Cellular synchronisationFate decisionGenetic oscillatorNeurogenesisPattern formation

Identifiers

PMID40379916
PMCPMC12084287

What OpenQuestion holds

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Registered trials

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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.