Evidence map›Paper›PMID 41143898›Full record

ArticleJournal of mathematical biology2025

Structural causes of pattern formation and loss through model-independent bifurcation analysis.

Liam D O'Brien, Adriana T Dawes

Abstract read
In one paragraph

Article in Journal of mathematical biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Liam D O'BrienDepartment of Mathematics, The Ohio State University, 231 W 18th Ave, Columbus, 43210, Ohio, USA. obrien.1093@osu.edu.ORCID 0009-0007-3827-9771
Adriana T DawesDepartment of Mathematics, The Ohio State University, 231 W 18th Ave, Columbus, 43210, Ohio, USA.ORCID 0000-0001-6055-2868

Funding

Mathematical investigation of dynein-mediated centrosome positioning in polarized cellsR01GM132651 · NIGMS · OHIO STATE UNIVERSITY · PI DAWES, ADRIANA · 2019 to 2022
$1.4M
NIGMS NIH HHS R01 GM132651NIH NIGMS 1R01GM132651
6 · The paper itself

Abstract

During development, precise cellular patterning is essential for the formation of functional tissues and organs. These patterns arise from conserved signaling networks that regulate communication both within and between cells. Here, we develop and present a model-independent ordinary differential equation (ODE) framework for analyzing pattern formation in a homogeneous cell array. In contrast to traditional approaches that focus on specific equations, our method relies solely on general assumptions about global intercellular communication (between cells) and qualitative properties of local intracellular biochemical signaling (within cells). Prior work has shown that global intercellular communication networks alone determine the possible emergent patterns in a generic system. We build on these results by demonstrating that additional constraints on the local intracellular signaling network lead to a single stable pattern which depends on the qualitative features of the network. Our framework enables the prediction of cell fate patterns with minimal modeling assumptions, and provides a powerful tool for inferring unknown interactions within signaling networks by analyzing tissue-level patterns.

Indexed as

Body PatterningModels, BiologicalAnimalsCell CommunicationComputer SimulationHumansMathematical ConceptsSignal TransductionBifurcation theoryDevelopmental biologyNetwork dynamicsPattern formationSignaling networks

Identifiers

PMID41143898
PMCPMC12559148

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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.