Evidence map›Paper›PMID 40158772›Full record

ArticleMathematical biosciences2025

Characterizing symmetry transitions in systems with dynamic morphology.

Maria-Veronica Ciocanel, Punit Gandhi, Karl Niklas, Adriana T Dawes

Abstract read
In one paragraph

Article in Mathematical biosciences, 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

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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. 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

4 authors.

Maria-Veronica CiocanelDepartment of Mathematics, Duke University, Durham, NC, USA; Department of Biology, Duke University, Durham, NC, USA.
Punit GandhiDepartment of Mathematics and Applied Mathematics, Virginia Commonwealth University, Richmond, VA, USA.
Karl NiklasSchool of Integrative Plant Science, Cornell University, Ithaca, NY, USA.
Adriana T DawesDepartment of Mathematics, The Ohio State University, Columbus, OH, USA; Department of Molecular Genetics, The Ohio State University, Columbus, OH, USA. Electronic address: dawes.33@osu.edu.

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 GM132651
6 · The paper itself

Abstract

The accurate quantification of symmetry is a key goal in biological inquiries because symmetry can affect biological performance and can reveal insights into development and evolutionary history. Recently, we proposed a versatile measure of symmetry, transformation information (TI), which provides an entropy-based measure of deviations from exact symmetry with respect to a parameterized family of transformations. Here we develop this measure further to quantify approximate symmetries and maximal symmetries represented by critical points in TI as a function of a transformation parameter. This framework allows us to characterize the evolution of symmetry by tracking qualitative changes with respect to these critical points. We apply TI to increasingly complex settings, from mathematically tractable probability distributions to differential equation models with emergent behaviors that are inspired by developmental biology and formulated in both static and growing domains. Our analysis of the qualitative changes in symmetry properties indicates a potential pathway toward a general mathematical framework for characterizing symmetry transitions akin to bifurcation theory for dynamical systems. The results reveal deep connections between observed symmetry transitions, subtle changes in morphology, and the underlying mechanisms that govern the dynamics of the system.

Indexed as

Models, BiologicalMorphogenesisAnimalsBiological EvolutionDevelopmental BiologyApproximate symmetryBifurcationsDevelopmental biologyInformation theoryPattern formation

Identifiers

PMID40158772
PMCPMC13242633

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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.