<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Alsous JI</submitter><funding>Javna Agencija za Raziskovalno Dejavnost RS</funding><funding>NIGMS NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | National Institutes of Health</funding><pagination>1391-1395</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8887698</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(12)</volume><pubmed_abstract>Clonal dominance arises when the descendants (clones) of one or a few founder cells contribute disproportionally to the final structure during collective growth [1-8]. In contexts such as bacterial growth, tumorigenesis, and stem cell reprogramming [2-4], this phenomenon is often attributed to pre-existing propensities for dominance, while in stem cell homeostasis, neutral drift dynamics are invoked [5,6]. The mechanistic origin of clonal dominance during development, where it is increasingly documented [1,6-8], is less understood. Here, we investigate this phenomenon in the &lt;i>Drosophila melanogaster&lt;/i> follicle epithelium, a system in which the joint growth dynamics of cell lineage trees can be reconstructed. We demonstrate that clonal dominance can emerge spontaneously, in the absence </pubmed_abstract><journal>Nature physics</journal><pubmed_title>Clonal dominance in excitable cell networks.</pubmed_title><pmcid>PMC8887698</pmcid><funding_grant_id>NIH R01GM134204-02</funding_grant_id><funding_grant_id>R01 GM134204</funding_grant_id><funding_grant_id>P1-0055</funding_grant_id><pubmed_authors>Alsous JI</pubmed_authors><pubmed_authors>Shvartsman SY</pubmed_authors><pubmed_authors>Rozman J</pubmed_authors><pubmed_authors>Kosmrlj A</pubmed_authors><pubmed_authors>Marmion RA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clonal dominance in excitable cell networks.</name><description>Clonal dominance arises when the descendants (clones) of one or a few founder cells contribute disproportionally to the final structure during collective growth [1-8]. In contexts such as bacterial growth, tumorigenesis, and stem cell reprogramming [2-4], this phenomenon is often attributed to pre-existing propensities for dominance, while in stem cell homeostasis, neutral drift dynamics are invoked [5,6]. The mechanistic origin of clonal dominance during development, where it is increasingly documented [1,6-8], is less understood. Here, we investigate this phenomenon in the &lt;i>Drosophila melanogaster&lt;/i> follicle epithelium, a system in which the joint growth dynamics of cell lineage trees can be reconstructed. We demonstrate that clonal dominance can emerge spontaneously, in the absence </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2025-04-25T22:29:12.12Z</modification><creation>2025-04-06T09:03:51.958Z</creation></dates><accession>S-EPMC8887698</accession><cross_references><pubmed>35242199</pubmed><doi>10.1038/s41567-021-01383-0</doi></cross_references></HashMap>