Author

Eve A. Maunders

The University of QueenslandORCID 0000-0003-2812-6943Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cell Biology· 1 Developmental Biology· 1 Evolutionary Biology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:cell-cell communication· 2 Approach:experimental assay· 2 Organism:non-human primate· 2 Approach:statistical model· 2 Approach:biophysical modeling· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1

Frequent Co-Authors

Bernard M. DegnaniD· 2 shared Xueyan XiangiD· 2 shared Andrew J. MasseyiD· 1 shared David C. HornigoldiD· 1 shared Elizabeth Hampson· 1 shared Elpida TsonouiD· 1 shared Heidi C. E. WelchiD· 1 shared Kirsti Hornigold· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersDevelopmental Biology

Bernard M. DegnanORCID

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3 papers

Recent·Most cited

Developmental BiologybioRxivPreprintSep 30, 2026

Symbiont biosynthetic output tracks host developmental stage in a marine sponge holobiont

Eve A. Maunders, Zhee Sheen Wong, Rebecca A. Fieth…·Bernard M. Degnan

The paper tracks how symbiont biosynthetic output aligns with host developmental stages in a marine sponge holobiont, showing transcriptional changes in symbionts correlate with host metabolic needs.

DOI 10.64898/2026.09.29.755549

non-human primatebulk RNA-seq

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Evolutionary BiologybioRxivPreprintAug 11, 2026

A partner-resolved marine sponge hologenome reveals that three bacterial symbionts disproportionately expand holobiont metabolism via enriched membrane transporter repertoires

Xueyan Xiang, Eve A. Maunders, Bernard M. Degnan

The paper analyzes the hologenome of a marine sponge and its three symbionts, revealing that these symbionts disproportionately expand holobiont metabolism through enriched membrane transporter genes.

DOI 10.64898/2026.08.05.743132

non-human primatebulk RNA-seq

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Cell BiologybioRxivPreprintApr 14, 2025

P-Rex1 Limits the Agonist-Induced Internalisation of GPCRs Independently of its Rac-GEF Activity

Martin J. Baker, Elizabeth Hampson, Priota Islam…·Heidi C. E. Welch

This paper shows P-Rex1 limits agonist-induced GPCR internalisation through its PDZ, DEP, and IP4P domains, independent of its Rac-GEF activity, by inhibiting phosphorylation and interacting with Grk2.

3 citations

humanproteomics

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