Author

María Borja-Gonzalez

Ollscoil na Gaillimhe – University of GalwayORCID 0000-0001-9703-9064Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 2 Research Focus:development & morphogenesis· 2 Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Organism:C. elegans· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Approach:genetic perturbation / CRISPR· 1

Frequent Co-Authors

Brian McDonaghiD· 2 shared Katarzyna Goljanek‐WhysalliD· 2 shared Afshin Samali AiD· 1 shared Anthony J. SannicandroiD· 1 shared Antonio Miranda‐VizueteiD· 1 shared Chao SuiD· 1 shared Clara Sanz‐NoguésiD· 1 shared Elan C. McCarthyiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersCell Biology

Brian McDonaghORCID

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2 papers

Recent·Most cited

Cell BiologyCell Death and DifferentiationPeer-reviewedNov 1, 2025

PERK orchestrates MERCS formation and mitochondrial remodelling promoting physiological adaptations during adaptive UPR signalling

José C. Casas-Martinez, Xia Qin, Penglin Li…·Brian McDonagh

This study shows PERK promotes MERCS formation and mitochondrial remodelling during adaptive UPR signalling in myoblasts and C. elegans, enhancing physiological function.

17 citationstop 1%

C. eleganshuman

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Cancer BiologybioRxivPreprintJan 11, 2025

miR-379-3p counteracts cancer cachexia through regulation of pyrimidinergic receptor, mitochondrial stress and interferon response.

María Borja-Gonzalez, Raúl González, Anthony J. Sannicandro…·Katarzyna Goljanek‐Whysall

This study identifies miR-379-3p as a regulator of cancer cachexia by modulating purinergic receptors, mitochondrial function, and inflammatory responses in a sex-dependent manner.

DOI 10.1101/2025.01.11.632559

mousebulk RNA-seq

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