Author

Anne‐Pascale Bouin

Centre National de la Recherche ScientifiqueORCID 0000-0002-9616-6173Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cell Biology· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:mouse· 3 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Assay:proteomics· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1

Frequent Co-Authors

Christiane I. OddouiD· 2 shared Emmanuelle PlanusiD· 2 shared Fabrice SengeriD· 2 shared Olivier DestaingiD· 2 shared A. Ahmed· 1 shared A. Onisiforou· 1 shared A. Samii· 1 shared Alexeï GrichineiD· 1 shared

Activity by Year

2023-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 32 mutual co-author links

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2 shared papersCell Biology

Christiane I. OddouORCID

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3 papers

Recent·Most cited

Cell BiologybioRxivPreprintOct 5, 2026

Endothelial gain of PIEZO/TRPV mechanosensors drives cavernous malformations

J de Jong, Candice Pasquier, T. Manicom Ramsamy…·Eva Faurobert

This study identifies PIEZO1, TRPV2, and TRPV4 as mechanosensors overexpressed in CCM lesions, showing their role in driving disease through altered adhesion and matrix degradation.

DOI 10.64898/2026.10.01.756057

mousezebrafish

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Cell BiologybioRxivPreprintSep 7, 2026

Hck signaling drives long-distance ECM degradation through endo-exocytosis coupling in macrophages.

Cristina Torres Torres, Marco Ruscone, Satish Babu Moparthi…·Olivier Destaing

This study identifies HCK signaling as a driver of long-distance ECM degradation in macrophages through endo-exocytosis coupling involving MMPs and cathepsins.

DOI 10.64898/2026.09.03.749091

mouseproteomics

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GeneticsbioRxivPreprintFeb 27, 2023

Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse

Jana Muroňová, Zine‐Eddine Kherraf, Elsa Giordani…·Christophe Arnoult

This study identifies bi-allelic CCDC146 mutations as a cause of non-syndromic male infertility in humans and mice, showing its role in sperm flagellum structure and microtubule organization.

1 citation

humanmouse

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