Author

Ines Akrouf

Inserm

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Pathology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Assay:proteomics· 1 Organism:rat· 1

Frequent Co-Authors

Bruno CadotiD· 1 shared Caroline Le GuineriD· 1 shared France Piétri‐RouxeliD· 1 shared Inès BarthélémyiD· 1 shared Jeanne Lainé· 1 shared Julie Chassagne· 1 shared Kamel MamchaouiiD· 1 shared Laura JulieniD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperPathology

Bruno CadotORCID

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1 paper

Recent·Most cited

Early endosome disturbance and endolysosomal pathway dysfunction in Duchenne muscular dystrophy

Julie Chassagne, Nathalie Da Silva, Ines Akrouf, Bruno Cadot, Laura Julien, Inès Barthélémy, Stéphane Blot, Caroline Le Guiner, Mai Thao Bui, Norma Beatriz Romero, Jeanne Lainé, France Piétri‐Rouxel, Pierre Meunier, Kamel Mamchaoui, Stéphanie Lorain, , Sofia Benkhelifa‐Ziyyat

This study identifies endosomal pathway dysfunction in DMD muscle cells and shows that Rab5 upregulation contributes to endosomal defects, which can be mitigated by Rab5 knock-down or dystrophin restoration.

American Journal Of Pathology · Jun 9, 2025Peer-reviewedPathology