Author

Colline Sanchez

Lyon 1 Université

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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Cell Biology· 1 Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Organism:mouse· 2 Assay:proteomics· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Organism:zebrafish· 1

Frequent Co-Authors

Candice KutchukianiD· 2 shared Vincent JacquemondiD· 2 shared Adelheid WeidingeriD· 1 shared Adrian Taylor· 1 shared Andrey V. KozloviD· 1 shared Anne Abott· 1 shared Anne Muesch· 1 shared Anne PetiotiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersGenetics

Candice KutchukianORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

ARHGAP20 organizes spatial Rap1-RhoA signaling coordination controlling adhesion dynamics during migration

Sandra Pagano, Colline Sanchez, Natasha Cox Cammer, Ravi M. Bhalla, Roshan Ravishankar, Deisy Segura-Villalobos, Anne Muesch, Julio Aguirre-Ghiso, Gaudenz M. Danuser, Louis Hodgson

This study identifies ARHGAP20 as a regulator of cell migration by modulating Rap1A-RhoA signaling coordination through vesicular trafficking.

bioRxiv · Jul 20, 2026 · PreprintCell Biology

Critical role of PCYT2 in muscle health and aging

Domagoj Cikes, Kareem Elsayad, Erdinç Sezgin, Erika Koltai, Ferenc Torma, Michael Orthofer, Rebecca Yarwood, Leonhard X. Heinz, Vitaly Sedlyarov, N. Darwish, Adrian Taylor, Sophie Grapentine, Fathiya M. Al-Murshedi, Anne Abott, Adelheid Weidinger, , Josef Martin Penninger

This study identifies PCYT2 as critical for muscle health and aging, showing its deficiency causes muscle weakness and aging, and demonstrates therapeutic potential through AAV-based delivery.

bioRxiv · Mar 2, 2022 · PreprintGenetics

In vivo RyR1 reduction in muscle triggers a core-like myopathy

Laurent Pelletier, Anne Petiot, Julie Brocard, Benoı̂t Giannesini, Diane Giovannini, Colline Sanchez, Lauriane Travard, Mathilde Chivet, Mathilde Beaufils, Candice Kutchukian, David Bendahan, Daniel METZGER, Clara Franzini Armstrong, Norma Beatriz Romero, John Rendu, , Isabelle Marty

This study shows that reducing RyR1 in mice causes muscle weakness, atrophy, and structural changes similar to Central Core Disease.

Acta Neuropathologica Communications · Nov 11, 2020Peer-reviewedNeuroscience