Author

S. Réty

Lyon 1 UniversitéORCID 0000-0002-2089-6727Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:metabolomics· 1 Approach:statistical model· 1 Organism:virus· 1

Frequent Co-Authors

Alessandra Maia‐GrondardiD· 1 shared Alexandra Desrames· 1 shared Amandine DavidiD· 1 shared Amandine VeltiD· 1 shared Anne HoudusseiD· 1 shared Armelle Roisin· 1 shared Arndt W. Schmidt· 1 shared Camille RustenholziD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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1 shared paperPlant Biology

Alessandra Maia‐GrondardORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Genetic analysis of grapevine wood composition identifies glycosyltransferases involved in the biosynthesis of stilbene glycosides

Hadrien Chepca, S. Réty, Catarina Branco, Jean‐François Chich, Geneviève Riveill, G. Arnold, Gisèle Butterlin, Vincent Dumas, Marie Lahaye, Amandine Velt, Zoé Postel, Éric Duchêne, Komlan Avia, Camille Rustenholz, Raquel Tavares, , Philippe Hugueney

The paper identifies glycosyltransferases involved in the biosynthesis of stilbene glycosides in grapevine wood through metabolomic and genetic analyses.

bioRxiv · Oct 27, 2026 · PreprintPlant Biology

Retroviral adapters hijack the RNA helicase UPF1 in a CRM1/XPO1 dependent manner and reveal proviral roles of UPF1.

Léa Prochasson, Makram Mghezzi-Habellah, Armelle Roisin, Martine Palma, Jean-Philippe Robin, Stève de Bossoreille, David Cluet, Malèke Mouelhi, Didier Décimo, Alexandra Desrames, Thibault Chaze, Mariette Matondo, Hélène Dutartre, Maria‐Isabel Thoulouze, Fabrice Lejeune, , Vincent Mocquet

This paper shows that HTLV-1 Rex hijacks CRM1 to retain UPF1 in the nucleus, inhibiting NMD and enabling UPF1 to support viral replication.

Nucleic Acids Research · May 10, 2025Peer-reviewedMolecular Biology

Omecamtiv mecarbil and Mavacamten target the same myosin pocket despite antagonistic effects in heart contraction

Daniel Auguin, Julien Robert‐Paganin, S. Réty, Carlos Massayuki Kikuti, Amandine David, Gabriele Theumer, Arndt W. Schmidt, Hans‐Joachim Knölker, Anne Houdusse

This study shows Omecamtiv mecarbil and Mavacamten target the same myosin pocket but have antagonistic effects on heart contraction through structural and simulation analyses.

bioRxiv · Nov 15, 2023 · PreprintMolecular Biology