Author

S. Pradervand

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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Plant Biology· 2 Physiology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

L. Wigger· 2 shared A. Naldi· 1 shared A.-S. Fiorucci· 1 shared B. Desvergne· 1 shared C. Casals Casas· 1 shared C. De Jesus Vieira Teixeira· 1 shared C. Fankhauser· 1 shared C. Nawrath· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 15 mutual co-author links

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2 shared papersPlant Biology

L. Wigger

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Reduced light access promotes hypocotyl growth via autophagy-mediated recycling

Y. Ince, A.-S. Fiorucci, M. Trevisan, V. C. Galvao, K. Johanna, L. Wigger, S. Pradervand, L. Fouillen, P. Van Delft, S. MONGRAND, H. Gallart-Ayala, J. Ivanisevic, C. Fankhauser

This study shows that reduced light and LRFR promote hypocotyl growth through distinct metabolic pathways: autophagy-mediated recycling and plasma membrane lipid biosynthesis.

Nature Communications · Oct 10, 2022Peer-reviewedPlant Biology

GDSL-domain containing proteins mediate suberin biosynthesis and degradation, enabling developmental plasticity of the endodermis during lateral root emergence

R. Ursache, C. De Jesus Vieira Teixeira, V. Denervaud Tendon, K. Gully, D. De Bellis, E. Schmid-Siegert, T. Grube Andersen, V. Shekhar, S. Calderon, S. Pradervand, C. Nawrath, N. Geldner, J. E. M. Vermeer

The paper identifies GDSL-lipases involved in suberin biosynthesis and degradation, enabling endodermal plasticity during lateral root emergence.

bioRxiv · Jun 25, 2020 · PreprintPlant Biology

System analysis of cross-talk between nuclear receptors reveals an opposite regulation of the cell cycle by LXR and FXR in human HepaRG liver cells

L. Wigger, C. Casals Casas, M. Baruchet, K. B. Trang, S. Pradervand, A. Naldi, B. Desvergne

The paper analyzes the cross-talk between nuclear receptors LXR, FXR, and PPAR in HepaRG liver cells, revealing opposite effects of FXR and LXR on cell cycle regulation and hepatocyte differentiation.

bioRxiv · Mar 25, 2019Physiology